{"title":"HEADACHE","description":null,"products":[{"product_id":"clevia-20-capsule","title":"CLEVIA 20 CAPSULES","description":"\u003ch1\u003eClevia\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Food supplement with Ginkgo biloba, Commiphora myrrha, coenzyme Q10 and vitamin B2.\u003cbr\u003e Ginkgo biloba: for memory and cognitive function, normal blood circulation, and microcirculation.\u003cbr\u003e Commiphora: for the function of the oropharyngeal mucosa and the digestive system.\u003cbr\u003e Vitamin B2: riboflavin contributes to the normal functioning of the nervous system and to the reduction of tiredness and fatigue.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIngredients\u003c\/b\u003e\u003cbr\u003e Ginkgo (Ginkgo biloba L.) leaves d.e. titrated to 24% in ginkgoflavonoid glucosides and to 6% in total terpene lactones, myrrh [Commiphora myrrha (Nees) Engl] oleo-gum-resin d.e.; bulking agent: cellulose; anti-caking agent: magnesium salts of fatty acids (vegetable); coenzyme Q10 (ubidecarenone), riboflavin (vitamin B2); casing: vegetable capsule (hydroxypropyl methylcellulose).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eGluten-free\u003c\/b\u003e and \u003cb\u003elactose-free\u003c\/b\u003e.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eNutritional characteristics\u003c\/b\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=3\"\u003e\n\n\u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e Average values \u003c\/td\u003e\n\n\u003ctd\u003e per 1 capsule \u003c\/td\u003e\n\n\u003ctd\u003e %NRV* \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Ginkgo leaves d.e.; of which:\u003cbr\u003eginkgoflavonoid glucosides\u003cbr\u003eof which total terpene lactones \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 150 mg\u003cbr\u003e36 mg\u003cbr\u003e9 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Myrrh gum resin d.e. \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 150 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Coenzyme Q10 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 10 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Riboflavin \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 2.4 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 171 \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e *NRV: Nutrient Reference Values\u003cbr\u003e \u003cbr\u003e \u003cb\u003eDirections for use\u003c\/b\u003e\u003cbr\u003e It is recommended to take 1 capsule per day.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Keep out of reach of children under 3 years of age. Do not exceed the recommended daily dose. Supplements are not intended as a substitute for a varied and balanced diet and a healthy lifestyle.\u003cbr\u003e If you are taking anticoagulant or antiplatelet drugs, consult your doctor before taking the product.\u003cbr\u003e The use of the product during pregnancy and breastfeeding is not recommended.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store in a cool, dry place.\u003cbr\u003e Shelf life unopened: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Bottle containing 20 capsules of 500 mg.\u003cbr\u003e Net weight: 10 g.\u003c\/div\u003e","brand":"AISAL S.A.","offers":[{"title":"Default Title","offer_id":45800060453131,"sku":"972050912","price":20.25,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_25dbd7ce-b4ee-4a0d-9cdb-47456a698686.jpg?v=1724850116"},{"product_id":"tensiva-40-bustine-da-3-g","title":"TENSIVA 40 SACHETS OF 3 G","description":"\u003ch1\u003eTensiva\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Food supplement with sweetener based on calcium, magnesium, vitamin D, which contribute to the maintenance of normal muscle function.\u003cbr\u003e The vitamin complex composed of vitamin B3 (niacin), B2, B6 and B12 contributes to the reduction of tiredness and fatigue.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIngredients\u003c\/b\u003e\u003cbr\u003e Potassium citrate, magnesium bisglycinate, maltodextrin; acidifier: tartaric acid; dibasic calcium phosphate, L-tryptophan, citrus flavor, vitamin B3 (niacin); sweetener: sucralose; vitamin D (cholecalciferol), vitamin B2 (riboflavin phosphate), vitamin B6 (pyridoxine hydrochloride), vitamin B12 (cyanocobalamin).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNutritional characteristics\u003c\/b\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=3\"\u003e\n\n\u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e Average values \u003c\/td\u003e\n\n\u003ctd\u003e per 1 sachet \u003c\/td\u003e\n\n\u003ctd\u003e %NRV* \u003c\/td\u003e\n\n\u003ctd\u003e per 2 sachets \u003c\/td\u003e\n\n\u003ctd\u003e %NRV* \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Calcium phosphate\u003cbr\u003eof which calcium \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 430 mg\u003cbr\u003e120 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e \u003cbr\u003e15% \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 860 mg\u003cbr\u003e240 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e \u003cbr\u003e30% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Magnesium bisglycinate\u003cbr\u003eof which magnesium \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 500 mg\u003cbr\u003e56 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e \u003cbr\u003e15% \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 1,000 mg\u003cbr\u003e112 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e \u003cbr\u003e30% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Tryptophan \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 140 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 280 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin PP \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 18 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 113% \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 36 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 226% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin B2 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 2.4 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 171% \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 4.8 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 342% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin B6 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 1.4 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 100% \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 2.8 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 200% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin D3 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 10 mcg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 200% \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 20 mcg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 400% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin B12 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 2.5 mcg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 100% \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 5 mcg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 200% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e *NRV: Nutrient Reference Values\u003cbr\u003e \u003cbr\u003e \u003cb\u003eDirections for use\u003c\/b\u003e\u003cbr\u003e It is recommended to take 1 or 2 sachets per day according to medical advice. Dissolve the content in a glass of water, stir well and drink immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Do not exceed the recommended daily dose. Keep out of reach of children under 3 years of age. Food supplements are not intended as substitutes for a varied and balanced diet and a healthy lifestyle. Do not take in case of ascertained hypersensitivity or allergy to one of the components. Do not use if the package is not intact. Do not use beyond the expiry date.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store in a cool, dry place away from light and heat sources.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e 40 sachets of 3.5 g.\u003cbr\u003e Net weight: 140 g.\u003c\/div\u003e","brand":"DISAL Srl","offers":[{"title":"Default Title","offer_id":45943151165707,"sku":"971953740","price":18.92,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_fbeee473-ee32-4440-bfab-f6f58e95eb6e.jpg?v=1727807501"},{"product_id":"biosline-migralen-12-bustine","title":"BIOSLINE MIGRALEN 12 SACHETS","description":"\u003ch1\u003eBIOS LINE \u003cbr\u003e migralen \u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Food supplement based on plant extracts of feverfew, lemon balm, chaste tree, cola, ginger and vitamin B2. \u003cbr\u003e Vitamin B2 contributes to the normal functioning of the nervous system, while ginger and feverfew extracts help to counteract localized tension.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eIngredients\u003c\/b\u003e\u003cbr\u003e Sweeteners: sorbitol, sucralose; feverfew [Tanacetum parthenium (L.) Sch. Bip.] herb with flowers e.g., cola [Cola nitida (Vent.) Schott et Endl.) seeds e.g. titrated to 10% in caffeine, chaste tree (Vitex agnus-castus L.) fruits e.g. titrated to 2.5% in agnusides, lemon balm (Melissa officinalis L.) leaves e.g. titrated to 0.5% in rosmarinic acid; anti-caking agent: silicon dioxide; flavorings, ginger (Zingiber officinale Rosc.) rhizome e.g. titrated to 5% in gingerols, vitamin B2 (riboflavin, corn starch).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eGluten\u003c\/b\u003e and \u003cb\u003elactose\u003c\/b\u003e free. \u003cbr\u003e \u003cbr\u003e \u003cb\u003eNutritional characteristics\u003c\/b\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=3\"\u003e\n\n\u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e Average values \u003c\/td\u003e\n\n\u003ctd\u003e per 2 sachets \u003c\/td\u003e\n\n\u003ctd\u003e %NRV* \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin B2 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 1.4 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 100 \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Feverfew herb with flowers e.g. \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 125.0 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Cola seeds e.g. titrated to 10% in caffeine\u003cbr\u003eequal to caffeine \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 100.0 mg\u003cbr\u003e10.0 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Chaste tree fruits e.g. tit. \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 32.0 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Lemon balm leaves e.g. tit. \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 25.0 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Ginger rhizome e.g. tit. \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 10.0 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e *Nutrient Reference Values \u003cbr\u003e \u003cbr\u003e \u003cb\u003eDirections for use\u003c\/b\u003e\u003cbr\u003e Dissolve 1 sachet under the tongue; if necessary, take a second sachet after 1-2 hours.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Keep out of reach of children under 3 years of age; do not exceed the recommended daily dose. Food supplements are not intended as a substitute for a varied, balanced diet and a healthy lifestyle. Contains polyols, excessive consumption may have laxative effects. Contains caffeine (10 mg\/daily dose), not recommended for children and during pregnancy and breastfeeding.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store in a cool, dry place at room temperature.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack of 12 orosoluble sachets.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e BL801 \u003c\/div\u003e","brand":"BIOS LINE SpA","offers":[{"title":"Default Title","offer_id":45944471650571,"sku":"932087760","price":7.81,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_98d96224-4829-4188-8501-befea2b3e6a3.jpg?v=1727816360"},{"product_id":"raihuen-balsamo-tigre-rosso-30-ml","title":"RAIHUEN RED TIGER BALM 30 ML","description":"\u003ch1\u003eRed Tiger Balm\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Cosmetic product indicated for providing immediate relief from muscle pain.\u003cbr\u003e Contains cinnamon essential oil.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e Apply a very small amount of cream to the affected area. For greater effect, cover with a gauze pad soaked in warm, wrung-out water.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIngredients\u003c\/b\u003e\u003cbr\u003e Petrolatum, camphor, Cinnamomum cassia, Eugenia caryophyllus, Melaleuca leucadendron, Mentha piperita oil, stearic acid, eugenol, alcohol, Glycine soja, limonene, Cera alba, palmitic acid, Daucus carota, Capsicum frutescens, menthol, myristic acid, linalool, benzyl benzoate, cinnamal, Juglans regia, arachidic acid, BHA, BHT, cinnamyl alcohol, diethyl phthalate, coumarin, isoeugenol, t-butyl alcohol, geraniol.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Avoid contact with eyes and mucous membranes.\u003cbr\u003e Do not use on particularly sensitive skin prone to irritation.\u003cbr\u003e Product is sensitive to high temperatures: avoid thermal shock.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Post-opening validity: 12 months.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e 30 ml jar.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e TIGRER\u003c\/div\u003e","brand":"NATUR-FARMA Srl","offers":[{"title":"Default Title","offer_id":45944492523787,"sku":"906808124","price":7.88,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_4881b3e6-d091-481d-928f-6ce38a93a48e.jpg?v=1727816687"},{"product_id":"migrasoll-30-capsule","title":"MIGRASOLL 30 CAPSULES","description":"\u003ch1\u003eMigraSoll \u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Food supplement based on:\u003cbr\u003e- Ginkgo Biloba: promotes normal blood circulation and microcirculation and contributes to normal cognitive and memory functions.\u003cbr\u003e- Coenzyme Q10.\u003cbr\u003e- Vitamin B2: contributes to the protection of cells from oxidative stress.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eIngredients\u003c\/b\u003e\u003cbr\u003eBulking agents: calcium phosphate, microcrystalline cellulose; coating agents: animal gelatin; Ginkgo biloba leaves (Ginkgo biloba L. dry extract titled 3% bilobalide), coenzyme Q10 (ubidecarenone); stabilizer: cross-linked sodium carboxymethylcellulose; anti-caking agents: magnesium stearate, silicon dioxide; vitamin B2 (riboflavin 5'-phosphate, sodium); coloring: titanium dioxide.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eGluten-free\u003c\/b\u003e.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003eIt is suggested to take 1 capsule per day. For optimal use of the product, follow your doctor's instructions.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003eKeep out of reach of children under 3 years of age. Do not exceed the recommended daily dose. Supplements are not intended as substitutes for a varied and balanced diet and a healthy lifestyle.\u003cbr\u003eIf you are taking anticoagulant or antiplatelet drugs, consult your doctor before taking the product. The use of the product during pregnancy and breastfeeding is not recommended.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003eStore at a temperature below 25°C. Avoid exposure to localized heat sources, sunlight, and keep away from humidity. The minimum shelf life refers to the product correctly stored, in an intact package.\u003cbr\u003eShelf life when unopened: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Blister pack of 30 capsules.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e ELY120\u003c\/div\u003e","brand":"PURYTRA FARMACEUTICI SpA","offers":[{"title":"Default Title","offer_id":45944718688523,"sku":"930668355","price":21.37,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_1abb3fe3-87e3-400f-9502-bac627abd2e7.jpg?v=1727817961"},{"product_id":"raihuen-balsamo-tigre-bianco-30-ml","title":"RAIHUEN WHITE TIGER BALM 30 ML","description":"\u003ch1\u003eTIGER BALM\u003c\/h1\u003e \u003cb\u003eCod.\u003c\/b\u003e TIGRE","brand":"NATUR-FARMA Srl","offers":[{"title":"Default Title","offer_id":45945831588107,"sku":"906808112","price":8.17,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_2552e426-77ac-4a3f-aab9-1454833d0a90.jpg?v=1727821417"},{"product_id":"cefalt-20-stick","title":"CEFALT 20 STICK","description":"\u003ch1\u003eCefalt\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Dietary supplement with L-tryptophan, magnesium bisglycinate, vitamins D3, B3 and B2, and Boswellia serrata BosPure, useful in cases of low dietary intake or increased need for these nutrients.\u003cbr\u003e Boswellia can counteract localized tension.\u003cbr\u003e Magnesium, vitamin B3, and B2 contribute to the normal functioning of the nervous system.\u003cbr\u003e Vitamin D3 and magnesium contribute to normal muscle function.\u003cbr\u003e With sweeteners.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIngredients\u003c\/b\u003e\u003cbr\u003e Magnesium bisglycinate, bulking agent: isomalt; acidifier: citric acid; Boswellia serrata BosPure [Boswellia resin (Boswellia serrata Roxb.) dry extract titrated to 40% boswellic acids], L-tryptophan, anti-caking agent: silicon dioxide; emulsifier: sucrose esters of fatty acids; bulking agent: sorbitol powder; flavor, beetroot root (Beta vulgaris L.) powder, anti-caking agent: talc; vitamin B3 (nicotinamide), safflower flowers (Chartamus tinctorius L.) dry extract, sweetener: sucralose; vitamin D (cholecalciferol), sweetener: steviol glycosides from stevia leaves (Stevia rebaudiana Bertoni); vitamin B2 (Riboflavin).\u003cbr\u003e \u003cb\u003eGluten-free\u003c\/b\u003e.\u003cbr\u003e Naturally \u003cb\u003elactose-free\u003c\/b\u003e.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNutritional characteristics\u003c\/b\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"400\"\u003e \u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e\u003cb\u003eNutrients\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003eper dose (1 stick)\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003e%NRV*\u003c\/b\u003e\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMagnesium\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e225 mg\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e60%\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eVitamin B3\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e16 mg\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e100%\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eVitamin D3\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e10 mcg\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e200%\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eVitamin B2\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e1.4 mg\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e100%\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBoswellia serrata BosPure\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e200 mg\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e-\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eL-tryptophan\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e150 mg\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e-\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003c\/table\u003e*NRV: Nutrient Reference Values.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eDirections for use\u003c\/b\u003e\u003cbr\u003e It is recommended to take 1 stick per day. Dissolve the content in a glass of water, mix well and consume immediately after preparation.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Supplements should not be considered a substitute for a varied, balanced diet and a healthy lifestyle. Do not exceed the recommended doses. Keep out of reach of children under three years of age.\u003cbr\u003e The product contains polyols: excessive consumption may have laxative effects.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store in a cool, dry place.\u003cbr\u003e Shelf life unopened: 36 months.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack containing 20 single-dose sticks of 3.8 g.\u003cbr\u003e Net weight: 76 g.\u003c\/div\u003e","brand":"MINERVA MEDICA Srl","offers":[{"title":"Default Title","offer_id":45946865811723,"sku":"934546058","price":18.27,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_d6a850b8-2e65-4986-b51d-02d0938a070c.jpg?v=1727831003"},{"product_id":"cefalt-20-bustine","title":"CEFALT 20 SACHETS","description":"\u003ch1\u003eCefalt\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Food supplement, with sweetener, based on magnesium bisglycinate, Boswellia serrata, L-tryptophan and vitamins D3, B3 and B2, useful in cases of reduced dietary intake or increased need for these nutrients. Boswellia serrata counteracts localized tension states. Magnesium and vitamins B3 and B2 contribute to the normal functioning of the nervous system. Magnesium and vitamin D3 contribute to normal muscle function. Magnesium and vitamin B3 contribute to normal psychological function.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eGluten\u003c\/b\u003e-free.\u003cbr\u003e Naturally \u003cb\u003elactose\u003c\/b\u003e-free.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIngredients\u003c\/b\u003e\u003cbr\u003e Magnesium bisglycinate, maltodextrins; acidity regulator: citric acid; Boswellia serrata e.s. (Boswellia serrata Roxb. ex Colebr., gum resin) titrated to 65% in boswellic acids; colourings: beta-carotene, beetroot red; L-tryptophan, flavouring, sucrose esters of fatty acids; sweetener: sucralose; vitamin B3 (niacin), vitamin D3 (cholecalciferol); anti-caking agent: silicon dioxide; vitamin B2 (riboflavin).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNutritional characteristics\u003c\/b\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=3\"\u003e\n\n\u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e Average values \u003c\/td\u003e\n\n\u003ctd\u003e per 1 sachet (3.5 g) \u003c\/td\u003e\n\n\u003ctd\u003e %NRV* \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Magnesium bisglycinate \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 225 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Boswellia serrata e.s. \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 200 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e L-tryptophan \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 150 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e   \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin B3 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 16 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 100% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin B2 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 1.4 mg \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 100% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\n\u003ctd\u003e Vitamin D3 \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 10 mcg\u003cbr\u003e400 I.U. \u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e 200% \u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e *NRV: Nutrient Reference Values\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e We recommend taking 1 sachet per day, regardless of meals. Dissolve the contents of the sachet in a glass of water, stir very well and consume immediately after preparation.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Supplements should not be intended as substitutes for a varied, balanced diet and a healthy lifestyle. Do not exceed the recommended doses. Keep out of reach of children under three years of age.\u003cbr\u003e The product contains polyols: excessive consumption may have laxative effects. Do not use the product if the package is not intact. Use is not recommended in cases of confirmed hypersensitivity to one or more of the ingredients listed. Given the nature of the ingredients contained, the product may have a different appearance from batch to batch: this does not affect the quality of the product.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store in a dry place, away from heat sources, in a temperature range between 8° and 25°C.\u003cbr\u003e The expiry date refers to the product correctly stored, in an unopened package.\u003cbr\u003e Validity in intact packaging: 36 months.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e 20 sachets of 3.5 g.\u003cbr\u003e Net weight: 70 g.\u003c\/div\u003e","brand":"MINERVA MEDICA Srl","offers":[{"title":"Default Title","offer_id":46041833013515,"sku":"934546058","price":18.96,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_050ad48c-de75-412f-9d41-0047a238e188.jpg?v=1729665716"},{"product_id":"okitask-os-grat-20bust-40mg","title":"OKITASK*OS GRAN 20SACH 40MG","description":"\u003cp\u003e\u003cb\u003eOkitask 40 mg granules\u003c\/b\u003e\u003cbr\u003e ketoprofen lysine salt\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eOkitask contains ketoprofen, which belongs to a group of medicines called \"Non-Steroidal Anti-Inflammatory Drugs\" (NSAIDs). Ketoprofen blocks the chemicals that cause inflammation.\u003cbr\u003e Okitask is indicated for the treatment of pain of various origins and natures, and in particular: headache, toothache, neuralgia (nerve pain), menstrual pain, muscle pain and musculoskeletal pain (bone and joint pain).\u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after a few days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Okitask:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ketoprofen, other non-steroidal anti-inflammatory drugs (NSAIDs) or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you have a history of hypersensitivity (allergy) reactions triggered by the use of ketoprofen or substances with a similar mechanism of action, for example acetylsalicylic acid or other NSAIDs (other anti-inflammatories) such as asthma (bronchial inflammation and narrowing of the airways), bronchospasm (constriction of the bronchi), allergic rhinitis (allergic inflammation of the nasal mucosa), urticaria, skin rashes, nasal polyps, angioneurotic oedema (swelling of the skin and mucous membranes) or other allergic reactions;\u003cbr\u003e - if you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways);\u003cbr\u003e - if you have severe heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs);\u003cbr\u003e - if you suffer from gastritis (inflammation of the stomach lining);\u003cbr\u003e - if you currently have a peptic ulcer (a lesion of the stomach or the first part of the intestine) or bleeding, or if you have suffered in the past from bleeding or recurrent peptic ulcer (two or more distinct, proven episodes of bleeding or ulceration);\u003cbr\u003e - if you have suffered in the past from gastrointestinal bleeding (stomach or intestinal bleeding), ulceration, perforation or chronic dyspepsia (difficult digestion);\u003cbr\u003e - if you have a history of gastrointestinal bleeding or perforation following previous NSAID therapy;\u003cbr\u003e - if you suffer from Crohn's disease (inflammation of the intestine) or ulcerative colitis (inflammation of the intestine with ulcers);\u003cbr\u003e - if you have severe liver (reduced liver function due to liver cirrhosis, severe hepatitis) or kidney (reduced kidney function) failure;\u003cbr\u003e - if you suffer from leucopenia (reduction in the number of white blood cells) or thrombocytopenia (reduction in the number of platelets);\u003cbr\u003e - if you suffer from haemorrhagic diathesis (predisposition to the development of haemorrhages) and other coagulation disorders or if you have haemostatic disorders (difficulty in stopping bleeding);\u003cbr\u003e - if you are taking a high dose of diuretics;\u003cbr\u003e - if you are in the third trimester of pregnancy;\u003cbr\u003e - if the person to be treated is under 15 years of age.\u003cbr\u003e\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Okitask.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eWarnings\u003c\/u\u003e\u003cbr\u003e Undesirable effects can be minimised by using the lowest effective dose for the shortest possible duration of treatment needed to control symptoms (see \"How to take Okitask\" and the paragraphs below on gastrointestinal and cardiovascular risks).\u003cbr\u003e Concomitant use of Okitask with other anti-inflammatories should be avoided.\u003cbr\u003e During treatment with all NSAIDs, such as Okitask, at any time, with or without warning symptoms or a previous history of serious gastrointestinal events, gastrointestinal bleeding, ulceration and perforation, which can be fatal, have been reported. Patients who have previously suffered from these conditions have a higher risk (see \"Do not take Okitask\").\u003cbr\u003e Report any abdominal signs or symptoms (including gastrointestinal bleeding) even at the beginning of treatment.\u003cbr\u003e Inform your doctor if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (medicines used to treat inflammatory conditions), anticoagulants (medicines that delay blood clotting), such as warfarin, selective serotonin reuptake inhibitors (medicines used to treat depression), or antiplatelet agents (medicines that prevent platelet aggregation) such as acetylsalicylic acid (see \"Other medicines and Okitask\").\u003cbr\u003e The elderly are at greater risk of developing adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which can be fatal.\u003cbr\u003e \u003cb\u003eImmediately stop treatment with Okitask at the first signs of gastrointestinal bleeding or ulceration.\u003c\/b\u003e\u003cbr\u003e Severe skin reactions (of the skin), some of which fatal, such as exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see \"Possible side effects\"). The reaction occurs in most cases in the initial stages of treatment. Stop using Okitask if a rash, mucosal lesions or any other sign of hypersensitivity (allergic reaction) appears.\u003cbr\u003e\u003cbr\u003e \u003cu\u003ePrecautions\u003c\/u\u003e\u003cbr\u003e\u003cb\u003e Ask your doctor or pharmacist for advice before taking Okitask:\u003c\/b\u003e\u003cbr\u003e - If your kidneys are not working well, as Okitask should be taken with caution in this case. If you use Okitask, you should monitor your kidneys, especially if you are elderly or if you are taking diuretics (medicines that lower blood pressure).\u003cbr\u003e - If you have liver problems, you should have periodic check-ups.\u003cbr\u003e - If you have an infection - see section ''Infections'' below.\u003cbr\u003e - If you suffer from uncontrolled hypertension (high blood pressure), congestive heart failure (fluid accumulation in the lungs, abdominal organs and peripheral tissues due to inadequate pumping function of the heart), confirmed ischemic heart disease (heart disease that appears following reduced blood flow due to narrowing of the coronary arteries), peripheral arterial disease and\/or cerebrovascular disease (disease of the arteries and vessels of the brain), as you should only take Okitask after careful evaluation by your doctor.\u003cbr\u003e - If you have risk factors for these conditions, for example if you have high blood pressure, diabetes (disease caused by high blood glucose levels), hyperlipidemia (high levels of fats in the blood), or if you smoke.\u003cbr\u003e - If you have allergic manifestations or have suffered from allergies in the past, as the medicine should be administered with caution.\u003cbr\u003e - If you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways) or with allergic diathesis (predisposition to the onset of allergy), chronic rhinitis (inflammation of the nasal mucosa) and allergic rhinitis (allergic inflammation of the nasal mucosa), chronic sinusitis and\/or nasal polyposis.\u003cbr\u003e - If you suffer from haematopoietic alterations (which modify the formation and maturation of blood cells), systemic lupus erythematosus (immune system disease) or mixed connective tissue disorders, as Okitask should be used with caution.\u003cbr\u003e - If you have hepatic porphyria (a rare blood disease characterised by altered activity of one of the liver enzymes), as the medicine could trigger an attack.\u003cbr\u003e Some NSAIDs may be associated with an increased risk of arterial thrombotic events (e.g. heart attack or stroke). Currently, insufficient data are available to rule out a similar risk for OKITASK.\u003cbr\u003e An increased risk of atrial fibrillation (alteration of heart rhythm) associated with the use of NSAIDs has been reported.\u003cbr\u003e Hyperkalaemia (increased amount of potassium in the blood) may occur, especially if you suffer from diabetes, kidney failure and\/or are taking medicines that may cause hyperkalaemia (see \"Other medicines and Okitask\"). In these circumstances, potassium levels should be monitored periodically.\u003cbr\u003e Okitask can mask the symptoms of infections such as fever and pain. It is therefore possible that Okitask may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e Contact your doctor if you experience vision problems, such as blurred vision, as treatment should be stopped.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everyone gets them.\u003cbr\u003e The most commonly observed adverse events are gastrointestinal in nature.\u003cbr\u003e The following adverse reactions have been observed with the use of ketoprofen in adults:\u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e - dyspepsia (difficult digestion), nausea, abdominal pain and vomiting\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e - headache, dizziness, drowsiness\u003cbr\u003e - constipation, diarrhoea, flatulence (emission of intestinal gas from the anus), gastritis (inflammation of the stomach lining)\u003cbr\u003e - rash, itching and fatigue\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e - haemorrhagic anaemia (reduction of haemoglobin in the blood, substance that transports oxygen in the blood caused by bleeding)\u003cbr\u003e - paraesthesia (sensation of numbness, tingling)\u003cbr\u003e - blurred vision (see Warnings and precautions)\u003cbr\u003e - tinnitus (persistent perception of noises in the ear)\u003cbr\u003e - asthma (bronchial inflammation and narrowing of the airways)\u003cbr\u003e - stomatitis (inflammation of the mucous membranes lining the mouth), peptic ulcer (lesion of the stomach or the first part of the intestine)\u003cbr\u003e - hepatitis (inflammation of the liver), increased transaminases (increase in certain enzymes that indicate liver function), increased bilirubin (a substance that indicates liver function)\u003cbr\u003e - increased weight\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e - facial oedema (swelling) and erythema (skin redness)\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFrequency not known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e - thrombocytopenia (reduction in the number of platelets), agranulocytosis (severe reduction in the number of a type of white blood cells), bone marrow failure (reduction in the production of blood cells by the bone marrow), haemolytic anaemia (reduction of haemoglobin in the blood, substance that transports oxygen in the blood, caused by the destruction of red blood cells), leucopenia (decrease in the number of white blood cells), neutropenia (decrease in the number of a type of white blood cells), aplastic anaemia (reduction of haemoglobin in the blood, substance that transports oxygen in the blood, caused by insufficient production of blood cells by the bone marrow), leucocytosis (increase in the number of white blood cells), thrombocytopenic purpura (presence of skin spots due to a reduction in the number of platelets)\u003cbr\u003e - anaphylactic reaction (severe allergic reaction, including shock), hypersensitivity (allergy)\u003cbr\u003e - jaundice (yellowing of the skin and the white part of the eyes)\u003cbr\u003e - depression, hallucination (perception of non-existent things in reality), confusional state, altered mood, agitation, insomnia, convulsions (uncontrolled body movements), dizziness, dysgeusia (altered taste), tremor, dyskinesia (involuntary movements), syncope (fainting), hyperkinesia (involuntary and uncoordinated movements), periorbital oedema (swelling around the eye), peripheral oedema\u003cbr\u003e - chills, asthenia (weakness)\u003cbr\u003e - heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs), atrial fibrillation (alteration of heart rhythm), palpitations (perception of heart beat), tachycardia (increase in the number of heart beats), hypertension (high blood pressure), hypotension (low blood pressure)\u003cbr\u003e - vasodilation (dilation of blood vessels), vasculitis (inflammation of vessels), including leukocytoclastic vasculitis (inflammation of small vessels)\u003cbr\u003e - bronchospasm (constriction of the bronchi), especially in patients with confirmed hypersensitivity to acetylsalicylic acid and other NSAIDs, rhinitis (inflammation of the nasal mucosa), dyspnoea (difficult breathing), laryngeal oedema (swelling of the throat due to fluid accumulation), laryngospasm (narrowing of the larynx), acute respiratory failure (one fatal case has been reported in an asthmatic patient sensitive to acetylsalicylic acid)\u003cbr\u003e - exacerbation of colitis (worsening of inflammation of the intestine), exacerbation of Crohn's disease (worsening of inflammation of the intestine), gastrointestinal bleeding (stomach or intestinal bleeding), gastrointestinal perforation (sometimes fatal, particularly in the elderly, see Warnings), gastric ulcer (lesion of the stomach), mouth ulceration, duodenal ulcer (lesion of the first part of the intestine), duodenal perforation, heartburn (heartburn), mouth oedema (swelling), pancreatitis (inflammation of the pancreas), melaena (presence of digested blood in the stools), haematemesis (vomiting blood), abdominal discomfort, colitis, hyperchlorhydria (excess acid in the stomach), gastric pain (stomach pain), erosive gastritis (severe inflammation of the stomach lining), tongue oedema (swelling of the tongue)\u003cbr\u003e - photosensitivity reactions (reaction to sensitivity to sunlight or UV lamps), alopecia (hair loss), urticaria, angioedema (swelling of face, lips, mouth, tongue or throat that can cause difficulty breathing and swallowing), bullous eruptions including Stevens-Johnson syndrome, Lyell's syndrome and toxic epidermal necrolysis (severe skin reactions), oedema (fluid retention), exanthema (skin rash), maculopapular exanthema (skin rash with patches), purpura (purple spots on the skin due to abnormal blood accumulation), acute generalised exanthematous pustulosis (skin rash with formation of purulent collections), dermatitis (skin irritation)\u003cbr\u003e - acute kidney failure (reduced kidney function), tubulointerstitial nephritis, nephritis and nephritic syndrome (inflammation of the kidneys), nephrotic syndrome (kidney alteration involving protein loss with urine), glomerulonephritis (inflammatory kidney disease), water\/sodium retention with possible oedema (accumulation of water and sodium causing swelling), acute tubular necrosis and renal papillary necrosis (severe kidney damage), oliguria (decreased urine production), abnormal kidney function test, haematuria (presence of blood in urine)\u003cbr\u003e - aseptic meningitis (inflammation of the membranes lining the brain not caused by infections), lymphangitis (inflammation of the lymphatic vessels)\u003cbr\u003e - hyperkalaemia (increased amount of potassium in the blood), hyponatremia (decreased amount of sodium in the blood)\u003cbr\u003e \u003cbr\u003e Compliance with the instructions contained in the package leaflet reduces the risk of side effects.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"DOMPE' FARMACEUTICI SpA","offers":[{"title":"Default Title","offer_id":46290062049547,"sku":"042028023","price":7.85,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_36c67b3d-a63a-4e8b-aa1a-3d8062f9baf3.png?v=1734079956"},{"product_id":"benatia-bb-150ml-100mg-5ml-fra","title":"BENATIA*BB 150ML 100MG\/5ML FRA","description":"\u003cp\u003e\u003cb\u003eBENATIA Children 100mg\/5ml oral suspension strawberry flavour sugar-free\u003cbr\u003e BENATIA Children 100mg\/5ml oral suspension orange flavour sugar-free\u003cbr\u003e\u003c\/b\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eBENATIA contains ibuprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action reduces pain, fever, and inflammation. BENATIA is indicated for children aged 3 months to 12 years for the symptomatic treatment of fever, including post-vaccination fever, and mild to moderate pain (such as headache, toothache, sore throat, earache).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not give BENATIA to your child:\u003c\/b\u003e\u003cbr\u003e - if they are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if they experience or have experienced in the past allergic reactions such as wheezing, rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or urticaria, especially if associated with nasal polyps and asthma, after taking other analgesics, other antipyretics, acetylsalicylic acid and other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e - if they suffer from severe kidney or liver disease (renal or hepatic insufficiency);\u003cbr\u003e - if they suffer from severe heart disease (heart failure);\u003cbr\u003e - if they suffer or have suffered from stomach and\/or intestinal bleeding (gastrointestinal haemorrhage) or perforation following previous NSAID treatments;\u003cbr\u003e - if they suffer or have suffered from gastric\/duodenal ulcers (peptic ulcers) or active or recurrent bleeding (at least two distinct episodes of demonstrated ulceration or bleeding);\u003cbr\u003e - if they are taking other non-steroidal anti-inflammatory drugs (NSAIDs, including selective COX-2 inhibitors) (see section Other medicines and BENATIA);\u003cbr\u003e - if they have any disease that increases the risk of bleeding;\u003cbr\u003e - in case of unexplained blood disorders;\u003cbr\u003e - if they are severely dehydrated, for example, have had severe episodes of vomiting, diarrhoea, or drink very little;\u003cbr\u003e - if they are under 3 months of age or weigh less than 5.6 kg;\u003cbr\u003e - if they are in the last trimester of pregnancy (see section Pregnancy and breastfeeding).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before giving BENATIA to your child.\u003cbr\u003e • if they suffer or have suffered from allergies to medicines used to treat fever, pain, and inflammation (non-steroidal anti-inflammatory drugs) and if they suffer from breathing difficulties (asthma), seasonal allergies (hay fever), nasal polyps, if they have severe respiratory or chest problems, e.g. chronic obstructive pulmonary disease, swelling of the face, lips, and throat (angioedema);\u003cbr\u003e • if they are taking other medicines used for the treatment of pain, to reduce fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, including COX-2 inhibitors) (see section Other medicines and BENATIA);\u003cbr\u003e • if they have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation, as an increase in gastrointestinal bleeding and perforations may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if low doses of aspirin or other drugs that may increase the risk of stomach and intestinal diseases are taken (see section Other medicines and BENATIA). During treatment with all NSAIDs, at any time, with or without warning symptoms or previous history of serious gastrointestinal events, bleeding, ulceration, and perforation of the stomach or intestine may occur, which can be fatal. Therefore, inform your doctor of any unusual gastrointestinal symptoms (especially gastrointestinal bleeding) particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, discontinue treatment with BENATIA and contact your doctor;\u003cbr\u003e • if they suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease) as these diseases may worsen (see section Possible side effects);\u003cbr\u003e • if they are taking medicines that could increase the risk of ulcer or bleeding, such as medicines used to treat inflammation and some immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section Other medicines and BENATIA);\u003cbr\u003e • if they have heart disease (uncontrolled hypertension, congestive heart failure, confirmed ischemic heart disease, peripheral arterial disease) or have suffered from reduced blood flow to the brain (stroke), or if you think the child may be at risk for these conditions (for example, if they have high blood pressure, if they have high sugar levels (diabetes) or fats in the blood, or if they smoke). Medicines like BENATIA may be associated with a slight increase in the risk of heart attack or reduced blood flow to the brain: the risk is more likely with high doses and prolonged therapies. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • if they suffer or have suffered from high blood pressure and\/or severe heart disease (heart failure) because, in association with NSAID therapy, fluid retention, high blood pressure, and swelling (oedema) have been reported;\u003cbr\u003e • if they have an infection (see section Infections below);\u003cbr\u003e • if they have chickenpox, in which case, it is advisable to avoid the use of BENATIA.\u003cbr\u003e \u003cbr\u003e The use of BENATIA requires adequate precautions, especially if the child:\u003cbr\u003e • suffers or has suffered from asthma because breathing difficulties could worsen;\u003cbr\u003e • suffers from clotting problems or hypertension;\u003cbr\u003e • suffers from kidney, heart, liver diseases if taking drugs that increase urine production (diuretics), or if they have undergone major surgery with consequent fluid loss, since in these cases your doctor will advise you to perform periodic blood and urine tests on the child;\u003cbr\u003e • has undergone major surgery;\u003cbr\u003e • suffers from certain congenital diseases affecting blood formation (e.g. acute intermittent porphyria); is dehydrated (e.g. due to fever, vomiting, or diarrhoea), in this case, rehydrate them before and during treatment to avoid the risk of kidney function alteration.\u003cbr\u003e \u003cbr\u003e During prolonged treatments with BENATIA, you must pay particular attention and immediately notify the doctor if:\u003cbr\u003e • signs or symptoms of ulcerations or bleeding of the stomach and intestine appear (e.g. black and foul-smelling stools, vomiting with blood);\u003cbr\u003e • signs or symptoms of liver damage appear (e.g. hepatitis and jaundice);\u003cbr\u003e • signs or symptoms of kidney damage appear (e.g. increased urine production, blood in the urine);\u003cbr\u003e • visual disturbances (blurred or reduced vision, areas of complete or partial blindness, altered colour perception);\u003cbr\u003e • symptoms such as frequent or daily headaches despite regular use of medicines for headache, as these could be caused by excessive use of these medicines;\u003cbr\u003e • symptoms such as headache, disorientation, nausea, vomiting, stiff neck, and fever, as these could be symptoms due to aseptic meningitis (more frequent if the child suffers from systemic lupus erythematosus or other collagenopathies).\u003cbr\u003e\u003cbr\u003e Skin reactions\u003cbr\u003e Severe skin reactions have been reported in association with BENATIA treatment. Stop taking BENATIA and consult your doctor immediately if you experience rash, mucosal lesions, blisters, or other signs of allergy, as these may be the first signs of a very severe skin reaction.\u003cbr\u003e See section 4.\u003cbr\u003e \u003cbr\u003e Infections\u003cbr\u003e BENATIA can mask the symptoms of infections such as fever and pain. It is therefore possible that BENATIA may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents, there is a risk of impaired kidney function.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e \u003cb\u003eIf your child experiences any of the following serious side effects, stop administering the tablets and inform the doctor immediately or go to the nearest hospital:\u003c\/b\u003e\u003cbr\u003e • severe alterations of the skin and mucous membranes characterized by rashes, redness, itching, and blisters (bullous and exfoliative dermatitides including erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis);\u003cbr\u003e • allergic reactions, even severe, which may include: urticaria, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnoea), altered heart rate (tachycardia), low blood pressure (hypotension), anaphylaxis, severe shock, and worsening of asthma;\u003cbr\u003e • aseptic meningitis with symptoms such as disorientation, headache, nausea, vomiting, stiff neck, and fever (more frequent if the child suffers from systemic lupus erythematosus or other collagenopathies). Further side effects include:\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • headache, dizziness, drowsiness, and convulsions;\u003cbr\u003e • stomach pain, nausea, and indigestion (dyspepsia);\u003cbr\u003e • skin rashes;\u003cbr\u003e • vision disturbances.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • cystitis, rhinitis;\u003cbr\u003e • depression, insomnia, difficulty concentrating, unstable mood, hearing disturbances;\u003cbr\u003e • cerebrovascular haemorrhage;\u003cbr\u003e • dry eyes;\u003cbr\u003e • sensation of one's own heartbeat (palpitations);\u003cbr\u003e • diarrhoea, flatulence, dry mouth, constipation, and vomiting;\u003cbr\u003e • hair loss (alopecia);\u003cbr\u003e • skin becomes sensitive to light;\u003cbr\u003e • severe kidney diseases including tubular necrosis, glomerulonephritis, blood in the urine, and increased urine production;\u003cbr\u003e • decreased haematocrit levels.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells (anaemia, leukopenia, thrombocytopenia, eosinophilia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe fatigue, nosebleeds, and haemorrhages;\u003cbr\u003e • signs or symptoms of ulcerations or bleeding of the stomach and intestine, black and foul-smelling stools, vomiting with blood;\u003cbr\u003e • lesions with bleeding of the mouth, heartburn (gastritis);\u003cbr\u003e • simultaneous kidney and liver disease (hepatorenal syndrome), death of some liver cells (hepatic necrosis), liver disease (hepatic insufficiency, hepatic dysfunction, hepatitis, jaundice);\u003cbr\u003e • severe kidney diseases (acute renal failure, papillary necrosis) particularly following long-term treatments, associated with an increase in blood urea concentration and swelling (oedema);\u003cbr\u003e • decreased haemoglobin levels in the blood;\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • severe skin infections and soft tissue complications during chickenpox infection;\u003cbr\u003e • worsening of infection-related inflammations (e.g. necrotizing fasciitis) associated with the use of certain non-steroidal anti-inflammatory drugs (NSAIDs). If signs of an infection appear or worsen, you should consult your doctor immediately to assess if anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • irritability;\u003cbr\u003e • fluid retention and decreased appetite;\u003cbr\u003e • abnormal perception of noises such as buzzing, ringing, or rustling (tinnitus);\u003cbr\u003e • severe heart disease (heart failure) and swelling (oedema);\u003cbr\u003e • increased blood pressure (hypertension) and reduced blood flow to the body (shock);\u003cbr\u003e • respiratory tract disorders including asthma, laryngeal obstruction, wheezing (bronchospasm), temporary cessation of breathing (apnoea), and difficulty breathing (dyspnoea);\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease), inflammation of the pancreas (pancreatitis), inflammation of the duodenum (duodenitis), inflammation of the oesophagus (oesophagitis);\u003cbr\u003e • a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swelling of the lymph nodes, and an increase in eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, and scaly rash, with pustules forming under the skin and vesicles located mainly on skin folds, torso, and upper limbs accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • skin becomes sensitive to light.\u003cbr\u003e \u003cbr\u003e Stop using BENATIA if you develop these symptoms and contact your doctor immediately.\u003cbr\u003e See also section 2.\u003cbr\u003e The use of ibuprofen, especially at high doses (2400 mg\/day), may be associated with a modest increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including those not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"DYMALIFE PHARMACEUTICAL Srl","offers":[{"title":"Default Title","offer_id":46290069160203,"sku":"043186016","price":10.77,"currency_code":"EUR","in_stock":true}]},{"product_id":"enantyum-10cpr-riv-25mg","title":"ENANTYUM*10FC TAB 25MG","description":"\u003cp\u003e\u003cb\u003eEnantyum 25 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Dexketoprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Enantyum is a painkiller belonging to the group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs).\u003cbr\u003e It is used for the treatment of mild to moderate pain, such as muscle pain, painful menstruation (dysmenorrhea), and toothache.\u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 - 4 days.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Enantyum:\u003c\/b\u003e\u003cbr\u003e • If you are allergic to dexketoprofen or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e • If you are allergic to acetylsalicylic acid or other non-steroidal anti-inflammatory drugs;\u003cbr\u003e • If you have asthma or have suffered from asthma attacks, acute allergic rhinitis (a short period of inflammation of the nasal mucosa), nasal polyps (polypoid masses in the nose due to allergy), urticaria (skin rash), angioedema (swelling of the face, eyes, lips, or tongue, or difficulty breathing) or wheezing in the chest, after taking acetylsalicylic acid or other non-steroidal anti-inflammatory drugs;\u003cbr\u003e • If you have suffered from photoallergic or phototoxic reactions (a particular form of skin redness and\/or blistering after exposure to sunlight) during treatment with ketoprofen (a non-steroidal anti-inflammatory drug) or with fibrates (medicines used to lower blood fat levels);\u003cbr\u003e • If you suffer from a peptic ulcer\/bleeding in the stomach or intestine or if you have suffered in the past from stomach or intestinal bleeding, ulceration or perforation;\u003cbr\u003e • If you suffer from chronic digestive problems (e.g. indigestion, heartburn);\u003cbr\u003e • If you have suffered in the past from bleeding or perforation in the stomach or intestine due to previous use of non-steroidal anti-inflammatory drugs (NSAIDs) used for pain;\u003cbr\u003e • If you suffer from inflammatory bowel diseases (Crohn's disease or ulcerative colitis);\u003cbr\u003e • If you suffer from severe heart failure, or have moderate to severe kidney problems or serious liver problems;\u003cbr\u003e • If you have bleeding problems or coagulation disorders;\u003cbr\u003e • If you are severely dehydrated (have lost a large amount of body fluids) due to vomiting, diarrhoea or insufficient fluid intake;\u003cbr\u003e • If you are in the third trimester of pregnancy or are breastfeeding.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Consult your doctor or pharmacist before using Enantyum:\u003cbr\u003e • If you suffer from allergies, or have had problems due to allergies in the past;\u003cbr\u003e • If you have kidney problems, liver problems or heart problems (hypertension and\/or heart failure) or fluid retention, or have previously suffered from any of these conditions;\u003cbr\u003e • If you are on diuretic therapy or have very poor hydration problems or a reduced blood volume due to excessive fluid loss (for example due to excessive urination, diarrhoea, vomiting);\u003cbr\u003e • If you suffer from heart conditions, if you have had a stroke or if you think you may be at risk for these conditions (for example if you have high blood pressure, diabetes or high cholesterol or if you are a smoker) you should discuss therapy with your doctor or pharmacist; medicines such as Enantyum may be associated with a small increased risk of heart attack (myocardial infarction) or stroke. These risks are more likely with high doses of the drug and with prolonged therapy. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • If you are elderly: there is a greater chance of being subject to side effects (see section 4); In the event that these occur, consult your doctor immediately;\u003cbr\u003e • If you are a woman with fertility problems (this medicine may reduce your fertility, therefore you should not take the medicine if you are planning a pregnancy or if you are undergoing fertility investigations);\u003cbr\u003e • If you suffer from a blood and blood cell formation disorder;\u003cbr\u003e • If you suffer from systemic lupus erythematosus or mixed connective tissue disease (immune system disorders affecting connective tissue);\u003cbr\u003e • If you have suffered in the past from a chronic inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • If you have or have suffered in the past from other stomach or intestinal disorders;\u003cbr\u003e • If you have an infection - see the Infections section below;\u003cbr\u003e • If you are taking other medicines that increase the risk of peptic ulcer or bleeding, for example oral steroids, some antidepressants (SSRI type, i.e. Selective Serotonin Reuptake Inhibitors), medicines that prevent blood clots from forming such as aspirin or anticoagulants such as warfarin. In these cases, consult your doctor before taking this medicine: they may prescribe an additional medicine to protect your stomach (for example misoprostol or other medicines that block the production of gastric acids);\u003cbr\u003e • If you suffer from asthma associated with chronic rhinitis, chronic sinusitis, and\/or nasal polyposis, as you have a greater risk of allergy to acetylsalicylic acid and\/or NSAIDs compared to the rest of the population. The administration of this medicine can cause asthma attacks or bronchospasm, particularly in subjects allergic to acetylsalicylic acid or NSAIDs.\u003cbr\u003e \u003cbr\u003e\u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e Dexketoprofen can mask the symptoms of infection such as fever and pain. It is therefore possible that this medicine may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the infection symptoms persist or worsen, consult your doctor immediately.\u003cbr\u003e The use of this medicine is not recommended during chickenpox virus infection.\u003cbr\u003e \u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e This medicine has not been studied in children and adolescents. Therefore, safety and efficacy have not been established and the product should not be used in children and adolescents.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everyone experiences them.\u003cbr\u003e The possible side effects are listed below, ordered by the probability with which they may occur.\u003cbr\u003e \u003cbr\u003e\u003cb\u003eCommon side effects: may affect up to 1 in 10 patients\u003c\/b\u003e\u003cbr\u003e Nausea and\/or vomiting, abdominal pain mainly in the upper quadrants, diarrhoea, digestive problems (dyspepsia).\u003cbr\u003e \u003cbr\u003e\u003cb\u003eUncommon side effects: may affect up to 1 in 100 patients\u003c\/b\u003e\u003cbr\u003e Dizziness, lightheadedness, drowsiness, sleep disturbances, nervousness, headache, palpitations, hot flashes, inflammation of the stomach wall (gastritis), constipation, dry mouth, flatulence, skin rash, fatigue, pain, feeling of fever and chills, feeling of general malaise.\u003cbr\u003e \u003cbr\u003e\u003cb\u003eRare side effects: may affect up to 1 in 1,000 patients\u003c\/b\u003e\u003cbr\u003e Peptic ulcer, bleeding or perforated peptic ulcer (which may manifest with traces of blood in vomit or stools), fainting, high blood pressure, slow breathing, fluid retention and peripheral edema (e.g. swollen ankles), laryngeal edema, loss of appetite (anorexia), altered sensitivity (paresthesia), itchy rash, acne, increased sweating, back pain, frequent urination, menstrual disorders, prostate problems, abnormal liver function tests (blood tests), hepatocellular damage (hepatitis), acute renal failure.\u003cbr\u003e \u003cbr\u003e\u003cb\u003eVery rare side effects: may affect up to 1 in 10,000 patients\u003c\/b\u003e\u003cbr\u003e Anaphylactic reaction (hypersensitivity reaction that can also lead to collapse), ulceration of the skin, mouth, eyes and genital area (Stevens-Johnson and Lyell syndromes), facial edema or swelling of the lips and throat (angioedema), difficulty breathing due to contraction of the muscles surrounding the airways (bronchospasm), shortness of breath, fast heartbeat, low blood pressure, pancreatitis, blurred vision, ringing in the ears (tinnitus), skin reactions, light hypersensitivity, itching, kidney problems. Decrease in white blood cells in the blood (neutropenia), decrease in platelets in the blood (thrombocytopenia).\u003cbr\u003e \u003cbr\u003e Inform your doctor immediately if you notice side effects in the stomach or intestine at the beginning of treatment (for example stomach pain, acidity or bleeding), if you have previously suffered from any of these side effects due to prolonged use of anti-inflammatory drugs, and especially if you are elderly.\u003cbr\u003e \u003cbr\u003e Stop using this medicine as soon as you notice the appearance of a skin rash, or any lesion on the inner surface of the mouth or genitals, or any sign of allergy.\u003cbr\u003e \u003cbr\u003e During treatment with non-steroidal anti-inflammatory drugs, fluid retention and swelling effects (particularly in the ankles and legs), an increase in blood pressure and heart failure have been reported.\u003cbr\u003e \u003cbr\u003e Medicines like this may be associated with a small increased risk of heart attack (myocardial infarction) or cerebrovascular accidents (stroke).\u003cbr\u003e \u003cbr\u003e In patients suffering from immune system disorders affecting connective tissue (systemic lupus erythematosus or mixed connective tissue disease), anti-inflammatory medicines can rarely cause fever, headache and neck stiffness.\u003cbr\u003e \u003cbr\u003e The most frequently observed adverse events are gastrointestinal in nature. Peptic ulcers, perforation or gastrointestinal bleeding may occur, sometimes fatal, especially for the elderly. Nausea, vomiting, diarrhoea, flatulence, constipation, dyspepsia, abdominal pain, melaena, haematemesis, ulcerative stomatitis, worsening of colitis and Crohn's disease have been reported following administration. Less frequently, inflammation of the stomach wall (gastritis) has been observed.\u003cbr\u003e \u003cbr\u003e As with other NSAIDs, haematological reactions may occur (purpura, aplastic and haemolytic anaemia and rarely agranulocytosis and bone marrow hypoplasia).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"A.MENARINI IND.FARM.RIUN.Srl","offers":[{"title":"Default Title","offer_id":46290072568075,"sku":"033656430","price":4.46,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_e4571164-845c-4107-b0bd-7b36163a37d1.png?v=1734080039"},{"product_id":"moment-36cpr-riv-200mg","title":"MOMENT*36COATED TABS 200MG","description":"\u003cp\u003e\u003cb\u003eMOMENT 200 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMoment contains ibuprofen, a medicine belonging to the class of analgesic-anti-inflammatory drugs, i.e., drugs that combat pain and inflammation.\u003cbr\u003e \u003cbr\u003e Moment is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for: - treating pain of various origins and types (headache, toothache, neuralgia, osteoarticular and muscle pain, menstrual pain);\u003cbr\u003e - reducing the symptoms of fever and flu-like conditions.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Moment:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to other anti-rheumatic medicines (e.g., acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see section Other medicines and Moment);\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breastfeeding (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have previously had bleeding or perforation of the stomach or intestine after taking medicines;\u003cbr\u003e - if you have previously had two or more distinct episodes of ulcer or stomach bleeding;\u003cbr\u003e - in the presence of severe heart disease (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhea or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck area (angioedema), and chest pain. Stop Moment immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e Skin reactions\u003cbr\u003e Severe skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.\u003cbr\u003e \u003cbr\u003e Talk to your doctor or pharmacist before taking Moment:\u003cbr\u003e - if you have experienced difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, runny nose (chronic rhinitis), nasal polyps (nasal polyposis) or inflammation of the paranasal sinus mucosa (sinusitis) or suffer\/have suffered from allergies, because you may experience difficulty breathing (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section Other medicines and Moment);\u003cbr\u003e - if you are elderly or have suffered from ulcers, especially if the ulcer has also manifested with bleeding or perforation (see section Do not take Moment), as the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly consult your doctor to have a medicine prescribed that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you take low doses of acetylsalicylic acid or medicines that may increase the risk of stomach and\/or intestinal diseases (see section Other medicines and Moment);\u003cbr\u003e - if you have suffered or suffer from chronic bowel diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 Possible side effects);\u003cbr\u003e - if you have had stomach and intestinal diseases related to the use of medicines, and in particular if you are elderly, you must report any unusual intestinal symptoms (especially bleeding) to your doctor, particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of stomach and\/or intestinal ulcers or bleeding, such as oral corticosteroids (e.g., cortisone), anticoagulants (e.g., warfarin), antidepressants (selective serotonin reuptake inhibitors), or antiplatelet agents (e.g., acetylsalicylic acid). See also the section Other medicines and Moment. If gastrointestinal bleeding or ulceration occurs in patients taking Moment, treatment should be discontinued;\u003cbr\u003e - if you have high blood pressure and the medicines you are taking are not able to lower it and\/or you have heart disease or blood circulation problems in the brain or other body districts or you think you may be at risk for these diseases (for example if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or have heart disease, as fluid retention, increased blood pressure, and swelling have been observed following treatment with NSAIDs. NSAIDs can reduce the action of medicines to lower blood pressure (see section Other medicines and Moment);\u003cbr\u003e - if you have lost a significant amount of fluids, or if swelling, heart problems or high blood pressure appear;\u003cbr\u003e - if you have decreased kidney function, heart or liver malfunction, or if you are elderly or undergoing treatment with medicines for high blood pressure, as you may be more prone to the onset of kidney problems. Furthermore, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e - if you suffer from a coagulation disorder or are taking medicines that slow down blood clotting (anticoagulants) (see section Other medicines and Moment);\u003cbr\u003e - if you suffer from a disease that can affect various organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as in rare occasions, symptoms of aseptic meningitis have been observed in patients treated with ibuprofen. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients who did not have concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section Other medicines and Moment);\u003cbr\u003e - if you intend to become pregnant (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have problems getting pregnant or are undergoing fertility investigations (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have an infection - see the section Infections below.\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller medicines such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss your therapy with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation to the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Medicines like Moment can:\u003cbr\u003e - be associated with the appearance of kidney diseases, even serious ones (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e - cause eye disorders, therefore, in case of prolonged treatments, periodic eye checks are recommended. If visual disturbances occur, stop treatment with Moment.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment can mask the symptoms of infections such as fever and pain. Therefore, Moment may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003e If the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Moment can cause side effects, although not everybody gets them.\u003cbr\u003e The side effects of the medicine can be minimized if you use the lowest dose among those recommended, and if you use the medicine only for the period necessary to control your symptoms.\u003cbr\u003e \u003cbr\u003e If you develop an ulcer, or stomach and\/or intestinal bleeding, or skin and\/or mucous membrane lesions, you must stop treatment with Moment and contact your doctor. These side effects are usually more common in the elderly.\u003cbr\u003e \u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate, or more severe reactions, even allergic ones, although rarely.\u003cbr\u003e \u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP using Moment immediately\u003c\/b\u003e and contact your doctor or the nearest hospital immediately where you will be given appropriate and specific treatment:\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucous membrane lesions;\u003cbr\u003e • signs of an allergic reaction, even severe (erythema, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • peeling skin;\u003cbr\u003e • reddish, non-raised, target-shaped or circular spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e • widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e • visual disturbances;\u003cbr\u003e • liver disease (hepatic dysfunction);\u003cbr\u003e • bleeding, ulceration and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e \u003cbr\u003e If one of the allergic reactions described above occurs, go to the hospital as it is necessary to have immediate availability of equipment, medicines and personnel suitable for emergency treatment, since in rare cases, following the use of ibuprofen, serious side effects, sometimes fatal, have been reported, even in the absence of known allergy.\u003cbr\u003e \u003cbr\u003e The risk of experiencing such symptoms is higher in the early stages of therapy: in most cases, the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e Furthermore, you may experience other side effects that have also been reported with other medicines similar to Moment and are listed below according to frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue;\u003cbr\u003e \u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis);\u003cbr\u003e • insomnia, anxiety;\u003cbr\u003e • numbness of the limbs or other parts of the body (paresthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • momentary cessation of breathing (apnea);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • vertigo;\u003cbr\u003e • liver disorders (altered liver function);\u003cbr\u003e • liver inflammation (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney diseases (renal function damage and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure);\u003cbr\u003e • hypersensitivity reactions such as rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnea), asthma attacks with possible drop in blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity);\u003cbr\u003e \u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction of white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusional state, hallucinations;\u003cbr\u003e • inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section Warnings and precautions), with symptoms of neck stiffness, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect various organs and tissues of the body (lupus erythematosus syndrome);\u003cbr\u003e • worsening of inflammation caused by an existing infection (e.g., development of necrotizing fasciitis);\u003cbr\u003e • high blood nitrogen levels;\u003cbr\u003e • altered liver function tests (increased transaminases, increased alkaline phosphatase);\u003cbr\u003e • abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e \u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling one's own heartbeat (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (hepatic insufficiency);\u003cbr\u003e • hypertension;\u003cbr\u003e • severe allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making it difficult to breathe, fast heart rate, severe rapidly appearing allergic reaction that can cause death (anaphylaxis), severe skin rash or peeling skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • severe skin infections and soft tissue disorders may occur during chickenpox infection.\u003cbr\u003e \u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomiting;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in stools;\u003cbr\u003e • blood in vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory colon and bowel diseases (colitis, Crohn's disease);\u003cbr\u003e • increased risk of sudden reduction in brain blood circulation (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red and scaly rash, with pustules under the skin and blisters located mainly on skin lesions, on the trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using Moment if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290077712651,"sku":"025669185","price":11.36,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_bed3aee4-a790-424d-b5fd-4a18962f36f3.jpg?v=1734080110"},{"product_id":"momendol-24cpr-riv-220mg","title":"MOMENDOL*24FILMTABS 220MG","description":"\u003cp\u003e\u003cb\u003eMOMENDOL 220 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003eNaproxen sodium\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMomendol belongs to the class of analgesic-anti-inflammatory-antirheumatic non-steroidal drugs, i.e., medicines that fight pain, inflammation, fever and are useful in the symptomatic treatment of rheumatic diseases.\u003cbr\u003eMomendol is used for the short-term symptomatic treatment of mild to moderate pain, such as muscle and joint pain (e.g., back pain, stiff neck), headache, toothache, and menstrual pain.\u003cbr\u003eMomendol can also be used for the treatment of fever.\u003cbr\u003eConsult your doctor if you do not feel better or if you feel worse after 7 days of treatment for pain, and after 3 days of treatment for fever.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take MOMENDOL\u003c\/b\u003e\u003cbr\u003e• If you are allergic to naproxen sodium or any of the other ingredients of this medicine (listed in section 6), or to other chemically related substances.\u003cbr\u003e• If you suffer from allergic manifestations, such as asthma, urticaria, rhinitis, nasal polyps, angioedema, and allergic reactions induced by acetylsalicylic acid, analgesics, anti-inflammatory and\/or antirheumatic drugs.\u003cbr\u003e• If you have a history of gastrointestinal bleeding or perforation, recurrent active or previous peptic ulcer, chronic inflammatory bowel diseases (ulcerative colitis, Crohn's disease), severe hepatic insufficiency, severe heart failure, severe renal insufficiency (creatinine clearance \u0026lt;30 ml\/min), angioedema, during intensive diuretic therapy, in subjects with active bleeding and at risk of bleeding during anticoagulant therapy (See \"Other medicines and MOMENDOL\" and \"Warnings and precautions\").\u003cbr\u003e• During pregnancy, from the third trimester, and during breastfeeding (See \"Pregnancy, breastfeeding and fertility\").\u003cbr\u003e• The medicine cannot be administered to children under 12 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Momendol:\u003cbr\u003e• As there is a close correlation between dosage and the occurrence of severe gastrointestinal side effects. Therefore, the lowest effective dose should always be used.\u003cbr\u003e• Medicines such as MOMENDOL may be associated with a modest increased risk of heart attack (\"myocardial infarction\") or stroke. Any risk is more likely with high doses and prolonged treatments. Do not exceed the recommended dose or duration of treatment (7 days for pain and 3 days for fever treatment).\u003cbr\u003e• When MOMENDOL is used in hypertensive patients and\/or in patients with reduced cardiac and\/or renal function. During treatment with MOMENDol, diuresis and renal function should be closely monitored, particularly in the elderly, in patients with heart failure or chronic renal failure, and in patients undergoing diuretic therapy, after major surgeries involving significant blood loss.\u003cbr\u003e• If you have heart problems, or a history of stroke, or think you may be at risk for these conditions (for example, if you have high blood pressure, diabetes, or high cholesterol, or if you smoke), you should discuss your treatment with your doctor or pharmacist.\u003cbr\u003e• When MOMENDOL is used in patients with severe heart failure, a worsening of the condition may occur.\u003cbr\u003e• When MOMENDOL is used in patients with a history of gastrointestinal diseases or liver failure and in patients with active or previous allergic manifestations, as in these subjects the product may cause bronchospasm, asthma, or other allergic phenomena. In these cases, particular caution is advised.\u003cbr\u003e• MOMENDOL should be discontinued at the first appearance of skin rash, mucosal lesions, or any other sign of allergy and\/or hypersensitivity.\u003cbr\u003e• If visual disturbances occur, treatment with MOMENDOL should be discontinued.\u003cbr\u003e• As naproxen, like any other anti-inflammatory drug, can mask the concomitant symptoms of infectious diseases.\u003cbr\u003e• As in isolated cases, an aggravation of infectious inflammations has been reported in temporal connection with the use of anti-inflammatory drugs.\u003cbr\u003e• If used in elderly patients, who generally present some degree of impairment of renal, hepatic and cardiac functions, since this group of patients is more exposed to the risk of onset of side effects related to the use of anti-inflammatory drugs. Prolonged use of anti-inflammatory drugs in the elderly is not recommended.\u003cbr\u003e• As naproxen inhibits platelet aggregation and can prolong bleeding time. Patients with coagulation disorders or on therapy with medicines that interfere with coagulation should be carefully monitored while taking MOMENDOL.\u003cbr\u003e• When MOMENDOL is used by habitual consumers of high daily doses of alcohol, there is a high risk of stomach bleeding.\u003cbr\u003e• The use of the product should be avoided in cases of pain of gastrointestinal origin. It is known that in patients taking anti-inflammatory drugs, stomach or intestinal bleeding may occur.\u003cbr\u003e• In asthmatic patients, the product is generally contraindicated.\u003cbr\u003e• When MOMENDOL is used in combination with other drugs requiring caution, see \"Other medicines and MOMENDOL\".\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003eFor children under 16 years of age, it is recommended to contact a doctor.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everyone gets them.\u003cbr\u003eThe most commonly observed side effects are gastrointestinal.\u003cbr\u003eThe following side effects have been reported with NSAIDs and naproxen:\u003cbr\u003e\u003cbr\u003e\u003cb\u003eCommon (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e- Headache, drowsiness, dizziness\u003cbr\u003e- Nausea, dyspepsia, vomiting, heartburn, gastralgia, flatulence.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e- Allergic reaction (including facial oedema and angioedema)\u003cbr\u003e- Sleep disorders, excitement\u003cbr\u003e- Visual disturbances\u003cbr\u003e- Tinnitus, hearing disturbances\u003cbr\u003e- Contusion\u003cbr\u003e- Diarrhoea, constipation\u003cbr\u003e- Rash\/itching\u003cbr\u003e- Abnormal kidney function\u003cbr\u003e- Chills, oedema (including peripheral oedema).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e- Peptic ulcer, perforation or gastrointestinal bleeding, sometimes fatal, may occur especially in elderly subjects, haematemesis, ulcerative stomatitis, aggravated colitis and aggravated Crohn's disease.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e- Haemolytic or aplastic anaemia, thrombocytopenia, granulocytopenia\u003cbr\u003e- Meningitis-like reaction\u003cbr\u003e- In association with NSAID treatment, tachycardia, oedema, hypertension and heart failure have been observed\u003cbr\u003e- Dyspnoea, asthma\u003cbr\u003e- Colitis, stomatitis. Gastritis has been observed less frequently\u003cbr\u003e- Jaundice, hepatitis, reduced liver function\u003cbr\u003e- Photosensitivity, alopecia, bullous disorder including Stevens-Johnson syndrome and toxic epidermal necrolysis\u003cbr\u003e- Increased blood pressure.\u003cbr\u003e\u003cbr\u003eAs with other anti-inflammatory drugs, anaphylactic or anaphylactoid allergic reactions may occur in patients with or without previous exposure to drugs of the same class.\u003cbr\u003eThe characteristic symptoms of an anaphylactic reaction are: severe and sudden hypotension, acceleration or slowing of the heartbeat, unusual tiredness or weakness, anxiety, agitation, loss of consciousness, difficulty breathing or swallowing, itching, urticaria with or without angioedema, skin redness, nausea, vomiting, crampy abdominal pain, diarrhoea.\u003cbr\u003eMedicines such as MOMENDOL may be associated with a modest increased risk of heart attack (\"myocardial infarction\") or stroke.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290088001803,"sku":"025829185","price":11.51,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_403f8e5b-f0dd-4d48-abaf-f485ca4b027a.png?v=1734080148"},{"product_id":"spididol-os-grat-12bs-400mg-al","title":"SPIDIDOL*OS GRA 12SACH 400MG AL","description":"\u003cp\u003e\u003cb\u003eSPIDIDOL 400 mg film-coated tablets\u003cbr\u003e SPIDIDOL 400 mg granules for oral solution apricot flavour\u003c\/b\u003e\u003cbr\u003e Ibuprofen arginine salt\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e This medicine contains the active ingredient ibuprofen, belonging to a group of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs) which act by relieving pain (analgesic action) and reducing the symptoms of inflammation (anti-inflammatory action).\u003cbr\u003e \u003cbr\u003e SPIDIDOL is indicated for the treatment of pain or inflammatory conditions in the following cases:\u003cbr\u003e - \u003cb\u003ePain treatment:\u003c\/b\u003e headache, toothache, menstrual pain, neuralgia, osteoarticular (bone) and muscle pain.\u003cbr\u003e - \u003cb\u003eTreatment of febrile and flu-like conditions\u003c\/b\u003e, in addition to other medicines.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not notice any improvement or if your symptoms worsen.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take SPIDIDOL\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen, other similar medicines or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you have previously suffered from stomach and intestinal disorders associated with bleeding (gastrointestinal bleeding or perforation related to previous treatments with anti-inflammatory drugs (NSAIDs) or a history of recurrent peptic haemorrhage\/ulcer, with two or more distinct episodes of demonstrated ulceration or bleeding);\u003cbr\u003e - if you suffer from stomach and intestinal disorders associated with the presence of lesions and bleeding (active and recurrent peptic ulcer);\u003cbr\u003e - if you suffer from stomach or intestinal bleeding (gastrointestinal bleeding);\u003cbr\u003e - if you have other bleeding such as cerebrovascular bleeding;\u003cbr\u003e - if you suffer from ulcerative colitis or Crohn's disease;\u003cbr\u003e - if you suffer from severe liver or kidney problems (severe hepatic and renal insufficiency);\u003cbr\u003e - if you suffer from haemorrhages (haemorrhagic diathesis);\u003cbr\u003e - if you suffer from severe heart problems (severe heart failure);\u003cbr\u003e - if in the past, after taking acetylsalicylic acid or other anti-inflammatory medicines (NSAIDs), you have experienced facial swelling due to fluid accumulation, especially around the mouth and eyes (angioedema), severe respiratory difficulty (bronchospasm), breathing problems (asthma), skin irritation (urticaria), inflammation of the nasal mucous membranes (rhinitis) or nasal polyps;\u003cbr\u003e - if you suffer from systemic lupus erythematosus or other skin diseases (collagen diseases);\u003cbr\u003e - if you are in the third trimester of pregnancy (See paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - before or after heart surgery;\u003cbr\u003e - if you suffer from phenylketonuria, a condition in which the levels of certain substances in the urine and blood are altered. This warning refers only to the granules for oral solution as it contains aspartame.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e Consult your doctor or pharmacist before taking SPIDIDOL if you have an infection (see paragraph Infections).\u003cbr\u003e \u003cbr\u003e \u003cu\u003eTake special care with SPIDIDOL\u003c\/u\u003e:\u003cbr\u003e Severe skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Stop using SPIDIDOL and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in paragraph 4.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eTake this medicine with caution if:\u003c\/b\u003e\u003cbr\u003e - you are already taking other anti-inflammatory medicines (including selective COX-2 inhibitors, see paragraph Other medicines and SPIDIDOL);\u003cbr\u003e - you are taking other medicines that could increase the risk of ulceration or bleeding, such as oral corticosteroids, anticoagulants such as warfarin, selective serotonin reuptake inhibitors or antiplatelet agents such as aspirin (See paragraph Other medicines and SPIDIDOL);\u003cbr\u003e - you have suffered from high blood pressure (hypertension) because, in association with NSAID therapy, you may have problems eliminating fluids (fluid retention) and experience swelling due to the accumulation of fluids (edema);\u003cbr\u003e - you have previously suffered from intestinal disorders (ulcerative colitis, Crohn's disease);\u003cbr\u003e - you suffer from heart problems (mild to moderate congestive heart failure);\u003cbr\u003e - you have suffered from breathing problems (bronchospasm) especially if due to the use of medicines. In patients who suffer or have suffered from bronchial asthma or allergic diseases, bronchospasm could worsen. In these cases, especially for prolonged treatments, your doctor may suggest periodic tests;\u003cbr\u003e - you suffer from coagulation disorders or a decrease in heart, liver or kidney function; in these cases, especially for prolonged treatments, periodic tests may be necessary. Hypersensitivity to SPIDIDOL can cause liver problems (hepatotoxic reactions);\u003cbr\u003e - you suffer from lupus erythematosus, a chronic autoimmune disease that can affect various organs and tissues and causes facial lesions and pain, or you suffer from other skin diseases (collagen diseases). In this case, you must consult your doctor before taking SPIDIDOL. The risk of developing skin disorders may increase;\u003cbr\u003e - you intend to become pregnant, as the use of SPIDIDOL may impair female fertility; the use of SPIDIDOL must be discontinued in women who have fertility problems or who are undergoing fertility investigations.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRisks of Stroke and Heart Attack\u003c\/b\u003e\u003cbr\u003e Anti-inflammatory\/pain relief drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e You should discuss your therapy with your doctor or pharmacist before taking SPIDIDOL if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema) and chest pain, have been reported with ibuprofen. Stop SPIDIDOL immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eGastrointestinal risks\u003c\/b\u003e\u003cbr\u003e At any time, with or without warning symptoms or a previous history of serious gastrointestinal diseases, stomach and intestinal bleeding (gastrointestinal haemorrhage), severe lesion formation (ulceration and perforation), which can be fatal, may occur. If you have previously suffered from an ulcer, the risk of gastrointestinal bleeding, ulceration or perforation is higher with increased doses of NSAIDs. Your doctor will suggest taking specific medicines to protect the stomach such as misoprostol or proton pump inhibitors, especially if you are taking other medicines (e.g., aspirin or medicines that increase the risk of gastrointestinal problems).\u003cbr\u003e If you suffer or have suffered from stomach or intestinal problems (gastrointestinal toxicity), especially at the beginning of treatment with SPIDIDOL, tell your doctor about any gastrointestinal symptoms you experience (especially bleeding). At doses greater than 1000 mg per day, a prolongation of bleeding time may occur.\u003cbr\u003e If you experience gastrointestinal bleeding or ulceration, stop treatment with SPIDIDOL and contact your doctor or the nearest hospital.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVision problems\u003c\/b\u003e\u003cbr\u003e If you experience vision problems, stop treatment with this medicine and consult an ophthalmologist.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eElderly patients\u003c\/b\u003e\u003cbr\u003e If you are an elderly person, the risk of side effects is greater, especially bleeding and perforations in the stomach and intestines (gastrointestinal events) which can be fatal. The risk of gastrointestinal bleeding, ulceration or perforation is higher with increased doses of NSAIDs.\u003cbr\u003e Therefore, start treatment with the lowest available dose and take SPIDIDOL for the shortest possible period to control symptoms. Your doctor may indicate medicines that have a protective action on the stomach (misoprostol or proton pump inhibitors), especially if you are taking other medicines (e.g., aspirin or medicines that increase the risk of gastrointestinal problems). If you suffer or have suffered from stomach or intestinal problems (gastrointestinal toxicity), especially at the beginning of treatment with SPIDIDOL, tell your doctor about any gastrointestinal symptoms you experience (especially bleeding). At doses greater than 1000 mg per day, a prolongation of bleeding time may occur.\u003cbr\u003e If you experience gastrointestinal bleeding or ulceration, stop treatment with SPIDIDOL and contact your doctor or the nearest hospital.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e This medicine should be administered with caution in dehydrated adolescents because there is an increased risk of kidney problems (see paragraph 3 Use in adolescents aged 12 to 18 years).\u003cbr\u003e \u003cbr\u003e Use caution when starting ibuprofen treatment if you suffer from severe dehydration.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e SPIDIDOL can mask the symptoms of infections such as fever and pain. It is therefore possible that SPIDIDOL may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e Therefore, in case of infection, use ibuprofen therapy with caution.\u003cbr\u003e \u003cbr\u003e NSAIDs can cause an increase in liver function test results.\u003cbr\u003e You should avoid alcohol because it can increase the side effects of NSAIDs, especially those affecting the gastrointestinal tract or the central nervous system.\u003cbr\u003e If you experience a hypersensitivity reaction after taking ibuprofen, stop treatment immediately.\u003cbr\u003e Medically assisted measures should be initiated by specialised medical personnel, in line with the symptomatology.\u003cbr\u003e Ibuprofen acid can cause a prolongation of bleeding time because it reversibly inhibits platelet aggregation.\u003cbr\u003e \u003cbr\u003e \u003cem\u003ePay particular attention in the aforementioned cases, bearing in mind that any risk is more likely when using this medicine at high doses and in prolonged therapies.\u003c\/em\u003e\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everyone gets them.\u003cbr\u003e \u003cbr\u003e Stop using ibuprofen and consult your doctor immediately if you notice any of the following symptoms:\u003cbr\u003e • reddish, non-raised, target-shaped or circular patches on the trunk, often with central blisters, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalised exanthematous pustulosis).\u003cbr\u003e \u003cbr\u003e The following side effects may occur:\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery common\u003c\/b\u003e (may affect more than 1 in 10 people)\u003cbr\u003e - indigestion (dyspepsia);\u003cbr\u003e - diarrhoea.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCommon\u003c\/b\u003e (may affect up to 1 in 10 people)\u003cbr\u003e - abdominal pain or discomfort, heartburn, nausea, flatulence;\u003cbr\u003e - headache, dizziness;\u003cbr\u003e - skin disease, rash.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon\u003c\/b\u003e (may affect up to 1 in 100 people)\u003cbr\u003e - formation of lesions in the stomach or intestines (peptic ulcers or haemorrhages) sometimes fatal, especially in the elderly;\u003cbr\u003e - vomiting;\u003cbr\u003e - blood in the stools (melena);\u003cbr\u003e - inflammation of the stomach (gastritis);\u003cbr\u003e - inflammation of the mouth (stomatitis);\u003cbr\u003e - confusion;\u003cbr\u003e - drowsiness;\u003cbr\u003e - itching, skin irritation (urticaria, exanthema), severe skin problem associated with bleeding (purpura);\u003cbr\u003e - swelling of the face, lips, mouth, tongue or throat that can cause difficulty in breathing and swallowing (angioedema);\u003cbr\u003e - allergic reactions;\u003cbr\u003e - difficulty breathing (asthma, worsening of asthma, bronchospasm, dyspnea).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare\u003c\/b\u003e (may affect up to 1 in 1,000 people)\u003cbr\u003e - formation of lesions in the stomach or intestines (gastrointestinal perforation);\u003cbr\u003e - constipation;\u003cbr\u003e - blood in vomit (haematemesis);\u003cbr\u003e - inflammation of the mouth associated with the presence of lesions (ulcerative stomatitis);\u003cbr\u003e - worsening of certain chronic inflammatory bowel diseases (colitis and Crohn's disease);\u003cbr\u003e - hearing disorders, perception of ringing in the ear (tinnitus);\u003cbr\u003e - vision disorders (blurred vision, amblyopia and difficulty distinguishing colours);\u003cbr\u003e - alteration of platelet, white blood cell and red blood cell levels (thrombocytopenia, agranulocytosis, aplastic anaemia, haemolytic anaemia, granulocytopenia);\u003cbr\u003e - blood in the urine (haematuria);\u003cbr\u003e - difficulty passing urine (dysuria);\u003cbr\u003e - liver problems (hepatotoxicity);\u003cbr\u003e - altered liver function tests (elevated transaminases);\u003cbr\u003e - altered diagnostic tests (increased alkaline phosphatase, reduced haematocrit, prolonged bleeding time, decreased blood calcium*, increased uric acid*);\u003cbr\u003e - severe allergic reaction (anaphylaxis);\u003cbr\u003e - cerebrovascular accident*.\u003cbr\u003e * Effect of the NSAID class\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare\u003c\/b\u003e (may affect up to 1 in 10,000 people)\u003cbr\u003e - weakening of sensory and orientation functions (clouding of consciousness);\u003cbr\u003e - severe skin disorders (exfoliative dermatitis, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, allergic vasculitis);\u003cbr\u003e - kidney problems (interstitial nephritis, papillary necrosis, renal failure, including acute form);\u003cbr\u003e - altered diagnostic tests (decrease in haemoglobin level in the blood).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNot known\u003c\/b\u003e (frequency cannot be estimated from the available data)\u003cbr\u003e - decreased appetite and body weight (anorexia);\u003cbr\u003e - swelling of a part of the body due to fluid accumulation (edema);\u003cbr\u003e - fever;\u003cbr\u003e - heart problems (heart failure);\u003cbr\u003e - increased blood pressure (hypertension);\u003cbr\u003e - blood circulation problems (thrombosis);\u003cbr\u003e - decreased blood pressure (hypotension);\u003cbr\u003e - depression and mental problems (psychotic reaction);\u003cbr\u003e - infection of the membranes surrounding the brain without bacterial growth in culture (aseptic meningitis);\u003cbr\u003e - swelling affecting the connection point between the optic nerve and the eye (papilledema);\u003cbr\u003e - drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell);\u003cbr\u003e - worsening of skin rashes;\u003cbr\u003e - unexpected and exaggerated skin manifestations on exposure to the sun (photosensitivity reaction);\u003cbr\u003e - anaemia;\u003cbr\u003e - muscle stiffness;\u003cbr\u003e - increased uric acid levels in the blood (hyperuricemia);\u003cbr\u003e - poor elimination of sodium and fluids manifested by swelling (edema);\u003cbr\u003e - menstrual cycle disorders;\u003cbr\u003e - liver inflammation (hepatitis), liver damage, jaundice;\u003cbr\u003e - altered kidney function test;\u003cbr\u003e - severe clinical reaction triggered in a sensitised subject on contact with a specific allergen (anaphylactic shock);\u003cbr\u003e - burning and pain in the throat (throat irritation);\u003cbr\u003e - a widespread, red and scaly rash, with the formation of pustules under the skin and blisters located mainly on skin folds, on the trunk and on the upper limbs accompanied by fever at the beginning of treatment (acute generalised exanthematous pustulosis). Stop using SPIDIDOL if you develop these symptoms and contact your doctor immediately.\u003cbr\u003e See also paragraph 2;\u003cbr\u003e - chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ZAMBON ITALIA Srl","offers":[{"title":"Default Title","offer_id":46290094489867,"sku":"039600022","price":7.29,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_3301695d-2d46-48d9-befb-4c8c9b06beb5.png?v=1734080197"},{"product_id":"aspirina-dolore-inf-8cpr-500mg","title":"ASPIRIN PAIN INF*8TAB 500MG","description":"\u003cp\u003e\u003cb\u003eAspirin Pain and Inflammation\u003c\/b\u003e\u003cbr\u003e500 mg film-coated tablets\u003cbr\u003eAcetylsalicylic acid\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eAspirin Pain and Inflammation contains acetylsalicylic acid. Acetylsalicylic acid is an analgesic (reduces pain) and antipyretic (reduces fever).\u003cbr\u003eAspirin Pain and Inflammation is used for the symptomatic treatment of fever and\/or mild to moderate pain, such as headache, flu syndrome, toothache, muscle pain.\u003cbr\u003e\u003cb\u003eAspirin Pain and Inflammation is specifically reserved for adults and adolescents aged 16 years and over.\u003c\/b\u003e\u003cbr\u003ePlease consult your doctor or pharmacist for other forms of acetylsalicylic acid for patients weighing less than 40 kg.\u003cbr\u003e\u003cbr\u003eConsult your doctor if you do not notice improvement or if your symptoms worsen after 3 days (for fever) or 3-4 days (for pain).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Aspirin Pain and Inflammation:\u003c\/b\u003e\u003cbr\u003e• if you are allergic to acetylsalicylic acid or other salicylates or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e• if you have suffered from asthma or allergic reactions (e.g. urticaria, angioedema, severe rhinitis, shock) induced by the administration of acetylsalicylic acid or related medicines (in particular non-steroidal anti-inflammatory drugs);\u003cbr\u003e• if you suffer from a gastric or intestinal ulcer (including duodenal);\u003cbr\u003e• if you suffer from a bleeding condition or are at risk of bleeding;\u003cbr\u003e• if you suffer from severe liver, kidney or heart failure;\u003cbr\u003e• if you are taking methotrexate therapy in doses greater than 15 mg\/week;\u003cbr\u003e• if you are taking oral anticoagulants (medicines to thin the blood and prevent clot formation);\u003cbr\u003e• if you are beyond the 5th month of pregnancy (more than 24 weeks of amenorrhea);\u003cbr\u003e• Children and adolescents under 16 years of age.\u003cbr\u003e\u003cbr\u003eIf in doubt, consult your doctor or pharmacist before taking this medicine.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Aspirin Pain and Inflammation:\u003cbr\u003e\u003cbr\u003e• if you are taking other products containing acetylsalicylic acid, to avoid the risk of overdose;\u003cbr\u003e• if you experience a headache while taking high doses of acetylsalicylic acid for a prolonged period of time, do not increase the dosage but rather seek advice from your doctor or pharmacist;\u003cbr\u003e• if you use painkillers regularly, especially different painkillers in combination, this can lead to reduced kidney function;\u003cbr\u003e• if you have G6PD deficiency (Glucose-6-phosphate dehydrogenase), a hereditary disease affecting red blood cells, because high doses of acetylsalicylic acid could lead to hemolysis (destruction of red blood cells);\u003cbr\u003e• if you have a history of gastric or intestinal ulcers, or gastric or intestinal bleeding or gastritis;\u003cbr\u003e• if you suffer from liver or kidney failure;\u003cbr\u003e• if you suffer from asthma: the occurrence of an asthma attack, in some patients, may be linked to an allergic reaction to non-steroidal anti-inflammatory drugs or acetylsalicylic acid. In this case, the use of this medicine is not recommended;\u003cbr\u003e• in case of heavy menstruation;\u003cbr\u003e• if gastrointestinal bleeding occurs during treatment (blood loss from the mouth, blood in the stools, dark stools): stop treatment and immediately call your doctor or emergency room;\u003cbr\u003e• if you are also taking medicines that thin the blood and prevent its coagulation (anticoagulants);\u003cbr\u003e• if you suffer from mild or moderate renal impairment;\u003cbr\u003e• if you suffer from impaired cardiovascular circulation;\u003cbr\u003e• acetylsalicylic acid increases the risk of bleeding even at low doses and even several days after taking it. Inform your doctor, surgeon or anaesthetist or dentist if surgery is planned, even minor surgery;\u003cbr\u003e• acetylsalicylic acid changes the amount of uric acid in the blood. This must be taken into account if you are taking medication for gout;\u003cbr\u003e• It is recommended not to take this medicine during breastfeeding;\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren\u003c\/b\u003e\u003cbr\u003eReye's syndrome (a rare but very serious disease mainly associated with neurological and liver damage) has been observed in children with viral diseases who have been given acetylsalicylic acid. Consequently:\u003cbr\u003e• in case of viral disease such as flu or chickenpox, acetylsalicylic acid should not be given to a child without first consulting a doctor;\u003cbr\u003e• if signs of dizziness or fainting, behavioural changes or vomiting appear in a child taking acetylsalicylic acid, immediately notify the doctor.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everyone gets them.\u003cbr\u003eFrequencies: not known: frequency cannot be estimated from the available data.\u003cbr\u003e\u003cbr\u003e\u003cb\u003ePossible side effects due to acetylsalicylic acid are:\u003c\/b\u003e\u003cbr\u003eThese side effects are all very serious and you may need urgent medical attention or hospitalisation. Immediately inform your doctor or go to the nearest hospital if you notice any of the following symptoms:\u003cbr\u003e• bleeding (blood loss from the nose or gums, red spots under the skin);\u003cbr\u003e• allergic reactions such as skin rash, asthma attack or facial swelling accompanied by difficulty breathing;\u003cbr\u003e• headache, dizziness, sensation of hearing loss, tinnitus (ringing in the ears) which are usually signs of overdose;\u003cbr\u003e• cerebral haemorrhage;\u003cbr\u003e• stomach ache;\u003cbr\u003e• gastrointestinal haemorrhage. See Warnings and precautions section. These occur more frequently when high doses are taken;\u003cbr\u003e• Increase in liver enzymes, generally reversible upon discontinuation of treatment, altered liver function (particularly liver cells);\u003cbr\u003e• urticaria, skin reactions;\u003cbr\u003e• Reye's syndrome (altered state of consciousness or abnormal behaviour, or vomiting) in children with viral diseases taking acetylsalicylic acid (see Section 2: What you need to know before taking Aspirin Pain and Inflammation);\u003cbr\u003e• kidney impairment and acute kidney damage;\u003cbr\u003e• intestinal diaphragm disease (a narrowing of the intestine), especially in long-term treatment.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"BAYER SpA","offers":[{"title":"Default Title","offer_id":46290094752011,"sku":"041962010","price":4.36,"currency_code":"EUR","in_stock":true}]},{"product_id":"momendol-12cps-molli-220mg","title":"MOMENDOL*12 SOFTGELS 220MG","description":"\u003cp\u003e\u003cb\u003eMOMENDOL 220 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Naproxen sodium\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e Momendol contains naproxen, a medicine that belongs to the class of analgesic-anti-inflammatory drugs, which are drugs that fight pain and inflammation.\u003cbr\u003e Momendol is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 16 and over\u003c\/b\u003e for the short-term treatment of:\u003cbr\u003e - mild to moderate pain such as headaches, joint and muscle pain (e.g., back pain, stiff neck), toothaches, and menstrual pain;\u003cbr\u003e - fever.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse.\u003cbr\u003e Do not prolong treatment with Momendol for:\u003cbr\u003e - more than 7 days for pain;\u003cbr\u003e - more than 3 days for fever.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Momendol\u003c\/b\u003e\u003cbr\u003e - if you are allergic to naproxen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to substances closely related to naproxen from a chemical point of view;\u003cbr\u003e - if you suffer from allergic diseases, such as asthma, hives, runny nose (rhinitis), nasal polyps, swelling of the skin and mucous membranes (angioedema);\u003cbr\u003e - if you have had allergic reactions caused by acetylsalicylic acid, painkillers, anti-inflammatories or drugs used to treat rheumatism;\u003cbr\u003e - if you have suffered from gastrointestinal or other bleeding, such as cerebrovascular;\u003cbr\u003e - if you have had bleeding or perforation of the stomach or intestines in the past after taking medicines;\u003cbr\u003e - if you have had two or more distinct episodes of stomach ulcer or bleeding in the past;\u003cbr\u003e - if you have suffered from inflammation of the stomach lining (e.g., congestive gastropathy, atrophic gastritis);\u003cbr\u003e - if you have an active stomach or duodenal ulcer;\u003cbr\u003e - if you suffer from inflammatory bowel diseases (e.g., ulcerative colitis and Crohn's disease);\u003cbr\u003e - if you are under 16 years of age;\u003cbr\u003e - if you are pregnant or breastfeeding (see section Pregnancy and breastfeeding);\u003cbr\u003e - if you have severe heart disease;\u003cbr\u003e - if you have severe liver or kidney disease;\u003cbr\u003e - if you are taking high doses of diuretics (medicines to treat high blood pressure) (see section Other medicines and Momendol);\u003cbr\u003e - if you have ongoing bleeding or are taking anticoagulants (blood thinners) and are at risk of bleeding.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e In general, side effects can be minimized by using the lowest effective dose for the shortest possible duration of treatment needed to control symptoms, especially in elderly patients.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eConsult your doctor or pharmacist before taking Momendol:\u003c\/b\u003e\u003cbr\u003e - if you are taking other anti-inflammatory medicines (including selective COX-2 inhibitors and some NSAIDs) because they could cause a modest increased risk of heart attack (myocardial infarction) or lack of blood supply to the brain (stroke) (see section Other medicines and Momendol);\u003cbr\u003e - if you suffer from high blood pressure and\/or have non-severe heart disease, as fluid retention, increased blood pressure, and swelling have been observed following treatment with NSAIDs;\u003cbr\u003e - if you suspect you have an infection;\u003cbr\u003e - if you are elderly, know you have non-severe kidney, liver or heart problems, or are using an anti-inflammatory medicine for a prolonged period; in these cases, your doctor will advise you to start treatment with the lowest dose and possibly the simultaneous use of stomach-protective drugs;\u003cbr\u003e - if you habitually drink high doses of alcohol;\u003cbr\u003e - if you want to take Momendol for stomach pain;\u003cbr\u003e - if in the past you suffered from non-severe stomach and\/or intestinal problems due to a medicine;\u003cbr\u003e - if you are taking anti-inflammatory drugs (oral corticosteroids), blood thinners (anticoagulants such as warfarin) or antidepressants (selective serotonin reuptake inhibitors);\u003cbr\u003e - if you are taking Aspirin\/acetylsalicylic acid to prevent blood clots;\u003cbr\u003e - severe skin reactions, including exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in association with Momendol. If you notice any of the symptoms related to these severe skin reactions, described in section 4, stop treatment with Momendol and contact your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStop treatment with Momendol and consult your doctor or pharmacist if, during the use of Momendol:\u003c\/b\u003e\u003cbr\u003e - visual disturbances appear;\u003cbr\u003e - you have an infection or notice an worsening of an infection;\u003cbr\u003e - in case of a wound, you notice a prolonged bleeding time;\u003cbr\u003e - you experience sudden and intense abdominal pain;\u003cbr\u003e - particularly in the first few days of treatment, any unusual symptoms in the stomach and\/or intestines (especially bleeding) appear;\u003cbr\u003e - particularly in the first month of treatment, changes in the skin or mucous membranes or any other sign of hypersensitivity appear, which could be signs of severe allergic reactions (exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis).\u003cbr\u003e \u003cbr\u003e Your doctor will monitor your kidney function:\u003cbr\u003e - if you are elderly;\u003cbr\u003e - if you suffer from diseases that impair kidney function and diuresis (the process that allows urine formation);\u003cbr\u003e - if you are taking diuretics (medicines used to treat high blood pressure and that increase the amount of urine);\u003cbr\u003e - if you have recently undergone surgery involving hypovolemia (decrease in blood volume).\u003cbr\u003e \u003cbr\u003e During treatment with Momendol, your doctor will monitor you carefully:\u003cbr\u003e - if you have diseases that affect blood clotting;\u003cbr\u003e - if you are taking medicines that can affect blood clotting.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Momendol can be used in adolescents aged 16 and over.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e \u003cbr\u003e The use of Momendol can cause side effects that are generally mild to moderate (nausea, vomiting, diarrhea, flatulence, constipation, dyspepsia (indigestion), abdominal pain), or more serious, allergic reactions.\u003cbr\u003e \u003cbr\u003e If you develop an ulcer, or stomach bleeding with melena (black stools), hematemesis (vomiting blood) and\/or intestinal bleeding, or skin and\/or mucous membrane lesions, you should stop treatment with Momendol and contact your doctor.\u003cbr\u003e Furthermore, if you experience any of the following symptoms, \u003cb\u003eSTOP using\u003c\/b\u003e Momendol immediately and contact your doctor or the nearest hospital where you will undergo appropriate and specific treatment:\u003cbr\u003e • skin rashes or lesions\u003cbr\u003e • mucous membrane lesions\u003cbr\u003e • signs of allergic reaction (erythema, itching, hives)\u003cbr\u003e • peeling skin\u003cbr\u003e • severe skin rash or skin exfoliation (toxic epidermal necrolysis, Stevens-Johnson syndrome)\u003cbr\u003e • bleeding, ulcer and perforation of the stomach and intestines, which can be fatal, particularly in the elderly\u003cbr\u003e • visual disturbances\u003cbr\u003e • edema, hypertension and heart failure.\u003cbr\u003e \u003cbr\u003e The risk of experiencing such symptoms is higher in the early stages of therapy. In most cases, the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e Side effects can be minimized by using the lowest effective dose for the shortest possible duration of treatment needed to control symptoms.\u003cbr\u003e \u003cbr\u003e In addition, you may experience other side effects, listed below by frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • nausea\u003cbr\u003e • indigestion (dyspepsia)\u003cbr\u003e • vomiting\u003cbr\u003e • heartburn (pyrosis)\u003cbr\u003e • stomach pain (gastralgia)\u003cbr\u003e • gas (flatulence)\u003cbr\u003e • headache (cephalalgia)\u003cbr\u003e • drowsiness\u003cbr\u003e • dizziness\u003cbr\u003e • lightheadedness\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • diarrhea\u003cbr\u003e • constipation\u003cbr\u003e • sleep disorders, insomnia and somnolence\u003cbr\u003e • excitement\u003cbr\u003e • visual disturbances\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • hearing disturbances\u003cbr\u003e • allergic reactions with swelling and angioedema\u003cbr\u003e • chills\u003cbr\u003e • skin rash\u003cbr\u003e • itching\u003cbr\u003e • swelling (edema)\u003cbr\u003e • bruising (ecchymosis)\u003cbr\u003e • reduced kidney function\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • stomach or intestinal ulcer\u003cbr\u003e • stomach or intestinal bleeding\u003cbr\u003e • stomach or intestinal perforation\u003cbr\u003e • blood in vomit (hematemesis)\u003cbr\u003e • lesions inside the mouth (ulcerative stomatitis)\u003cbr\u003e • worsening of colitis\u003cbr\u003e • worsening of a chronic inflammatory bowel disease (Crohn's disease)\u003cbr\u003e • kidney inflammation (glomerulonephritis)\u003cbr\u003e • muscle weakness and pain (myalgia)\u003cbr\u003e • fever\u003cbr\u003e • increase and decrease in blood glucose\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation inside the mouth (stomatitis), aphthous ulcers\u003cbr\u003e • inflammatory disease of the colon and intestine (colitis), pancreas (pancreatitis) and esophagus (esophagitis)\u003cbr\u003e • yellowish skin discoloration (jaundice)\u003cbr\u003e • liver inflammation (hepatitis)\u003cbr\u003e • reduced liver function\u003cbr\u003e • decrease in hemoglobin, a substance that carries oxygen in the blood (aplastic or hemolytic anemia)\u003cbr\u003e • reduction in the number of platelets in the blood (thrombocytopenia)\u003cbr\u003e • decreased number of white blood cells (granulocytopenia, leukopenia) up to complete absence (agranulocytosis)\u003cbr\u003e • increase in blood cells called eosinophils (eosinophilia)\u003cbr\u003e • difficulty breathing (dyspnea, asthma), eosinophilic pneumonia, alveolitis\u003cbr\u003e • sensitivity to light (photosensitivity)\u003cbr\u003e • decrease in the amount of hair (alopecia)\u003cbr\u003e • skin rash with blisters (vesicular eruption) or with nodules, pustules or reddish spots\u003cbr\u003e • reddish cockade-like patches on the skin (erythema multiforme)\u003cbr\u003e • redness and blisters (fixed erythema)\u003cbr\u003e inflammatory reaction with the formation of small purplish papules (lichen planus)\u003cbr\u003e • sweating\u003cbr\u003e • systemic lupus erythematosus (chronic autoimmune disease)\u003cbr\u003e • accelerated heartbeat (tachycardia)\u003cbr\u003e • swelling (edema) and inflammation of the vessels (vasculitis)\u003cbr\u003e • high blood pressure (hypertension)\u003cbr\u003e • heart failure (severe heart disease)\u003cbr\u003e • kidney failure\u003cbr\u003e • inflammation or damage to the kidney with loss of protein and blood in the urine\u003cbr\u003e • increase in blood potassium\u003cbr\u003e • increase in blood creatinine\u003cbr\u003e • symptoms such as fever, drowsiness, headache, sensitivity to light in patients with immune system diseases (meningitis-like symptoms) and convulsions\u003cbr\u003e • cognitive disorders\u003cbr\u003e • thirst and malaise\u003cbr\u003e • depression and difficulty concentrating and thinking\u003cbr\u003e • inflammation of the anterior part of the optic nerve (papillitis)\u003cbr\u003e • inflammation of the posterior part of the optic nerve (retrobulbar optic neuritis)\u003cbr\u003e • swelling of the papilla at the back of the eye (papilledema)\u003cbr\u003e • hearing loss.\u003cbr\u003e \u003cbr\u003e Not known: frequency cannot be estimated from the available data\u003cbr\u003e \u003cbr\u003e Stop taking Momendol and contact your doctor immediately if you notice any of the following side effects:\u003cbr\u003e \u003cbr\u003e -Extensive skin rash, high body temperature, increased liver enzymes, blood abnormalities (eosinophilia), enlarged lymph nodes and involvement of other organs (drug reaction with eosinophilia and systemic symptoms, also known as DRESS). See also section 2.\u003cbr\u003e \u003cbr\u003e -A distinctive allergic skin reaction known as fixed drug eruption, which usually recurs in the same location(s) upon re-exposure to the medicine and may appear as round or oval patches with redness and skin swelling, rash with blisters (hives), itching sensation.\u003cbr\u003e \u003cbr\u003e • stomach inflammation (gastritis)\u003cbr\u003e \u003cbr\u003e Other side effects that have been reported with other medicines similar to Momendol and which therefore may also be potential side effects of Momendol:\u003cbr\u003e • allergic reactions, including severe ones.\u003cbr\u003e Characteristic symptoms of a severe allergic reaction are: severe and sudden low blood pressure, accelerated or slowed heartbeat, unusual tiredness or weakness, anxiety, agitation, loss of consciousness, difficulty breathing or swallowing, itching, hives with or without skin swelling, skin redness, nausea, vomiting, abdominal pain with cramps, diarrhea.\u003cbr\u003e Medicines similar to Momendol may be associated with a modest increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290098684171,"sku":"025829223","price":8.81,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_38ad55e3-b4cf-4727-9a42-44ac5cd8abba.png?v=1734080281"},{"product_id":"okitask-10cpr-riv-40mg","title":"OKITASK*10FC 40MG","description":"\u003cp\u003e\u003cb\u003eOkitask 40 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ketoprofen lysine salt\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eOkitask contains ketoprofen, which belongs to a group of medicines called \"Non-Steroidal Anti-Inflammatory Drugs\" (NSAIDs). Ketoprofen blocks the chemicals that cause inflammation.\u003cbr\u003e Okitask is indicated for treating pain of various origins and natures, and in particular: headaches, toothaches, neuralgia (nerve pain), menstrual pain, muscle pain, and osteoarticular pain (bone and joint pain).\u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Okitask:\u003c\/b\u003e\u003cbr\u003e - If you are allergic to ketoprofen, other non-steroidal anti-inflammatory drugs (NSAIDs), or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - If you have a history of hypersensitivity reactions (allergy) triggered by the use of ketoprofen or substances with a similar mechanism of action, for example, acetylsalicylic acid or other NSAIDs (other anti-inflammatories) such as asthma (bronchial inflammation and airway narrowing), bronchospasm (constriction of the bronchi), allergic rhinitis (allergic inflammation of the nasal mucosa), urticaria, skin rashes, nasal polyps, angioneurotic edema (swelling of the skin and mucous membranes) or other allergic reactions;\u003cbr\u003e - If you suffer from bronchial asthma (bronchial inflammation and airway narrowing);\u003cbr\u003e - If you have severe heart failure (inability of the heart to pump the adequate amount of blood needed by the body's needs);\u003cbr\u003e - If you suffer from gastritis (inflammation of the stomach lining);\u003cbr\u003e - If you currently have a peptic ulcer (a lesion of the stomach or the first part of the intestine) or bleeding, or if you have suffered in the past from recurrent bleeding or peptic ulcer (two or more distinct, proven episodes of bleeding or ulceration);\u003cbr\u003e - If you have suffered in the past from gastrointestinal bleeding, ulceration, or perforation or chronic dyspepsia (difficult digestion);\u003cbr\u003e - If you have a history of gastrointestinal bleeding or perforation resulting from previous NSAID therapy;\u003cbr\u003e - If you suffer from Crohn's disease (inflammation of the intestine) or ulcerative colitis (inflammation of the intestine with ulcers);\u003cbr\u003e - If you have severe hepatic insufficiency (reduced liver function due to liver cirrhosis, severe hepatitis) or renal insufficiency (reduced kidney function);\u003cbr\u003e - If you suffer from leukopenia (reduction in the number of white blood cells) or thrombocytopenia (reduction in the number of platelets);\u003cbr\u003e - If you suffer from hemorrhagic diathesis (predisposition to develop hemorrhages) and other coagulation disorders or if you have hemostatic disorders (difficulty in stopping bleeding);\u003cbr\u003e - If you are being treated with a high dose of diuretics;\u003cbr\u003e - If you are in the third trimester of pregnancy;\u003cbr\u003e - If the person to be treated is under 15 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Okitask.\u003cbr\u003e  \u003cu\u003e\u003cem\u003eWarnings\u003c\/em\u003e\u003c\/u\u003e\u003cbr\u003e  Undesirable effects can be minimized by using the lowest effective dose for the shortest possible duration of treatment needed to control symptoms (see How to take Okitask and the paragraphs below on gastrointestinal and cardiovascular risks).\u003cbr\u003e  The concomitant use of Okitask with other anti-inflammatories should be avoided. During treatment with all NSAIDs, such as Okitask, at any time, with or without warning symptoms or a previous history of serious gastrointestinal events, gastrointestinal bleeding, ulceration, and perforation, which can be fatal, have been reported. Patients who have previously suffered from these conditions have a higher risk (see Do not take Okitask).\u003cbr\u003e  Report any abdominal signs or symptoms (including gastrointestinal bleeding) even at the beginning of treatment. Inform your doctor if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (medicines used for the treatment of inflammatory conditions), anticoagulants (medicines that slow down blood clotting), such as warfarin, selective serotonin reuptake inhibitors (medicines used for the treatment of depression), or antiplatelet agents (medicines that prevent platelet aggregation) such as acetylsalicylic acid (see Other medicines and Okitask).\u003cbr\u003e  The elderly are more exposed to the risk of developing adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforations, which can be fatal. \u003cb\u003eImmediately suspend treatment with Okitask at the first signs of gastrointestinal bleeding or ulceration.\u003c\/b\u003e\u003cbr\u003e  Severe skin reactions, some of which fatal, such as exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see Possible side effects). The reaction occurs in most cases in the early stages of treatment. Discontinue the use of Okitask if a rash, mucosal lesions, or any other sign of hypersensitivity (allergic reaction) appears.\u003cbr\u003e  \u003cbr\u003e  \u003cem\u003ePrecautions\u003c\/em\u003e\u003cbr\u003e  \u003cb\u003eAsk your doctor or pharmacist for advice before taking Okitask\u003c\/b\u003e\u003cbr\u003e  - If your kidneys are not working well because in this case Okitask should be taken with caution. If you use Okitask, you should monitor your kidneys, especially if you are elderly or if you are being treated with diuretics (medicines that lower blood pressure).\u003cbr\u003e  - If you have liver problems, you should have periodic check-ups.\u003cbr\u003e  - If you have an infection - see the Infections paragraph below.\u003cbr\u003e  - If you suffer from uncontrolled hypertension (high blood pressure), congestive heart failure (accumulation of fluid in the lungs, abdominal organs, and peripheral tissues due to inadequate heart pump function), confirmed ischemic heart disease (heart disease that occurs following a reduction in blood flow due to narrowing of the coronary arteries), peripheral arterial disease and\/or cerebrovascular disease (disease of the arteries and blood vessels of the brain), as you should only take Okitask after careful medical evaluation.\u003cbr\u003e  - If you have risk factors for these conditions, for example, if you have high blood pressure, diabetes (disease caused by high blood glucose levels), hyperlipidemia (high levels of fats in the blood), if you smoke.\u003cbr\u003e  - If you have allergic manifestations or have suffered from allergies in the past, as the medicine should be administered with caution.\u003cbr\u003e  - If you suffer from bronchial asthma (bronchial inflammation and airway narrowing) or allergic diathesis (predisposition to the onset of allergy), chronic rhinitis (inflammation of the nasal mucosa) and allergic rhinitis (allergic inflammation of the nasal mucosa), chronic sinusitis and\/or nasal polyposis.\u003cbr\u003e  - If you suffer from hematopoietic alterations (which modify the formation and maturation of blood cells), systemic lupus erythematosus (immune system disease) or mixed connective tissue diseases, as Okitask should be used with caution.\u003cbr\u003e  - If you have hepatic porphyria (rare blood disease characterized by altered activity of one of the liver enzymes), as the medicine could trigger an attack.\u003cbr\u003e  Some NSAIDs may be associated with an increased risk of arterial thrombotic events (e.g., heart attack or stroke). Currently, there is insufficient data to exclude a similar risk for OKITASK. An increased risk of atrial fibrillation (alteration of the heart rhythm) associated with the use of NSAIDs has been reported. Hyperkalemia (increased amount of potassium in the blood) may occur, especially if you suffer from diabetes, renal insufficiency, and\/or are being treated with medicines that can cause hyperkalemia (see Other medicines and Okitask). In these circumstances, potassium levels should be monitored periodically.\u003cbr\u003e  \u003cbr\u003e  Infections\u003cbr\u003e  Okitask can mask the symptoms of infections such as fever and pain. Therefore, it is possible that Okitask may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the infection symptoms persist or worsen, contact your doctor immediately.\u003cbr\u003e  Consult your doctor if you experience vision problems, such as blurred vision, as treatment must be discontinued.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everyone gets them.\u003cbr\u003e  The most commonly observed adverse events are gastrointestinal in nature.\u003cbr\u003e  The following adverse reactions have been observed with the use of ketoprofen in adults:\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eCommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e  - dyspepsia (difficult digestion), nausea, abdominal pain and vomiting.\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e  - headache, dizziness, drowsiness, constipation, diarrhea, flatulence (emission of intestinal gas from the anus), gastritis (inflammation of the stomach lining)\u003cbr\u003e  - rash, itching and fatigue\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e  - hemorrhagic anemia (reduction of hemoglobin in the blood, a substance that carries oxygen in the blood caused by bleeding)\u003cbr\u003e  - paraesthesia (sensation of numbness, tingling)\u003cbr\u003e  - blurred vision (see Warnings and precautions)\u003cbr\u003e  - tinnitus (persistent perception of noises in the ear)\u003cbr\u003e  - asthma (bronchial inflammation and airway narrowing)\u003cbr\u003e  - stomatitis (inflammation of the mucous membranes lining the mouth), peptic ulcer (lesion of the stomach or the first part of the intestine)\u003cbr\u003e  - hepatitis (inflammation of the liver), increased transaminases (increase in certain enzymes indicating liver function), increased bilirubin (a substance indicating liver function)\u003cbr\u003e  - increased weight.\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e  - edema (swelling) of the face and erythema (redness of the skin)\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eFrequency not known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e  - thrombocytopenia (reduction in the number of platelets), agranulocytosis (severe reduction in the number of a type of white blood cells), bone marrow failure (reduction in the production of blood cells by the bone marrow), hemolytic anemia (reduction of hemoglobin in the blood, a substance that carries oxygen in the blood, caused by the destruction of red blood cells), leukopenia (decrease in the number of white blood cells), neutropenia (decrease in the number of a type of white blood cells), aplastic anemia (reduction of hemoglobin in the blood, a substance that carries oxygen in the blood, caused by insufficient production of blood cells by the bone marrow), leukocytosis (increase in the number of white blood cells), thrombocytopenic purpura (presence of spots on the skin due to a reduction in the number of platelets)\u003cbr\u003e  - anaphylactic reaction (severe allergic reaction, including shock), hypersensitivity (allergy)\u003cbr\u003e  - jaundice (yellowing of the skin and the whites of the eyes)\u003cbr\u003e  - depression, hallucination (perception of non-existent things in reality), confusional state, altered mood, agitation, insomnia, convulsions (uncontrolled body movements), dizziness, dysgeusia (altered taste), tremor, dyskinesia (involuntary movements), syncope (fainting), hyperkinesia (involuntary and uncoordinated movements), periorbital edema (swelling around the eye), peripheral edema\u003cbr\u003e  - chills, asthenia (weakness)\u003cbr\u003e  - heart failure (inability of the heart to pump the adequate amount of blood needed by the body's needs), atrial fibrillation (altered heart rhythm), palpitations (perception of heart beat), tachycardia (increase in heart rate), hypertension (high blood pressure), hypotension (low blood pressure)\u003cbr\u003e  - vasodilation (dilation of blood vessels), vasculitis (inflammation of vessels), including leukocytoclastic vasculitis (inflammation of small vessels)\u003cbr\u003e  - bronchospasm (constriction of the bronchi), especially in patients with confirmed hypersensitivity to acetylsalicylic acid and other NSAIDs, rhinitis (inflammation of the nasal mucosa), dyspnea (difficult breathing), laryngeal edema (swelling of the throat due to fluid accumulation), laryngospasm (narrowing of the larynx), acute respiratory failure (one fatal case has been reported in an asthmatic patient sensitive to acetylsalicylic acid)\u003cbr\u003e  - exacerbation of colitis (worsening of intestinal inflammation), exacerbation of Crohn's disease (worsening of intestinal inflammation), gastrointestinal bleeding (stomach or intestinal bleeding), gastrointestinal perforation (sometimes fatal, particularly in the elderly, see Warnings), gastric ulcer (stomach lesion), mouth ulceration, duodenal ulcer (lesion of the first part of the intestine), duodenal perforation, heartburn (stomach burning), mouth edema (swelling of the mouth), pancreatitis (inflammation of the pancreas), melena (presence of digested blood in stools), hematemesis (vomiting blood), abdominal discomfort, colitis, hyperchlorhydria (excess stomach acid), stomach pain, erosive gastritis (severe inflammation of the stomach lining), tongue edema (swelling of the tongue)\u003cbr\u003e  - photosensitivity reactions (sensitivity reaction to sunlight or UV lamps), alopecia (hair loss), urticaria, angioedema (swelling of the face, lips, mouth, tongue or throat that can cause difficulty breathing and swallowing), bullous eruptions including Stevens-Johnson syndrome, Lyell's syndrome and toxic epidermal necrolysis (severe skin reactions), edema (fluid retention), exanthema (skin rash), maculopapular exanthema (skin rash with patches), purpura (purplish spots on the skin due to abnormal blood accumulation), acute generalized exanthematous pustulosis (skin rash with formation of purulent collections), dermatitis (skin irritation)\u003cbr\u003e  - acute renal failure (reduced kidney function), tubulointerstitial nephritis, nephritis and nephritic syndrome (inflammation of the kidneys), nephrotic syndrome (renal disorder involving protein loss in the urine), glomerulonephritis (inflammatory kidney disease), water\/sodium retention with possible edema (accumulation of water and sodium causing swelling), acute tubular necrosis and renal papillary necrosis (severe kidney damage), oliguria (decreased urine production), abnormal kidney function test, hematuria (presence of blood in the urine)\u003cbr\u003e  - aseptic meningitis (inflammation of the membranes covering the brain not caused by infection), lymphangitis (inflammation of the lymphatic vessels)\u003cbr\u003e  - hyperkalemia (increased amount of potassium in the blood) and hyponatremia (decreased amount of sodium in the blood).\u003cbr\u003e  \u003cbr\u003e  Adherence to the instructions in the package leaflet reduces the risk of side effects.\u003cbr\u003e  \u003cbr\u003e   \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"DOMPE' FARMACEUTICI SpA","offers":[{"title":"Default Title","offer_id":46290104713483,"sku":"042028035","price":5.12,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_6bf2cfa2-7c02-43ca-9787-c37e32be478a.png?v=1734080361"},{"product_id":"momentact-30cpr-riv-400mg","title":"MOMENTACT*30COATED TABS 400MG","description":"\u003cp\u003e\u003cb\u003eMOMENTACT 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMomentact contains ibuprofen, a medicine belonging to the class of analgesic-anti-inflammatory drugs, i.e., medicines that fight pain and inflammation.\u003cbr\u003e \u003cbr\u003e Momentact is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents from 12 years of age\u003c\/b\u003e to treat:\u003cbr\u003e - various types of pain (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain) and to help reduce the symptoms of fever and flu.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Momentact:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to other anti-rheumatic medicines (e.g., acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see section Other medicines and Momentact), or allergic to any of the other ingredients of this medicine;\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breastfeeding (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have previously experienced bleeding or perforation of the stomach or intestine after taking medicines;\u003cbr\u003e - if you have previously had two or more distinct episodes of ulcer or stomach bleeding;\u003cbr\u003e - in the presence of severe heart disease;\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea, or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eWhat you need to know before taking Momentact\u003cbr\u003e \u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck (angioedema), and chest pain, have been reported with ibuprofen. Stop Momentact immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003e Severe skin reactions have been reported in association with ibuprofen treatment, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalised exanthematous pustulosis (AGEP).\u003cbr\u003e Stop taking Momentact and consult your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.\u003cbr\u003e \u003cbr\u003e Talk to your doctor or pharmacist before taking Momentact:\u003cbr\u003e - if you have had episodes of breathing difficulties (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, runny nose (chronic rhinitis), nasal polyps (nasal polyposis) or inflammation of the nasal mucosa (sinusitis) or suffer\/have suffered from allergies, as you may experience breathing difficulties (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used to treat joint or muscle pain, fever or inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as the risk of ulcers and bleeding may increase in these cases (see section Other medicines and Momentact);\u003cbr\u003e - if you are elderly or if you have suffered from ulcers, especially if the ulcer has also manifested with bleeding or perforation (see section Do not take Momentact), as the risk of bleeding, ulcer or perforation is higher with high doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly consult your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you are taking low doses of acetylsalicylic acid or medicines that may increase the risk of stomach and\/or intestinal diseases (see section Other medicines and Momentact);\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 Possible side effects);\u003cbr\u003e - if you have had stomach and intestinal diseases related to the use of medicines, and in particular if you are elderly, you should report any unusual intestinal symptoms (especially bleeding) to your doctor, particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcers or bleeding of the stomach and\/or intestine, such as oral corticosteroids (e.g., cortisone), anticoagulants (e.g., warfarin), antidepressants (serotonin inhibitors), or antiplatelet agents (e.g., acetylsalicylic acid). See also section Other medicines and Momentact. If gastrointestinal bleeding or ulceration occurs in patients taking Momentact, treatment should be discontinued;\u003cbr\u003e - if you have high blood pressure and the medicines you are taking cannot lower it and\/or you have heart or blood circulation diseases in the brain or periphery or think you may be at risk for these diseases (for example, if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or have heart disease, as fluid retention, increased blood pressure, and swelling have been observed after treatment with NSAIDs. NSAIDs can reduce the action of medicines to lower blood pressure (see section Other medicines and Momentact);\u003cbr\u003e - if you have lost a considerable amount of fluids, or if you experience swelling, heart problems or high blood pressure;\u003cbr\u003e - if you have reduced kidney function, heart or liver malfunction, or if you are elderly or are being treated with medicines for high blood pressure, as you may be more predisposed to kidney problems. In addition, the habitual concomitant use of several painkillers may further increase this risk;\u003cbr\u003e - if you suffer from heart disease;\u003cbr\u003e - if you suffer from liver diseases (hepatic dysfunction);\u003cbr\u003e - if you are elderly, as the risk of bleeding, ulcers and perforations is increased compared to other patients;\u003cbr\u003e - if you suffer from a coagulation disorder or are taking medicines to make the blood thinner (anticoagulants) (see section Other medicines and Momentact);\u003cbr\u003e - if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of aseptic meningitis have been observed in patients treated with ibuprofen.\u003cbr\u003e Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients who did not have concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section Other medicines and Momentact);\u003cbr\u003e - if you intend to become pregnant (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have difficulty becoming pregnant or are undergoing fertility investigations (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - If you have an infection - see section Infections below;\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if given in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss your therapy with your doctor or pharmacist before taking Momentact if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Medicines such as Momentact can:\u003cbr\u003e - be associated with the onset of even severe kidney diseases (such as renal papillary necrosis, analgesic nephropathy and kidney failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e - cause eye disorders, therefore in case of prolonged treatments, regular eye check-ups are recommended. If visual disturbances occur, stop treatment with Momentact.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Momentact can mask the symptoms of infections such as fever and pain. It is therefore possible that Momentact may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003e If the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Momentact can cause side effects, although not everyone gets them. The side effects of the medicine can be minimised if you use the lowest recommended dose, and if you use the medicine only for the period necessary to control your symptoms.\u003cbr\u003e \u003cbr\u003e If you get an ulcer, or stomach and\/or intestinal bleeding, or skin and\/or mucous membrane lesions appear, you must stop treatment with Momentact and contact your doctor. Usually, these side effects are more frequent in the elderly.\u003cbr\u003e \u003cbr\u003e The use of Momentact can cause side effects that are generally mild or moderate or more severe, allergic reactions, albeit rarely.\u003cbr\u003e \u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP IMMEDIATELY\u003c\/b\u003e using Momentact and contact your doctor or the nearest hospital where you will undergo appropriate and specific treatment:\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucous membrane lesions;\u003cbr\u003e • signs of an allergic reaction, even severe (rashes, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • peeling skin;\u003cbr\u003e • reddish, non-raised, target-shaped or circular spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson syndrome);\u003cbr\u003e • widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalised exanthematous pustulosis);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • liver disease (hepatic dysfunction);\u003cbr\u003e • bleeding, ulcer and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e \u003cbr\u003e In the event of an allergic reaction among those listed above, go to the hospital as immediate availability of appropriate equipment, medicines and personnel suitable for emergency treatment is necessary, as in rare cases, following the use of ibuprofen, serious, sometimes fatal, side effects have been reported, even in the absence of known allergy.\u003cbr\u003e \u003cbr\u003e The risk of experiencing these symptoms is higher in the early stages of therapy: in most cases, the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e In addition, you may experience further side effects that have also been reported with other medicines similar to Momentact and which are listed below according to frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness\u003cbr\u003e • malaise\u003cbr\u003e • fatigue\u003cbr\u003e \u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the stomach (gastritis)\u003cbr\u003e • insomnia, anxiety\u003cbr\u003e • numbness of the limbs or other parts of the body, drowsiness\u003cbr\u003e • nasal congestion (rhinitis)\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnoea)\u003cbr\u003e • momentary interruption of breathing (apnoea)\u003cbr\u003e • hearing impairment\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • vertigo\u003cbr\u003e • liver disorders (altered liver function)\u003cbr\u003e • inflammation of the liver (hepatitis)\u003cbr\u003e • yellowing of the skin and eyes (jaundice)\u003cbr\u003e • kidney diseases (damage to kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and kidney failure)\u003cbr\u003e • hypersensitivity reactions such as skin rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), asthma, difficulty breathing (bronchospasm or dyspnoea), asthma attacks with lowering of blood pressure\u003cbr\u003e • skin reactions to light (photosensitivity)\u003cbr\u003e \u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leucopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia)\u003cbr\u003e • depression, confusion, hallucinations\u003cbr\u003e • inflammation of the optic nerve (optic neuritis)\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis), especially in patients with pre-existing autoimmune disorders (see section Warnings and precautions), with symptoms of neck stiffness, headache, nausea, vomiting, fever or disorientation\u003cbr\u003e • eye disorders with visual disturbances and optic nerve pathology (toxic optic neuropathy)\u003cbr\u003e • swelling due to fluid accumulation in the tissues\u003cbr\u003e • disease that can affect various organs and tissues of the body (lupus erythematosus)\u003cbr\u003e • worsening of inflammation caused by an existing infection (e.g., development of necrotising fasciitis)\u003cbr\u003e \u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis)\u003cbr\u003e • sensation of feeling one's own heartbeat (palpitations)*\u003cbr\u003e • heart disease (heart failure)*\u003cbr\u003e • heart attack (myocardial infarction)*\u003cbr\u003e • increased fluid around the lungs (acute pulmonary oedema)*\u003cbr\u003e • liver disease (hepatic failure)\u003cbr\u003e • hypertension*\u003cbr\u003e • severe allergic reactions, which may include symptoms such as swelling of the face, tongue and throat that make breathing difficult, rapid heartbeat, severe allergic reaction of rapid onset and that can cause death (anaphylaxis), severe skin rash or exfoliation of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme)\u003cbr\u003e • severe skin and soft tissue infections can occur during chickenpox infection\u003cbr\u003e \u003cbr\u003e \u003cb\u003e*these side effects tend to resolve with discontinuation of treatment\u003cbr\u003e \u003cbr\u003e not known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach\u003cbr\u003e • nausea\u003cbr\u003e • vomiting\u003cbr\u003e • diarrhoea\u003cbr\u003e • flatulence\u003cbr\u003e • constipation\u003cbr\u003e • difficulty digesting\u003cbr\u003e • abdominal pain\u003cbr\u003e • heartburn\u003cbr\u003e • blood in the stools\u003cbr\u003e • blood in the vomit\u003cbr\u003e • lesions inside the mouth\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis, Crohn's disease)\u003cbr\u003e • increased risk of heart attack (myocardial infarction), or lack of blood flow to the brain (stroke)\u003cbr\u003e • high blood pressure\u003cbr\u003e • severe heart disease (heart failure)\u003cbr\u003e • a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swelling of the lymph nodes and an increase in eosinophils (a type of white blood cell)\u003cbr\u003e • a widespread, red and scaly rash, with the formation of pustules under the skin and vesicles located mainly on the skin folds, on the trunk and on the upper limbs accompanied by fever at the beginning of treatment (acute generalised exanthematous pustulosis). Stop using Momentact if you develop these symptoms and contact your doctor immediately. See also section 2\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290106220811,"sku":"035618204","price":11.85,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_da9ce2fa-7264-44e4-89ed-aff4dfc21bc9.png?v=1734080371"},{"product_id":"moment-24cpr-riv-200mg","title":"MOMENT*24FC 200MG","description":"\u003cp\u003e\u003cb\u003eMOMENT 200 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMoment contains ibuprofen, a medicine belonging to the class of analgesic-anti-inflammatories, i.e., drugs that combat pain and inflammation.\u003cbr\u003e \u003cbr\u003e Moment is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents from 12 years of age\u003c\/b\u003e for: - treatment of pain of various origins and natures (headaches, toothaches, neuralgia, osteo-articular and muscular pain, menstrual pain);\u003cbr\u003e - reduction of symptoms of feverish and flu-like states.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Moment:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you are allergic to other antirheumatic medicines (e.g., acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see paragraph Other medicines and Moment);\u003cbr\u003e - if the patient is under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breastfeeding (see paragraph Pregnancy, breastfeeding, and fertility);\u003cbr\u003e - if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have previously had bleeding or perforation of the stomach or intestines following the intake of medicines;\u003cbr\u003e - if you have previously had two or more distinct episodes of stomach ulcer or bleeding;\u003cbr\u003e - in the presence of severe heart diseases (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhea, or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. Stop Moment immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e Skin reactions\u003cbr\u003e Severe skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in paragraph 4.\u003cbr\u003e \u003cbr\u003e Talk to your doctor or pharmacist before taking Moment:\u003cbr\u003e - if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, runny nose (chronic rhinitis), nasal polyps (nasal polyposis) or inflammation of the paranasal sinus mucosa (sinusitis) or suffer\/have suffered from allergies because you could experience difficulty breathing (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see paragraph Other medicines and Moment);\u003cbr\u003e - if you are elderly or have suffered from an ulcer, especially if the ulcer has also manifested with bleeding or perforation (see paragraph Do not take Moment), as the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly contact your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you take low doses of acetylsalicylic acid or drugs that can increase the risk of stomach and\/or intestinal diseases (see paragraph Other medicines and Moment);\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see paragraph 4 Possible side effects);\u003cbr\u003e - if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report any unusual intestinal symptoms (especially bleeding) to your doctor, particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of stomach and\/or intestinal ulcer or bleeding, such as oral corticosteroids (e.g., cortisone), anticoagulants (e.g., warfarin), antidepressants (selective serotonin reuptake inhibitors), or antiplatelet agents (e.g., acetylsalicylic acid). See also paragraph Other medicines and Moment. If gastrointestinal bleeding or ulceration occurs in patients taking Moment, treatment must be discontinued;\u003cbr\u003e - if you have high blood pressure and the medicines you are taking cannot lower it and\/or you have heart diseases or blood circulation problems in the brain or other body parts or think you may be at risk for these diseases (for example if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or have heart diseases, as fluid retention, increased blood pressure, and swelling have been found following treatment with NSAIDs. NSAIDs can reduce the action of medicines to lower blood pressure (see paragraph Other medicines and Moment);\u003cbr\u003e - if you have lost a considerable amount of fluids, or if swelling, heart problems, or high blood pressure appear;\u003cbr\u003e - if you have decreased kidney function, heart or liver malfunction, or if you are elderly or undergoing treatment with high blood pressure medications, as you may be more predisposed to the onset of kidney problems. Furthermore, the usual concomitant use of several painkillers can further increase this risk;\u003cbr\u003e - if you suffer from a coagulation disorder or are taking medicines that slow down blood clotting (anticoagulants) (see paragraph Other medicines and Moment);\u003cbr\u003e - if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as in rare occasions in patients undergoing treatment with ibuprofen, symptoms of aseptic meningitis have been observed. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue pathologies, it has also been observed in patients who did not manifest concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease, or high blood pressure (see paragraph Other medicines and Moment);\u003cbr\u003e - if you intend to become pregnant (see paragraph Pregnancy, breastfeeding, and fertility);\u003cbr\u003e - if you have difficulty becoming pregnant or are undergoing fertility investigations (see paragraph Pregnancy, breastfeeding, and fertility);\u003cbr\u003e - if you have an infection - see paragraph Infections below.\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss your therapy with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Medicines like Moment can:\u003cbr\u003e - be associated with the appearance of even severe kidney diseases (such as renal papillary necrosis, analgesic nephropathy, and kidney failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e - cause eye disorders, therefore, in case of prolonged treatments, periodic eye checks are recommended. If visual disturbances occur, stop treatment with Moment.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment can mask the symptoms of infections such as fever and pain. It is therefore possible that Moment may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003e If the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Moment can cause side effects, although not everybody gets them.\u003cbr\u003e The side effects of the drug can be minimized if you use the lowest recommended dose, and if you use the drug only for the period necessary to control your symptoms.\u003cbr\u003e \u003cbr\u003e If you develop an ulcer, or stomach and\/or intestinal bleeding, or skin and\/or mucous membrane lesions, you must stop treatment with Moment and contact your doctor. These side effects are usually more frequent in the elderly.\u003cbr\u003e \u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate, or more severe reactions, including allergic reactions, albeit rarely.\u003cbr\u003e \u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eIMMEDIATELY STOP using\u003c\/b\u003e Moment and contact your doctor or the nearest hospital immediately where you will undergo appropriate and specific treatment:\u003cbr\u003e • chest pain, which can be a sign of a potentially severe allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucous membrane lesions;\u003cbr\u003e • signs of an allergic reaction, even severe (erythema, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • peeling skin;\u003cbr\u003e • non-raised reddish spots, target-shaped or circular on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals, and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e • widespread rash, high body temperature, and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red, and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • liver disease (hepatic dysfunction);\u003cbr\u003e • bleeding, ulcer, and perforation of the stomach and intestines, which can be fatal, particularly in the elderly.\u003cbr\u003e \u003cbr\u003e In the event of an allergic reaction among those listed above, go to the hospital as it is necessary to have immediate availability of equipment, drugs, and personnel suitable for emergency treatment, as in rare cases, following the use of ibuprofen, severe adverse effects, sometimes fatal, have been reported even in the absence of known allergy.\u003cbr\u003e \u003cbr\u003e The risk of experiencing these symptoms is higher in the early stages of therapy: in most cases, the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e Furthermore, you may experience further side effects that have also been reported with other medicines similar to Moment and which are listed below according to frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue;\u003cbr\u003e \u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • stomach inflammation (gastritis);\u003cbr\u003e • insomnia, anxiety;\u003cbr\u003e • numbness of the limbs or other parts of the body (paresthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • temporary cessation of breathing (apnea);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • vertigo;\u003cbr\u003e • liver disorders (altered liver function);\u003cbr\u003e • liver inflammation (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney diseases (renal function damage and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome, and kidney failure);\u003cbr\u003e • hypersensitivity reactions such as skin rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnea), asthma attacks with possible lowering of blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity);\u003cbr\u003e \u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction of white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusion, hallucinations;\u003cbr\u003e • inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see paragraph Warnings and precautions), with symptoms of neck stiffness, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve pathology (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect several organs and tissues of the body (systemic lupus erythematosus syndrome);\u003cbr\u003e • worsening of inflammations caused by an already existing infection (e.g., development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase);\u003cbr\u003e • abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e \u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling one's own heartbeat (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (liver failure);\u003cbr\u003e • hypertension;\u003cbr\u003e • severe allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue, and throat making it difficult to breathe, fast heartbeat, severe rapidly developing allergic reaction that can cause death (anaphylaxis), severe rash or skin exfoliation (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • severe skin infections and soft tissue pathologies may occur during chickenpox infection.\u003cbr\u003e \u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomiting;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stools;\u003cbr\u003e • blood in the vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease);\u003cbr\u003e • increased risk of sudden reduction of blood circulation in the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red, and scaly rash, with pustules forming under the skin and blisters located mainly on skin lesions, on the trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using Moment if you develop these symptoms and contact your doctor immediately. See also paragraph 2.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290106319115,"sku":"025669072","price":10.09,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_a4a8199f-e5f4-4a00-9937-49bef25bc834.png?v=1734080378"},{"product_id":"brufen-analges-12cpr-riv-400mg","title":"BRUFEN ANALGES*12FC TAB 400MG","description":"\u003cp\u003e\u003cb\u003eBRUFEN ANALGESICO 200 mg film-coated tablets\u003cbr\u003eBRUFEN ANALGESICO 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003eIbuprofen (as lysine salt)\u003c\/p\u003e\n\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eBRUFEN ANALGESICO contains the active substance ibuprofen. It belongs to a group of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs). NSAIDs provide relief by modifying the body's response to pain and fever.\u003cbr\u003e\u003cbr\u003eBRUFEN ANALGESICO tablets are used for the symptomatic treatment of mild to moderate pain, such as headache, dental pain, menstrual pain, and pain and fever associated with the common cold.\u003c\/p\u003e\n\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take BRUFEN ANALGESICO:\u003c\/b\u003e\u003cbr\u003e• if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e• if you have suffered an allergic reaction, such as asthma, difficulty breathing, swelling of the face, tongue or throat, hives, runny and itchy nose, caused by acetylsalicylic acid (ASA) or other NSAIDs;\u003cbr\u003e• if you have (or have had two or more episodes of) stomach ulcer or bleeding;\u003cbr\u003e• if you have had gastrointestinal perforation or bleeding while using NSAIDs;\u003cbr\u003e• if you suffer from cerebrovascular bleeding or other active bleeding;\u003cbr\u003e• if you suffer from blood formation disorders of unknown nature;\u003cbr\u003e• if you have severe dehydration (caused by vomiting, diarrhoea or insufficient fluid intake);\u003cbr\u003e• if you suffer from severe liver, kidney or heart failure;\u003cbr\u003e• if you are in the last 3 months of pregnancy.\u003c\/p\u003e\n\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking BRUFEN ANALGESICO:\u003cbr\u003e• if you have recently undergone major surgery;\u003cbr\u003e• if you suffer or have suffered from asthma or an allergic disease, as difficulty breathing may occur;\u003cbr\u003e• if you suffer from hay fever, nasal polyps or chronic obstructive respiratory disease, as there is an increased risk of allergic reactions. Allergic reactions can occur as asthma attacks (so-called analgesic asthma), Quincke's oedema or hives;\u003cbr\u003e• if you suffer from heart problems;\u003cbr\u003e• if you have a history of gastrointestinal diseases (such as ulcerative colitis, Crohn's disease);\u003cbr\u003e• if you suffer from systemic lupus erythematosus or mixed connective tissue disease (a disease affecting the skin, joints and kidneys);\u003cbr\u003e• if you suffer from certain hereditary blood formation disorders (e.g. acute intermittent porphyria);\u003cbr\u003e• if you suffer from blood clotting disorders;\u003cbr\u003e• if you are taking other NSAIDs. Concomitant use with other NSAIDs, including specific cyclo-oxygenase-2 inhibitors, increases the risk of adverse reactions (see section Other medicines and BRUFEN ANALGESICO, below) and should be avoided;\u003cbr\u003e• if you have chickenpox, it is advisable to avoid using BRUFEN ANALGESICO;\u003cbr\u003e• if you are elderly;\u003cbr\u003e• if you have an infection - see paragraph Infections below.\u003cbr\u003e\u003cbr\u003ePatients with kidney or liver problems should consult a doctor before taking ibuprofen tablets.\u003cbr\u003e\u003cbr\u003eAnti-inflammatories such as ibuprofen may be associated with a small increased risk of heart attack (myocardial infarction) or stroke, particularly if given in high doses.\u003cbr\u003eDo not exceed the recommended dose or duration of treatment (see paragraph 3).\u003cbr\u003e\u003cbr\u003eYou should discuss treatment with your doctor or pharmacist before taking BRUFEN ANALGESICO if:\u003cbr\u003e• you have heart problems, including heart failure, angina (chest pain), or a history of heart attack, bypass surgery, peripheral artery disease (circulation problems in the legs or feet due to narrowing or blockage of the arteries), or any type of stroke (including mini-stroke or transient ischaemic attack, TIA);\u003cbr\u003e• you suffer from high blood pressure, diabetes, high cholesterol, have a family history of heart disease or stroke, or are a smoker.\u003cbr\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema) and chest pain. Stop BRUFEN ANALAGESICO immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e\u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003eSevere skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment.\u003cbr\u003eStop using BRUFEN ANALGESICO and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in paragraph 4.\u003cbr\u003e\u003cbr\u003e\u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003eBRUFEN ANALGESICO can hide the symptoms of infections such as fever and pain. It is therefore possible that BRUFEN ANALGESICO could delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003eUndesirable effects can be minimised by using the lowest effective dose for the shortest period of time. Elderly people have an increased risk of undesirable effects.\u003cbr\u003e\u003cbr\u003eIn general, habitual use of analgesics (even of different types) can lead to serious and persistent kidney problems. This risk can increase during physical exercise associated with salt loss and dehydration. Therefore, it should be avoided. There is a risk of impaired kidney function in dehydrated children and adolescents.\u003cbr\u003e\u003cbr\u003eProlonged use of any type of analgesic for headache can make it worse. If such a situation is present or suspected, medical advice should be sought and treatment should be stopped. The diagnosis of headache from overuse of medicines should be suspected in patients who have headaches despite (or because of) regular use of headache medicines.\u003cbr\u003e\u003cbr\u003eDuring prolonged administration of BRUFEN ANALGESICO, regular checks of the liver, kidney function and blood cell count are required. Your doctor may ask you to undergo blood tests during treatment.\u003c\/p\u003e\n\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003eSide effects can be minimised by taking the lowest dose for the shortest period of time necessary to relieve symptoms. Elderly people using this product have a higher risk of developing problems associated with side effects.\u003cbr\u003e\u003cbr\u003eMedicines such as BRUFEN ANALGESICO may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003eSome of the side effects listed below are less frequent when the maximum daily dose is 1200 mg compared to high-dose therapy in rheumatic patients.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eIf you think you have any of the following side effects or symptoms, stop taking this medicine and seek immediate medical attention:\u003c\/b\u003e\u003cbr\u003e• stomach or intestinal ulcers, sometimes with bleeding and perforation, blood vomiting or tarry black stools (common: may affect up to 1 in 10 people)\u003cbr\u003e• kidney disorders with blood in the urine that may be associated with kidney failure (uncommon: may affect up to 1 in 100 people)\u003cbr\u003e• severe allergic reactions (very rare: may affect up to 1 in 10,000 people) such as:\u003cbr\u003e- difficulty breathing or unexplained wheezing\u003cbr\u003e- dizziness or fast heartbeat\u003cbr\u003e- drop in blood pressure causing shock\u003cbr\u003e- swelling of the face, tongue and throat.\u003cbr\u003e• reddish non-raised, target-shaped or circular patches on the trunk, often with central blisters, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis] (very rare: may affect up to 1 in 10,000 people)\u003cbr\u003e• severe skin condition that can affect the mouth and other parts of the body with symptoms including red patches, often itchy, similar to measles rash, starting on the limbs and sometimes on the face and rest of the body. The spots can swell or can progress to form raised, red, pale-centred spots. Affected patients may have fever, sore throat, headache and\/or diarrhoea (very rare: may affect up to 1 in 10,000 people)\u003cbr\u003e• severe peeling or flaking of the skin (very rare: may affect up to 1 in 10,000 people)\u003cbr\u003e• Widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome) (not known: frequency cannot be estimated from the available data).\u003cbr\u003e• inflammation of the pancreas with severe epigastric pain, often with nausea and vomiting (very rare: may affect up to 1 in 10,000 people)\u003cbr\u003e• nausea, vomiting, loss of appetite, general feeling of ill health, fever, itching, yellowing of the skin and eyes, light-coloured stools, dark-coloured urine, which may be signs of hepatitis or liver failure (very rare: may affect up to 1 in 10,000 people)\u003cbr\u003e• heart disorder with shortness of breath and swelling of the feet or legs due to fluid retention (heart failure) (not known: frequency cannot be estimated from the available data)\u003cbr\u003e• aseptic meningitis (infection around the brain or spinal cord, with symptoms including: fever, nausea, vomiting, headache, stiff neck and extreme sensitivity to bright light and clouded mental state such that you are not fully aware of your surroundings (very rare: may affect up to 1 in 10,000 people)\u003cbr\u003e• heart attack (myocardial infarction, very rare: may affect up to 1 in 10,000 people) or stroke (frequency not known: cannot be estimated from the available data)\u003cbr\u003e• severe kidney damage (papillary necrosis, particularly with long-term use (rare: may affect up to 1 in 1,000 people)\u003cbr\u003e• worsening of infection-related inflammation (e.g. development of flesh-eating bacteria syndrome) particularly with the use of other NSAIDs (very rare: may affect up to 1 in 10,000 people)\u003cbr\u003e• Chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome (not known: frequency cannot be estimated from the available data)\u003cbr\u003e\u003cbr\u003e\u003cb\u003eStop taking\u003c\/b\u003e the medicine and tell your doctor if the following occur:\u003cbr\u003eVery common: (may affect more than 1 in 10 people)\u003cbr\u003e• indigestion or heartburn\u003cbr\u003e• abdominal pain (stomach pain) or other stomach abnormalities\u003cbr\u003e\u003cbr\u003eNot known (frequency cannot be estimated from the available data)\u003cbr\u003e• visual disturbances\u003cbr\u003e• a widespread, red, scaly rash, with pustules under the skin and blisters located mainly on the skin folds, trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using BRUFEN ANALGESICO if you develop these symptoms and contact your doctor immediately. See also paragraph 2.\u003cbr\u003e\u003cbr\u003eTell your doctor if any of the following side effects occur:\u003cbr\u003eVery common (may affect more than 1 in 10 people)\u003cbr\u003e• nausea, flatulence, diarrhoea, constipation, vomiting\u003cbr\u003e\u003cbr\u003eCommon (may affect up to 1 in 10 people)\u003cbr\u003e• headache, drowsiness, dizziness, spinning sensation, tiredness, agitation, inability to sleep, irritability\u003cbr\u003e• stomach and duodenal ulcers, sometimes with bleeding and perforation, occult blood loss which can lead to anaemia, a condition in which there is a decrease in red blood cells (symptoms include tiredness, headache, shortness of breath during exercise, dizziness and pallor), tarry black stools, vomiting with blood, mouth ulcers and herpes, inflammation of the colon (symptoms include diarrhoea, usually with blood and mucus, stomach pain and fever), worsening of inflammatory bowel disease, inflammation of the intestinal wall\u003cbr\u003e\u003cbr\u003eUncommon (may affect up to 1 in 100 people)\u003cbr\u003e• hives, itching, unusual bleeding or bruising under the skin, rash, asthma attack (sometimes with hypotension)\u003cbr\u003e• runny or blocked nose, sneezing, facial pain or pressure, difficulty breathing\u003cbr\u003e• inflammation of the stomach (symptoms include: pain, nausea, vomiting, blood vomiting, blood in stools)\u003cbr\u003e• increased skin sensitivity to the sun\u003cbr\u003e• swelling of the face, lips, mouth, tongue or throat, which may cause difficulty swallowing or breathing, sometimes with high blood pressure\u003cbr\u003e• fluid retention in body tissues, especially in patients with high blood pressure or kidney problems\u003cbr\u003e\u003cbr\u003eRare (may affect up to 1 in 1,000 people)\u003cbr\u003e• a disease affecting the skin, joints and kidneys (lupus erythematosus syndrome)\u003cbr\u003e• depression, confusion, hallucinations, mental illness with strange or disturbing thoughts or mood\u003cbr\u003e• ringing, hissing, whistling, sounds or other persistent noises in the ears\u003cbr\u003e• increased urea nitrogen, transaminases and alkaline phosphatase, decreased haemoglobin and haematocrit values, inhibition of platelet aggregation, prolonged bleeding time, decreased serum calcium, increased serum uric acid, all observed with a blood test\u003cbr\u003e• loss of visual capacity\u003cbr\u003e\u003cbr\u003eVery rare (may affect up to 1 in 10,000 people)\u003cbr\u003e• rapid or irregular heartbeat (palpitations)\u003cbr\u003e• increased fluid in body tissues\u003cbr\u003e• inflammation of the oesophagus, narrowing of the intestine\u003cbr\u003e• liver disorders, liver damage (especially with long-term use), liver failure, yellowing of the skin and\/or eyes, also called jaundice\u003cbr\u003e• severe skin infections, with soft tissue complications, may occur if you have chickenpox\u003cbr\u003e• fluid accumulation in the lungs, symptoms include shortness of breath, which can be very severe and usually worsens when lying down\u003cbr\u003e\u003cbr\u003eNot known (frequency cannot be estimated from the available data)\u003cbr\u003e• worsening of an inflammatory disease that can affect any part of the gastrointestinal tract (symptoms include pain, fever, diarrhoea and weight loss), worsening of inflammation of the colon (symptoms: diarrhoea, usually with blood and mucus, stomach pain, fever)\u003cbr\u003e• high blood pressure\u003cbr\u003e• unusual hair loss or incipient baldness\u003cbr\u003e• menstrual disorders\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including those not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\n\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"MYLAN SpA","offers":[{"title":"Default Title","offer_id":46290106908939,"sku":"042386348","price":6.82,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/analgesico_400.png?v=1734111864"},{"product_id":"brufenlik-20bust-400mg-10ml","title":"BRUFENLIK*20SACHETS 400MG 10ML","description":"\u003cp\u003e\u003cb\u003eBrufenlik 400 mg oral suspension in sachet\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eThe active ingredient in this medicine is ibuprofen. It belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). Brufenlik reduces fever and relieves pain.\u003cbr\u003e \u003cbr\u003e Brufenlik is used for the short-term treatment of mild to moderate pain such as\u003cbr\u003e - Headache and migraine\u003cbr\u003e - Toothache\u003cbr\u003e - Dysmenorrhea (painful periods)\u003cbr\u003e - Muscle, joint and back pain\u003cbr\u003e - Fever associated with the common cold.\u003cbr\u003e \u003cbr\u003e Brufenlik 400 mg is used in adults and adolescents over 12 years of age (weighing more than 40 kg).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Brufenlik\u003c\/b\u003e\u003cbr\u003e • if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you have ever had an allergic reaction (such as asthma, rash, swollen face or lips or shortness of breath) after taking ibuprofen, acetylsalicylic acid or other NSAIDs;\u003cbr\u003e • severe heart failure;\u003cbr\u003e • severe liver or kidney failure;\u003cbr\u003e • active bleeding or an increased tendency to bleed;\u003cbr\u003e • have (or have had two or more episodes of) stomach ulcer, duodenal ulcer or bleeding;\u003cbr\u003e • have or have ever had an ulcer or bleeding in the stomach or small intestine while taking NSAIDs;\u003cbr\u003e • after the sixth month of pregnancy.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eAlways administer the lowest effective dose for the shortest possible treatment duration to reduce the risk of side effects. Doses higher than recommended may lead to risks. This also means that taking multiple NSAIDs simultaneously should be avoided.\u003cbr\u003e \u003cbr\u003e Talk to your doctor or pharmacist before taking Brufenlik:\u003cbr\u003e - if you have certain immune system disorders (mixed connective tissue disorders and systemic lupus erythematosus (SLE), immune system conditions affecting connective tissue resulting in joint pain, skin changes and disorders of other organs) as there may be an increased risk of aseptic meningitis;\u003cbr\u003e - if you suffer from kidney or liver failure;\u003cbr\u003e - if you have heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including \"mini-stroke\" or \"TIA\", transient ischemic attack);\u003cbr\u003e - if you have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker;\u003cbr\u003e - if you suffer from asthma, chronic rhinitis (chronic stuffy and runny nose) or allergic diseases as Brufenlik may cause breathing difficulties, hives or a severe allergic reaction in the presence of one of these conditions;\u003cbr\u003e - if you have inflammatory bowel diseases, previous stomach ulcer or an increased tendency to bleeding of another nature;\u003cbr\u003e - if you have an infection - see section \u0026lt;infections\u0026gt; below.\u003cbr\u003e \u003cbr\u003e Ibuprofen can cause severe allergic reactions; especially if you are allergic to acetylsalicylic acid. Symptoms may include hives, swelling of the face, tongue or throat, difficulty swallowing, difficulty breathing. \u003cb\u003eStop taking Brufenlik and contact a doctor immediately\u003c\/b\u003e if you experience any of these symptoms (see section 4 Possible side effects).\u003cbr\u003e \u003cbr\u003e \u003cem\u003eSkin reactions\u003c\/em\u003e\u003cbr\u003e Severe skin reactions have been reported in association with Brufenlik treatment. Stop taking Brufenlik and consult your doctor immediately if a rash, mucosal lesions, blisters or other signs of allergy appear, as these may be the first signs of a very severe skin reaction. See section 4.\u003cbr\u003e \u003cbr\u003e \u003cem\u003eUlcers and bleeding in the gastrointestinal tract\u003c\/em\u003e\u003cbr\u003e • Patients who have previously had problems with the gastrointestinal tract, especially elderly patients, should contact a doctor in case of abdominal symptoms (especially gastrointestinal bleeding), particularly at the start of treatment. Bleeding, ulceration or perforation in the stomach or intestine can occur without warning signs even in patients who have never had such problems before.\u003cbr\u003e \u003cbr\u003e • Elderly patients should be aware of their increased risk of adverse events, particularly bleeding and perforation of the digestive tract, which can be fatal.\u003cbr\u003e \u003cbr\u003e • Stop treatment and consult a doctor if gastrointestinal bleeding or ulceration occurs during Brufenlik treatment.\u003cbr\u003e \u003cbr\u003e \u003cem\u003eCardiovascular effects\u003c\/em\u003e\u003cbr\u003e • Anti-inflammatory\/pain-relieving medicines such as ibuprofen may be associated with a slight increase in the risk of heart attack or stroke, particularly if used at high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e \u003cem\u003eInfections\u003c\/em\u003e\u003cbr\u003e • Brufenlik can mask the symptoms of infections such as fever and pain. It is therefore possible that Brufenlik may delay adequate treatment of the infection, which could increase the risk of complications.\u003cbr\u003e This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e • During chickenpox, it is advisable to avoid the use of this medicine.\u003cbr\u003e \u003cbr\u003e \u003cem\u003eIf you are dehydrated\u003c\/em\u003e\u003cbr\u003e • Particular caution should be exercised in dehydrated patients, as there is a risk of kidney failure, especially in dehydrated adolescents and the elderly.\u003cbr\u003e \u003cbr\u003e \u003cem\u003eHeadache\u003c\/em\u003e\u003cbr\u003e • Prolonged use of any type of painkiller for headaches can worsen the situation. If this situation occurs or is suspected, a doctor should be consulted and treatment should be discontinued.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e In dehydrated children and adolescents, there is a risk of impaired kidney function.\u003cbr\u003e Brufenlik 400 mg should not be taken by children under 12 years of age (weighing less than 40 kg).\u003cbr\u003e Other dosage forms and strengths are more appropriate for children.\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"MYLAN SpA","offers":[{"title":"Default Title","offer_id":46290113429771,"sku":"048424042","price":4.42,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/1901120053.webp?v=1734111730"},{"product_id":"enantyum-20cpr-riv-25mg","title":"ENANTYUM*20FC 25MG","description":"\u003cp\u003e\u003cb\u003eEnantyum 25 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Dexketoprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eEnantyum is a painkiller belonging to the group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs).\u003cbr\u003e It is used for the treatment of mild to moderate pain, such as muscle pain, painful menstruation (dysmenorrhea), toothache.\u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 - 4 days.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Enantyum:\u003c\/b\u003e\u003cbr\u003e • If you are allergic to dexketoprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • If you are allergic to acetylsalicylic acid or other non-steroidal anti-inflammatory drugs;\u003cbr\u003e • If you have asthma or have suffered from asthma attacks, acute allergic rhinitis (a short period of inflammation of the nasal mucosa), nasal polyps (polypoid masses in the nose due to allergy), urticaria (skin rash), angioedema (swelling of the face, eyes, lips, or tongue, or difficulty breathing) or wheezing in the chest, after taking acetylsalicylic acid or other non-steroidal anti-inflammatory drugs;\u003cbr\u003e • If you have suffered from photoallergic or phototoxic reactions (a particular form of skin redness and\/or blistering following exposure to sunlight) during treatment with ketoprofen (a non-steroidal anti-inflammatory drug) or with fibrates (drugs used to reduce blood fat levels);\u003cbr\u003e • If you suffer from peptic ulcer\/bleeding of the stomach or intestine or if you have suffered in the past from stomach or intestinal bleeding, ulceration or perforation;\u003cbr\u003e • If you suffer from chronic digestive problems (e.g. indigestion, heartburn);\u003cbr\u003e • If you have suffered in the past from stomach or intestinal bleeding or perforation due to previous use of non-steroidal anti-inflammatory drugs (NSAIDs) used for pain;\u003cbr\u003e • If you suffer from chronic inflammatory bowel diseases (Crohn's disease or ulcerative colitis);\u003cbr\u003e • If you suffer from severe heart failure, or have moderate to severe kidney problems or serious liver problems;\u003cbr\u003e • If you have bleeding problems or clotting disorders;\u003cbr\u003e • If you are severely dehydrated (you have lost a large amount of body fluids) due to vomiting, diarrhea or insufficient fluid intake;\u003cbr\u003e • If you are in the third trimester of pregnancy or are breastfeeding.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before using Enantyum:\u003cbr\u003e • If you suffer from allergies, or have had problems due to allergies in the past;\u003cbr\u003e • If you have kidney disorders, liver or heart problems (hypertension and\/or heart failure) or fluid retention, or have previously suffered from any of these disorders;\u003cbr\u003e • If you are being treated with diuretics or have very poor hydration problems or have a reduced blood volume due to excessive fluid loss (for example, due to excessive urination, diarrhea, vomiting);\u003cbr\u003e • If you suffer from heart disorders, if you have had a stroke or if you think you may be at risk for these conditions (for example, if you have high blood pressure, diabetes or high cholesterol or if you are a smoker) you should discuss the therapy with your doctor or pharmacist; medicines like Enantyum may be associated with a small increased risk of heart attack (myocardial infarction) or stroke. These risks are more likely with high doses of the drug and with prolonged therapy. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • If you are elderly: there is a greater probability of being subject to side effects (see section 4);\u003cbr\u003e In the event that these occur, consult your doctor immediately;\u003cbr\u003e • If you are a woman with fertility problems (this medicine may reduce your fertility, therefore you should not take the medicine if you are planning a pregnancy or if you are undergoing fertility investigations);\u003cbr\u003e • If you suffer from a disorder of blood and blood cell formation;\u003cbr\u003e • If you suffer from systemic lupus erythematosus or mixed connective tissue disease (immune system disorders affecting connective tissue);\u003cbr\u003e • If you have previously suffered from chronic inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • If you have or have previously suffered from other stomach or intestinal disorders;\u003cbr\u003e • If you have an infection - see Infections section below;\u003cbr\u003e • If you are taking other medicines that increase the risk of peptic ulcer or bleeding, such as oral steroids, some antidepressants (of the SSRI type, i.e. Selective Serotonin Reuptake Inhibitors), medicines that prevent blood clots from forming such as aspirin or anticoagulants such as warfarin. In these cases, consult your doctor before taking this medicine: this may prescribe an additional medicine to protect your stomach (for example misoprostol or other medicines that block the production of gastric acids);\u003cbr\u003e • If you suffer from asthma associated with chronic rhinitis, chronic sinusitis, and\/or nasal polyposis as you have a greater risk of allergy to acetylsalicylic acid and\/or NSAIDs compared to the rest of the population. The administration of this medicine can cause asthma attacks or bronchospasm, particularly in subjects allergic to acetylsalicylic acid or NSAIDs.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e Dexketoprofen can mask the symptoms of infection such as fever and pain. It is therefore possible that this medicine may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e The use of this medicine is not recommended during chickenpox virus infection.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e This medicine has not been studied in children and adolescents. Therefore, safety and efficacy have not been established and the product should not be used in children and adolescents.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e The possible side effects are listed below, ordered by their probability of occurring.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCommon side effects: may affect up to 1 in 10 patients\u003c\/b\u003e\u003cbr\u003e Nausea and\/or vomiting, abdominal pain mainly in the upper quadrants, diarrhea, digestive problems (dyspepsia).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon side effects: may affect up to 1 in 100 patients\u003c\/b\u003e\u003cbr\u003e Dizziness, light-headedness, drowsiness, sleep disturbances, nervousness, headache, palpitations, hot flashes, inflammation of the stomach lining (gastritis), constipation, dry mouth, flatulence, skin rash, fatigue, pain, feeling of fever and chills, general feeling of malaise.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare side effects: may affect up to 1 in 1,000 patients\u003c\/b\u003e\u003cbr\u003e Peptic ulcer, bleeding or perforated peptic ulcer (which may manifest with traces of blood in vomit or stools), fainting, high blood pressure, slow breathing, fluid retention and peripheral edema (e.g. swollen ankles), laryngeal edema, loss of appetite (anorexia), altered sensation (paresthesia), itchy rash, acne, increased sweating, back pain, frequent urination, menstrual disorders, prostate problems, abnormal liver function tests (blood tests), hepatocellular damage (hepatitis), acute kidney failure.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare side effects: may affect up to 1 in 10,000 patients\u003c\/b\u003e\u003cbr\u003e Anaphylactic reaction (hypersensitivity reaction that can also lead to collapse), ulceration of the skin, mouth, eyes and genital area (Stevens-Johnson and Lyell syndromes), facial edema or swelling of the lips and throat (angioedema), difficulty breathing due to contraction of the muscles surrounding the airways (bronchospasm), shortness of breath, rapid heartbeat, low blood pressure, pancreatitis, blurred vision, ringing in the ears (tinnitus), skin reactions, light hypersensitivity, itching, kidney problems. Decrease in white blood cells in the blood (neutropenia), decrease in platelets in the blood (thrombocytopenia).\u003cbr\u003e \u003cbr\u003e Inform your doctor immediately if you notice side effects in the stomach or intestine at the beginning of treatment (for example stomach pain, acidity or bleeding), if you have previously suffered from any of these side effects due to prolonged use of anti-inflammatory drugs, and particularly if you are elderly.\u003cbr\u003e \u003cbr\u003e Stop using this medicine as soon as you notice the appearance of a skin rash, or any lesion on the inner surface of the mouth or genitals, or any sign of allergy.\u003cbr\u003e \u003cbr\u003e During treatment with non-steroidal anti-inflammatory drugs, fluid retention and swelling (particularly of the ankles and legs), increased blood pressure and heart failure have been reported.\u003cbr\u003e \u003cbr\u003e Medicines like this may be associated with a small increased risk of heart attack (myocardial infarction) or cerebrovascular accidents (stroke).\u003cbr\u003e \u003cbr\u003e In patients with immune system disorders affecting connective tissue (systemic lupus erythematosus or mixed connective tissue disease), anti-inflammatory medicines can rarely cause fever, headache and neck stiffness.\u003cbr\u003e \u003cbr\u003e The most frequently observed adverse events are gastrointestinal in nature. Peptic ulcers, perforation or gastrointestinal bleeding may occur, sometimes fatal, especially in the elderly. Nausea, vomiting, diarrhea, flatulence, constipation, dyspepsia, abdominal pain, melena, hematemesis, ulcerative stomatitis, worsening of colitis and Crohn's disease have been reported following administration. Less frequently, inflammation of the stomach wall (gastritis) has been observed.\u003cbr\u003e \u003cbr\u003e As with other NSAIDs, hematological reactions may occur (purpura, aplastic and hemolytic anemia and rarely agranulocytosis and bone marrow hypoplasia).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"https:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"A.MENARINI IND.FARM.RIUN.Srl","offers":[{"title":"Default Title","offer_id":46290113724683,"sku":"033656442","price":7.44,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_5c9aa596-9222-48f2-882e-1ec75aa34c06.png?v=1734080445"},{"product_id":"momentact-20cpr-riv-400mg","title":"MOMENTACT*20COATED TABS 400MG","description":"\u003cp\u003e\u003cb\u003eMOMENTACT 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMomentact contains ibuprofen, a medicine belonging to the class of analgesic-anti-inflammatory drugs, which means drugs that fight pain and inflammation.\u003cbr\u003e \u003cbr\u003e Momentact is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 and over\u003c\/b\u003e to treat:\u003cbr\u003e - pain of various origins and natures (headaches, toothaches, neuralgia, osteo-articular and muscular pain, menstrual pain) and to help reduce the symptoms of feverish and flu-like states.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Momentact:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to other anti-rheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see section Other medicines and Momentact), or allergic to any of the other ingredients of this medicine;\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breastfeeding (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have a history of bleeding or perforation of the stomach or intestine following the use of medicines;\u003cbr\u003e - if you have a history of two or more distinct episodes of ulcer or stomach bleeding;\u003cbr\u003e - if you have severe heart disease;\u003cbr\u003e - if you have severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eWhat you need to know before taking Momentact\u003cbr\u003e \u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck region (angioedema) and chest pain, have been reported with ibuprofen. Stop Momentact immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003e Severe skin reactions have been reported in association with ibuprofen treatment, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP).\u003cbr\u003e Stop taking Momentact and consult your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.\u003cbr\u003e \u003cbr\u003e Consult your doctor or pharmacist before taking Momentact:\u003cbr\u003e - if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, runny nose (chronic rhinitis), presence of nasal polyps (nasal polyposis) or inflammation of the nasal mucosa (sinusitis) or suffer\/have suffered from allergies because you could experience difficulty breathing (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section Other medicines and Momentact);\u003cbr\u003e - if you are elderly or if you have suffered from an ulcer, especially if the ulcer also manifested with bleeding or perforation (see section Do not take Momentact), as the risk of bleeding, ulcer or perforation is higher with high doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly consult your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you are taking low doses of acetylsalicylic acid or drugs that can increase the risk of stomach and\/or intestinal diseases (see section Other medicines and Momentact);\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 Possible side effects);\u003cbr\u003e - if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report any unusual intestinal symptoms (especially haemorrhage) to your doctor, particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcer or bleeding of the stomach and\/or intestine, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (serotonin inhibitors), or antiplatelet drugs (e.g. acetylsalicylic acid). See also section Other medicines and Momentact. If gastrointestinal haemorrhage or ulceration occurs in patients taking Momentact, treatment must be discontinued;\u003cbr\u003e - if you have high blood pressure and the medicines you are taking are unable to lower it and\/or you have heart disease or blood circulation problems in the brain or periphery or you think you may be at risk for these diseases (for example, if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or have heart disease, as fluid retention, increased blood pressure and swelling have been observed following treatment with NSAIDs. NSAIDs can reduce the action of medicines to lower blood pressure (see section Other medicines and Momentact);\u003cbr\u003e - if you have lost a considerable amount of fluids, or if you experience swelling, heart problems or high blood pressure;\u003cbr\u003e - if you have reduced kidney function, heart or liver malfunction, or if you are elderly or are being treated with medicines for high blood pressure, as you may be more prone to the onset of kidney problems. Furthermore, the habitual concomitant use of several painkillers can further increase this risk;\u003cbr\u003e - if you suffer from heart disease;\u003cbr\u003e - if you suffer from liver diseases (hepatic dysfunction);\u003cbr\u003e - if you are elderly, as the risk of haemorrhage, ulcers and perforations is increased compared to other patients;\u003cbr\u003e - if you suffer from a coagulation disorder or are taking medicines to thin the blood (anticoagulants) (see section Other medicines and Momentact);\u003cbr\u003e - if you suffer from a disease that can affect various organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of aseptic meningitis have been observed in patients treated with ibuprofen.\u003cbr\u003e Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients who did not have concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section Other medicines and Momentact);\u003cbr\u003e - if you intend to become pregnant (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have problems getting pregnant or are undergoing fertility investigations (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - If you have an infection - see section Infections below;\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss your therapy with your doctor or pharmacist before taking Momentact if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary artery bypass surgery, peripheral arterial disease (poor circulation to the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Medicines such as Momentact can:\u003cbr\u003e - be associated with the appearance of even serious kidney diseases (such as renal papillary necrosis, analgesic nephropathy and kidney failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e - cause eye disorders, therefore, in the case of prolonged treatments, periodic eye examinations are recommended. If visual disturbances occur, stop treatment with Momentact.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Momentact can hide the symptoms of infections such as fever and pain. It is therefore possible that Momentact may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003e If the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Momentact can cause side effects, although not everyone gets them. The side effects of the drug can be minimised if you use the lowest recommended dose, and if you use the drug only for the period necessary to control your symptoms.\u003cbr\u003e \u003cbr\u003e If you develop an ulcer, or stomach and\/or intestinal bleeding, or skin and\/or mucous membrane lesions, you must stop treatment with Momentact and consult your doctor. These side effects are usually more frequent in the elderly.\u003cbr\u003e \u003cbr\u003e The use of Momentact can cause generally mild or moderate side effects or more serious, allergic reactions, albeit rarely.\u003cbr\u003e \u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eIMMEDIATELY STOP using\u003c\/b\u003e Momentact and contact your doctor or the nearest hospital where you will receive appropriate and specific treatment:\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucous membrane lesions;\u003cbr\u003e • signs of an allergic reaction, even severe (erythema, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • peeling skin;\u003cbr\u003e • non-raised reddish spots, target-shaped or circular on the trunk, often with central vesicles, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson syndrome);\u003cbr\u003e • widespread rash, elevated body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and vesicles, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalised exanthematous pustulosis);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • liver disease (hepatic dysfunction);\u003cbr\u003e • bleeding, ulcer and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e \u003cbr\u003e In case of an allergic reaction among those listed above, go to the hospital as it is necessary to have immediate availability of equipment, drugs and personnel suitable for emergency treatment, as in rare cases severe side effects, sometimes fatal, have been reported following the use of ibuprofen, even in the absence of known allergy.\u003cbr\u003e \u003cbr\u003e The risk of developing such symptoms is higher in the early stages of therapy: in most cases, the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e Furthermore, you may experience further side effects that have also been reported with other medicines similar to Momentact and are listed below by frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness\u003cbr\u003e • malaise\u003cbr\u003e • fatigue\u003cbr\u003e \u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • stomach inflammation (gastritis)\u003cbr\u003e • insomnia, anxiety\u003cbr\u003e • numbness of the limbs or other parts of the body, drowsiness\u003cbr\u003e • nasal congestion (rhinitis)\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnoea)\u003cbr\u003e • momentary cessation of breathing (apnoea)\u003cbr\u003e • hearing impairment\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • vertigo\u003cbr\u003e • liver disorders (impaired liver function)\u003cbr\u003e • liver inflammation (hepatitis)\u003cbr\u003e • yellowing of skin and eyes (jaundice)\u003cbr\u003e • kidney diseases (damage to kidney function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and kidney failure)\u003cbr\u003e • hypersensitivity reactions such as skin rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), asthma, difficulty breathing (bronchospasm or dyspnoea), asthma attacks with lowering of blood pressure\u003cbr\u003e • skin reactions to light (photosensitivity)\u003cbr\u003e \u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (haemolytic anaemia, aplastic anaemia), platelets (thrombocytopenia)\u003cbr\u003e • depression, confused state, hallucinations\u003cbr\u003e • inflammation of the optic nerve (optic neuritis)\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis), especially in patients with pre-existing autoimmune disorders (see section Warnings and precautions), with symptoms of stiff neck, headache, nausea, vomiting, fever or disorientation\u003cbr\u003e • eye disorders with visual disturbances and optic nerve pathology (toxic optic neuropathy)\u003cbr\u003e • swelling due to fluid accumulation in the tissues\u003cbr\u003e • disease that can affect various organs and tissues of the body (lupus erythematosus)\u003cbr\u003e • worsening of inflammations caused by an existing infection (e.g. development of necrotizing fasciitis)\u003cbr\u003e \u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis)\u003cbr\u003e • sensation of feeling one's heartbeat (palpitations)*\u003cbr\u003e • heart disease (heart failure)*\u003cbr\u003e • heart attack (myocardial infarction)*\u003cbr\u003e • increased fluid around the lungs (acute pulmonary oedema)*\u003cbr\u003e • liver disease (hepatic insufficiency)\u003cbr\u003e • hypertension*\u003cbr\u003e • severe allergic reactions, which may include symptoms such as swelling of the face, tongue and throat making breathing difficult, fast heartbeat, severe allergic reaction with rapid onset that can cause death (anaphylaxis), severe rash or skin exfoliation (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme)\u003cbr\u003e • severe skin infections and soft tissue disorders can occur during chickenpox infection\u003cbr\u003e \u003cbr\u003e \u003cb\u003e*these side effects tend to resolve with discontinuation of treatment\u003cbr\u003e \u003cbr\u003e not known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach\u003cbr\u003e • nausea\u003cbr\u003e • vomiting\u003cbr\u003e • diarrhoea\u003cbr\u003e • flatulence\u003cbr\u003e • constipation\u003cbr\u003e • indigestion\u003cbr\u003e • abdominal pain\u003cbr\u003e • heartburn\u003cbr\u003e • blood in stools\u003cbr\u003e • blood in vomit\u003cbr\u003e • lesions inside the mouth\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease)\u003cbr\u003e • increased risk of heart attack (myocardial infarction), or lack of blood supply to the brain (stroke)\u003cbr\u003e • high blood pressure\u003cbr\u003e • severe heart disease (heart failure)\u003cbr\u003e • a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell)\u003cbr\u003e • a widespread, red and scaly rash, with the formation of pustules under the skin and vesicles located mainly on the skin folds, on the trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalised exanthematous pustulosis). Stop using Momentact if you develop these symptoms and contact your doctor immediately. See also section 2\u003cbr\u003e • chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290126274827,"sku":"035618053","price":11.12,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_53c20ff3-967d-4c98-9ff5-5ec49a311465.png?v=1734080506"},{"product_id":"moment-10cps-molli-200mg","title":"MOMENT*10 SOFT CAPSULES 200MG","description":"\u003cp\u003e\u003cb\u003eMOMENT 200 mg soft capsules\u003c\/b\u003e\u003cbr\u003eIbuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMoment contains ibuprofen, a medicine belonging to the class of analgesics-anti-inflammatories, i.e., drugs that fight pain and inflammation.\u003cbr\u003e \u003cbr\u003e Moment is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 and over\u003c\/b\u003e for:\u003cbr\u003e - treatment of pain of various origins and nature (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain);\u003cbr\u003e - reduction of fever and flu symptoms.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Moment\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you are allergic to other anti-rheumatic medicines (e.g., acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see paragraph Other medicines and Moment);\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breastfeeding (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have previously experienced bleeding or perforation of the stomach or intestine following taking medicines;\u003cbr\u003e - if you have previously had two or more separate episodes of ulcer or stomach bleeding;\u003cbr\u003e - in the presence of severe heart disease (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhea or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eWhat you need to know before taking Moment\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck region (angioedema) and chest pain, have been reported with ibuprofen. Stop Moment immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e Skin reactions\u003cbr\u003e Severe skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment.\u003cbr\u003e Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in paragraph 4.\u003cbr\u003e \u003cbr\u003e Consult your doctor or pharmacist before taking Moment:\u003cbr\u003e - if you have experienced breathing difficulties (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, runny nose (chronic rhinitis), presence of polyps in the nose (nasal polyposis) or inflammation of the paranasal sinus mucosa (sinusitis) or suffer\/have suffered from allergies because you could experience breathing difficulties (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see paragraph Other medicines and Moment);\u003cbr\u003e - if you are elderly or if you have suffered from an ulcer, especially if the ulcer has also manifested with bleeding or perforation (see paragraph Do not take Moment), as the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly consult your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you are taking low doses of acetylsalicylic acid or drugs that can increase the risk of stomach and\/or intestinal diseases (see paragraph Other medicines and Moment);\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see paragraph 4 Possible side effects);\u003cbr\u003e - if you have had stomach and intestinal diseases related to the use of medicines, and in particular if you are elderly, you must report any unusual intestinal symptoms (especially bleeding) to your doctor, particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcer or bleeding of the stomach and\/or intestine, such as oral corticosteroids (e.g., cortisone), anticoagulants (e.g., warfarin), antidepressants (selective serotonin reuptake inhibitors), or blood antiplatelets (e.g., acetylsalicylic acid). See also the paragraph Other medicines and Moment. If gastrointestinal bleeding or ulceration occurs in patients taking Moment, treatment must be suspended;\u003cbr\u003e - if you have high blood pressure and the medicines you are taking are unable to lower it and\/or you have heart disease or blood circulation problems in the brain or other body districts or you think you may be at risk for these diseases (for example, if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or have heart disease, as fluid retention, increased blood pressure and swelling have been observed following treatment with NSAIDs. NSAIDs can reduce the action of medicines to lower blood pressure (see paragraph Other medicines and Moment);\u003cbr\u003e - if you have lost a considerable amount of fluid or you develop swelling, heart problems or high blood pressure;\u003cbr\u003e - if you have decreased kidney function, heart or liver malfunction or if you are elderly or on treatment with medicines for high blood pressure as you may be more predisposed to the onset of kidney problems. Furthermore, the habitual concomitant use of different painkillers can further increase this risk;\u003cbr\u003e - if you suffer from a coagulation disorder or are taking medicines that slow blood coagulation (anticoagulants) (see paragraph Other medicines and Moment);\u003cbr\u003e - if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as in rare occasions in patients treated with ibuprofen, symptoms of aseptic meningitis have been observed. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue disorders, it has also been observed in patients who did not manifest concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see paragraph Other medicines and Moment). - if you intend to become pregnant (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have difficulty becoming pregnant or are undergoing fertility investigations (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have an infection - see paragraph Infections below.\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss therapy with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Medicines like Moment can:\u003cbr\u003e - be associated with the appearance of even serious kidney diseases (such as renal papillary necrosis, analgesic nephropathy and kidney failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e - give rise to eye disorders, therefore, in case of prolonged treatments, periodic eye checks are recommended. If visual disturbances occur, stop treatment with Moment.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment can mask the symptoms of infections such as fever and pain. It is therefore possible that Moment may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003e If the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Moment can cause side effects, although not everyone gets them.\u003cbr\u003e The side effects of the drug can be minimized if you use the lowest recommended dose and if you use the drug only for the period necessary to control your symptoms.\u003cbr\u003e \u003cbr\u003e If you develop an ulcer or stomach and\/or intestinal bleeding or skin and\/or mucous membrane lesions, you must stop treatment with Moment and consult your doctor. These side effects are usually more common in the elderly.\u003cbr\u003e \u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate or more serious reactions, even of an allergic type, albeit rarely.\u003cbr\u003e \u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP immediately\u003c\/b\u003e using Moment and contact your doctor or the nearest hospital immediately where you will undergo appropriate and specific treatment:\u003cbr\u003e • chest pain, which may be a sign of a potentially severe allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucous membrane lesions;\u003cbr\u003e • signs of allergic reaction, even severe (erythema, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • peeling skin;\u003cbr\u003e • non-raised, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e • widespread rash, elevated body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • liver disease (hepatic dysfunction);\u003cbr\u003e • bleeding, ulcer and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e \u003cbr\u003e If one of the allergic reactions listed above occurs, go to the hospital as it is necessary to have immediate availability of equipment, drugs and personnel suitable for emergency treatment, as in rare cases, following the use of ibuprofen, serious side effects have been reported, sometimes fatal, even in the absence of known allergy.\u003cbr\u003e \u003cbr\u003e The risk of manifesting such symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e Furthermore, you may experience further side effects that have also been reported with other medicines similar to Moment and which are listed below according to frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue.\u003cbr\u003e \u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • stomach inflammation (gastritis);\u003cbr\u003e • insomnia, anxiety;\u003cbr\u003e • numbness of the limbs or other parts of the body (paresthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • breathing difficulties (bronchospasm, dyspnea);\u003cbr\u003e • momentary cessation of breathing (apnea);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • vertigo;\u003cbr\u003e • liver disorders (altered liver function);\u003cbr\u003e • liver inflammation (hepatitis);\u003cbr\u003e • yellowing of skin and eyes (jaundice);\u003cbr\u003e • kidney diseases (kidney function damage and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and kidney failure);\u003cbr\u003e • hypersensitivity reactions such as rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), breathing difficulties (bronchospasm or dyspnea), asthma attacks with possible lowering of blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity).\u003cbr\u003e \u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction of white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusion, hallucinations;\u003cbr\u003e • inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see paragraph Warnings and precautions), with symptoms of neck stiffness, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve pathology (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect several organs and tissues of the body (lupus erythematosus syndrome);\u003cbr\u003e • worsening of inflammations caused by an existing infection (e.g., development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • alteration of liver function tests (increased transaminases, increased alkaline phosphatase);\u003cbr\u003e • abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e \u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling one's heartbeat (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (hepatic insufficiency);\u003cbr\u003e • hypertension;\u003cbr\u003e • severe allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making breathing difficult, fast heartbeat, severe rapidly occurring allergic reaction that can cause death (anaphylaxis), severe skin rash or peeling skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • severe skin infections and soft tissue disorders can occur during chickenpox infection.\u003cbr\u003e \u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomiting;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • difficulty digesting;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stools;\u003cbr\u003e • blood in the vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease);\u003cbr\u003e • increased risk of sudden reduction of blood circulation in the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell).\u003cbr\u003e a widespread, red and scaly rash, with pustules forming under the skin and blisters located mainly on skin lesions, on the trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis) Stop using Moment if you develop these symptoms and contact your doctor immediately. See also paragraph 2.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290126405899,"sku":"025669197","price":6.39,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_42d06793-319a-4e97-9135-2ee4e3f9dbcb.jpg?v=1734080515"},{"product_id":"enantyum-10bust-os-grat-25mg","title":"ENANTYUM*10SACH ORAL GRANULES 25MG","description":"\u003cp\u003e\u003cb\u003eEnantyum 25 mg granules for oral solution\u003c\/b\u003e\u003cbr\u003e Dexketoprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it's for\u003c\/b\u003e\u003cbr\u003eEnantyum is a painkiller belonging to the group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs).\u003cbr\u003e It is used for the short-term symptomatic treatment of mild to moderate pain, such as acute muscle pain, joint pain, painful menstruation (dysmenorrhea), and toothache.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Enantyum:\u003c\/b\u003e\u003cbr\u003e • if you are allergic to dexketoprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you are allergic to acetylsalicylic acid or other non-steroidal anti-inflammatory drugs;\u003cbr\u003e • if you suffer from asthma or have suffered from asthma attacks, acute allergic rhinitis (short periods of nasal mucous membrane inflammation), nasal polyps (polypoid masses in the nose due to allergy), urticaria (skin rash), angioedema (swelling of the face, eyes, lips or tongue, or breathing difficulties) or wheezing in the chest, after taking acetylsalicylic acid or other non-steroidal anti-inflammatory drugs;\u003cbr\u003e • if you have suffered from photoallergic or phototoxic reactions (a particular form of redness and\/or irritation of the skin exposed to sunlight) in conjunction with taking ketoprofen (an NSAID) or fibrates (medicines used to lower blood lipid levels);\u003cbr\u003e • if you suffer from peptic ulcer\/stomach or intestinal bleeding or if you have a history of stomach or intestinal bleeding, ulceration or perforation;\u003cbr\u003e • if you have chronic digestive problems (e.g. indigestion, heartburn);\u003cbr\u003e • if you have a history of stomach or intestinal bleeding or perforation due to the use of non-steroidal anti-inflammatory drugs (NSAIDs) for pain;\u003cbr\u003e • if you suffer from chronic inflammatory bowel diseases (Crohn's disease or ulcerative colitis);\u003cbr\u003e • if you suffer from severe heart failure, moderate or severe kidney failure, severe liver failure;\u003cbr\u003e • if you have bleeding problems or coagulation disorders;\u003cbr\u003e • if you are severely dehydrated (have lost a lot of fluids) due to vomiting, diarrhea or insufficient fluid intake;\u003cbr\u003e • if you are in the third trimester of pregnancy or if you are breastfeeding.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Enantyum:\u003cbr\u003e • if you suffer from allergies, or have had allergy problems in the past;\u003cbr\u003e • if you have kidney, liver or heart conditions (hypertension and\/or heart failure) and fluid retention, or if you have a history of any of these disorders;\u003cbr\u003e • if you are on diuretics or if you are poorly hydrated and have reduced blood volume due to excessive fluid loss (e.g. due to excessive urination, diarrhea, vomiting);\u003cbr\u003e • if you have heart disease, have had a stroke or think you may be at risk for these conditions (e.g. if you have high blood pressure, diabetes or high cholesterol or if you are a smoker), discuss treatment with your doctor or pharmacist; medicines like Enantyum may be associated with a slight increased risk of heart attack (myocardial infarction) or cerebrovascular accident (stroke).\u003cbr\u003e These risks are more likely with high doses of the medicine and with prolonged therapy. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • if you are elderly: the risk of side effects is higher (see point 4). If they occur, consult your doctor immediately;\u003cbr\u003e • if you are a woman with fertility problems (Enantyum may reduce female fertility, therefore you should not take the medicine if you are planning a pregnancy or are undergoing fertility investigations);\u003cbr\u003e • if you suffer from a disorder of blood and blood cell formation;\u003cbr\u003e • if you suffer from systemic lupus erythematosus or mixed connective tissue disease (immune system disorders affecting connective tissue);\u003cbr\u003e • if you have a history of chronic inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • if you have a history of other stomach or intestinal disorders;\u003cbr\u003e • if you have an infection – see section \"Infections\" below;\u003cbr\u003e • if you are taking other medicines that increase the risk of peptic ulcer or bleeding, e.g. oral steroids, some antidepressants (e.g. SSRIs, selective serotonin reuptake inhibitors), antiplatelet agents like aspirin or anticoagulants like warfarin. In these cases, consult your doctor before taking Enantyum: they may prescribe an additional medicine to protect your stomach (e.g. misoprostol or other medicines that reduce gastric acid production);\u003cbr\u003e • if you suffer from asthma associated with chronic rhinitis, chronic sinusitis and\/or nasal polyposis, as you have a higher risk of allergy to acetylsalicylic acid and\/or NSAIDs compared to the rest of the population. The administration of this medicine may cause asthma attacks or bronchospasm, especially in subjects allergic to acetylsalicylic acid or NSAIDs.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e Enantyum can mask the symptoms of infection such as fever and pain. It is therefore possible that Enantyum may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e The use of this medicine is not recommended during chickenpox virus infection.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e The use of Enantyum has not been studied in children and adolescents. Therefore, safety and efficacy have not been established and the medicine should not be used in children and adolescents.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e The possible side effects are listed below, ordered according to their probability of occurrence. Since the list is partly based on the side effects of the tablet formulation of Enantyum, and Enantyum in granules is absorbed more quickly than tablets, it is possible that the actual frequency of side effects (gastrointestinal) may be higher with Enantyum in granules.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCommon side effects (may affect up to 1 in 10 patients)\u003c\/b\u003e\u003cbr\u003e Nausea and\/or vomiting, abdominal pain mainly in the upper quadrants, diarrhea, digestive problems (dyspepsia).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon side effects (may affect up to 1 in 100 patients)\u003c\/b\u003e\u003cbr\u003e Dizziness (vertigo), dizziness, drowsiness, insomnia, nervousness, headache, palpitations, hot flashes, inflammation of the stomach lining (gastritis), constipation, dry mouth, flatulence, skin rash, fatigue, pain, fever and chills, general feeling of unwellness (malaise).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare side effects (may affect up to 1 in 1,000 patients)\u003c\/b\u003e\u003cbr\u003e Peptic ulcer, bleeding or perforated peptic ulcer (manifesting as hematemesis, i.e. vomiting blood, or black stools), fainting, hypertension, slowed breathing, fluid retention and peripheral edema (e.g. swollen ankles), laryngeal edema, loss of appetite (anorexia), altered sensation (particularly touch), itchy rash, acne, increased sweating, back pain, frequent urination, menstrual disorders, prostate problems, abnormal liver function test (blood analysis), hepatocellular damage (hepatitis), acute kidney failure.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 patients)\u003c\/b\u003e\u003cbr\u003e Anaphylactic reactions (hypersensitivity reactions that can also lead to collapse), open sores on the skin, mouth, eyes and genital area (Stevens-Johnson and Lyell syndromes), facial edema or swelling of the lips and throat (angioedema), shortness of breath due to contraction of the muscles surrounding the airways (bronchospasm), shortness of breath, rapid heartbeat, hypotension, pancreatitis, blurred vision, ringing in the ears (tinnitus), sensitive skin, light sensitivity, itching, kidney problems. Reduced number of white blood cells (neutropenia), decreased blood platelets (thrombocytopenia).\u003cbr\u003e \u003cbr\u003e Inform your doctor immediately if you notice any stomach or intestinal side effects at the start of treatment (e.g. stomach pain, acidity or bleeding), if you have previously suffered from these side effects due to prolonged use of anti-inflammatory drugs and particularly if you are elderly.\u003cbr\u003e \u003cbr\u003e Stop using Enantyum as soon as you notice a skin rash or any lesion inside the mouth or genitals, or any sign of allergy.\u003cbr\u003e \u003cbr\u003e During treatment with non-steroidal anti-inflammatory drugs, fluid retention and swelling (particularly of the ankles and legs), increased blood pressure and heart failure have been reported.\u003cbr\u003e \u003cbr\u003e Medicines like Enantyum may be associated with a small increased risk of heart attack (myocardial infarction) or cerebrovascular accident (stroke).\u003cbr\u003e \u003cbr\u003e In patients suffering from immune system disorders affecting connective tissue (systemic lupus erythematosus or mixed connective tissue disease), anti-inflammatory drugs can, in rare cases, cause fever, headache and neck stiffness.\u003cbr\u003e \u003cbr\u003e The most commonly observed adverse events are gastrointestinal in nature. Peptic ulcers, perforation or gastrointestinal bleeding may occur, sometimes fatal, especially for the elderly. Nausea, vomiting, diarrhea, flatulence, constipation, dyspepsia, abdominal pain, melena, hematemesis, ulcerative stomatitis, worsening of colitis and Crohn's disease have been reported following administration. Less frequently, inflammation of the stomach lining (gastritis) has been observed.\u003cbr\u003e \u003cbr\u003e As with other NSAIDs, hematological reactions may occur (purpura, aplastic and hemolytic anemia and rarely agranulocytosis and bone marrow hypoplasia).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"A.MENARINI IND.FARM.RIUN.Srl","offers":[{"title":"Default Title","offer_id":46290133647627,"sku":"033656214","price":5.29,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_d7c27c9e-a9c2-431b-a10f-3cc3a975e01e.jpg?v=1734080599"},{"product_id":"nurofenteen-12cpr-oro-200mg-li","title":"NUROFENTEEN*12ORO TAB 200MG LI","description":"\u003cp\u003e\u003cb\u003eNUROFENTEEN 200 mg orodispersible lemon tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eNUROFENTEEN contains 200 mg of ibuprofen. Ibuprofen belongs to a group of medicines called Non-Steroidal Anti-Inflammatory Drugs (NSAIDs). These medicines work by changing the body's response to pain, swelling, and high temperature.\u003cbr\u003e \u003cbr\u003e NUROFENTEEN is used for:\u003cbr\u003e • relieving symptoms of mild to moderate pain such as headache, toothache, and menstrual pain\u003cbr\u003e • reducing fever\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days in adolescents, or after 3 days in case of fever or after 4 days for pain treatment in adults.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take NUROFENTEEN if:\u003c\/b\u003e\u003cbr\u003e • you are allergic (hypersensitive) to ibuprofen or any of the other ingredients of NUROFENTEEN (listed in section 6)\u003cbr\u003e • you have suffered from breathing difficulties, asthma, rhinitis, swelling of the face and\/or hands, or hives after taking ibuprofen, acetylsalicylic acid, or other similar analgesics (NSAIDs)\u003cbr\u003e • you suffer from severe liver failure, severe kidney failure, or severe heart failure\u003cbr\u003e • you have (or have had) two or more episodes of stomach ulcer or stomach bleeding\u003cbr\u003e • you have experienced gastrointestinal bleeding or perforation following previous NSAID treatments\u003cbr\u003e • you have cerebrovascular hemorrhage or other types of active bleeding\u003cbr\u003e • you suffer from unexplained blood formation disorders\u003cbr\u003e • you suffer from severe dehydration (caused by vomiting, diarrhea, or insufficient fluid intake)\u003cbr\u003e • you are in the last 3 months of pregnancy (see below).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eConsult your doctor or pharmacist before taking NUROFENTEEN\u003c\/b\u003e\u003cbr\u003e • if you have an infection - see section Infections below\u003cbr\u003e • if you suffer from certain skin diseases (systemic lupus erythematosus (SLE) or mixed connective tissue disease)\u003cbr\u003e • if you suffer from a hereditary blood formation disorder (Acute intermittent porphyria)\u003cbr\u003e • if you have blood clotting problems\u003cbr\u003e • if you suffer or have suffered from gastrointestinal tract disorders (ulcerative colitis or Crohn's disease)\u003cbr\u003e • if you suffer from reduced kidney function\u003cbr\u003e • if you suffer from liver disorders\u003cbr\u003e • if you are planning a pregnancy\u003cbr\u003e • if you suffer or have suffered from asthma or allergic diseases, as you may experience shortness of breath\u003cbr\u003e • if you suffer from hay fever, nasal polyps, or chronic obstructive respiratory diseases, as there is an increased risk of developing allergic reactions. Allergic reactions can manifest as asthma attacks (so-called analgesic asthma), skin swelling (Quincke's edema) or hives\u003cbr\u003e • it is advisable to avoid taking NUROFENTEEN if you have chickenpox\u003cbr\u003e • if NUROFENTEEN is taken for long periods of time, regular tests to evaluate liver and kidney function, and blood cell count should be performed\u003cbr\u003e • undesirable effects can be minimized by using the lowest effective dose for the shortest possible time\u003cbr\u003e • elderly people are at higher risk of developing adverse reactions\u003cbr\u003e • in general, habitual use of (different types of) analgesics can lead to serious permanent kidney problems. This risk may increase in case of physical exertion associated with salt loss and dehydration. Therefore, it should be avoided.\u003cbr\u003e • prolonged use of any type of analgesic for headaches can worsen the symptoms. If this occurs or this situation is suspected, you should stop taking NUROFENTEEN and consult your doctor. The diagnosis of medication overuse headache (MOH) should be suspected in patients who have frequent or daily headaches despite (or because of) the regular use of analgesic medicines\u003cbr\u003e • concomitant use with other NSAIDs, including selective cyclooxygenase 2 inhibitors, may increase the risk of undesirable effects and should be avoided (see section Taking with other medicines)\u003cbr\u003e • in dehydrated adolescents, there is a risk of kidney impairment\u003cbr\u003e • particular caution is required if you have recently undergone major surgery\u003cbr\u003e • anti-inflammatory\/pain relief medicines such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking NUROFENTEEN if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary artery bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including 'mini-stroke' or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Infections\u003cbr\u003e NUROFENTEEN can hide symptoms of infections such as fever and pain. Therefore, NUROFENTEEN may delay appropriate treatment of an infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the infection symptoms persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions have been reported in association with NUROFENTEEN treatment. Stop taking NUROFENTEEN and consult your doctor immediately if you experience a rash, mucosal lesions, blisters, or other signs of allergy as these may be the first signs of a very serious skin reaction. See section 4.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, NUROFENTEEN can cause side effects, although not everybody gets them.\u003cbr\u003e Undesirable effects can be minimized by using the lowest effective dose for the shortest possible time for symptom relief.\u003cbr\u003e You may experience one of the known side effects of NSAIDs (see below). If this happens, or if you have concerns about it, stop taking this medicine and inform your doctor as soon as possible. Elderly people taking this medicine are more at risk of developing problems associated with side effects.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStop taking this medicine and consult your doctor immediately if you experience:\u003cbr\u003e • signs of intestinal bleeding\u003c\/b\u003e such as: severe abdominal pain, dark stools, vomiting with blood or dark particles resembling coffee grounds;\u003cbr\u003e • \u003cb\u003esigns of very rare but serious allergic reactions\u003c\/b\u003e such as worsening of asthma, unexplained wheezing or shortness of breath, swelling of the face, tongue or throat, breathing difficulties, accelerated heartbeat, drop in blood pressure leading to shock. These symptoms can also occur with the first use of this medicine;\u003cbr\u003e • \u003cb\u003esevere skin reactions\u003c\/b\u003e such as rashes all over the body, peeling, blistering or flaking of the skin.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eConsult your doctor if you experience any of the following adverse reactions\u003cbr\u003e \u003cbr\u003e Common (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • gastrointestinal problems, such as heartburn, abdominal pain and nausea, indigestion, diarrhea, vomiting, flatulence (wind) and constipation and slight blood loss in the stomach and\/or intestine which in exceptional cases can cause anemia.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • Gastrointestinal ulcers, bleeding and perforation, inflammation of the oral mucosa with ulceration, worsening of existing intestinal disorders (ulcerative colitis or Crohn's disease), gastritis\u003cbr\u003e • Central nervous system disorders such as headache, dizziness, insomnia, agitation, irritability or fatigue\u003cbr\u003e • Vision disorders\u003cbr\u003e • Various skin rashes\u003cbr\u003e • Hypersensitivity reactions with hives and itching\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • Tinnitus (ringing in the ears)\u003cbr\u003e • Increased uric acid levels in the blood, flank and\/or abdominal pain, blood in the urine and fever may be signs of kidney damage (papillary necrosis).\u003cbr\u003e • Decreased hemoglobin levels\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • esophagitis, pancreatitis, formation of membranous strictures in the intestine (diaphragm-like intestinal strictures)\u003cbr\u003e • heart failure, heart attack and swelling of the face and hands (edema)\u003cbr\u003e • reduced urine output and swelling (especially in patients with high blood pressure or reduced kidney function); swelling (edema) and cloudy urine (nephrotic syndrome); inflammatory kidney disease (interstitial nephritis) which can lead to acute kidney failure. If any of the above symptoms occur or if you have a general feeling of ill health, stop taking NUROFENTEEN and consult your doctor immediately as these could be the first signs of kidney damage or kidney failure.\u003cbr\u003e • psychotic reactions and depression\u003cbr\u003e • high blood pressure and vasculitis\u003cbr\u003e • palpitations\u003cbr\u003e • liver dysfunction, liver damage (first sign may be skin discoloration), especially for long periods of treatment, liver failure, acute inflammation of the liver (hepatitis).\u003cbr\u003e • problems in blood cell production - first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe exhaustion, bleeding from the nose and skin and unexplained bruising. In these cases, you should stop taking NUROFENTEEN and consult your doctor immediately. No self-medication treatment with analgesics and fever-reducing drugs (antipyretic medicines) should be carried out\u003cbr\u003e • severe skin infections and soft tissue complications have been observed during a chickenpox infection\u003cbr\u003e • the worsening of inflammation related to infections (e.g. necrotizing fasciitis) associated with the use of some analgesics (NSAIDs) has been described. If signs of an infection appear or worsen, contact your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e • symptoms of aseptic meningitis with stiff neck, headache, nausea, vomiting, fever or disorientation have been observed during the use of ibuprofen. Patients with autoimmune diseases (SLE, mixed connective tissue disease) may be more susceptible. Contact your doctor immediately if these symptoms occur.\u003cbr\u003e • severe forms of skin reactions such as skin rashes with redness and blistering (e.g. Stevens-Johnson syndrome, toxic epidermal necrolysis\/Lyell's syndrome), hair loss (alopecia)\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • Respiratory tract reactivity including asthma, bronchospasm and dyspnea\u003cbr\u003e • A severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: skin rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell).\u003cbr\u003e • A widespread, red, scaly rash with bumps under the skin and blisters located mainly on the skin folds, trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using NUROFENTEEN if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e • The skin becomes sensitive to light;\u003cbr\u003e \u003cbr\u003e Medicines such as NUROFENTEEN may be associated with a slight increased risk of heart attack (myocardial infarction) or stroke. \u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"RECKITT BENCKISER H.(IT.) SpA","offers":[{"title":"Default Title","offer_id":46290141872395,"sku":"035677145","price":5.91,"currency_code":"EUR","in_stock":true}]},{"product_id":"nurofencaps-10cps-molli-400mg","title":"NUROFENCAPS*10 SOFT CAPSULES 400MG","description":"\u003cp\u003e\u003cb\u003eNurofencaps 400 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eIbuprofen belongs to a group of medicines called Non-Steroidal Anti-Inflammatory Drugs (NSAIDs). These medicines provide relief by changing the body's response to pain and fever.\u003cbr\u003e \u003cbr\u003e Nurofencaps is used in adults and adolescents weighing over 40 kg (from 12 years of age) for the short-term symptomatic treatment of:\u003cbr\u003e • mild to moderate pain such as headache, menstrual pain and toothache;\u003cbr\u003e • fever and pain associated with the common cold.\u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days in adolescents or after 3 days for fever and 4 days for pain treatment in adults.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Nurofencaps if:\u003c\/b\u003e\u003cbr\u003e • you are allergic to the active ingredient or any of the other ingredients of this medicine (listed in section 6)\u003cbr\u003e • you have ever suffered from breathing difficulties, asthma, runny nose, swelling or hives after taking acetylsalicylic acid or similar analgesics (NSAIDs)\u003cbr\u003e • you have (or have had two or more separate episodes of) stomach\/duodenal ulcer (peptic ulcer) or stomach bleeding\u003cbr\u003e • you have had gastrointestinal bleeding or perforation following previous treatment with NSAIDs (non-steroidal anti-inflammatory drugs)\u003cbr\u003e • you suffer from unexplained blood formation disorders\u003cbr\u003e • you suffer from severe liver, kidney or heart failure\u003cbr\u003e • you are in the last 3 months of pregnancy (see section Pregnancy and breastfeeding)\u003cbr\u003e • you suffer from severe dehydration (caused by vomiting, diarrhoea or insufficient fluid intake)\u003cbr\u003e • you suffer from bleeding in the brain (cerebrovascular bleeding) or other active bleeding.\u003cbr\u003e \u003cbr\u003e Do not administer to adolescents weighing less than 40 kg or children under 12 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Nurofencaps if:\u003cbr\u003e • you have an infection - see section Infections below.\u003cbr\u003e • you suffer from systemic lupus erythematosus (SLE) or mixed connective tissue disease (immune system conditions causing joint pain, skin rashes and fever).\u003cbr\u003e • you suffer from a certain hereditary blood formation disorder (e.g. acute intermittent porphyria) or have blood clotting problems.\u003cbr\u003e • you have or have had intestinal diseases (ulcerative colitis or Crohn's disease).\u003cbr\u003e • you have reduced kidney function.\u003cbr\u003e • you have liver problems.\u003cbr\u003e • you have recently undergone major surgery.\u003cbr\u003e • you suffer or have suffered from asthma or allergy, as you may experience shortness of breath.\u003cbr\u003e • you suffer from hay fever, nasal polyps or chronic obstructive respiratory disorders, as there is an increased risk of developing allergic reactions. Allergic reactions may manifest as asthma attacks (so-called analgesic asthma), acute swelling (Quincke's edema) or skin rash.\u003cbr\u003e • you are taking other medicines that could increase the risk of ulceration or bleeding such as oral corticosteroids, blood thinners (like warfarin), selective serotonin reuptake inhibitors (medicines for depression) or antiplatelet agents such as acetylsalicylic acid.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eOther warnings\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e • Prolonged use of analgesics for headaches can worsen the symptoms. If this occurs or is suspected, you should stop taking Nurofencaps and consult your doctor.\u003cbr\u003e • You should avoid taking Nurofencaps if you have chickenpox.\u003cbr\u003e • If Nurofencaps is taken for long periods of time, regular blood tests and regular liver and kidney checks are necessary.\u003cbr\u003e • Taking Nurofencaps in combination with other NSAIDs, including selective cyclooxygenase 2 inhibitors, may increase the risk of adverse effects and should be avoided (see section Other medicines and Nurofencaps).\u003cbr\u003e • In general, the habitual use of (different types of) analgesics can lead to severe lasting kidney problems and should be avoided. The risk is further increased by salt loss and dehydration.\u003cbr\u003e • In dehydrated adolescents, there is a risk of impaired kidney function.\u003cbr\u003e \u003cbr\u003e Infections\u003cbr\u003e Nurofencaps can mask the symptoms of infections such as fever and pain. Therefore, it is possible that Nurofencaps may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the infection symptoms persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e Skin reactions\u003cbr\u003e Serious skin reactions have been reported in association with Nurofencaps treatment. Stop taking Nurofencaps and consult your doctor immediately if you develop a rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very serious skin reaction. See section 4.\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/pain relief medicines such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially when given in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss your therapy with your doctor or pharmacist before taking Nurofencaps if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or blockage of arteries) or any type of stroke (including mini-stroke or TIA, transient ischaemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eSide effects can be minimized by using the lowest effective dose for the shortest period of time. Elderly people are more at risk of experiencing side effects.\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e Consult your doctor before taking Nurofencaps if any of the above conditions concern you.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Nurofencaps can cause side effects, although not everybody gets them.\u003cbr\u003e \u003cbr\u003e Side effects can be minimized by using the lowest effective dose for the shortest possible time to relieve symptoms.\u003cbr\u003e You may experience one of the known side effects of NSAIDs (see below). If this happens, or if you have any concerns about it, stop taking this medicine and tell your doctor as soon as possible. Elderly people taking this medicine are at greater risk of developing problems associated with side effects.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eSTOP TAKING this medicine and consult your doctor immediately if you experience:\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e • \u003cb\u003esigns of intestinal bleeding\u003c\/b\u003e such as: severe abdominal pain, dark stools, vomiting blood or dark particles similar to coffee grounds;\u003cbr\u003e • \u003cb\u003esigns of very rare but severe allergic reactions\u003c\/b\u003e such as worsening asthma, unexplained wheezing or shortness of breath, swelling of the face, tongue or throat, breathing difficulties, rapid heartbeat, drop in blood pressure leading to shock. These symptoms may also occur on first use of this medicine;\u003cbr\u003e • \u003cb\u003esevere skin reactions\u003c\/b\u003e such as skin rashes all over the body, peeling, blistering or flaking of the skin.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eConsult your doctor if you experience any of the following adverse reactions, if they become severe or if you notice any adverse reaction not listed in the leaflet.\u003cbr\u003e \u003cbr\u003e Common (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • Gastrointestinal disorders such as heartburn, abdominal pain, nausea, and indigestion, vomiting, flatulence, diarrhoea, constipation and mild blood loss in the stomach and\/or intestines which in exceptional cases can cause anaemia.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • Gastric or intestinal ulcers, sometimes with bleeding and perforation, inflammation of the oral mucosa with ulceration (ulcerative stomatitis), inflammation of the stomach (gastritis) worsening of colitis and Crohn's disease\u003cbr\u003e • Central nervous system disorders such as headache, dizziness, insomnia, agitation, irritability or fatigue\u003cbr\u003e • Visual disturbances\u003cbr\u003e • Allergic reactions, such as skin rashes, itching and asthma attacks. You should stop taking Nurofencaps and consult your doctor immediately\u003cbr\u003e • Various skin rashes\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • Tinnitus (ringing in the ears)\u003cbr\u003e • Kidney damage (papillary necrosis) and high uric acid concentrations in the blood\u003cbr\u003e • Impaired hearing\u003cbr\u003e • Increased urea concentration in the blood\u003cbr\u003e • Reduced haemoglobin levels\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • Swelling (oedema), high blood pressure (hypertension) and heart failure have been reported in association with NSAID treatment\u003cbr\u003e • Inflammation of the oesophagus or pancreas, formation of membranous strictures in the small and large intestine (diaphragm-like intestinal strictures).\u003cbr\u003e • Severe skin infections and soft tissue complications have been observed during a chickenpox infection.\u003cbr\u003e • Reduced urine output and swelling (especially in patients with high blood pressure or reduced kidney function); swelling (oedema) and cloudy urine (nephrotic syndrome); inflammatory kidney disease (interstitial nephritis) which may lead to acute kidney failure. If any of the above symptoms occur or if you have a general feeling of being unwell, stop taking Nurofencaps and consult your doctor immediately as these could be the first signs of kidney damage or kidney failure.\u003cbr\u003e • Blood cell production disorders. The first signs are: fever, sore throat, superficial ulcers of the oral cavity, flu-like symptoms, severe exhaustion, nose and skin bleeding. In these cases, you must stop treatment immediately and consult your doctor. Do not treat these symptoms with analgesics or medicines that reduce fever (antipyretics).\u003cbr\u003e • Psychotic reactions and depression.\u003cbr\u003e • Worsening of infection-related inflammation (e.g. necrotising fasciitis) has been described in association with the use of certain analgesics (NSAIDs). If signs of an infection appear or worsen while using Nurofencaps, consult your doctor immediately to assess whether anti-infective\/antibiotic therapy is necessary.\u003cbr\u003e • High blood pressure, palpitations, heart failure, myocardial infarction.\u003cbr\u003e • Liver dysfunction, liver damage, especially for long periods of treatment, liver failure, acute inflammation of the liver (hepatitis).\u003cbr\u003e • Symptoms of aseptic meningitis with neck stiffness, headache, feeling unwell, nausea, fever or disorientation have been observed during the use of ibuprofen. Patients with autoimmune disorders (SLE, mixed connective tissue disease) may be more susceptible. Contact your doctor immediately if these symptoms occur.\u003cbr\u003e • Severe forms of skin reactions such as rashes with redness and blistering (e.g. Stevens-Johnson syndrome, toxic epidermal necrolysis\/Lyell's syndrome), hair loss (alopecia).\u003cbr\u003e • Severe generalized hypersensitivity reactions.\u003cbr\u003e • Worsening of asthma and bronchospasm.\u003cbr\u003e • Inflammation of blood vessels (vasculitis).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • A severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: skin rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell).\u003cbr\u003e • A widespread, red, scaly rash with bumps under the skin and blisters located mainly on the skin folds, trunk and upper extremities accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using Nurofencaps if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e • the skin becomes sensitive to light.\u003cbr\u003e \u003cbr\u003e Nurofencaps contains Ponceau 4R (E124) which may cause allergic reactions.\u003cbr\u003e \u003cbr\u003e Medicines such as Nurofencaps may be associated with a slight increase in the risk of heart attack (myocardial infarction) or stroke. \u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"RECKITT BENCKISER H.(IT.) SpA","offers":[{"title":"Default Title","offer_id":46290141905163,"sku":"041860053","price":7.29,"currency_code":"EUR","in_stock":true}]},{"product_id":"okitask-20cpr-riv-40mg","title":"OKITASK*20COATED TABS 40MG","description":"\u003cp\u003e\u003cb\u003eOkitask 40 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ketoprofen lysine salt\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eOkitask contains ketoprofen, which belongs to a group of medicines called \"Non-Steroidal Anti-Inflammatory Drugs\" (NSAIDs). Ketoprofen blocks the chemicals that cause inflammation.\u003cbr\u003e Okitask is indicated for treating pain of various origins and natures, and in particular: headache, toothache, neuralgia (nerve pain), menstrual pain, muscle and osteoarticular pain (of the bones and joints).\u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Okitask:\u003c\/b\u003e\u003cbr\u003e - If you are allergic to ketoprofen, other non-steroidal anti-inflammatory drugs (NSAIDs) or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - If you have a history of hypersensitivity reactions (allergy) triggered by the use of ketoprofen or substances with a similar mechanism of action, for example, acetylsalicylic acid or other NSAIDs (other anti-inflammatories) such as asthma (bronchial inflammation and narrowing of the airways), bronchospasm (constriction of the bronchi), allergic rhinitis (allergic inflammation of the nasal mucosa), urticaria, skin rashes, nasal polyps, angioneurotic edema (swelling of the skin and mucous membranes) or other allergic-type reactions;\u003cbr\u003e - If you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways);\u003cbr\u003e - If you have severe heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs);\u003cbr\u003e - If you suffer from gastritis (inflammation of the stomach lining);\u003cbr\u003e - If you currently have a peptic ulcer (a lesion of the stomach or the first part of the intestine) or bleeding, or if you have suffered in the past from recurrent bleeding or peptic ulcer (two or more distinct, proven episodes of bleeding or ulceration);\u003cbr\u003e - If you have suffered in the past from gastrointestinal bleeding or perforation or chronic dyspepsia (difficult digestion) as a result of previous NSAID therapy;\u003cbr\u003e - If you have a history of gastrointestinal bleeding or perforation following previous NSAID therapy;\u003cbr\u003e - If you suffer from Crohn's disease (inflammation of the intestine) or ulcerative colitis (inflammation of the intestine with ulcers);\u003cbr\u003e - If you have severe hepatic (reduced liver function due to liver cirrhosis, severe hepatitis) or renal (reduced kidney function) insufficiency;\u003cbr\u003e - If you suffer from leukopenia (reduction in the number of white blood cells) or thrombocytopenia (reduction in the number of platelets);\u003cbr\u003e - If you suffer from hemorrhagic diathesis (predisposition to the development of hemorrhages) and other coagulation disorders or if you have hemostatic disorders (difficulty in stopping bleeding);\u003cbr\u003e - If you are on high-dose diuretic therapy;\u003cbr\u003e - If you are in the third trimester of pregnancy;\u003cbr\u003e - If the person to be treated is under 15 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Okitask.\u003cbr\u003e  \u003cu\u003e\u003cem\u003eWarnings\u003c\/em\u003e\u003c\/u\u003e\u003cbr\u003e  Undesirable effects can be minimised by using the lowest effective dose for the shortest possible duration of treatment needed to control symptoms (see How to take Okitask and the sections below on gastrointestinal and cardiovascular risks).\u003cbr\u003e  The concomitant use of Okitask with other anti-inflammatories should be avoided. During treatment with all NSAIDs, such as Okitask, at any time, with or without warning symptoms or a previous history of serious gastrointestinal events, gastrointestinal bleeding, ulceration and perforation, which can be fatal, have been reported. Patients who have already suffered from these conditions in the past have a greater risk (see Do not take Okitask).\u003cbr\u003e  Report any abdominal signs or symptoms (including gastrointestinal bleeding) even at the start of treatment. Inform your doctor if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (medicines used to treat inflammatory conditions), anticoagulants (medicines that delay blood clotting), such as warfarin, selective serotonin reuptake inhibitors (medicines used to treat depression), or antiplatelet agents (medicines that prevent platelet aggregation) such as acetylsalicylic acid (see Other medicines and Okitask).\u003cbr\u003e  The elderly are at greater risk of developing adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforations, which can be fatal. \u003cb\u003eImmediately stop treatment with Okitask at the first signs of gastrointestinal bleeding or ulceration.\u003c\/b\u003e\u003cbr\u003e  Severe skin reactions, some of which fatal, such as exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see Possible side effects). The reaction occurs in most cases in the initial stages of treatment. Discontinue the use of Okitask if a rash, mucosal lesions or any other sign of hypersensitivity (allergic reaction) appears.\u003cbr\u003e  \u003cbr\u003e  \u003cem\u003ePrecautions\u003c\/em\u003e\u003cbr\u003e  \u003cb\u003eAsk your doctor or pharmacist for advice before taking Okitask\u003c\/b\u003e\u003cbr\u003e  - If your kidneys are not working well, as Okitask should be taken with caution in this case. If you use Okitask, you should monitor your kidneys, especially if you are elderly or if you are on diuretic therapy (medicines that lower blood pressure).\u003cbr\u003e  - If you have liver problems, you should undergo periodic checks.\u003cbr\u003e  - If you have an infection - see the Infections section below.\u003cbr\u003e  - If you suffer from uncontrolled hypertension (high blood pressure), congestive heart failure (fluid accumulation in the lungs, abdominal organs and peripheral tissues due to inadequate pumping function of the heart), confirmed ischemic heart disease (heart condition that occurs after a reduction in blood flow due to narrowing of the coronary arteries), peripheral arterial disease and\/or cerebrovascular disease (disease of the arteries and blood vessels of the brain), as you should take Okitask only after careful medical evaluation.\u003cbr\u003e  - If you have risk factors for these conditions, for example if you have high blood pressure, diabetes (disease caused by high blood glucose levels), hyperlipidemia (high levels of fats in the blood), if you smoke.\u003cbr\u003e  - If you have allergic manifestations or have suffered from allergies in the past, as the medicine should be administered with caution.\u003cbr\u003e  - If you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways) or with allergic diathesis (predisposition to the onset of allergy), chronic rhinitis (inflammation of the nasal mucosa) and allergic rhinitis (allergic inflammation of the nasal mucosa), chronic sinusitis and\/or nasal polyposis.\u003cbr\u003e  - If you suffer from hematopoietic disorders (which modify the formation and maturation of blood cells), systemic lupus erythematosus (disease of the immune system) or mixed connective tissue diseases, as Okitask should be used with caution.\u003cbr\u003e  - If you have hepatic porphyria (rare blood disease characterised by altered activity of one of the liver enzymes), as the medicine could trigger an attack.\u003cbr\u003e  Some NSAIDs may be associated with an increased risk of arterial thrombotic events (e.g. heart attack or stroke). There are currently insufficient data to exclude a similar risk for OKITASK. An increased risk of atrial fibrillation (alteration of the heart rhythm) associated with the use of NSAIDs has been reported. Hyperkalemia (increased amount of potassium in the blood) may occur, especially if you suffer from diabetes, kidney failure and\/or are on therapy with medicines that can cause hyperkalemia (see Other medicines and Okitask). In these circumstances, potassium levels should be monitored periodically.\u003cbr\u003e  \u003cbr\u003e  Infections\u003cbr\u003e  Okitask can mask the symptoms of infections such as fever and pain. It is therefore possible that Okitask may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e  Consult your doctor if you experience vision disturbances, such as blurred vision, as treatment must be discontinued.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everyone experiences them.\u003cbr\u003e  The most commonly observed adverse events are gastrointestinal in nature.\u003cbr\u003e  The following adverse reactions have been observed with the use of ketoprofen in adults:\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eCommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e  - dyspepsia (difficult digestion), nausea, abdominal pain and vomiting.\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e  - headache, dizziness, drowsiness, constipation, diarrhoea, flatulence (emission of intestinal gas from the anus), gastritis (inflammation of the stomach lining)\u003cbr\u003e  - rash, itching and fatigue\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e  - hemorrhagic anaemia (reduction of haemoglobin in the blood, a substance that carries oxygen in the blood caused by bleeding)\u003cbr\u003e  - paraesthesia (sensation of numbness, tingling)\u003cbr\u003e  - blurred vision (see Warnings and precautions)\u003cbr\u003e  - tinnitus (persistent perception of noises in the ear)\u003cbr\u003e  - asthma (bronchial inflammation and narrowing of the airways)\u003cbr\u003e  - stomatitis (inflammation of the mucous membranes lining the mouth), peptic ulcer (lesion of the stomach or the first part of the intestine)\u003cbr\u003e  - hepatitis (inflammation of the liver), increased transaminases (increase in certain enzymes that indicate liver function), increased bilirubin (a substance that indicates liver function)\u003cbr\u003e  - increased weight.\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e  - facial edema (swelling) and erythema (skin redness)\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003eFrequency not known (frequency cannot be defined on the basis of available data)\u003c\/b\u003e\u003cbr\u003e  - thrombocytopenia (reduction in the number of platelets), agranulocytosis (severe reduction in the number of a type of white blood cells), bone marrow failure (reduction in the production of blood cells by the bone marrow), hemolytic anaemia (reduction in haemoglobin in the blood, a substance that carries oxygen in the blood, caused by the destruction of red blood cells), leukopenia (decrease in the number of white blood cells), neutropenia (decrease in the number of a type of white blood cells), aplastic anaemia (reduction in haemoglobin in the blood, a substance that carries oxygen in the blood, caused by insufficient production of blood cells by the bone marrow), leukocytosis (increase in the number of white blood cells), thrombocytopenic purpura (presence of spots on the skin due to a reduction in the number of platelets)\u003cbr\u003e  - anaphylactic reaction (severe allergic reaction, including shock), hypersensitivity (allergy)\u003cbr\u003e  - jaundice (yellowing of the skin and the whites of the eyes)\u003cbr\u003e  - depression, hallucination (perception of non-existent things in reality), confusional state, altered mood, agitation, insomnia, convulsions (uncontrolled body movements), dizziness, dysgeusia (altered taste), tremor, dyskinesia (involuntary movements), syncope (fainting), hyperkinesia (involuntary and uncoordinated movements), periorbital edema (swelling around the eye), peripheral edema\u003cbr\u003e  - chills, asthenia (weakness)\u003cbr\u003e  - heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs), atrial fibrillation (altered heart rhythm), palpitations (perception of heart beat), tachycardia (increased heart rate), hypertension (high blood pressure), hypotension (low blood pressure)\u003cbr\u003e  - vasodilation (dilation of blood vessels), vasculitis (inflammation of vessels), including leukocytoclastic vasculitis (inflammation of small vessels)\u003cbr\u003e  - bronchospasm (constriction of the bronchi), especially in patients with confirmed hypersensitivity to acetylsalicylic acid and other NSAIDs, rhinitis (inflammation of the nasal mucosa), dyspnea (difficult breathing), laryngeal edema (swelling of the throat due to fluid accumulation), laryngospasm (narrowing of the larynx), acute respiratory failure (one case, with fatal outcome, has been reported in an asthmatic patient sensitive to acetylsalicylic acid)\u003cbr\u003e  - exacerbation of colitis (worsening of intestinal inflammation, exacerbation of Crohn's disease (worsening of intestinal inflammation), gastrointestinal bleeding (bleeding of the stomach or intestine), gastrointestinal perforation (sometimes fatal, particularly in the elderly, see Warnings), gastric ulcer (lesion of the stomach), mouth ulceration, duodenal ulcer (lesion of the first part of the intestine), duodenal perforation, heartburn (stomach acid), mouth edema (swelling of the mouth), pancreatitis (inflammation of the pancreas), melena (presence of digested blood in the stool), hematemesis (vomiting of blood), abdominal discomfort, colitis, hyperchlorhydria (excess stomach acid), gastric pain (stomach ache), erosive gastritis (severe inflammation of the stomach lining), tongue edema (swelling of the tongue)\u003cbr\u003e  - photosensitivity reactions (reaction of sensitivity to sunlight or UV lamps), alopecia (hair loss), urticaria, angioedema (swelling of the face, lips, mouth, tongue or throat that can cause difficulty in breathing and swallowing), bullous eruptions including Stevens-Johnson syndrome, Lyell's syndrome and toxic epidermal necrolysis (severe skin reactions), edema (fluid retention), exanthema (skin rash), maculopapular exanthema (skin rash with patches), purpura (purplish spots on the skin due to abnormal blood accumulation), acute generalised exanthematous pustulosis (skin rash with pus formation), dermatitis (skin irritation)\u003cbr\u003e  - acute renal failure (reduced kidney function), tubulointerstitial nephritis, nephritis and nephritic syndrome (inflammation of the kidneys), nephrotic syndrome (renal disorder involving protein loss in the urine), glomerulonephritis (inflammatory kidney disease), water\/sodium retention with possible edema (accumulation of water and sodium causing swelling), acute tubular necrosis and renal papillary necrosis (severe kidney damage), oliguria (decreased urine production), abnormal kidney function test, hematuria (presence of blood in the urine)\u003cbr\u003e  - aseptic meningitis (inflammation of the membranes covering the brain not caused by infections), lymphangitis (inflammation of the lymphatic vessels)\u003cbr\u003e  - hyperkalemia (increase in the amount of potassium in the blood) and hyponatremia (decrease in the amount of sodium in the blood).\u003cbr\u003e  \u003cbr\u003e  Compliance with the instructions contained in the leaflet reduces the risk of side effects.\u003cbr\u003e  \u003cbr\u003e   \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"DOMPE' FARMACEUTICI SpA","offers":[{"title":"Default Title","offer_id":46290146754827,"sku":"042028047","price":7.91,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_568fcd05-8f23-4b8e-9701-269a20fb07b5.png?v=1734080755"},{"product_id":"momendol-12cpr-riv-220mg","title":"MOMENDOL*12COATED TABS 220MG","description":"\u003cp\u003e\u003cb\u003eMOMENDOL 220 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003eNaproxen sodium\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMomendol belongs to the class of analgesic-anti-inflammatory-antirheumatic non-steroidal drugs, i.e., medicines that combat pain, inflammation, fever, and are useful in the symptomatic treatment of rheumatic diseases.\u003cbr\u003eMomendol is used for the short-term symptomatic treatment of mild to moderate pain, such as muscle and joint pain (e.g., backache, stiff neck), headache, toothache, and menstrual pain.\u003cbr\u003eMomendol can also be used for the treatment of fever.\u003cbr\u003eConsult your doctor if you do not feel better or if you feel worse after 7 days of pain treatment, and after 3 days of fever treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take MOMENDOL\u003c\/b\u003e\u003cbr\u003e• If you are allergic to naproxen sodium or any of the other ingredients of this medicine (listed in section 6), or to other chemically related substances.\u003cbr\u003e• If you suffer from allergic manifestations, such as asthma, urticaria, rhinitis, nasal polyps, angioedema, and allergic reactions induced by acetylsalicylic acid, analgesics, anti-inflammatory and\/or antirheumatic drugs.\u003cbr\u003e• If you have a history of gastrointestinal bleeding or perforation, recurrent active or previous peptic ulcer, chronic inflammatory bowel diseases (ulcerative colitis, Crohn's disease), severe hepatic insufficiency, severe cardiac insufficiency, severe renal insufficiency (creatinine clearance \u0026lt;30 ml\/min), angioedema, during intensive diuretic therapy, in subjects with active bleeding and at risk of bleeding during anticoagulant therapy (See \"Other medicines and MOMENDOL\" and \"Warnings and precautions\").\u003cbr\u003e• During pregnancy, from the third trimester, and during breastfeeding (See \"Pregnancy, breastfeeding and fertility\").\u003cbr\u003e• The medicine cannot be administered to children under 12 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Momendol:\u003cbr\u003e• As there is a strong correlation between dosage and the appearance of severe gastrointestinal side effects. Therefore, the minimum effective dose should always be used.\u003cbr\u003e• Medicines such as MOMENDol may be associated with a modest increased risk of heart attack (\"myocardial infarction\") or stroke. Any risk is more likely with high doses and prolonged treatment. Do not exceed the recommended dose or duration of treatment (7 days for pain and 3 days for fever treatment).\u003cbr\u003e• When MOMENDOL is used in hypertensive patients and\/or in patients with reduced cardiac and\/or renal function. During treatment with MOMENDOL, diuresis and renal function should be closely monitored, particularly in the elderly, in patients with heart failure or chronic renal failure, and in patients undergoing diuretic treatment, following major surgical interventions involving significant blood loss.\u003cbr\u003e• If you have heart problems, or a history of stroke or think you may be at risk for these conditions (for example, if you have high blood pressure, diabetes, or high cholesterol, or if you smoke) you should discuss your therapy with your doctor or pharmacist.\u003cbr\u003e• When MOMENDOL is used in patients with severe heart failure, a worsening of the condition may occur.\u003cbr\u003e• When MOMENDOL is used in patients with a history of gastrointestinal diseases or liver failure and in patients with current or previous allergic manifestations, as in these subjects the product may cause bronchospasm, asthma, or other allergic phenomena. In these cases, particular caution is advised.\u003cbr\u003e• MOMENDOL should be discontinued at the first appearance of skin rash, mucosal lesions, or any other sign of allergy and\/or hypersensitivity.\u003cbr\u003e• If visual disturbances occur, treatment with MOMENDOL should be discontinued.\u003cbr\u003e• Since naproxen, like any other anti-inflammatory drug, can mask the concomitant symptoms of infectious diseases.\u003cbr\u003e• Since in isolated cases, in temporal connection with the use of anti-inflammatory drugs, an aggravation of infection-based inflammations has been reported.\u003cbr\u003e• If used in elderly patients, who generally have some degree of impaired renal, hepatic, and cardiac function, as this group of patients is more exposed to the risk of onset of side effects related to the use of anti-inflammatory drugs. Prolonged use of anti-inflammatory drugs in the elderly is not recommended.\u003cbr\u003e• Since naproxen inhibits platelet aggregation and can prolong bleeding time. Patients with coagulation disorders or on therapy with medicines that interfere with coagulation should be carefully monitored while taking MOMENDOL.\u003cbr\u003e• When MOMENDOL is used by habitual consumers of high daily doses of alcohol, there is a high risk of stomach bleeding.\u003cbr\u003e• The use of the product should be avoided in cases of pain of gastrointestinal origin. It is known that in patients taking anti-inflammatory drugs, stomach or intestinal bleeding may occur.\u003cbr\u003e• In asthmatic patients, the product is generally contraindicated.\u003cbr\u003e• When MOMENDOL is used in combination with other drugs that require caution, see \"Other medicines and MOMENDOL\".\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003eBelow 16 years of age, it is advisable to contact a doctor.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003eThe most commonly observed side effects are gastrointestinal.\u003cbr\u003eThe following side effects have been reported with NSAIDs and naproxen:\u003cbr\u003e\u003cbr\u003e\u003cb\u003eCommon (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e- Headache, drowsiness, dizziness\u003cbr\u003e- Nausea, dyspepsia, vomiting, heartburn, gastralgia, flatulence.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e- Allergic reaction (including facial edema and angioedema)\u003cbr\u003e- Sleep disturbances, agitation\u003cbr\u003e- Vision disturbances\u003cbr\u003e- Tinnitus, hearing disturbances\u003cbr\u003e- Contusion\u003cbr\u003e- Diarrhea, constipation\u003cbr skin rash\u003e- Abnormal kidney function\u003cbr\u003e- Chills, edema (including peripheral edema).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare (may affect up to 1 in 1000 people):\u003c\/b\u003e\u003cbr\u003e- Peptic ulcer, gastrointestinal perforation or bleeding, sometimes fatal, may occur especially in elderly subjects, hematemesis, ulcerative stomatitis, aggravated colitis and aggravated Crohn's disease.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e- Hemolytic or aplastic anemia, thrombocytopenia, granulocytopenia\u003cbr\u003e- Meningitis-like reaction\u003cbr\u003e- Tachycardia, edema, hypertension and heart failure have been observed in association with NSAID treatment\u003cbr\u003e- Dyspnoea, asthma\u003cbr\u003e- Colitis, stomatitis. Gastritis has been observed less frequently\u003cbr\u003e- Jaundice, hepatitis, reduced liver function\u003cbr\u003e- Photosensitivity, alopecia, blistering disorder including Stevens-Johnson syndrome and toxic epidermal necrolysis\u003cbr\u003e- Increased blood pressure.\u003cbr\u003e\u003cbr\u003eAs with other anti-inflammatory drugs, anaphylactic or anaphylactoid allergic reactions may occur in patients with or without previous exposure to drugs of the same class.\u003cbr\u003eThe characteristic symptoms of an anaphylactic reaction are: severe and sudden hypotension, acceleration or slowing of the heart rate, unusual fatigue or weakness, anxiety, agitation, loss of consciousness, difficulty breathing or swallowing, itching, urticaria with or without angioedema, skin redness, nausea, vomiting, cramping abdominal pain, diarrhea.\u003cbr\u003eMedicines such as MOMENDOL may be associated with a modest increased risk of heart attack (\"myocardial infarction\") or stroke.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290155110667,"sku":"025829084","price":8.35,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_8d9b165b-c040-4abb-bc5f-fd16ee4e049b.png?v=1734080796"},{"product_id":"enantyum-10bs-soluz-25mg-10ml","title":"ENANTYUM*10SA SOL 25MG 10ML","description":"\u003cp\u003e\u003cb\u003eEnantyum 25 mg oral solution in sachet\u003c\/b\u003e\u003cbr\u003e Dexketoprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eThis medicine is a painkiller belonging to the group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs).\u003cbr\u003e It is used for the short-term symptomatic treatment of acute pain of mild to moderate intensity, such as acute muscular pain, joint pain, painful menstruation (dysmenorrhoea), toothache. This medicine is indicated for adults.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Enantyum\u003c\/b\u003e\u003cbr\u003e • if you are allergic to dexketoprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • if you are allergic to acetylsalicylic acid or other non-steroidal anti-inflammatory drugs;\u003cbr\u003e • if you suffer from asthma or have suffered from asthma attacks, acute allergic rhinitis (short periods of nasal mucous membrane inflammation), nasal polyps (polypoid masses in the nose due to allergy), urticaria (skin rash), angioedema (swelling of the face, eyes, lips or tongue, or breathing difficulties) or wheezing in the chest, after taking acetylsalicylic acid or other non-steroidal anti-inflammatory drugs;\u003cbr\u003e • if you have suffered from photoallergic or phototoxic reactions (a particular form of redness and\/or irritation of the skin exposed to sunlight) in conjunction with the use of ketoprofen (an NSAID) or fibrates (medicines used to lower blood lipid levels);\u003cbr\u003e • if you suffer from peptic ulcer\/bleeding of the stomach or intestine or if you have a history of bleeding, ulceration or perforation of the stomach or intestine;\u003cbr\u003e • if you have chronic digestive problems (e.g. indigestion, heartburn);\u003cbr\u003e • if you have a history of stomach or intestinal bleeding or perforation due to the use of non-steroidal anti-inflammatory drugs (NSAIDs) for pain;\u003cbr\u003e • if you suffer from chronic inflammatory bowel diseases (Crohn's disease or ulcerative colitis);\u003cbr\u003e • if you suffer from severe heart failure, moderate or severe kidney failure, severe liver failure;\u003cbr\u003e • if you have bleeding problems or coagulation disorders;\u003cbr\u003e • if you are severely dehydrated (have lost a lot of fluids) due to vomiting, diarrhoea or insufficient fluid intake;\u003cbr\u003e • if you are in the third trimester of pregnancy or if you are breastfeeding.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Enantyum:\u003cbr\u003e • if you suffer from allergies, or have had allergy problems in the past;\u003cbr\u003e • if you have kidney, liver or heart conditions (hypertension and\/or heart failure) and fluid retention, or if you have suffered from any of these conditions in the past;\u003cbr\u003e • if you are on diuretics or if you are poorly hydrated and have reduced blood volume due to excessive fluid loss (e.g. excessive urination, diarrhoea, vomiting);\u003cbr\u003e • if you suffer from heart conditions, if you have had a stroke or if you think you may be at risk for these conditions (for example, if you have high blood pressure, diabetes or high cholesterol or if you are a smoker), discuss the therapy with your doctor or pharmacist; medicines like Enantyum may be associated with a slight increase in the risk of heart attack (myocardial infarction) or cerebrovascular accident (stroke). These risks are more likely with high doses of the drug and with prolonged therapy. Do not exceed the recommended dose or duration of treatment;\u003cbr\u003e • if you are elderly, the risk of side effects is higher (see point 4); if they occur, consult your doctor immediately;\u003cbr\u003e • if you are a woman with fertility problems (this medicine may reduce female fertility, therefore you should not take the medicine if you are planning a pregnancy or if you are undergoing fertility investigations);\u003cbr\u003e • if you suffer from a disorder of blood and blood cell formation;\u003cbr\u003e • if you suffer from systemic lupus erythematosus or mixed connective tissue disease (immune system disorders affecting connective tissue);\u003cbr\u003e • if you have a history of chronic inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • if you suffer or have suffered in the past from other stomach or intestinal disorders;\u003cbr\u003e • if you have an infection – see paragraph \"Infections\" below;\u003cbr\u003e • if you are taking other medicines that increase the risk of peptic ulcer or bleeding, e.g. oral steroids, some antidepressants (e.g. SSRIs, selective serotonin reuptake inhibitors), antiplatelet agents such as aspirin or anticoagulants such as warfarin. In these cases, consult your doctor before taking this medicine: they may prescribe an additional medicine to protect your stomach (e.g. misoprostol or other medicines that reduce gastric acid production);\u003cbr\u003e • if you suffer from asthma associated with chronic rhinitis, chronic sinusitis and\/or nasal polyposis, as you have a higher risk of allergy to acetylsalicylic acid and\/or NSAIDs compared to the rest of the population. The administration of this medicine may cause asthma attacks or bronchospasm, especially in subjects allergic to acetylsalicylic acid or NSAIDs.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e Dexketoprofen can mask the symptoms of infections such as fever and pain. Therefore, this medicine may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e The use of dexketoprofen has not been studied in children and adolescents. Therefore, safety and efficacy have not been established and the medicine should not be used in children and adolescents.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Enantyum can cause side effects, although not everybody gets them.\u003cbr\u003e The possible side effects are listed below, ordered according to the probability with which they may occur. Since the list is partly based on the side effects of the tablet formulation of Enantyum, and Enantyum oral solution is absorbed more rapidly than tablets, it is possible that the actual frequency of (gastrointestinal) side effects may be higher with Enantyum oral solution in sachet.\u003cbr\u003e \u003cbr\u003e\u003cb\u003e Common side effects (may affect up to 1 in 10 patients):\u003c\/b\u003e\u003cbr\u003e Nausea and\/or vomiting, abdominal pain mainly in the upper quadrants, diarrhoea, digestive problems (dyspepsia).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon side effects (may affect up to 1 in 100 patients):\u003c\/b\u003e\u003cbr\u003e Dizziness (vertigo), dizziness, drowsiness, insomnia, nervousness, headache, palpitations, flushing, inflammation of the gastric wall (gastritis), constipation, dry mouth, flatulence, skin rash, fatigue, pain, feverish sensation and chills, general malaise (malaise).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare side effects (may affect up to 1 in 1,000 patients):\u003c\/b\u003e\u003cbr\u003e Peptic ulcer, bleeding or perforated peptic ulcer (manifested by haematemesis, i.e. vomiting blood, or black stools), fainting, hypertension, slowed breathing, fluid retention and peripheral oedema (e.g. swollen ankles), laryngeal oedema, loss of appetite (anorexia), altered sensation, pruritic rash, acne, increased sweating, back pain, frequent urination, menstrual disorders, prostate problems, abnormal liver function tests (blood tests), hepatocellular damage (hepatitis), acute kidney failure.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 patients):\u003c\/b\u003e\u003cbr\u003e Anaphylactic reactions (hypersensitivity reactions that can also lead to collapse), open wounds on the skin, mouth, eyes and genital area (Stevens-Johnson and Lyell syndromes), facial oedema or swelling of the lips and throat (angioneurotic oedema), shortness of breath due to muscle contraction surrounding the airways (bronchospasm), rapid heartbeat, hypotension, pancreatitis, blurred vision, ringing in the ears (tinnitus), sensitive skin, sensitivity to light, itching, kidney problems. Reduced white blood cell count (neutropenia), decreased blood platelets (thrombocytopenia).\u003cbr\u003e \u003cbr\u003e Inform your doctor immediately if you notice any stomach or intestinal side effects at the beginning of treatment (e.g. stomach pains, heartburn or bleeding), if you have previously suffered from these side effects due to prolonged use of anti-inflammatory drugs, and especially if you are elderly.\u003cbr\u003e \u003cbr\u003e Stop using this medicine as soon as you notice a skin rash or any lesion inside the mouth or genitals, or any sign of allergy.\u003cbr\u003e \u003cbr\u003e During treatment with non-steroidal anti-inflammatory drugs, fluid retention and swelling (particularly of the ankles and legs), increased blood pressure and heart failure have been reported.\u003cbr\u003e \u003cbr\u003e Medicines like Enantyum may be associated with a small increased risk of heart attack (myocardial infarction) or cerebrovascular accident (stroke).\u003cbr\u003e \u003cbr\u003e In patients suffering from immune system disorders affecting connective tissue (systemic lupus erythematosus or mixed connective tissue disease), anti-inflammatory drugs may, in rare cases, cause fever, headache and neck stiffness.\u003cbr\u003e \u003cbr\u003e The most commonly observed adverse events are gastrointestinal in nature. Peptic ulcers, perforation or gastrointestinal bleeding may occur, sometimes fatal, especially for the elderly. Nausea, vomiting, diarrhoea, flatulence, constipation, dyspepsia, abdominal pain, melaena, haematemesis, ulcerative stomatitis, worsening of colitis and Crohn's disease have been reported following administration. Less frequently, inflammation of the gastric wall (gastritis) has been observed. \u003cbr\u003e \u003cbr\u003e As with other NSAIDs, aseptic meningitis may occur, which may occur predominantly in patients with systemic lupus erythematosus or mixed connective tissue disease and haematological reactions (purpura, aplastic and haemolytic anaemia, and more rarely agranulocytosis and bone marrow hypoplasia).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"A.MENARINI IND.FARM.RIUN.Srl","offers":[{"title":"Default Title","offer_id":46290158977291,"sku":"033656416","price":5.58,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_1f1c9e1c-5933-4e4d-87aa-786ddd1189cf.png?v=1734080839"},{"product_id":"neonisidina-12cpr","title":"NEONISIDINA*12TABLETS","description":"\u003cp\u003e\u003cb\u003eNEO NISIDINA tablets\u003c\/b\u003e\u003cbr\u003eAcetylsalicylic acid + paracetamol + caffeine\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eNEO NISIDINA is an oral medicine that relieves pain (analgesic) and reduces fever (antipyretic), containing three active ingredients: acetylsalicylic acid, paracetamol, and caffeine.\u003cbr\u003e\u003cbr\u003eNEO NISIDINA is used for the treatment of headaches, nerve inflammation (neuralgia), toothache, menstrual pain, joint pain, feverish states, and common colds.\u003cbr\u003e\u003cbr\u003eConsult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take NEO NISIDINA\u003c\/b\u003e\u003cbr\u003e- if you are allergic to acetylsalicylic acid, paracetamol, caffeine, or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e- if you are allergic to medicines belonging to the salicylate group or non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e- if you have previously developed symptoms such as asthma, swelling of the face, tongue, and throat (angioedema) and hives after taking non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e- if you have lesions in your stomach or the first part of your intestine (gastric or duodenal ulcer);\u003cbr\u003e- if you have a predisposition to bleeding (hemorrhages), for example, if you suffer from blood clotting disorders (hemophilia);\u003cbr\u003e- if you are in the third trimester of pregnancy;\u003cbr\u003e- if you are under 16 years of age;\u003cbr\u003e- if you are between 16 and 18 years old and have chickenpox or the flu virus, as it can cause serious complications (see section \"Children and adolescents\");\u003cbr\u003e- if you suffer from asthma;\u003cbr\u003e- if you suffer from severe kidney, liver, or heart problems;\u003cbr\u003e- if you are taking methotrexate (at doses of 15 mg\/week or more) (see section \"Other medicines and NEO NISIDINA\");\u003cbr\u003e- if you suffer from a disease caused by glucose-6-phosphate dehydrogenase deficiency;\u003cbr\u003e- if you suffer from a blood disorder characterized by a low number of red blood cells (severe hemolytic anemia).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking NEO NISIDINA.\u003cbr\u003e\u003cbr\u003eAvoid using this medicine for more than 3 days without first consulting your doctor and without their direct supervision. If pain or fever persist or worsen, if new symptoms appear, or if there is redness or swelling, consult your doctor immediately as these could be signs of an worsening of the existing condition.\u003cbr\u003e\u003cbr\u003eTake this medicine \u003cb\u003ewith caution\u003c\/b\u003e and only on your doctor's advice in the following cases:\u003cbr\u003e- if you suffer from allergic rhinitis and nasal polyps;\u003cbr\u003e- if you have chronic or recurrent stomach or intestinal problems or if you have previously suffered from ulcers, bleeding, or perforation in the stomach or intestine;\u003cbr\u003e- if you suspect you are allergic to other similar medicines (analgesic antipyretics or non-steroidal anti-inflammatory drugs (NSAIDs));\u003cbr\u003e- if you regularly consume alcoholic beverages;\u003cbr\u003e- if you suffer from liver problems (mild or moderate liver failure, altered liver function, e.g., due to chronic alcohol abuse, hepatitis, Gilbert's syndrome);\u003cbr\u003e- if you have kidney problems (altered kidney function and mild or moderate kidney failure);\u003cbr\u003e- if you are taking blood thinners (oral anticoagulants, antiplatelet agents, systemic heparin, thrombolytics, or other drugs) (see section \"Other medicines and NEO NISIDINA\");\u003cbr\u003e- if you are scheduled for surgery or an invasive diagnostic examination, as blood clotting problems could occur;\u003cbr\u003e- if you are in the first or second trimester of pregnancy;\u003cbr\u003e- if you are elderly and over 70 years old, especially if you are taking other medicines simultaneously.\u003cbr\u003e\u003cbr\u003eAvoid prolonged or frequent use of the medicine without first consulting your doctor and do not take other paracetamol-containing products simultaneously, as serious side effects can occur if paracetamol is taken in high doses. The risk of serious side effects is also increased when NEO NISIDINA is taken together with other medicines used to relieve pain (analgesics) or lower fever (antipyretics), therefore avoid the concomitant use of these medicines.\u003cbr\u003e\u003cbr\u003eAbrupt discontinuation of analgesics after a prolonged period of incorrect use at high doses can cause headaches, fatigue, nervousness, and withdrawal symptoms that resolve within a few days. Until then, avoid taking other painkillers and do not resume taking them without consulting your doctor.\u003cbr\u003e\u003cbr\u003eIncorrect use of the medicine (for doses or durations higher than indicated) can cause serious damage, particularly to the liver, kidneys (analgesic nephropathy), or blood, which could be life-threatening for the patient.\u003cbr\u003eAcetylsalicylic acid can decrease uric acid elimination and cause a gout attack in susceptible individuals, and can also mask the symptoms of an infection.\u003cbr\u003e\u003cbr\u003eTaking this medicine may alter the results of some laboratory tests, such as the measurement of uric acid (uricemia) or sugar (glycemia) levels in the blood.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003eThis medicine is contraindicated in children and adolescents under 16 years of age, but in cases of suspected viral infection, such as the flu or chickenpox, NEO NISIDINA should not be taken even by adolescents aged between 16 and 18 years (see section \"Do not use NEO NISIDINA\"). In this case, there is a risk of a rare and life-threatening disease characterized by vomiting, headache, loss of consciousness, liver failure, and central nervous system problems (Reye's syndrome), which requires immediate medical attention.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003eYou may experience:\u003cbr\u003e- stomach upset, nausea, vomiting, stomach and intestinal lesions (gastroduodenal ulcers) and inflammation of the stomach (erosive gastritis) which can lead to severe bleeding. These effects occur mainly after the use of high doses but can also occur at low doses;\u003cbr\u003e- severe allergic reactions with symptoms such as low blood pressure (hypotension), breathing problems (dyspnea, bronchoconstriction), anaphylactic shock, swelling of the face, lips and throat (angioneurotic edema), skin reactions;\u003cbr\u003e\u003cbr\u003eFurthermore, after using NEO NISIDINA, you may experience the following side effects:\u003cbr\u003e\u003cb\u003eCommon\u003c\/b\u003e (may affect up to 1 in 10 people):\u003cbr\u003e- nervousness;\u003cbr\u003e- dizziness;\u003cbr\u003e- abdominal pain, indigestion (dyspepsia), nausea.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon\u003c\/b\u003e (may affect up to 1 in 100 people):\u003cbr\u003e- feeling of rapid heartbeat (palpitations);\u003cbr\u003e- vomiting, diarrhea.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare\u003c\/b\u003e (may affect up to 1 in 1000 people):\u003cbr\u003e- agitation, tremor;\u003cbr\u003e- dizziness caused by ear problems;\u003cbr\u003e- altered heart rate (tachycardia);\u003cbr\u003e- inflammation of the esophagus (esophagitis);\u003cbr\u003e- hyperhidrosis (increased sweating);\u003cbr\u003e- feeling of tiredness and fatigue;\u003cbr\u003e- altered liver function and increased levels of certain enzymes (transaminases);\u003cbr\u003e- stomach or intestinal lesions (gastrointestinal ulcer) and bleeding.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare\u003c\/b\u003e (may affect up to 1 in 10,000 people):\u003cbr\u003e- reduction of blood glucose levels (hypoglycemia);\u003cbr\u003e- severe lesions of the stomach or intestinal mucosa (gastrointestinal perforation); severe skin diseases (including erythema multiforme);\u003cbr\u003e- impaired kidney function;\u003cbr\u003e- decrease in the number of platelets, white blood cells, or all blood components, including red blood cells (hematocrit alterations, thrombocytopenia, leukopenia, agranulocytosis, pancytopenia);\u003cbr\u003e- allergic reactions such as erythema, urticaria, nausea, Quincke's edema, swelling, difficulty breathing (dyspnea) and anaphylactic shock;\u003cbr\u003e- difficulty breathing caused by bronchoconstriction in people allergic to non-steroidal anti-inflammatory drugs (NSAIDs).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eNot known\u003c\/b\u003e (frequency cannot be estimated from the available data):\u003cbr\u003e- increased risk of bleeding such as nosebleeds (epistaxis) and gum bleeding (gingivorrhagia) due to the antiplatelet effect of acetylsalicylic acid which can last for several days after discontinuation of treatment; headache, drowsiness, confusion;\u003cbr\u003e- vision disorders;\u003cbr\u003e- hearing problems, sound or noise perceived by the patient but not generated by the external environment (tinnitus);\u003cbr\u003e- prolongation of pregnancy and labor;\u003cbr\u003e- kidney problems (acute renal failure, interstitial nephritis, hematuria, anuria);\u003cbr\u003e- severe skin reactions (erythema multiforme, Stevens-Johnson syndrome and epidermal necrolysis);\u003cbr\u003e- iron deficiency anemia, due to bleeding in the digestive tract, especially after prolonged use of acetylsalicylic acid;\u003cbr\u003e\u003cbr\u003eIn cases of overdose, due to the presence of paracetamol, hepatic cytolysis can occur, which can progress to massive and irreversible necrosis.\u003cbr\u003e\u003cbr\u003eThe presence of caffeine, a central nervous system stimulant, can cause agitation, insomnia, tremor, dyspeptic symptoms and tachycardia.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"PHARMAIDEA Srl","offers":[{"title":"Default Title","offer_id":46290160091403,"sku":"004558185","price":6.2,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_225b2078-80df-4c57-8992-f203be7acfb3.jpg?v=1734080867"},{"product_id":"momentact-12cpr-riv-400mg","title":"MOMENTACT*12 FILM-COATED TABLETS 400MG","description":"\u003cp\u003e\u003cb\u003eMOMENTACT 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMomentact contains ibuprofen, a medicine belonging to the class of analgesic-anti-inflammatory drugs, meaning medicines that combat pain and inflammation.\u003cbr\u003e \u003cbr\u003e Momentact is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents from 12 years of age\u003c\/b\u003e, to treat:\u003cbr\u003e - pain of various origins and nature (headache, toothache, neuralgia, osteoarticular and muscular pain, menstrual pain) and to help reduce the symptoms of feverish and flu-like conditions.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Momentact:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you are allergic to other anti-rheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see paragraph Other medicines and Momentact), or allergic to any of the other ingredients of this medicine;\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breastfeeding (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have previously had bleeding or perforation of the stomach or intestine after taking medicines;\u003cbr\u003e - if you have previously had two or more distinct episodes of ulcer or stomach bleeding;\u003cbr\u003e - if you have severe heart disease;\u003cbr\u003e - if you have severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eWhat you need to know before taking Momentact\u003cbr\u003e \u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck region (angioedema) and chest pain, have been reported with ibuprofen. Stop Momentact immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003e Severe skin reactions have been reported in association with ibuprofen treatment, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP).\u003cbr\u003e Stop taking Momentact and consult your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in paragraph 4.\u003cbr\u003e \u003cbr\u003e Consult your doctor or pharmacist before taking Momentact:\u003cbr\u003e - if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, runny nose (chronic rhinitis), nasal polyps (nasal polyposis) or inflammation of the nasal mucosa (sinusitis) or suffer\/have suffered from allergies because you could experience difficulty breathing (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see paragraph Other medicines and Momentact);\u003cbr\u003e - if you are elderly or if you have suffered from an ulcer, especially if the ulcer also manifested with bleeding or perforation (see paragraph Do not take Momentact), as the risk of bleeding, ulcer or perforation is higher with high doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly consult your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you are taking low doses of acetylsalicylic acid or medicines that may increase the risk of stomach and\/or intestinal diseases (see paragraph Other medicines and Momentact);\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see paragraph 4 Possible side effects);\u003cbr\u003e - if you have had stomach and intestinal diseases related to the use of medicines, and in particular if you are elderly, you should report any unusual intestinal symptoms (especially bleeding) to your doctor, particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcer or stomach and\/or intestinal bleeding, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (serotonin inhibitors), or antiplatelet agents (e.g. acetylsalicylic acid). See also paragraph Other medicines and Momentact. If gastrointestinal bleeding or ulceration occurs in patients taking Momentact, treatment should be discontinued;\u003cbr\u003e - if you have high blood pressure and the medicines you are taking are unable to lower it and\/or you have heart disease or blood circulation problems in the brain or periphery or you think you may be at risk for these diseases (for example, if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or have heart disease, as fluid retention, increased blood pressure and swelling have been observed following treatment with NSAIDs. NSAIDs can reduce the action of medicines to lower blood pressure (see paragraph Other medicines and Momentact);\u003cbr\u003e - if you have lost a considerable amount of fluids, or if you experience swelling, heart problems or high blood pressure;\u003cbr\u003e - if you have decreased kidney function, heart or liver malfunction, or if you are elderly or on treatment with medicines for high blood pressure, as you may be more prone to kidney problems. Furthermore, the usual concomitant use of several painkillers can further increase this risk;\u003cbr\u003e - if you suffer from heart disease;\u003cbr\u003e - if you suffer from liver diseases (hepatic dysfunction);\u003cbr\u003e - if you are elderly, as the risk of bleeding, ulcers and perforations is increased compared to other patients;\u003cbr\u003e - if you suffer from a clotting disorder or are taking medicines to thin the blood (anticoagulants) (see paragraph Other medicines and Momentact);\u003cbr\u003e - if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of aseptic meningitis have been observed in patients treated with ibuprofen.\u003cbr\u003e Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients who did not manifest concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see paragraph Other medicines and Momentact);\u003cbr\u003e - if you intend to become pregnant (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have difficulty becoming pregnant or are undergoing fertility investigations (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - If you have an infection - see paragraph Infections below;\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss your therapy with your doctor or pharmacist before taking Momentact if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Medicines like Momentact can:\u003cbr\u003e - be associated with the appearance of even serious kidney diseases (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e - cause eye disorders, therefore, in case of prolonged treatments, periodic eye examinations are recommended. If you experience vision disturbances, stop treatment with Momentact.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Momentact can mask the symptoms of infections such as fever and pain. It is therefore possible that Momentact may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003e If the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Momentact can cause side effects, although not everyone experiences them. The side effects of the medicine can be minimised if you use the lowest recommended dose, and if you use the medicine only for the period necessary to control your symptoms.\u003cbr\u003e \u003cbr\u003e If you develop an ulcer, or stomach and\/or intestinal bleeding occurs, or skin and\/or mucous membrane lesions, you must stop treatment with Momentact and consult your doctor. Usually these side effects are more frequent in the elderly.\u003cbr\u003e \u003cbr\u003e The use of Momentact can cause generally mild or moderate side effects or more serious, allergic reactions, albeit rarely.\u003cbr\u003e \u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP using Momentact immediately\u003c\/b\u003e and consult your doctor or the nearest hospital where you will undergo appropriate and specific treatment:\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucous membrane lesions;\u003cbr\u003e • signs of an allergic reaction, even severe (erythema, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • peeling skin;\u003cbr\u003e • non-raised reddish patches, target-shaped or circular on the trunk, often with central vesicles, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson syndrome);\u003cbr\u003e • widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and vesicles, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • vision disturbances;\u003cbr\u003e • liver disease (hepatic dysfunction);\u003cbr\u003e • bleeding, ulcer and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e \u003cbr\u003e In case of an allergic reaction among those listed above, go to the hospital as it is necessary to have immediate availability of equipment, medicines and personnel suitable for emergency treatment, as in rare cases, following the use of ibuprofen, serious side effects, sometimes with fatal outcome, have been reported, even in the absence of known allergy.\u003cbr\u003e \u003cbr\u003e The risk of experiencing these symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e Furthermore, you may experience further side effects that have also been reported with other medicines similar to Momentact and which are listed below according to frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness\u003cbr\u003e • malaise\u003cbr\u003e • fatigue\u003cbr\u003e \u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • stomach inflammation (gastritis)\u003cbr\u003e • insomnia, anxiety\u003cbr\u003e • numbness of the limbs or other parts of the body, drowsiness\u003cbr\u003e • nasal congestion (rhinitis)\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnoea)\u003cbr\u003e • momentary interruption of breathing (apnoea)\u003cbr\u003e • hearing impairment\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • vertigo\u003cbr\u003e • liver disorders (impaired liver function)\u003cbr\u003e • liver inflammation (hepatitis)\u003cbr\u003e • yellowing of the skin and eyes (jaundice)\u003cbr\u003e • kidney diseases (kidney function damage and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure)\u003cbr\u003e • hypersensitivity reactions such as rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), asthma, difficulty breathing (bronchospasm or dyspnoea), asthma attacks with lowering of blood pressure\u003cbr\u003e • skin reactions to light (photosensitivity)\u003cbr\u003e \u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leucopenia, neutropenia, agranulocytosis), red blood cells (haemolytic anaemia, aplastic anaemia), platelets (thrombocytopenia)\u003cbr\u003e • depression, confusional state, hallucinations\u003cbr\u003e • inflammation of the optic nerve (optic neuritis)\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis), especially in patients with pre-existing autoimmune disorders (see paragraph Warnings and precautions), with symptoms of neck stiffness, headache, nausea, vomiting, fever or disorientation\u003cbr\u003e • eye disorders with vision disturbances and optic nerve pathology (toxic optic neuropathy)\u003cbr\u003e • swelling due to fluid accumulation in the tissues\u003cbr\u003e • disease that can affect various organs and tissues of the body (lupus erythematosus)\u003cbr\u003e • worsening of inflammations caused by an existing infection (e.g. development of necrotizing fasciitis)\u003cbr\u003e \u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis)\u003cbr\u003e • sensation of feeling one's own heartbeat (palpitations)*\u003cbr\u003e • heart disease (heart failure)*\u003cbr\u003e • heart attack (myocardial infarction)*\u003cbr\u003e • increased fluid around the lungs (acute pulmonary oedema)*\u003cbr\u003e • liver disease (hepatic insufficiency)\u003cbr\u003e • hypertension*\u003cbr\u003e • severe allergic reactions, which may include symptoms such as swelling of the face, tongue and throat making breathing difficult, fast heartbeat, severe rapidly occurring allergic reaction that can cause death (anaphylaxis), severe rash or skin exfoliation (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme)\u003cbr\u003e • severe skin and soft tissue infections can occur during chickenpox infection\u003cbr\u003e \u003cbr\u003e \u003cb\u003e*these side effects tend to resolve with the discontinuation of treatment\u003cbr\u003e \u003cbr\u003e not known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach\u003cbr\u003e • nausea\u003cbr\u003e • vomiting\u003cbr\u003e • diarrhoea\u003cbr\u003e • flatulence\u003cbr\u003e • constipation\u003cbr\u003e • indigestion\u003cbr\u003e • abdominal pain\u003cbr\u003e • heartburn\u003cbr\u003e • blood in stools\u003cbr\u003e • blood in vomit\u003cbr\u003e • lesions inside the mouth\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis, Crohn's disease)\u003cbr\u003e • increased risk of heart attack (myocardial infarction), or lack of blood supply to the brain (stroke)\u003cbr\u003e • high blood pressure\u003cbr\u003e • severe heart disease (heart failure)\u003cbr\u003e • a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell)\u003cbr\u003e • a widespread, red and scaly rash, with pustule formation under the skin and vesicles located mainly on the skin folds, trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalised exanthematous pustulosis). Stop using Momentact if you develop these symptoms and contact your doctor immediately. See also paragraph 2\u003cbr\u003e • chest pain, which can be a sign of a potentially severe allergic reaction called Kounis syndrome\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290160451851,"sku":"035618026","price":8.76,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_e09cbb42-8d2c-40b4-bce5-2aca0a6904e7.png?v=1734080884"},{"product_id":"nurofen-24cpr-riv-200mg","title":"NUROFEN*24FC 200MG","description":"\u003cp\u003e\u003cb\u003eNUROFEN 200 mg film-coated tablets\u003cbr\u003eNUROFEN 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003eIbuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eNurofen contains ibuprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action reduces pain and swelling caused by inflammation and fever.\u003cbr\u003e\u003cbr\u003eNurofen is indicated in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents over 12 years of age\u003c\/b\u003e for the treatment of various types of pain: headache, toothache, neuralgia, muscle, bone and joint pain, menstrual pain.\u003cbr\u003eNurofen is also indicated as an adjuvant for the symptomatic treatment of feverish and flu-like conditions.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen. Stop Nurofen immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eDo not take Nurofen if:\u003c\/b\u003e\u003cbr\u003e• you are allergic (hypersensitive) to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e• you have previously experienced allergic reactions such as breathing difficulties (bronchospasm, asthma), rhinitis (runny nose), swelling of the face, lips, and throat (angioedema), or hives after taking ibuprofen, acetylsalicylic acid, or other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e• you suffer from severe kidney or liver disease (renal or hepatic insufficiency);\u003cbr\u003e• you suffer from severe heart disease (severe heart failure);\u003cbr\u003e• you have suffered from stomach bleeding or perforation following previous NSAID treatments;\u003cbr\u003e• you suffer or have suffered from current or recurrent gastric\/duodenal ulcers (peptic ulcers) or bleeding (at least two distinct episodes of demonstrated ulceration or bleeding);\u003cbr\u003e• you are in the last trimester of pregnancy;\u003cbr\u003e• you are about to undergo or have undergone heart surgery.\u003cbr\u003e\u003cbr\u003eDo not administer Nurofen to children under 12 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Nurofen if:\u003cbr\u003e• you are taking other medicines used for pain treatment, to reduce fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section Other medicines and Nurofen);\u003cbr\u003e• you are elderly and\/or have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation, as an increase in gastrointestinal bleeding and perforations may occur. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low doses of aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section Other medicines and Nurofen).\u003cbr\u003eDuring treatment with all NSAIDs, at any time, with or without warning symptoms or previous history of serious gastrointestinal events, bleeding, ulceration, and perforation of the stomach or intestine may occur, which can be fatal. Therefore, inform your doctor of any unusual gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the early stages of treatment. If gastrointestinal bleeding or ulceration occurs, discontinue Nurofen and contact your doctor;\u003cbr\u003e• you suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e• you are taking medicines that could increase the risk of ulceration or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section Other medicines and Nurofen);\u003cbr\u003e• you suffer from high blood pressure and\/or severe heart disease (heart failure) since, in association with NSAID therapy, fluid retention, high blood pressure, and swelling have been reported;\u003cbr\u003e• you suffer from reduced liver and\/or kidney function, as habitual use of analgesic medicines like Nurofen can lead to severe permanent kidney problems (with possible onset of renal failure). Your doctor will advise you to perform periodic tests during treatment;\u003cbr\u003e• you suffer or have suffered from asthma (difficulty breathing) or allergic reactions as you may experience shortness of breath;\u003cbr\u003e• you suffer from coagulation problems;\u003cbr\u003e• you suffer from a chronic autoimmune disease that causes disorders in various parts of the body, particularly the skin (systemic lupus erythematosus) or from mixed connective tissue disease, as it increases the risk of aseptic meningitis; you experience the first signs of a hypersensitivity reaction after taking Nurofen. If this occurs or is suspected, you should stop taking Nurofen and consult your doctor. Medically assisted measures must be initiated by specialized medical personnel, in line with the symptomatology;\u003cbr\u003eAnti-inflammatory\/pain relief medicines based on ibuprofen can cause a prolongation of bleeding time by reversibly inhibiting platelet aggregation;\u003cbr\u003e• you have an infection - see section Infections below.\u003cbr\u003e\u003cbr\u003eAnti-inflammatory\/pain relief medicines like ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered at high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003eYou should discuss your therapy with your doctor or pharmacist before taking Nurofen if you have:\u003cbr\u003e• heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary artery bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e• high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003eSkin reactions\u003cbr\u003eSevere skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Stop using Nurofen and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003eInfections\u003cbr\u003eNurofen can mask the symptoms of infections such as fever and pain. Therefore, it is possible that Nurofen may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the infection symptoms persist or worsen, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003eDo not give this medicine to children under 12 years of age.\u003cbr\u003eCaution is required in dehydrated adolescents (12-18 years) as there is a risk of impaired renal function.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003eIf you experience any of the following side effects, \u003cb\u003eSTOP\u003c\/b\u003e treatment and contact your doctor:\u003cbr\u003e• allergic reactions, including severe ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnea), altered heart rate (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma.\u003cbr\u003e• reddish, non-raised, target-shaped or circular patches on the trunk, often with central blisters, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis].\u003cbr\u003e• widespread rash, high body temperature, and enlarged lymph nodes (DRESS syndrome).\u003cbr\u003e• widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003eFurther side effects include:\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e• stomach problems, such as heartburn, stomach pain, and nausea\u003cbr\u003e• headache\u003cbr\u003e• dizziness\u003cbr\u003e• skin rashes\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e• diarrhea, vomiting, flatulence, constipation\u003cbr\u003e• increased transaminases, increased alkaline phosphatase, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased uric acid\u003cbr\u003e• stroke\u003cbr\u003e• liver damage (hepatotoxicity)\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e• peptic ulcers, perforation and bleeding of the stomach and intestine, black stools and vomiting blood\u003cbr\u003e• lesions with bleeding of the mouth, heartburn (gastritis)\u003cbr\u003e• severe heart disease (heart failure), edema, and high blood pressure (hypertension)\u003cbr\u003e• severe kidney diseases (renal failure, papillary necrosis) particularly following long-term treatments, associated with an increase in blood urea concentration (the first signs are: urinating less than normal, general malaise). Presence of blood in the urine (hematuria), kidney inflammation (nephritis), a set of signs and symptoms such as protein loss in the urine, decreased protein levels in the blood, fluid accumulation in the body with consequent swelling, increased lipid or fat levels in the blood, blood hypercoagulability, related to kidney diseases (nephrotic syndrome)\u003cbr\u003e• liver damage, especially following long-term treatments, hepatitis, jaundice\u003cbr\u003e• reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe fatigue, nose and skin bleeding, skin bruises (hematomas)\u003cbr\u003e• aseptic meningitis with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (more frequent if you suffer from systemic lupus erythematosus or mixed connective tissue disease)\u003cbr\u003e• decreased hemoglobin levels in the blood\u003cbr\u003e• visual disturbances\u003cbr\u003e\u003cbr\u003e\u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e• Chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e• respiratory tract disorders including asthma, worsening of asthma, wheezing (bronchospasm) and difficulty breathing (dyspnea)\u003cbr\u003e• worsening of inflammatory bowel diseases (colitis and Crohn's disease)\u003cbr\u003e• a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes, and increased eosinophils (a type of white blood cell)\u003cbr\u003e• inflammation of the pancreas (pancreatitis)\u003cbr\u003e• a widespread, red and scaly rash, with the formation of pustules under the skin and blisters localized mainly on the skin folds, on the trunk and on the upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003eStop using Nurofen if you develop these symptoms and contact your doctor immediately.\u003cbr\u003eSee also section 2.\u003cbr\u003e• the skin becomes sensitive to light. The use of ibuprofen, especially at high doses (2400 mg\/day), may be associated with a modest increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"RECKITT BENCKISER H.(IT.) SpA","offers":[{"title":"Default Title","offer_id":46290170544395,"sku":"025634041","price":6.56,"currency_code":"EUR","in_stock":true}]},{"product_id":"aspirina-dolore-inf-20cpr500mg","title":"ASPIRIN PAIN INF*20TB500MG","description":"\u003cp\u003e\u003cb\u003eAspirin Pain and Inflammation\u003c\/b\u003e\u003cbr\u003e  500 mg film-coated tablets\u003cbr\u003e  Acetylsalicylic acid\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eAspirin Pain and Inflammation contains acetylsalicylic acid. Acetylsalicylic acid is an analgesic (reduces pain) and antipyretic (reduces fever).\u003cbr\u003e  Aspirin Pain and Inflammation is used for the symptomatic treatment of fever and\/or mild to moderate pain, such as headache, flu-like symptoms, toothache, muscle pain.\u003cbr\u003e  \u003cb\u003eAspirin Pain and Inflammation is specifically reserved for adults and adolescents aged 16 years and over.\u003c\/b\u003e\u003cbr\u003e  Consult your doctor or pharmacist for other forms of acetylsalicylic acid for patients weighing less than 40 kg.\u003cbr\u003e  \u003cbr\u003e  Consult your doctor if you do not notice improvements or if you notice a worsening of symptoms after 3 days (for fever) or 3-4 days (for pain).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Aspirin Pain and Inflammation:\u003c\/b\u003e\u003cbr\u003e  • if you are allergic to acetylsalicylic acid or other salicylates or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e  • if you have suffered from asthma or allergic reactions (e.g. urticaria, angioedema, severe rhinitis, shock) induced by the administration of acetylsalicylic acid or related medicines (in particular non-steroidal anti-inflammatory drugs);\u003cbr\u003e  • if you suffer from a stomach or intestinal ulcer (including duodenal ulcer);\u003cbr\u003e  • if you suffer from a bleeding condition or are at risk of bleeding;\u003cbr\u003e  • if you suffer from severe hepatic, renal, or cardiac insufficiency;\u003cbr\u003e  • if you are taking methotrexate in doses exceeding 15 mg\/week;\u003cbr\u003e  • if you are taking oral anticoagulants (medicines to thin the blood and prevent clot formation);\u003cbr\u003e  • if you are after the 5th month of pregnancy (more than 24 weeks without menstruation);\u003cbr\u003e  • Children and adolescents under 16 years of age.\u003cbr\u003e  \u003cbr\u003e  If in doubt, consult your doctor or pharmacist before taking this medicine.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Aspirin Pain and Inflammation:\u003cbr\u003e  \u003cbr\u003e  • if you are taking other products containing acetylsalicylic acid, to avoid the risk of overdose;\u003cbr\u003e  • if you experience headache while taking high doses of acetylsalicylic acid for a prolonged period of time, do not increase the dosage but rather ask your doctor or pharmacist for advice;\u003cbr\u003e  • if you use painkillers regularly, especially different painkillers in combination, this can lead to reduced kidney function;\u003cbr\u003e  • if you have a G6PD deficiency (Glucose-6-phosphate dehydrogenase), a hereditary disease affecting red blood cells, because high doses of acetylsalicylic acid could lead to hemolysis (destruction of red blood cells);\u003cbr\u003e  • if you have a history of stomach or intestinal ulcers, or stomach or intestinal bleeding or gastritis;\u003cbr\u003e  • if you suffer from hepatic or renal insufficiency;\u003cbr\u003e  • if you suffer from asthma: the occurrence of an asthma attack, in some patients, may be related to an allergic reaction to non-steroidal anti-inflammatory drugs or acetylsalicylic acid. In this case, the use of this medicine is not recommended;\u003cbr\u003e  • in case of heavy menstruation;\u003cbr\u003e  • if gastrointestinal bleeding occurs during treatment (blood loss from the mouth, blood in the stools, dark stool color): stop treatment and immediately call your doctor or emergency room;\u003cbr\u003e  • if you are also taking medicines that thin the blood and prevent clotting (anticoagulants);\u003cbr\u003e  • if you suffer from mild or moderate renal impairment;\u003cbr\u003e  • if you suffer from an alteration of cardiovascular circulation;\u003cbr\u003e  • acetylsalicylic acid increases the risk of bleeding even at low doses and even several days after intake. Inform your doctor, surgeon, or anesthetist or dentist if surgery is planned, even minor surgery;\u003cbr\u003e  • acetylsalicylic acid alters the amount of uric acid in the blood. This must be taken into consideration if you are taking a medication for gout;\u003cbr\u003e  • It is recommended not to take this medicine during breastfeeding;\u003cbr\u003e  \u003cbr\u003e\u003cb\u003e  Children\u003c\/b\u003e\u003cbr\u003e  Reye's syndrome (a rare but very serious disease mainly associated with neurological and liver damage) has been observed in children with viral diseases and undergoing acetylsalicylic acid administration. Therefore:\u003cbr\u003e  • in case of a viral disease such as flu or chickenpox, acetylsalicylic acid should not be administered to a child without first consulting a doctor;\u003cbr\u003e  • if signs of dizziness or fainting, behavioral changes, or vomiting occur in a child taking acetylsalicylic acid, immediately inform the doctor.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e  Frequencies: not known: frequency cannot be estimated from the available data.\u003cbr\u003e  \u003cbr\u003e  \u003cb\u003ePossible side effects due to acetylsalicylic acid are:\u003c\/b\u003e\u003cbr\u003e  These side effects are all very serious and you may urgently need medical attention or hospitalization. Immediately inform your doctor or go to the nearest hospital if you notice any of the following symptoms:\u003cbr\u003e  • bleeding (blood loss from the nose or gums, red spots under the skin);\u003cbr\u003e  • allergic reactions such as skin rash, asthma attack, or facial swelling accompanied by difficulty breathing;\u003cbr\u003e  • headache, dizziness, feeling of hearing loss, tinnitus (ringing in the ears) which are usually signs of overdose;\u003cbr\u003e  • cerebral hemorrhage;\u003cbr\u003e  • stomachache;\u003cbr\u003e  • gastrointestinal bleeding. See Warnings and precautions section. These occur more frequently when high doses are taken;\u003cbr\u003e  • Increase in liver enzymes generally reversible with discontinuation of treatment, alteration of liver function (particularly liver cells);\u003cbr\u003e  • urticaria, skin reactions;\u003cbr\u003e  • Reye's syndrome (altered state of consciousness or abnormal behavior, or vomiting) in children with viral diseases and taking acetylsalicylic acid (see Section 2: What you need to know before taking Aspirin Pain and Inflammation);\u003cbr\u003e  • renal impairment and acute kidney damage;\u003cbr\u003e  • intestinal diaphragm disease (a narrowing of the intestine), especially with long-term treatment.\u003cbr\u003e\u003cbr\u003e   \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including those not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"BAYER SpA","offers":[{"title":"Default Title","offer_id":46290171953419,"sku":"041962034","price":7.91,"currency_code":"EUR","in_stock":true}]},{"product_id":"nurofen-12cpr-riv-400mg-pvc-al","title":"NUROFEN*12 COATED TABLETS 400MG PVC\/AL","description":"\u003cp\u003e\u003cb\u003eNUROFEN 200 mg coated tablets\u003cbr\u003e NUROFEN 400 mg coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eNurofen contains ibuprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action helps reduce pain and swelling caused by inflammation and fever.\u003cbr\u003e \u003cbr\u003e Nurofen is indicated in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents over 12 years of age\u003c\/b\u003e for the treatment of various types of pain: headache, toothache, neuralgia, muscle, bone and joint pain, menstrual pain.\u003cbr\u003e Nurofen is also indicated as an adjunct for the symptomatic treatment of fever and flu-like conditions.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema), and chest pain. Stop Nurofen immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eDo not take Nurofen if:\u003c\/b\u003e\u003cbr\u003e • you are allergic (hypersensitive) to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • you have previously had allergic reactions such as breathing difficulties (bronchospasm, asthma), rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or urticaria after taking ibuprofen, acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e • you suffer from severe kidney or liver disease (renal or hepatic insufficiency);\u003cbr\u003e • you suffer from severe heart disease (severe heart failure);\u003cbr\u003e • you have had stomach bleeding or perforation following previous NSAID treatments;\u003cbr\u003e • you suffer or have suffered from current or recurrent gastric\/duodenal ulcers (peptic ulcers) or hemorrhages (at least two distinct episodes of proven ulceration or bleeding);\u003cbr\u003e • you are in the last trimester of pregnancy;\u003cbr\u003e • you are about to undergo or have undergone heart surgery.\u003cbr\u003e \u003cbr\u003e Do not administer Nurofen to children under 12 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Nurofen if:\u003cbr\u003e • you are taking other medicines used to treat pain, lower fever and\/or treat inflammation (non-steroidal anti-inflammatory drugs, NSAIDs including COX-2 inhibitors) (see section Other medicines and Nurofen);\u003cbr\u003e • you are elderly and\/or have suffered from stomach and bowel disorders (history of ulcer), especially if complicated by bleeding or perforation, as there may be an increase in gastrointestinal bleeding and perforations. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low doses of aspirin or other medicines that may increase the risk of stomach and bowel diseases (see section Other medicines and Nurofen).\u003cbr\u003e During treatment with all NSAIDs, at any time, with or without warning symptoms or previous history of serious gastrointestinal events, bleeding, ulceration and perforation of the stomach or intestine may occur, which can be fatal. Therefore, inform your doctor of any unusual gastrointestinal symptoms (especially gastrointestinal bleeding), particularly in the early stages of treatment. If gastrointestinal bleeding or ulceration occurs, discontinue Nurofen and contact your doctor;\u003cbr\u003e • you suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e • you are taking medicines that could increase the risk of ulceration or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section Other medicines and Nurofen);\u003cbr\u003e • you suffer from high blood pressure and\/or severe heart disease (heart failure) because, in association with NSAID therapy, fluid retention, high blood pressure and swelling have been reported;\u003cbr\u003e • you suffer from reduced liver and\/or kidney function, as the habitual use of analgesic medicines such as Nurofen can lead to severe permanent kidney problems (with possible onset of kidney failure). Your doctor will advise you to perform periodic tests during treatment;\u003cbr\u003e • you suffer or have suffered from asthma (difficulty breathing) or allergic reactions as you may experience shortness of breath;\u003cbr\u003e • you suffer from clotting problems;\u003cbr\u003e • you suffer from a chronic autoimmune disease that causes disorders in various parts of the body, particularly the skin (systemic lupus erythematosus) or mixed connective tissue disease, as it increases the risk of aseptic meningitis; you experience the first signs of a hypersensitivity reaction after taking Nurofen. If this occurs or this situation is suspected, you must stop taking Nurofen and consult your doctor. Medically assisted measures must be initiated by specialized medical personnel, in line with the symptomatology;\u003cbr\u003e Anti-inflammatory\/painkiller drugs containing ibuprofen can cause a prolongation of bleeding time by reversibly inhibiting platelet aggregation;\u003cbr\u003e • you have an infection - see section Infections below.\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller drugs like ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss therapy with your doctor or pharmacist before taking Nurofen if you have:\u003cbr\u003e • heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e • high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Skin reactions\u003cbr\u003e Severe skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Nurofen and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.\u003cbr\u003e \u003cbr\u003e Infections\u003cbr\u003e Nurofen can mask the symptoms of infections such as fever and pain. It is therefore possible that Nurofen may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e Do not give this medicine to children under 12 years of age.\u003cbr\u003e Caution is required in dehydrated adolescents (12-18 years) as there is a risk of impaired renal function.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e \u003cbr\u003e If you experience any of the following side effects, \u003cb\u003eSTOP\u003c\/b\u003e treatment and contact your doctor:\u003cbr\u003e • allergic reactions, including severe ones, which may include: urticaria, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnea), altered heart rate (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma.\u003cbr\u003e • non-raised, target-shaped or circular reddish patches on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis].\u003cbr\u003e • Widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome).\u003cbr\u003e • Widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e \u003cbr\u003e Other side effects include:\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • stomach upset, such as heartburn, stomach pain and nausea\u003cbr\u003e • headache\u003cbr\u003e • dizziness\u003cbr\u003e • skin rashes\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • diarrhea, vomiting, flatulence, constipation\u003cbr\u003e • increased transaminases, increased alkaline phosphatase, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased uric acid\u003cbr\u003e • stroke\u003cbr\u003e • liver damage (hepatotoxicity)\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • peptic ulcers, stomach and intestinal perforation and bleeding, black stools and vomiting blood\u003cbr\u003e • lesions with mouth bleeding, heartburn (gastritis)\u003cbr\u003e • severe heart disease (heart failure), edema and high blood pressure (hypertension)\u003cbr\u003e • severe kidney diseases (kidney failure, papillary necrosis) particularly following long-term treatments, associated with an increase in blood urea concentration (the first signs are: urinating less than normal, general malaise). Presence of blood in the urine (hematuria), kidney inflammation (nephritis), a set of signs and symptoms such as protein loss in the urine, decreased protein levels in the blood, fluid accumulation in the body with consequent swelling, increased levels of lipids or fats in the blood, hypercoagulability of the blood, related to kidney diseases (nephrotic syndrome)\u003cbr\u003e • liver damage especially following long-term treatments, hepatitis, jaundice\u003cbr\u003e • reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe fatigue, nose and skin bleeding, skin bruises (hematomas)\u003cbr\u003e • aseptic meningitis with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (more common if you suffer from systemic lupus erythematosus or mixed connective tissue disease)\u003cbr\u003e • decreased hemoglobin levels in the blood\u003cbr\u003e • visual disturbances\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • Chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e • respiratory tract disorders including asthma, worsening of asthma, wheezing (bronchospasm) and difficulty breathing (dyspnea)\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis and Crohn's disease)\u003cbr\u003e • a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swelling of the lymph nodes and increased eosinophils (a type of white blood cell)\u003cbr\u003e • inflammation of the pancreas (pancreatitis)\u003cbr\u003e • a widespread, red and scaly rash, with the formation of pustules under the skin and blisters located mainly on the skin folds, on the trunk and on the upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e Stop using Nurofen if you develop these symptoms and contact your doctor immediately.\u003cbr\u003e See also section 2.\u003cbr\u003e • skin becomes sensitive to light The use of ibuprofen, especially at high doses (2400 mg\/day) may be associated with a modest increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"RECKITT BENCKISER H.(IT.) SpA","offers":[{"title":"Default Title","offer_id":46290180342027,"sku":"025634128","price":6.01,"currency_code":"EUR","in_stock":true}]},{"product_id":"okitask-os-grat-30bust-40mg","title":"OKITASK*OS GRAT 30SACHETS 40MG","description":"\u003cp\u003e\u003cb\u003eOkitask 40 mg granules\u003c\/b\u003e\u003cbr\u003e ketoprofen lysine salt\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eOkitask contains ketoprofen, which belongs to a group of medicines called \"Non-Steroidal Anti-Inflammatory Drugs\" (NSAIDs). Ketoprofen blocks the chemicals that cause inflammation.\u003cbr\u003e Okitask is indicated for the treatment of pain of various origins and natures, and in particular: headache, toothache, neuralgia (nerve pain), menstrual pain, muscle and osteoarticular (bone and joint) pain.\u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after a few days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Okitask:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ketoprofen, other non-steroidal anti-inflammatory drugs (NSAIDs) or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you have a history of hypersensitivity (allergic) reactions triggered by the use of ketoprofen or substances with a similar mechanism of action, for example acetylsalicylic acid or other NSAIDs (other anti-inflammatory drugs) such as asthma (bronchial inflammation and airway narrowing), bronchospasm (bronchial constriction), allergic rhinitis (allergic inflammation of the nasal mucosa), urticaria, skin rashes, nasal polyps, angioneurotic edema (swelling of the skin and mucous membranes) or other allergic-type reactions;\u003cbr\u003e - if you suffer from bronchial asthma (bronchial inflammation and airway narrowing);\u003cbr\u003e - if you have severe heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs);\u003cbr\u003e - if you suffer from gastritis (inflammation of the stomach lining);\u003cbr\u003e - if you currently have a peptic ulcer (a lesion of the stomach or the first part of the intestine) or bleeding, or if you have suffered in the past from recurrent bleeding or peptic ulcer (two or more distinct, proven episodes of bleeding or ulceration);\u003cbr\u003e - if you have suffered in the past from gastrointestinal bleeding (stomach or intestinal bleeding), ulceration, perforation or chronic dyspepsia (difficult digestion);\u003cbr\u003e - if you have a history of gastrointestinal bleeding or perforation following previous NSAID therapy;\u003cbr\u003e - if you suffer from Crohn's disease (inflammation of the intestine) or ulcerative colitis (inflammation of the intestine with ulcers);\u003cbr\u003e - if you have severe hepatic (reduced liver function due to liver cirrhosis, severe hepatitis) or renal (reduced kidney function) insufficiency;\u003cbr\u003e - if you suffer from leukopenia (reduction in the number of white blood cells) or thrombocytopenia (reduction in the number of platelets);\u003cbr\u003e - if you suffer from hemorrhagic diathesis (predisposition to develop hemorrhages) and other coagulation disorders or if you have hemostatic disorders (difficulty stopping bleeding);\u003cbr\u003e - if you are on high-dose diuretic therapy;\u003cbr\u003e - if you are in the third trimester of pregnancy;\u003cbr\u003e - if the person to be treated is under 15 years of age.\u003cbr\u003e\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Okitask.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eWarnings\u003c\/u\u003e\u003cbr\u003e Undesirable effects can be minimized by using the lowest effective dose for the shortest possible duration of treatment needed to control symptoms (see \"How to take Okitask\" and the paragraphs below on gastrointestinal and cardiovascular risks).\u003cbr\u003e Concomitant use of Okitask with other anti-inflammatory drugs should be avoided.\u003cbr\u003e During treatment with all NSAIDs, such as Okitask, at any time, with or without warning symptoms or a history of serious gastrointestinal events, gastrointestinal bleeding, ulceration and perforation, which can be fatal, have been reported. Patients who have previously suffered from these conditions have a higher risk (see \"Do not take Okitask\").\u003cbr\u003e Report any abdominal signs or symptoms (including gastrointestinal bleeding) even at the start of treatment.\u003cbr\u003e Inform your doctor if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (medicines used to treat inflammatory conditions), anticoagulants (medicines that delay blood clotting), such as warfarin, selective serotonin reuptake inhibitors (medicines used to treat depression), or antiplatelet agents (medicines that prevent platelet aggregation) such as acetylsalicylic acid (see \"Other medicines and Okitask\").\u003cbr\u003e The elderly are at greater risk of developing adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which can be fatal.\u003cbr\u003e \u003cb\u003eImmediately stop treatment with Okitask at the first signs of gastrointestinal bleeding or ulceration.\u003c\/b\u003e\u003cbr\u003e Severe skin reactions, some of which fatal, such as exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see \"Possible side effects\"). The reaction occurs in most cases in the initial stages of treatment. Discontinue Okitask if a rash, mucosal lesions or any other sign of hypersensitivity (allergic reaction) appears.\u003cbr\u003e\u003cbr\u003e \u003cu\u003ePrecautions\u003c\/u\u003e\u003cbr\u003e\u003cb\u003e Ask your doctor or pharmacist for advice before taking Okitask:\u003c\/b\u003e\u003cbr\u003e - If your kidneys are not working well, as Okitask should be taken with caution in this case. If you use Okitask, you should monitor your kidneys, especially if you are elderly or if you are on diuretic therapy (medicines that lower blood pressure).\u003cbr\u003e - If you have liver problems, you should have regular check-ups.\u003cbr\u003e - If you have an infection - see section \"Infections\" below.\u003cbr\u003e - If you suffer from uncontrolled hypertension (high blood pressure), congestive heart failure (fluid accumulation in the lungs, abdominal organs and peripheral tissues due to inadequate heart pump function), confirmed ischemic heart disease (heart disease that appears following reduced blood flow due to narrowing of the coronary arteries), peripheral arterial disease and\/or cerebrovascular disease (disease of the arteries and vessels of the brain), as you should only take Okitask after careful evaluation by your doctor.\u003cbr\u003e - If you have risk factors for these conditions, for example if you have high blood pressure, diabetes (disease caused by high blood glucose levels), hyperlipidemia (high levels of fats in the blood), or if you smoke.\u003cbr\u003e - If you have allergic manifestations or have suffered from allergies in the past, as the medicine should be administered with caution.\u003cbr\u003e - If you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways) or allergic diathesis (predisposition to allergy), chronic rhinitis (inflammation of the nasal mucosa) and allergic rhinitis (allergic inflammation of the nasal mucosa), chronic sinusitis and\/or nasal polyposis.\u003cbr\u003e - If you suffer from hematopoietic alterations (which modify the formation and maturation of blood cells), systemic lupus erythematosus (disease of the immune system) or mixed connective tissue diseases, as Okitask should be used with caution.\u003cbr\u003e - If you have hepatic porphyria (a rare blood disease characterized by altered activity of one of the liver enzymes), as the medicine could trigger an attack.\u003cbr\u003e Some NSAIDs may be associated with an increased risk of arterial thrombotic events (e.g. heart attack or stroke). Currently, there is insufficient data to exclude a similar risk for OKITASK.\u003cbr\u003e An increased risk of atrial fibrillation (alteration of the heart rhythm) associated with the use of NSAIDs has been reported.\u003cbr\u003e Hyperkalemia (increased amount of potassium in the blood) may occur, especially if you suffer from diabetes, renal insufficiency and\/or are on therapy with medicines that may cause hyperkalemia (see \"Other medicines and Okitask\"). In these circumstances, potassium levels should be monitored periodically.\u003cbr\u003e Okitask can mask the symptoms of infections such as fever and pain. Therefore, Okitask may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e Consult your doctor if you experience visual disturbances, such as blurred vision, as treatment must be stopped.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everyone gets them.\u003cbr\u003e The most commonly observed adverse events are gastrointestinal in nature.\u003cbr\u003e The following adverse reactions have been observed with the use of ketoprofen in adults:\u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e - dyspepsia (difficult digestion), nausea, abdominal pain and vomiting\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e - headache, dizziness, drowsiness\u003cbr\u003e - constipation, diarrhea, flatulence (passage of intestinal gas from the anus), gastritis (inflammation of the stomach lining)\u003cbr\u003e - rash, itching and fatigue\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e - hemorrhagic anemia (reduction of hemoglobin in the blood, a substance that carries oxygen in the blood caused by bleeding)\u003cbr\u003e - paresthesia (sensation of numbness, tingling)\u003cbr\u003e - blurred vision (see Warnings and precautions)\u003cbr\u003e - tinnitus (persistent perception of noises in the ear)\u003cbr\u003e - asthma (bronchial inflammation and airway narrowing)\u003cbr\u003e - stomatitis (inflammation of the mucous membranes lining the mouth), peptic ulcer (lesion of the stomach or the first part of the intestine)\u003cbr\u003e - hepatitis (inflammation of the liver), increased transaminases (increase in certain enzymes indicating liver function), increased bilirubin (a substance that indicates liver function)\u003cbr\u003e - increased weight\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e - facial edema (swelling) and erythema (skin redness)\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFrequency not known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e - thrombocytopenia (reduction in the number of platelets), agranulocytosis (severe reduction in the number of a type of white blood cells), bone marrow failure (reduction in the production of blood cells by the bone marrow), hemolytic anemia (reduction of hemoglobin in the blood, a substance that carries oxygen in the blood, caused by the destruction of red blood cells), leukopenia (decrease in the number of white blood cells), neutropenia (decrease in the number of a type of white blood cells), aplastic anemia (reduction of hemoglobin in the blood, a substance that carries oxygen in the blood, caused by insufficient production of blood cells by the bone marrow), leukocytosis (increase in the number of white blood cells), thrombocytopenic purpura (presence of spots on the skin due to a reduction in the number of platelets)\u003cbr\u003e - anaphylactic reaction (severe allergic reaction, including shock), hypersensitivity (allergy)\u003cbr\u003e - jaundice (yellowing of the skin and the white part of the eyes)\u003cbr\u003e - depression, hallucination (perception of things that do not exist in reality), confusional state, altered mood, agitation, insomnia, convulsions (uncontrolled body movements), dizziness, dysgeusia (altered taste), tremor, dyskinesia (involuntary movements), syncope (fainting), hyperkinesia (involuntary and uncoordinated movements), periorbital edema (swelling around the eye), peripheral edema\u003cbr\u003e - chills, asthenia (weakness)\u003cbr\u003e - heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs), atrial fibrillation (alteration of heart rhythm), palpitations (perception of heart beat), tachycardia (increase in heart rate), hypertension (high blood pressure), hypotension (low blood pressure)\u003cbr\u003e - vasodilation (dilation of blood vessels), vasculitis (inflammation of vessels), including leukocytoclastic vasculitis (inflammation of small vessels)\u003cbr\u003e - bronchospasm (constriction of the bronchi), especially in patients with confirmed hypersensitivity to acetylsalicylic acid and other NSAIDs, rhinitis (inflammation of the nasal mucosa), dyspnea (difficult breathing), laryngeal edema (swelling of the throat due to fluid accumulation), laryngospasm (narrowing of the larynx), acute respiratory failure (one fatal case has been reported in an asthmatic patient sensitive to acetylsalicylic acid)\u003cbr\u003e - exacerbation of colitis (worsening of an inflammation of the intestine), exacerbation of Crohn's disease (worsening of an inflammation of the intestine), gastrointestinal bleeding (stomach or intestinal bleeding), gastrointestinal perforation (sometimes fatal, especially in the elderly, see Warnings), gastric ulcer (lesion of the stomach), oral ulceration, duodenal ulcer (lesion of the first part of the intestine), duodenal perforation, heartburn (stomach burning), oral edema (swelling of the mouth), pancreatitis (inflammation of the pancreas), melena (presence of digested blood in the stool), hematemesis (vomiting blood), abdominal discomfort, colitis, hyperchlorhydria (excess acid in the stomach), gastric pain (stomach ache), erosive gastritis (severe inflammation of the stomach lining), tongue edema (swelling of the tongue)\u003cbr\u003e - photosensitivity reactions (sensitivity reaction to sunlight or UV lamps), alopecia (hair loss), urticaria, angioedema (swelling of the face, lips, mouth, tongue or throat that can cause difficulty in breathing and swallowing), bullous eruptions including Stevens-Johnson syndrome, Lyell's syndrome and toxic epidermal necrolysis (severe skin reactions), edema (fluid retention), exanthema (skin rash), maculopapular exanthema (skin rash with patches), purpura (purplish spots on the skin due to abnormal blood accumulation), acute generalized exanthematous pustulosis (skin rash with pus formation), dermatitis (skin irritation)\u003cbr\u003e - acute renal failure (reduction of renal function), tubulointerstitial nephritis, nephritis and nephritic syndrome (inflammation of the kidneys), nephrotic syndrome (renal alteration that involves protein loss in the urine), glomerulonephritis (inflammatory kidney disease), water\/sodium retention with possible edema (accumulation of water and sodium causing swelling), acute tubular necrosis and renal papillary necrosis (severe kidney damage), oliguria (decreased urine production), abnormal renal function test, hematuria (presence of blood in the urine)\u003cbr\u003e - aseptic meningitis (inflammation of the membranes lining the brain not caused by infections), lymphangitis (inflammation of the lymphatic vessels)\u003cbr\u003e - hyperkalemia (increase in the amount of potassium in the blood), hyponatremia (decrease in the amount of sodium in the blood)\u003cbr\u003e \u003cbr\u003e Compliance with the instructions contained in the package leaflet reduces the risk of side effects.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"DOMPE' FARMACEUTICI SpA","offers":[{"title":"Default Title","offer_id":46290180997387,"sku":"042028050","price":15.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_6a4e7001-e0d1-47e5-8280-c10d3cb08554.png?v=1734081110"},{"product_id":"okitask-os-grat-10bust-40mg","title":"OKITASK*OS GRAT 10 SACHETS 40MG","description":"\u003cp\u003e\u003cb\u003eOkitask 40 mg granules\u003c\/b\u003e\u003cbr\u003e ketoprofen lysine salt\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eOkitask contains ketoprofen, which belongs to a group of medicines called \"Non-Steroidal Anti-Inflammatory Drugs\" (NSAIDs). Ketoprofen blocks the chemicals that cause inflammation.\u003cbr\u003e Okitask is indicated for the treatment of pain of various origins and natures, and in particular: headache, toothache, neuralgia (nerve pain), menstrual pain, muscle and osteoarticular (bone and joint) pain.\u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after a few days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Okitask:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ketoprofen, other non-steroidal anti-inflammatory drugs (NSAIDs) or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you have a history of hypersensitivity reactions (allergy) triggered by the use of ketoprofen or substances with a similar mechanism of action, for example acetylsalicylic acid or other NSAIDs (other anti-inflammatories) such as asthma (bronchial inflammation and narrowing of the airways), bronchospasm (constriction of the bronchi), allergic rhinitis (allergic inflammation of the nasal mucosa), urticaria, skin rashes, nasal polyps, angioneurotic edema (swelling of the skin and mucous membranes) or other allergic reactions;\u003cbr\u003e - if you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways);\u003cbr\u003e - if you have severe heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs);\u003cbr\u003e - if you suffer from gastritis (inflammation of the stomach lining);\u003cbr\u003e - if you currently have a peptic ulcer (a lesion of the stomach or the first part of the intestine) or bleeding, or if you have suffered in the past from bleeding or recurrent peptic ulcer (two or more distinct, proven episodes of bleeding or ulceration);\u003cbr\u003e - if you have suffered in the past from gastrointestinal bleeding (stomach or intestinal bleeding), ulceration, perforation or chronic dyspepsia (difficult digestion);\u003cbr\u003e - if you have a history of gastrointestinal bleeding or perforation following previous NSAID therapy;\u003cbr\u003e - if you suffer from Crohn's disease (inflammation of the intestine) or ulcerative colitis (inflammation of the intestine with ulcers);\u003cbr\u003e - if you have severe liver failure (reduced liver function due to liver cirrhosis, severe hepatitis) or kidney failure (reduced kidney function);\u003cbr\u003e - if you suffer from leukopenia (reduction in the number of white blood cells) or thrombocytopenia (reduction in the number of platelets);\u003cbr\u003e - if you suffer from hemorrhagic diathesis (predisposition to the development of hemorrhages) and other coagulation disorders or if you have hemostatic disorders (difficulty in stopping bleeding);\u003cbr\u003e - if you are on high-dose diuretic therapy;\u003cbr\u003e - if you are in the third trimester of pregnancy;\u003cbr\u003e - if the subject to be treated is under 15 years of age.\u003cbr\u003e\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Okitask.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eWarnings\u003c\/u\u003e\u003cbr\u003e Undesirable effects can be minimized by using the lowest effective dose for the shortest possible duration of treatment needed to control symptoms (see \"How to take Okitask\" and the paragraphs below on gastrointestinal and cardiovascular risks).\u003cbr\u003e Concomitant use of Okitask with other anti-inflammatories should be avoided.\u003cbr\u003e During treatment with all NSAIDs, such as Okitask, at any time, with or without warning symptoms or a prior history of serious gastrointestinal events, gastrointestinal bleeding, ulceration and perforation have been reported, which can be fatal. Patients who have previously suffered from these conditions have a higher risk (see \"Do not take Okitask\").\u003cbr\u003e Report any abdominal signs or symptoms (including gastrointestinal bleeding) even at the start of treatment.\u003cbr\u003e Inform your doctor if you are taking medicines that may increase the risk of ulceration or bleeding, such as oral corticosteroids (medicines used to treat inflammatory conditions), anticoagulants (medicines that delay blood clotting), such as warfarin, selective serotonin reuptake inhibitors (medicines used to treat depression), or antiplatelet agents (medicines that prevent platelet aggregation) such as acetylsalicylic acid (see \"Other medicines and Okitask\").\u003cbr\u003e The elderly are more exposed to the risk of developing adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which can be fatal.\u003cbr\u003e \u003cb\u003eImmediately stop treatment with Okitask at the first signs of gastrointestinal bleeding or ulceration.\u003c\/b\u003e\u003cbr\u003e Severe skin reactions, some of which fatal, such as exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see \"Possible side effects\"). The reaction occurs in most cases in the initial stages of treatment. Discontinue use of Okitask if a rash, mucosal lesions or any other sign of hypersensitivity (allergic reaction) appears.\u003cbr\u003e\u003cbr\u003e \u003cu\u003ePrecautions\u003c\/u\u003e\u003cbr\u003e\u003cb\u003e Ask your doctor or pharmacist before taking Okitask:\u003c\/b\u003e\u003cbr\u003e - If your kidneys are not working well because in this case Okitask must be taken with caution. If you use Okitask, you must monitor your kidneys, especially if you are elderly or if you are on diuretic therapy (medicines that lower blood pressure).\u003cbr\u003e - If you have liver problems, you should have periodic check-ups.\u003cbr\u003e - If you have an infection – see section \"Infections\" below.\u003cbr\u003e - If you suffer from uncontrolled hypertension (high blood pressure), congestive heart failure (fluid accumulation in the lungs, abdominal organs and peripheral tissues due to inadequate heart pump function), confirmed ischemic heart disease (heart disease that appears following a reduction in blood flow due to a narrowing of the coronary arteries), peripheral arterial disease and\/or cerebrovascular disease (disease of the arteries and vessels of the brain), as you should only take Okitask after careful evaluation by your doctor.\u003cbr\u003e - If you have risk factors for these conditions, for example if you have high blood pressure, diabetes (disease caused by high blood glucose levels), hyperlipidemia (high fat levels in the blood), or if you smoke.\u003cbr\u003e - If you have allergic manifestations or have suffered from allergies in the past, as the medicine should be administered with caution.\u003cbr\u003e - If you suffer from bronchial asthma (bronchial inflammation and narrowing of the airways) or with allergic diathesis (predisposition to the onset of allergy), chronic rhinitis (inflammation of the nasal mucosa) and allergic rhinitis (allergic inflammation of the nasal mucosa), chronic sinusitis and\/or nasal polyposis.\u003cbr\u003e - If you suffer from hematopoietic alterations (which modify the formation and maturation of blood cells), systemic lupus erythematosus (disease of the immune system) or mixed connective tissue affections, as Okitask should be used with caution.\u003cbr\u003e - If you have hepatic porphyria (a rare blood disease characterized by altered activity of one of the liver enzymes), as the medicine could trigger an attack.\u003cbr\u003e Some NSAIDs may be associated with an increased risk of arterial thrombotic events (e.g., heart attack or stroke). Currently, there are insufficient data to exclude a similar risk for OKITASK.\u003cbr\u003e An increased risk of atrial fibrillation (alteration of the heart's beating rhythm) associated with the use of NSAIDs has been reported.\u003cbr\u003e Hyperkalemia (increased amount of potassium in the blood) may occur, especially if you suffer from diabetes, kidney failure and\/or are on therapy with medicines that can cause hyperkalemia (see \"Other medicines and Okitask\"). In these circumstances, potassium levels must be monitored periodically.\u003cbr\u003e Okitask can mask the symptoms of infections such as fever and pain. It is therefore possible that Okitask may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e Consult your doctor if you experience vision problems, such as blurred vision, as treatment must be stopped.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everyone gets them.\u003cbr\u003e The most commonly observed adverse events are gastrointestinal in nature.\u003cbr\u003e The following adverse reactions have been observed with the use of ketoprofen in adults:\u003cbr\u003e \u003cb\u003eCommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e - dyspepsia (difficult digestion), nausea, abdominal pain and vomiting\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e - headache, dizziness, drowsiness\u003cbr\u003e - constipation, diarrhea, flatulence (emission of intestinal gas from the anus), gastritis (inflammation of the stomach lining)\u003cbr\u003e - skin rash, itching and fatigue\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e - hemorrhagic anemia (reduction of hemoglobin in the blood, a substance that carries oxygen in the blood caused by bleeding)\u003cbr\u003e - paresthesia (sensation of numbness, tingling)\u003cbr\u003e - blurred vision (see Warnings and precautions)\u003cbr\u003e - tinnitus (persistent perception of noises in the ear)\u003cbr\u003e - asthma (bronchial inflammation and narrowing of the airways)\u003cbr\u003e - stomatitis (inflammation of the mucous membranes lining the mouth), peptic ulcer (lesion of the stomach or the first part of the intestine)\u003cbr\u003e - hepatitis (inflammation of the liver), increased transaminases (increase in some enzymes that indicate liver function), increased bilirubin (a substance that indicates liver function)\u003cbr\u003e - increased weight\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e - facial edema (swelling) and erythema (skin redness)\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFrequency not known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e - thrombocytopenia (reduction in the number of platelets), agranulocytosis (severe reduction in the number of a type of white blood cells), bone marrow failure (reduction in the production of blood cells by the bone marrow), hemolytic anemia (reduction in hemoglobin in the blood, a substance that carries oxygen in the blood, caused by the destruction of red blood cells), leukopenia (decrease in the number of white blood cells), neutropenia (decrease in the number of a type of white blood cells), aplastic anemia (reduction in hemoglobin in the blood, a substance that carries oxygen in the blood, caused by insufficient production of blood cells by the bone marrow), leukocytosis (increase in the number of white blood cells), thrombocytopenic purpura (presence of spots on the skin due to a reduction in the number of platelets)\u003cbr\u003e - anaphylactic reaction (severe allergic reaction, including shock), hypersensitivity (allergy)\u003cbr\u003e - jaundice (yellowing of the skin and the white part of the eyes)\u003cbr\u003e - depression, hallucination (perception of things nonexistent in reality), confusional state, altered mood, agitation, insomnia, convulsions (uncontrolled body movements), dizziness, dysgeusia (altered taste), tremor, dyskinesia (involuntary movements), syncope (fainting), hyperkinesia (involuntary and uncoordinated movements), periorbital edema (swelling around the eye), peripheral edema\u003cbr\u003e - chills, asthenia (weakness)\u003cbr\u003e - heart failure (inability of the heart to pump the adequate amount of blood needed for the body's needs), atrial fibrillation (alteration of the heart rhythm), palpitations (perception of the heart beat), tachycardia (increase in the number of heart beats), hypertension (high blood pressure), hypotension (low blood pressure)\u003cbr\u003e - vasodilation (dilation of blood vessels), vasculitis (inflammation of vessels), including leukocytoclastic vasculitis (inflammation of small vessels)\u003cbr\u003e - bronchospasm (constriction of the bronchi), especially in patients with confirmed hypersensitivity to acetylsalicylic acid and other NSAIDs, rhinitis (inflammation of the nasal mucosa), dyspnea (difficulty breathing), laryngeal edema (swelling of the throat due to fluid accumulation), laryngospasm (narrowing of the larynx), acute respiratory failure (one case, with fatal outcome, was reported in an asthmatic patient sensitive to acetylsalicylic acid)\u003cbr\u003e - exacerbation of colitis (worsening of an inflammation of the intestine), exacerbation of Crohn's disease (worsening of an inflammation of the intestine), gastrointestinal hemorrhage (bleeding of the stomach or intestine), gastrointestinal perforation (sometimes fatal, especially in the elderly, see Warnings), gastric ulcer (lesion of the stomach), mouth ulceration, duodenal ulcer (lesion of the first part of the intestine), duodenal perforation, heartburn (stomach burning), mouth edema (swelling), pancreatitis (inflammation of the pancreas), melena (presence of digested blood in the stool), hematemesis (vomiting blood), abdominal discomfort, colitis, hyperchlorhydria (excess acid in the stomach), gastric pain (stomach ache), erosive gastritis (severe inflammation of the stomach lining), tongue edema (swelling of the tongue)\u003cbr\u003e - photosensitivity reactions (reaction of sensitivity to sunlight or UV lamps), alopecia (hair loss), urticaria, angioedema (swelling of the face, lips, mouth, tongue or throat which may cause difficulty in breathing and swallowing), bullous eruptions including Stevens-Johnson syndrome, Lyell's syndrome and toxic epidermal necrolysis (severe skin reactions), edema (fluid retention), exanthema (skin rash), maculopapular exanthema (skin rash with patches), purpura (purplish spots on the skin due to abnormal blood accumulation), acute generalized exanthematous pustulosis (skin rash with formation of purulent collections), dermatitis (skin irritation)\u003cbr\u003e - acute kidney failure (reduction of kidney function), tubulointerstitial nephritis, nephritis and nephritic syndrome (inflammation of the kidneys), nephrotic syndrome (kidney alteration involving protein loss in the urine), glomerulonephritis (inflammatory kidney disease), water\/sodium retention with possible edema (accumulation of water and sodium causing swelling), acute tubular necrosis and renal papillary necrosis (severe kidney damage), oliguria (decreased urine production), abnormal kidney function test, hematuria (presence of blood in the urine)\u003cbr\u003e - aseptic meningitis (inflammation of the membranes lining the brain not caused by infections), lymphangitis (inflammation of the lymphatic vessels)\u003cbr\u003e - hyperkalemia (increase in the amount of potassium in the blood), hyponatremia (decrease in the amount of sodium in the blood)\u003cbr\u003e \u003cbr\u003e Adherence to the instructions contained in the package leaflet reduces the risk of side effects.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"DOMPE' FARMACEUTICI SpA","offers":[{"title":"Default Title","offer_id":46290181095691,"sku":"042028011","price":5.24,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_b2babb9f-d441-4926-b9b9-5dde1000289f.png?v=1734081115"},{"product_id":"ketodol-20cpr-25mg-200mg","title":"KETODOL*20TAB 25MG+200MG","description":"\u003cp\u003e\u003cb\u003eKETODOL 25 mg + 200 mg tablets\u003c\/b\u003e\u003cbr\u003eketoprofen and sucralfate\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eKetodol belongs to a category of medicines called NSAIDs (non-steroidal anti-inflammatory drugs).\u003cbr\u003eKetodol contains the active ingredients ketoprofen and sucralfate. Ketoprofen is contained in the central core of the tablet and has analgesic and anti-inflammatory activity; sucralfate is contained in the coating of the tablet and has a protective effect on the inner surface of the stomach (gastric mucosa).\u003cbr\u003eFirst, sucralfate is released, which protects the gastric mucosa, and immediately after, ketoprofen, which performs its analgesic and anti-inflammatory activity.\u003cbr\u003e\u003cbr\u003eKetodol is used for pains of various origins and natures:\u003cbr\u003e• headache;\u003cbr\u003e• toothache;\u003cbr\u003e• nerve pain (neuralgia);\u003cbr\u003e• bone, joint, and muscle pain;\u003cbr\u003e• menstrual pain.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Ketodol\u003c\/b\u003e\u003cbr\u003e• if you are allergic to ketoprofen or sucralfate or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e• if you have previously had allergic reactions such as severe breathing difficulties (bronchospasm), asthmatic attacks, inflammation inside the nose (rhinitis), allergic skin manifestations (urticaria) or if substances with the same mechanism of action as Ketodol (for example, acetylsalicylic acid or other NSAIDs) have previously caused allergic reactions. Indeed, particularly severe (anaphylactic) allergic reactions, rarely fatal, have been observed in these patients (see \"Possible side effects\");\u003cbr\u003e• in the third trimester of pregnancy, during breastfeeding (see \"Pregnancy, breastfeeding and fertility\") and in children and adolescents under 15 years of age;\u003cbr\u003e• if you suffer from a severe reduction in the heart's ability to provide an adequate amount of blood to the body (heart failure);\u003cbr\u003e• if you suffer from open sores that develop on the inner lining of the stomach (active peptic ulcer) or have previously suffered from bleeding, ulceration or perforation of the stomach and intestine;\u003cbr\u003e• if you have previously suffered from bleeding or perforation of the stomach and intestine due to previous NSAID therapy;\u003cbr\u003e• in case of easy bleeding tendency;\u003cbr\u003e• in case of severe liver failure;\u003cbr\u003e• in case of severe kidney failure;\u003cbr\u003e• if you have acute kidney damage (renal hypoperfusion);\u003cbr\u003e• if you are taking medicines that cause an increase in urine elimination (intensive diuretic therapy);\u003cbr\u003e• in case of chronic digestive difficulties;\u003cbr\u003e• if you suffer from stomach inflammation (gastritis);\u003cbr\u003e• in case of low white blood cell and platelet counts (leukopenia and thrombocytopenia);\u003cbr\u003e• in case of hereditary abnormalities in hemoglobin formation (porphyria);\u003cbr\u003e• if you suffer from chronic liver inflammation (liver cirrhosis);\u003cbr\u003e• if you are taking antibiotics such as tetracyclines, as these may be ineffective.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Ketodol. To avoid any hypersensitivity reactions or sun allergies, it is advisable not to expose yourself to the sun during use.\u003cbr\u003e\u003cbr\u003eStop treatment with ketoprofen:\u003cbr\u003e• if you notice bleeding or experience severe stomach or intestinal pain (ulceration);\u003cbr\u003e• at the first appearance of skin allergies (rash), mucosal lesions or any other sign of hypersensitivity or allergic reaction;\u003cbr\u003e• in case of a significant increase in the values of certain liver parameters and transaminases (which are used to evaluate liver function);\u003cbr\u003e• in case of vision disturbances, such as blurred vision.\u003cbr\u003e\u003cbr\u003eAsk your doctor or pharmacist for advice before using KETODOL if:\u003cbr\u003e• you suffer from an intestinal disease (ulcerative colitis, Crohn's disease) as these conditions could worsen;\u003cbr\u003e• you suffer from asthma associated with chronic rhinitis, chronic sinusitis and\/or nasal polyps, because the use of this medicine can contribute to triggering asthmatic crises or bronchospasms;\u003cbr\u003e• you have kidney function problems as the medicine is mainly eliminated by the kidneys;\u003cbr\u003e• you have an infection - see paragraph \u0026lt;\u003cinfections\u003e\u0026gt; below;\u003cbr\u003e• you are in intensive care and especially if you receive enteral nutrition, or if you have predisposing factors such as delayed gastric emptying;\u003cbr\u003e• you are taking other medicines that could increase the risk of gastrointestinal events, ulceration or bleeding such as:\u003cbr\u003e• oral corticosteroids,\u003cbr\u003e• warfarin (anticoagulant),\u003cbr\u003e• antidepressant drugs (SSRI antidepressants),\u003cbr\u003e• antiplatelet agents such as aspirin (see \"Other medicines and Ketodol\").\u003cbr\u003e\u003cbr\u003eIn these cases, the concomitant use of stomach protectors (misoprostol or proton pump inhibitors) is useful.\u003cbr\u003e\u003cbr\u003eInfections\u003cbr\u003eKETODOL can hide the symptoms of infections such as fever and pain. It is therefore possible that KETODOL may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003eContact your doctor:\u003cbr\u003e• in case of any abdominal symptom (especially gastrointestinal bleeding), particularly in the early stages of treatment;\u003cbr\u003e• for adequate monitoring and appropriate instructions, if you suffer from high blood pressure and\/or congestive heart failure, if you have previously suffered from liver disease or if you have abnormal liver function values;\u003cbr\u003e• if you have certain risk factors associated with cardiovascular diseases (high blood pressure, high cholesterol, diabetes mellitus, smoking) before starting long-term treatment;\u003cbr\u003e• before taking this medicine, if you have hereditary problems of intolerance to certain sugars;\u003cbr\u003e• for adequate monitoring of blood potassium levels, if you suffer from diabetes, kidney failure or if you are being treated with medicines that increase blood potassium concentration.\u003cbr\u003e\u003cbr\u003e\u003cu\u003eElderly patients\u003c\/u\u003e\u003cbr\u003eUse the medicine with caution because you may experience an increase in side effects, especially bleeding and perforations in the stomach and intestine, which can also be fatal (see \"How to use Ketodol\").\u003cbr\u003eStart treatment with the lowest possible dose, because the risk of gastrointestinal bleeding, ulceration, perforation is greater with increased NSAID doses.\u003cbr\u003e\u003cbr\u003eAt the beginning of treatment, kidney function should be carefully monitored in patients with heart failure, chronic liver inflammation (cirrhosis) and severe kidney impairment (nephrosis), in subjects undergoing diuretic therapy or suffering from chronic kidney failure, especially if elderly. In these patients, the use of ketoprofen can cause a reduction in blood flow to the kidneys and lead to kidney decompensation.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003eDo not administer the medicine to children and adolescents up to 15 years of age because the safety and efficacy of the medicine have not been established for these age groups.\u003c\/infections\u003e\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003eSide effects can be minimized by using the lowest effective dose for the shortest possible duration of treatment.\u003cbr\u003e\u003cb\u003eSerious side effects\u003c\/b\u003e\u003cbr\u003eThe following side effects are serious or can become serious. If any of the following symptoms occur, stop taking Ketodol and contact your doctor immediately:\u003cbr\u003e• severe skin reactions (some of which are fatal) such as:\u003cbr\u003e- death of skin cells, accompanied by malaise, chills, muscle pain and fever (toxic epidermal necrolysis);\u003cbr\u003e- skin rashes with blistering (Stevens-Johnson syndrome);\u003cbr\u003e• severe skin reaction characterized by redness and swelling together with pustule formation (acute generalized exanthematous pustulosis);\u003cbr\u003e• severe inflammation with skin redness (exfoliative dermatitis);\u003cbr\u003e• continuous stomach pain, which worsens on an empty stomach (gastric ulcers);\u003cbr\u003e• vomiting blood, blood in stools (gastrointestinal bleeding);\u003cbr\u003e• throat swelling (laryngeal edema and\/or glottal edema), breathing difficulty (dyspnea), intense perception of heartbeat (palpitation) or increased heart rate (tachycardia).\u003cbr\u003e\u003cbr\u003eOther side effects are listed below:\u003cbr\u003e\u003cbr\u003e\u003cb\u003eCommon side effects\u003c\/b\u003e (may affect up to 1 in 10 people) include:\u003cbr\u003e• Nausea, vomiting, heartburn, indigestion, abdominal pain, stomach pain.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon side effects\u003c\/b\u003e (may affect up to 1 in 100 people) include:\u003cbr\u003e• Headache, dizziness, drowsiness.\u003cbr\u003e• Diarrhea, constipation, flatulence (gas), stomach inflammation (gastritis).\u003cbr\u003e• Skin irritation, itching.\u003cbr\u003e• Swelling (fluid accumulation under the skin), feeling of fatigue.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare side effects\u003c\/b\u003e (may affect up to 1 in 1000 people) include:\u003cbr\u003e• Anemia from bleeding, low white blood cell count (seen in blood tests).\u003cbr\u003e• Lack of sensation and tingling in some parts of the body, involuntary muscle movements.\u003cbr\u003e• Blurred vision.\u003cbr\u003e• Ringing in the ears, loss of balance (vertigo).\u003cbr\u003e• Wheezing and breathing difficulty (asthma).\u003cbr\u003e• Oral ulcerations, colitis.\u003cbr\u003e• Liver inflammation (hepatitis), increased transaminases and bilirubin (seen in blood tests), yellowish skin discoloration (jaundice).\u003cbr\u003e• Generalized weakness.\u003cbr\u003e• Weight gain.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare side effects\u003c\/b\u003e (may affect up to 1 in 10,000 people) include:\u003cbr\u003e• Presence of a mass of foreign material in the stomach (bezoar).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eSide effects with unknown frequency\u003c\/b\u003e (frequency cannot be estimated from available data):\u003cbr\u003e• Significant reduction in white blood cells, reduction in platelet count, inability of the bone marrow to produce normal amounts of blood cells, anemia due to red blood cell destruction (seen in blood tests).\u003cbr\u003e• Allergic hypersensitivity reactions (including anaphylactic shock).\u003cbr\u003e• Reduction in blood sodium levels (hyponatremia) and increase in blood potassium levels (hyperkalemia).\u003cbr\u003e• Depression, hallucinations, confusion, mood changes, insomnia.\u003cbr\u003e• Viral disease of the brain and spinal cord membranes (aseptic meningitis), involuntary muscle contraction (convulsions), altered sense of taste.\u003cbr\u003e• Insufficient heart function, atrial fibrillation (a form of arrhythmia that makes the heartbeat irregular).\u003cbr\u003e• Increased blood pressure (hypertension), increased blood vessels, inflammation of blood vessels (vasculitis).\u003cbr\u003e• Severe breathing difficulty (bronchospasm) particularly in patients with known hypersensitivity to acetylsalicylic acid and NSAIDs.\u003cbr\u003e• Internal inflammation of the nose (rhinitis).\u003cbr\u003e• Worsening of colitis and Crohn's disease, inflammation of the pancreas (pancreatitis).\u003cbr\u003e• Sun allergy reactions (photosensitivity), hair loss (alopecia), widespread urticaria with swelling, blistering eruptions, skin inflammation and redness (dermatitis, eczema, erythema).\u003cbr\u003e• Difficulty urinating, reduced kidney function, kidney inflammation, kidney damage (nephrotoxic syndrome), abnormal kidney function tests (seen in blood tests).\u003cbr\u003e• Arterial thrombotic events (e.g., heart attack or stroke).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"EG SpA","offers":[{"title":"Default Title","offer_id":46290188370187,"sku":"028561037","price":8.3,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_dd04c517-0f3d-492b-942d-5a5e644c2da9.jpg?v=1734081229"},{"product_id":"momentact-os-sosp-8bust-400mg","title":"MOMENTACT*OS SUSP 8SACH 400MG","description":"\u003cp\u003e\u003cb\u003eMOMENTACT 400 mg oral suspension in sachets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMomentact contains ibuprofen, a medicine belonging to the class of analgesic-anti-inflammatory drugs, which fight pain and inflammation.\u003cbr\u003e \u003cbr\u003e Momentact is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e for:\u003cbr\u003e - Treatment of pain of various origins and types (headache, toothache, neuralgia, musculoskeletal pain, menstrual pain);\u003cbr\u003e - Reduction of fever and flu symptoms.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Momentact:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are allergic to other anti-rheumatic medicines (e.g., acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see section Other medicines and Momentact);\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breastfeeding (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have previously had bleeding or perforation of the stomach or intestine after taking medicines;\u003cbr\u003e - if you have previously had two or more distinct episodes of ulcer or stomach bleeding;\u003cbr\u003e - in the presence of severe heart disease (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhea or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eWhat you need to know before taking Momentact\u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck (angioedema) and chest pain, have been reported with ibuprofen. Stop Momentact immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003e Severe skin reactions have been reported in association with ibuprofen treatment including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP).\u003cbr\u003e Stop taking Momentact and consult your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.\u003cbr\u003e \u003cbr\u003e Consult your doctor or pharmacist before taking Momentact:\u003cbr\u003e - if you have had episodes of difficulty breathing (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, runny nose (chronic rhinitis), presence of nasal polyps (nasal polyposis) or inflammation of the paranasal sinus mucosa (sinusitis) or suffer\/have suffered from allergies because you may experience difficulty breathing (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section Other medicines and Momentact);\u003cbr\u003e - if you are elderly or if you have suffered from an ulcer, especially if the ulcer has also manifested with bleeding or perforation (see section Do not take Momentact), as the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly contact your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you take low doses of acetylsalicylic acid or drugs that may increase the risk of stomach and\/or intestinal diseases (see section Other medicines and Momentact);\u003cbr\u003e - if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 Possible side effects);\u003cbr\u003e - if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report any unusual intestinal symptoms to your doctor (especially hemorrhage) particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of ulcer or stomach and\/or intestinal bleeding, such as oral corticosteroids (e.g., cortisone), anticoagulants (e.g., warfarin), antidepressants (selective serotonin reuptake inhibitors), or antiplatelet agents (e.g., acetylsalicylic acid). See also section Other medicines and Momentact. If gastrointestinal bleeding or ulceration occurs in patients taking Momentact, treatment should be discontinued. If you have high blood pressure and the medicines you are taking cannot lower it and\/or you have heart disease or blood circulation problems in the brain or other districts or you think you may be at risk for these diseases (for example, if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been found following treatment with NSAIDs.\u003cbr\u003e NSAIDs can reduce the action of medicines to lower blood pressure (see section Other medicines and Momentact);\u003cbr\u003e - if you have lost a considerable amount of fluid, or if swelling, heart problems or high blood pressure appear;\u003cbr\u003e - if you have decreased kidney function, heart or liver malfunction, or if you are elderly or on treatment with high blood pressure medications, as you may be more prone to kidney problems. Furthermore, the usual concomitant use of several painkillers can further increase this risk;\u003cbr\u003e - if you suffer from a coagulation disorder or are taking medicines that slow blood coagulation (anticoagulants) (see section Other medicines and Momentact);\u003cbr\u003e - if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as on rare occasions in patients treated with ibuprofen, symptoms of aseptic meningitis have been observed.\u003cbr\u003e Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients who did not manifest concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see section Other medicines and Momentact);\u003cbr\u003e - If you intend to become pregnant (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have difficulty becoming pregnant or are undergoing fertility investigations (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have an infection - see section Infections below.\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e You should discuss therapy with your doctor or pharmacist before taking Momentact if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Medicines such as Momentact can:\u003cbr\u003e - be associated with the appearance of kidney diseases, even serious ones (such as renal papillary necrosis, analgesic nephropathy and kidney failure), therefore the doctor will monitor your kidney function;\u003cbr\u003e - cause eye disorders, therefore, in case of prolonged treatments, periodic eye checks are recommended. If visual disturbances occur, stop treatment with Momentact.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Momentact can mask the symptoms of infections such as fever and pain. It is therefore possible that Momentact may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003e If the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Momentact can cause side effects, although not everybody gets them. The side effects of the drug can be minimized if you use the lowest recommended dose, and if you use the drug only for the period necessary to control your symptoms.\u003cbr\u003e If you develop an ulcer, or stomach and\/or intestinal bleeding, or skin and\/or mucous membrane lesions, you must stop treatment with Momentact and contact your doctor. Usually these side effects are more frequent in the elderly.\u003cbr\u003e The use of Momentact can cause side effects that are generally mild or moderate or more serious reactions, even allergic ones, although rarely.\u003cbr\u003e \u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP\u003c\/b\u003e using Momentact immediately and contact your doctor or the nearest hospital where you will be given appropriate and specific treatment:\u003cbr\u003e • skin rashes or lesions,\u003cbr\u003e • mucous membrane lesions,\u003cbr\u003e • signs of an allergic reaction, even severe (rashes, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock),\u003cbr\u003e • peeling skin,\u003cbr\u003e • non-raised, target-shaped or circular reddish spots on the trunk, often with central vesicles, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes can be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson syndrome),\u003cbr\u003e • widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome),\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and vesicles, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis),\u003cbr\u003e • visual disturbances,\u003cbr\u003e • liver disease (hepatic dysfunction),\u003cbr\u003e • bleeding, ulcer and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e \u003cbr\u003e In case of an allergic reaction among those listed above, go to the hospital as it is necessary to have immediate availability of equipment, drugs and personnel suitable for emergency treatment, as in rare cases, following the use of ibuprofen, serious side effects, sometimes fatal, have been reported, even in the absence of known allergy.\u003cbr\u003e The risk of experiencing such symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e Furthermore, you may experience additional side effects that have also been reported with other medicines similar to Momentact and are listed below by frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness\u003cbr\u003e • malaise\u003cbr\u003e • fatigue\u003cbr\u003e \u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • stomach inflammation (gastritis)\u003cbr\u003e • insomnia, anxiety\u003cbr\u003e • numbness of the limbs or other parts of the body (paresthesia), drowsiness\u003cbr\u003e • nasal mucosa inflammation (rhinitis) difficulty breathing (bronchospasm, dyspnea)\u003cbr\u003e • momentary cessation of breathing (apnea)\u003cbr\u003e • visual disturbances\u003cbr\u003e • hearing impairment\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • vertigo\u003cbr\u003e • liver disorders (impaired liver function)\u003cbr\u003e • liver inflammation (hepatitis)\u003cbr\u003e • yellowing of skin and eyes (jaundice)\u003cbr\u003e • kidney diseases (kidney function damage and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and kidney failure)\u003cbr\u003e • hypersensitivity reactions such as rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), asthma, difficulty breathing (bronchospasm or dyspnea), asthma attacks with possible blood pressure drop\u003cbr\u003e • skin reactions to light (photosensitivity)\u003cbr\u003e • allergic rash (erythema)\u003cbr\u003e \u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e • reduction in the number of blood cells: reduction of white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia)\u003cbr\u003e • reduced clotting ability\u003cbr\u003e • depression, confusion, hallucinations\u003cbr\u003e • inflammation of the optic nerve (optic neuritis)\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section Warnings and precautions), with symptoms of neck stiffness, headache, nausea, vomiting, fever or disorientation\u003cbr\u003e • eye disorders with visual disturbances and optic nerve pathology (toxic optic neuropathy)\u003cbr\u003e • swelling due to fluid accumulation in the tissues\u003cbr\u003e • lupus erythematosus syndrome (a disease that can affect various organs and tissues of the body)\u003cbr\u003e • worsening of inflammation caused by an existing infection (for example, development of necrotizing fasciitis)\u003cbr\u003e • high levels of nitrogen in the blood\u003cbr\u003e • altered liver function tests (increased transaminases, increased alkaline phosphatase)\u003cbr\u003e • abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid)\u003cbr\u003e \u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis)\u003cbr\u003e • sensation of feeling one's heartbeat (palpitations)\u003cbr\u003e • heart disease (heart failure)\u003cbr\u003e • heart attack (myocardial infarction)\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema)\u003cbr\u003e • liver disease (liver failure)\u003cbr\u003e • hypertension\u003cbr\u003e • severe allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat making breathing difficult, fast heartbeat, severe rapidly occurring allergic reaction that can cause death (anaphylaxis), severe rash or skin exfoliation (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme).\u003cbr\u003e • worsening of skin infections caused by chickenpox.\u003cbr\u003e • skin infection and soft tissue pathology\u003cbr\u003e \u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e • peptic ulcer, gastrointestinal hemorrhage.\u003cbr\u003e • feeling of heaviness in the stomach,\u003cbr\u003e • nausea,\u003cbr\u003e • vomiting,\u003cbr\u003e • diarrhea,\u003cbr\u003e • flatulence,\u003cbr\u003e • constipation,\u003cbr\u003e • difficulty digesting,\u003cbr\u003e • abdominal pain,\u003cbr\u003e • heartburn,\u003cbr\u003e • blood in stool,\u003cbr\u003e • blood in vomit,\u003cbr\u003e • lesions inside the mouth,\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis, Crohn's disease),\u003cbr\u003e • increased risk of sudden reduction of blood circulation in the brain (stroke),\u003cbr\u003e • allergic reactions, anaphylaxis\u003cbr\u003e • drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swelling of the lymph nodes and an increase in eosinophils (a type of white blood cell).\u003cbr\u003e • a widespread, red and scaly rash, with the formation of pustules under the skin and vesicles located mainly on the skin folds, trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using Momentact if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e • chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including those not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290197709067,"sku":"035618077","price":8.79,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_d6779a4d-0f9b-474c-92f4-ddf891efe0e3.png?v=1734081259"},{"product_id":"momentact-10cps-molli-400mg","title":"MOMENTACT*10 SOFTGELS 400MG","description":"\u003cp\u003e\u003cb\u003eMOMENTACT 400 mg soft capsules\u003c\/b\u003e\u003cbr\u003eIbuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMomentact contains ibuprofen, a medicine belonging to the class of analgesic-anti-inflammatory drugs, meaning drugs that fight pain and inflammation.\u003cbr\u003e\u003cbr\u003eMomentact is used in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 years and over\u003c\/b\u003e to treat:\u003cbr\u003e- pain of various origins and types (headache, toothache, neuralgia, osteoarticular and muscular pain, menstrual pain) and to help reduce the symptoms of feverish and flu-like conditions.\u003cbr\u003e\u003cbr\u003eContact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Momentact:\u003c\/b\u003e\u003cbr\u003e- if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e- if you are allergic to other anti-rheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see section Other medicines and Momentact), or allergic to any of the other ingredients of this medicine;\u003cbr\u003e- if the patient is a child under 12 years of age;\u003cbr\u003e- if you are in the last 3 months of pregnancy or are breastfeeding (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e- if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e- if you have had bleeding or perforation of the stomach or intestine in the past following the intake of medicines;\u003cbr\u003e- if you have had two or more distinct episodes of stomach ulcer or bleeding in the past;\u003cbr\u003e- in the presence of severe heart disease;\u003cbr\u003e- in the presence of severe liver or kidney disease;\u003cbr\u003e- if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eWhat you need to know before taking Momentact\u003cbr\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck (angioedema) and chest pain, have been reported with ibuprofen. Stop Momentact immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e\u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003eSerious skin reactions have been reported in association with ibuprofen treatment, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP). Stop taking Momentact and consult your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Momentact:\u003cbr\u003e- if you have experienced breathing difficulties (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e- if you suffer from asthma, runny nose (chronic rhinitis), presence of polyps in the nose (nasal polyposis) or inflammation of the nasal mucosa (sinusitis) or suffer\/have suffered from allergies because you could experience breathing difficulties (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs);\u003cbr\u003e- if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section Other medicines and Momentact);\u003cbr\u003e- if you are elderly or have suffered from an ulcer, especially if the ulcer has also manifested with bleeding or perforation (see section Do not take Momentact), as the risk of bleeding, ulcer or perforation is higher with high doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly consult your doctor to have a stomach-protecting medicine prescribed (misoprostol or proton pump inhibitors). This possibility should also be considered if you are taking low doses of acetylsalicylic acid or drugs that may increase the risk of stomach and\/or intestinal diseases (see section Other medicines and Momentact);\u003cbr\u003e- if you have suffered or suffer from chronic intestinal diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 Possible side effects);\u003cbr\u003e- if you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report any unusual intestinal symptoms (especially bleeding) to your doctor, particularly in the initial phases of treatment;\u003cbr\u003e- if you are taking other medicines that increase the risk of ulcer or stomach and\/or intestinal bleeding, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (serotonin inhibitors), or antiplatelet agents (e.g. acetylsalicylic acid). See also section Other medicines and Momentact. If gastrointestinal bleeding or ulceration occurs in patients taking Momentact, treatment must be discontinued;\u003cbr\u003e- if you have high blood pressure and the medicines you are taking cannot lower it and\/or you have heart or blood circulation diseases in the brain or periphery or think you may be at risk for these diseases (for example, if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e- if you suffer from high blood pressure and\/or have heart diseases, as fluid retention, increased blood pressure and swelling have been found following treatment with NSAIDs. NSAIDs can reduce the action of medicines to lower blood pressure (see section Other medicines and Momentact);\u003cbr\u003e- if you have lost a considerable amount of fluid, or if you develop swelling, heart problems or high blood pressure;\u003cbr\u003e- if you have decreased kidney function, heart or liver malfunction, or if you are elderly or are being treated with medicines for high blood pressure, as you may be more prone to the onset of kidney problems. Furthermore, the habitual concomitant use of several painkillers can further increase this risk;\u003cbr\u003e- if you suffer from heart disease;\u003cbr\u003e- if you suffer from liver diseases (hepatic dysfunction);\u003cbr\u003e- if you are elderly, as the risk of bleeding, ulcers and perforations is increased compared to other patients;\u003cbr\u003e- if you suffer from a coagulation disorder or are taking medicines to thin the blood (anticoagulants) (see section Other medicines and Momentact);\u003cbr\u003e- if you suffer from a disease that can affect various organs and tissues of the body (systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as on rare occasions symptoms of aseptic meningitis have been observed in patients treated with ibuprofen.\u003cbr\u003eAlthough this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients who did not manifest concomitant chronic diseases.\u003cbr\u003e- if you are taking medicines to treat pain, heart disease or high blood pressure (see section Other medicines and Momentact);\u003cbr\u003e- if you intend to become pregnant (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e- if you have difficulty becoming pregnant or are undergoing fertility investigations (see section Pregnancy, breastfeeding and fertility);\u003cbr\u003e- If you have an infection - see section Infections below.\u003cbr\u003e\u003cbr\u003eAnti-inflammatory\/painkiller drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003eYou should discuss therapy with your doctor or pharmacist before taking Momentact if you have:\u003cbr\u003e• heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e• high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003eMedicines like Momentact can:\u003cbr\u003e• be associated with the onset of even serious kidney diseases (such as renal papillary necrosis, analgesic nephropathy and kidney failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e• cause eye disorders, therefore, in case of prolonged treatments, periodic eye check-ups are recommended. If visual disturbances occur, stop treatment with Momentact.\u003cbr\u003e\u003cbr\u003e\u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003eMomentact can mask the symptoms of infections such as fever and pain. It is therefore possible that Momentact could delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003eIf the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Momentact can cause side effects, although not everybody gets them. The side effects of the drug can be minimised if you use the lowest recommended dose, and if you use the drug only for the period necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003eIf you get an ulcer, or stomach and\/or intestinal bleeding, or skin and\/or mucous membrane lesions, you must stop treatment with Momentact and contact your doctor. Usually these side effects are more frequent in the elderly.\u003cbr\u003e\u003cbr\u003eThe use of Momentact can cause generally mild or moderate side effects or more serious allergic reactions, even if rarely.\u003cbr\u003e\u003cbr\u003eIf you experience any of the following symptoms, \u003cb\u003eSTOP immediately\u003c\/b\u003e using Momentact and contact your doctor or the nearest hospital where you will undergo appropriate and specific treatment:\u003cbr\u003e• skin rashes or lesions,\u003cbr\u003e• mucous membrane lesions,\u003cbr\u003e• signs of an allergic reaction, even severe (erythema, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock),\u003cbr\u003e• peeling skin,\u003cbr\u003e• non-raised reddish spots, target-shaped or circular on the trunk, often with central vesicles, peeling of the skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes can be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson syndrome),\u003cbr\u003e• widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome),\u003cbr\u003e• widespread, red and scaly rash, with bumps under the skin and vesicles, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalised exanthematous pustulosis),\u003cbr\u003e• visual disturbances,\u003cbr\u003e• liver disease (hepatic dysfunction),\u003cbr\u003e• bleeding, ulceration and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e\u003cbr\u003eIn case of an allergic reaction among those listed above, go to the hospital as immediate availability of equipment, drugs and personnel suitable for emergency treatment is necessary, since in rare cases serious side effects, sometimes fatal, have been reported following the use of ibuprofen, even in the absence of known allergy.\u003cbr\u003e\u003cbr\u003eThe risk of manifesting such symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003eFurthermore, you may experience further side effects that have also been reported with other medicines similar to Momentact and which are listed below according to frequency:\u003cbr\u003e\u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e• dizziness\u003cbr\u003e• malaise\u003cbr\u003e• fatigue\u003cbr\u003e\u003cbr\u003e\u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e• inflammation of the stomach (gastritis)\u003cbr\u003e• insomnia, anxiety\u003cbr\u003e• numbness of the limbs or other parts of the body, drowsiness\u003cbr\u003e• nasal congestion (rhinitis)\u003cbr\u003e• breathing difficulties (bronchospasm, dyspnoea)\u003cbr\u003e• momentary interruption of breathing (apnoea)\u003cbr\u003e• hearing impairment\u003cbr\u003e• ringing in the ears (tinnitus)\u003cbr\u003e• vertigo\u003cbr\u003e• liver disorders (altered liver function)\u003cbr\u003e• inflammation of the liver (hepatitis)\u003cbr\u003e• yellowing of skin and eyes (jaundice)\u003cbr\u003e• kidney diseases (renal function damage and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and kidney failure)\u003cbr\u003e• hypersensitivity reactions such as skin rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), asthma, breathing difficulties (bronchospasm or dyspnoea), asthma attacks with lowering of blood pressure\u003cbr\u003e• skin reactions to light (photosensitivity)\u003cbr\u003e\u003cbr\u003e\u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e• reduction in the number of blood cells: reduction of white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (haemolytic anaemia, aplastic anaemia), platelets (thrombocytopenia)\u003cbr\u003e• depression, confusional state, hallucinations\u003cbr\u003e• inflammation of the optic nerve (optic neuritis)\u003cbr\u003e• inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see section Warnings and precautions) with symptoms of nuchal rigidity, headache, nausea, vomiting, fever or disorientation\u003cbr\u003e• eye disorders with visual disturbances and optic nerve pathology (toxic optic neuropathy)\u003cbr\u003e• swelling due to fluid accumulation in the tissues\u003cbr\u003e• disease that can affect various organs and tissues of the body (lupus erythematosus)\u003cbr\u003e• aggravation of inflammations caused by an existing infection (e.g. development of necrotizing fasciitis)\u003cbr\u003e\u003cbr\u003e\u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e• inflammation of the pancreas, a gland involved in digestive processes (pancreatitis)\u003cbr\u003e• sensation of feeling one's own heartbeat (palpitations)*\u003cbr\u003e• heart disease (heart failure)*\u003cbr\u003e• heart attack (myocardial infarction)*\u003cbr\u003e• increased fluid around the lungs (acute pulmonary oedema)*\u003cbr\u003e• liver disease (hepatic insufficiency)\u003cbr\u003e• hypertension*\u003cbr\u003e• severe allergic reactions, which may include symptoms such as swelling of the face, tongue and throat making breathing difficult, rapid heartbeat, severe rapidly developing allergic reaction that can cause death (anaphylaxis), severe skin rash or exfoliation of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme)\u003cbr\u003e• severe skin infections and soft tissue disorders can occur during chickenpox infection\u003cbr\u003e\u003cb\u003e*these side effects tend to regress with discontinuation of treatment\u003cbr\u003e\u003cbr\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e• feeling of heaviness in the stomach\u003cbr\u003e• nausea\u003cbr\u003e• vomiting\u003cbr\u003e• diarrhoea\u003cbr\u003e• flatulence\u003cbr\u003e• constipation\u003cbr\u003e• difficulty digesting\u003cbr\u003e• abdominal pain\u003cbr\u003e• heartburn\u003cbr\u003e• blood in stools\u003cbr\u003e• blood in vomit\u003cbr\u003e• lesions inside the mouth\u003cbr\u003e• worsening of inflammatory bowel and colon diseases (colitis, Crohn's disease)\u003cbr\u003e• increased risk of heart attack (myocardial infarction), or failure of blood to reach the brain (stroke)\u003cbr\u003e• high blood pressure\u003cbr\u003e• severe heart disease (heart failure)\u003cbr\u003e• a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: skin rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell)\u003cbr\u003e• a widespread, red and scaly rash, with pustules under the skin and vesicles located mainly on the skin folds, trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalised exanthematous pustulosis). Stop using Momentact if you develop these symptoms and contact your doctor immediately. See also section 2\u003cbr\u003e• chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290197807371,"sku":"035618038","price":9.24,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_9643422c-a677-4398-aebd-f17bb247b9fa.png?v=1734081265"},{"product_id":"nurofen-12cpr-riv-200mg","title":"NUROFEN*12 FC TAB 200MG","description":"\u003cp\u003e\u003cb\u003eNUROFEN 200 mg film-coated tablets\u003cbr\u003eNUROFEN 400 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003eIbuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eNurofen contains ibuprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) whose action reduces pain and swelling caused by inflammation and fever.\u003cbr\u003e\u003cbr\u003eNurofen is indicated in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents over 12 years of age\u003c\/b\u003e for the treatment of various types of pain: headache, toothache, neuralgia, muscle, bone and joint pain, menstrual pain.\u003cbr\u003eNurofen is also indicated as an adjunct for the symptomatic treatment of fever and flu-like states.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking this medicine\u003c\/b\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck (angioedema), and chest pain. Stop Nurofen immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eDo not take Nurofen if:\u003c\/b\u003e\u003cbr\u003e• you are allergic (hypersensitive) to ibuprofen or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e• you have previously experienced allergic reactions such as breathing difficulties (bronchospasm, asthma), rhinitis (runny nose), swelling of the face, lips and throat (angioedema) or hives after taking ibuprofen, acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e• you suffer from severe kidney or liver disease (kidney or liver failure);\u003cbr\u003e• you suffer from severe heart disease (severe heart failure);\u003cbr\u003e• you have suffered from stomach bleeding or perforation following previous NSAID treatments;\u003cbr\u003e• you suffer or have suffered from gastric\/duodenal ulcers (peptic ulcers) or ongoing or recurrent bleeding (at least two distinct episodes of proven ulceration or bleeding);\u003cbr\u003e• you are in the last trimester of pregnancy;\u003cbr\u003e• you are due to undergo or have undergone heart surgery.\u003cbr\u003e\u003cbr\u003eDo not administer Nurofen to children under 12 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Nurofen if:\u003cbr\u003e• you are taking other medicines used for pain relief, to reduce fever and\/or to treat inflammation (non-steroidal anti-inflammatory drugs, including COX-2 inhibitors) (see section Other medicines and Nurofen);\u003cbr\u003e• you are elderly and\/or have suffered from stomach and intestinal disorders (history of ulcer), especially if complicated by bleeding or perforation, as there may be an increase in gastrointestinal bleeding and perforations. In these cases, your doctor will advise you to start treatment with the lowest available dose and possibly the concomitant use of medicines that protect the stomach (misoprostol or proton pump inhibitors). This should also be considered if you are taking low doses of aspirin or other medicines that may increase the risk of stomach and intestinal diseases (see section Other medicines and Nurofen).\u003cbr\u003eDuring treatment with all NSAIDs, at any time, with or without warning symptoms or a history of serious gastrointestinal events, bleeding, ulceration and perforation of the stomach or intestine may occur, which can be fatal. Therefore, inform your doctor of any unusual gastrointestinal symptoms (especially gastrointestinal bleeding) particularly in the initial stages of treatment. If gastrointestinal bleeding or ulceration occurs, discontinue Nurofen and contact your doctor;\u003cbr\u003e• you suffer or have suffered from an inflammatory bowel disease (ulcerative colitis, Crohn's disease);\u003cbr\u003e• you are taking medicines that could increase the risk of ulceration or bleeding, such as medicines used to treat inflammation and certain immune system diseases (oral corticosteroids), anticoagulants such as warfarin, medicines that may have an antiplatelet effect such as aspirin, medicines to treat depression (selective serotonin reuptake inhibitors) (see section Other medicines and Nurofen);\u003cbr\u003e• you suffer from high blood pressure and\/or severe heart disease (heart failure) because, in association with NSAID therapy, fluid retention, high blood pressure and swelling have been reported;\u003cbr\u003e• you suffer from reduced liver and\/or kidney function, as the habitual use of analgesic medicines such as Nurofen can lead to serious permanent kidney problems (with possible onset of kidney failure). Your doctor will advise you to perform periodic tests during treatment;\u003cbr\u003e• you suffer or have suffered from asthma (difficulty breathing) or allergic reactions as you may experience shortness of breath;\u003cbr\u003e• you suffer from coagulation problems;\u003cbr\u003e• you suffer from a chronic autoimmune disease that causes disorders in various parts of the body, particularly the skin (systemic lupus erythematosus) or mixed connective tissue disease, as this increases the risk of aseptic meningitis; you experience the first signs of a hypersensitivity reaction after taking Nurofen. If this occurs or is suspected, you should stop taking Nurofen and consult your doctor. Medically assisted measures must be initiated by specialized medical personnel, in line with the symptomatology;\u003cbr\u003eAnti-inflammatory\/pain relief drugs based on ibuprofen can cause a prolongation of bleeding time by reversibly inhibiting platelet aggregation;\u003cbr\u003e• you have an infection - see section Infections below.\u003cbr\u003e\u003cbr\u003eAnti-inflammatory\/pain relief drugs such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003eYou should discuss your treatment with your doctor or pharmacist before taking Nurofen if you have:\u003cbr\u003e• heart problems including heart attack, angina (chest pain), or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e• high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003eSkin reactions\u003cbr\u003eSerious skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Nurofen and contact your doctor immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003eInfections\u003cbr\u003eNurofen can mask the symptoms of infections such as fever and pain. Therefore, Nurofen may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003eDo not give this medicine to children under 12 years of age.\u003cbr\u003eCaution is required in dehydrated adolescents (12-18 years) as there is a risk of impaired kidney function.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003eIf you experience any of the following side effects, \u003cb\u003eSTOP\u003c\/b\u003e treatment and contact your doctor:\u003cbr\u003e• allergic reactions, even serious ones, which may include: hives, itching, purpura, swelling of the face, mouth and throat (angioedema), difficulty breathing (bronchospasm or dyspnea), altered heart rate (tachycardia), low blood pressure (hypotension), anaphylaxis, shock and worsening of asthma.\u003cbr\u003e• non-raised, target-shaped or circular reddish patches on the trunk, often with central blisters, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis].\u003cbr\u003e• Widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome).\u003cbr\u003e• Widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003eAdditional side effects include:\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e• stomach problems, such as heartburn, stomach pain and nausea\u003cbr\u003e• headache\u003cbr\u003e• dizziness\u003cbr\u003e• skin rashes\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e• diarrhea, vomiting, flatulence, constipation\u003cbr\u003e• increased transaminases, increased alkaline phosphatase, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased uric acid\u003cbr\u003e• stroke\u003cbr\u003e• liver damage (hepatotoxicity)\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e• peptic ulcers, perforation and bleeding of the stomach and intestine, black stools and vomiting blood\u003cbr\u003e• bleeding lesions of the mouth, heartburn (gastritis)\u003cbr\u003e• severe heart disease (heart failure), edema and high blood pressure (hypertension)\u003cbr\u003e• severe kidney diseases (kidney failure, papillary necrosis) particularly following long-term treatments, associated with an increase in blood urea concentration (the first signs are: urinating less than normal, general malaise). Presence of blood in the urine (hematuria), kidney inflammation (nephritis), a set of signs and symptoms such as protein loss in the urine, decreased protein levels in the blood, fluid accumulation in the body resulting in swelling, increased levels of lipids or fats in the blood, hypercoagulability of the blood, related to kidney diseases (nephrotic syndrome)\u003cbr\u003e• liver damage especially following long-term treatments, hepatitis, jaundice\u003cbr\u003e• reduction in the number of blood cells (anemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis) - the first signs are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe fatigue, bleeding from the nose and skin, bruises on the skin (hematomas)\u003cbr\u003e• aseptic meningitis with symptoms such as stiff neck, headache, nausea, vomiting, fever or disorientation (more frequent if you suffer from systemic lupus erythematosus or mixed connective tissue disease)\u003cbr\u003e• decreased hemoglobin levels in the blood\u003cbr\u003e• visual disturbances\u003cbr\u003e\u003cbr\u003e\u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e• Chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome\u003cbr\u003e• respiratory tract disorders including asthma, worsening of asthma, wheezing (bronchospasm) and difficulty breathing (dyspnea)\u003cbr\u003e• worsening of inflammatory bowel diseases (colitis and Crohn's disease)\u003cbr\u003e• a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swelling of the lymph nodes and increased eosinophils (a type of white blood cell)\u003cbr\u003e• inflammation of the pancreas (pancreatitis)\u003cbr\u003e• a widespread, red and scaly rash, with pustules forming under the skin and blisters located mainly on skin folds, on the trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003eStop using Nurofen if you develop these symptoms and contact your doctor immediately.\u003cbr\u003eSee also section 2.\u003cbr\u003e• the skin becomes sensitive to light. The use of ibuprofen, especially at high doses (2400 mg\/day) may be associated with a modest increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"RECKITT BENCKISER H.(IT.) SpA","offers":[{"title":"Default Title","offer_id":46290202034443,"sku":"025634015","price":3.91,"currency_code":"EUR","in_stock":true}]},{"product_id":"spididol-12cpr-riv-400mg","title":"SPIDIDOL*12FC 400MG","description":"\u003cp\u003e\u003cb\u003eSPIDIDOL 400 mg film-coated tablets\u003cbr\u003e SPIDIDOL 400 mg granules for oral solution apricot flavour\u003c\/b\u003e\u003cbr\u003e Ibuprofen arginine salt\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eThis medicine contains the active ingredient ibuprofen, belonging to a group of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs) which act by relieving pain (analgesic action) and reducing the symptoms of inflammation (anti-inflammatory action).\u003cbr\u003e \u003cbr\u003e SPIDIDOL is indicated for the treatment of pain or inflammatory conditions in the following cases:\u003cbr\u003e - \u003cb\u003eTreatment of pain:\u003c\/b\u003e headache, toothache, menstrual pain, neuralgia, osteoarticular (bone) and muscle pain.\u003cbr\u003e - \u003cb\u003eTreatment of feverish and flu-like conditions\u003c\/b\u003e, in addition to other medicines.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not notice any improvement or if your symptoms worsen.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take SPIDIDOL\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen, other similar medicines or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you have suffered in the past from stomach and intestinal disorders associated with bleeding (gastrointestinal haemorrhage or perforation related to previous treatments with anti-inflammatory drugs (NSAIDs) or a history of recurrent peptic haemorrhage\/ulcer, with two or more distinct episodes of demonstrated ulceration or bleeding);\u003cbr\u003e - if you suffer from stomach and intestinal disorders associated with the presence of lesions and bleeding (active and recurrent peptic ulcer);\u003cbr\u003e - if you suffer from stomach or intestinal bleeding (gastrointestinal bleeding);\u003cbr\u003e - if you have other ongoing bleeding such as cerebrovascular bleeding;\u003cbr\u003e - if you suffer from ulcerative colitis or Crohn's disease;\u003cbr\u003e - if you suffer from severe liver or kidney problems (severe hepatic and renal insufficiency);\u003cbr\u003e - if you suffer from haemorrhages (haemorrhagic diathesis);\u003cbr\u003e - if you suffer from severe heart problems (severe heart failure);\u003cbr\u003e - if in the past, after taking acetylsalicylic acid or other anti-inflammatory drugs (NSAIDs), you have experienced facial swelling due to fluid accumulation, especially around the mouth and eyes (angioedema), severe respiratory distress (bronchospasm), breathing problems (asthma), skin irritation (urticaria), inflammation of the nasal mucous membranes (rhinitis) or nasal polyps;\u003cbr\u003e - if you suffer from systemic lupus erythematosus or other skin diseases (collagen diseases);\u003cbr\u003e - if you are in the third trimester of pregnancy (See paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - before or after heart surgery;\u003cbr\u003e - if you suffer from phenylketonuria, a condition in which the levels of certain substances in the urine and blood are altered. This warning refers only to the granules for oral solution as it contains aspartame.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking SPIDIDOL if you have an infection (see paragraph Infections).\u003cbr\u003e \u003cbr\u003e \u003cu\u003ePay particular attention with SPIDIDOL\u003c\/u\u003e:\u003cbr\u003e Severe skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using SPIDIDOL and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in paragraph 4.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eTake this medicine with caution if:\u003c\/b\u003e\u003cbr\u003e - you are already taking other anti-inflammatory medicines (including selective COX-2 inhibitors, see paragraph Other medicines and SPIDIDOL);\u003cbr\u003e - you are taking other medicines that could increase the risk of ulceration or bleeding, such as oral corticosteroids, anticoagulants such as warfarin, selective serotonin reuptake inhibitors or antiplatelet agents such as aspirin (See paragraph Other medicines and SPIDIDOL);\u003cbr\u003e - you have suffered from high blood pressure (hypertension) because, in association with NSAID therapy, you may have problems with fluid elimination (fluid retention) and experience swelling due to the accumulation of fluids (oedema);\u003cbr\u003e - you have suffered in the past from bowel disorders (ulcerative colitis, Crohn's disease);\u003cbr\u003e - you suffer from heart problems (mild to moderate congestive heart failure);\u003cbr\u003e - you have suffered from breathing problems (bronchospasm) especially if following the use of medicines. In patients suffering or having suffered from bronchial asthma or allergic diseases, bronchospasm could worsen. In these cases, especially for prolonged treatments, your doctor may suggest you undergo periodic examinations;\u003cbr\u003e - you suffer from coagulation disorders or a decrease in heart, liver or kidney function; in these cases, especially for prolonged treatments, periodic analyses may be necessary. Hypersensitivity to SPIDIDOL can cause liver problems (hepatotoxic reactions);\u003cbr\u003e - you suffer from lupus erythematosus, a chronic autoimmune disease that can affect various organs and tissues and causes facial lesions and pain, or you suffer from other skin diseases (collagen diseases). In this case, you must consult your doctor before taking SPIDIDOL. The risk of skin disorders may increase;\u003cbr\u003e - you intend to start a pregnancy, as the use of SPIDIDOL can compromise female fertility; the use of SPIDIDOL should be suspended in women who have fertility problems or who are undergoing fertility investigations.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRisk of Stroke and Heart Attack\u003c\/b\u003e\u003cbr\u003e Anti-inflammatory\/pain relief medications such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e You should discuss your therapy with your doctor or pharmacist before taking SPIDIDOL if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Signs of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema) and chest pain, have been reported with ibuprofen. Stop SPIDIDOL immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eGastrointestinal Risks\u003c\/b\u003e\u003cbr\u003e At any time, with or without warning symptoms or a previous history of serious gastrointestinal conditions, stomach and intestinal bleeding (gastrointestinal haemorrhage), severe lesions (ulceration and perforation), which can be fatal, may occur. If you have suffered from an ulcer in the past, the risk of gastrointestinal bleeding, ulceration or perforation is higher with increased doses of NSAIDs. Your doctor will suggest you take specific medicines to protect your stomach such as misoprostol or proton pump inhibitors, especially if you are taking other medicines (for example, aspirin or medicines that increase the risk of gastrointestinal problems).\u003cbr\u003e If you suffer or have suffered from stomach or intestinal problems (gastrointestinal toxicity), especially at the beginning of treatment with SPIDIDOL, tell your doctor about any gastrointestinal symptoms you experience (especially bleeding). At doses greater than 1000 mg per day, bleeding time may be prolonged.\u003cbr\u003e If you experience gastrointestinal bleeding or ulceration, stop treatment with SPIDIDOL and contact your doctor or the nearest hospital.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVision problems\u003c\/b\u003e\u003cbr\u003e If you experience vision problems, stop treatment with this medicine and consult an ophthalmologist.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eElderly patients\u003c\/b\u003e\u003cbr\u003e If you are an elderly person, the risk of side effects is greater, especially bleeding and perforations in the stomach and intestines (gastrointestinal events) which can be fatal. The risk of gastrointestinal bleeding, ulceration or perforation is higher with increased doses of NSAIDs.\u003cbr\u003e Therefore, start treatment with the lowest available dose and take SPIDIDOL for the shortest possible period to control symptoms. Your doctor may indicate medicines that have a protective action on the stomach (misoprostol or proton pump inhibitors), especially if you are taking other medicines (for example, aspirin or medicines that increase the risk of gastrointestinal problems). If you suffer or have suffered from stomach or intestinal problems (gastrointestinal toxicity), especially at the beginning of treatment with SPIDIDOL, tell your doctor about any gastrointestinal symptoms you experience (especially bleeding). At doses greater than 1000 mg per day, bleeding time may be prolonged.\u003cbr\u003e If you experience gastrointestinal bleeding or ulceration, stop treatment with SPIDIDOL and contact your doctor or the nearest hospital.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e This medicine should be administered with caution in dehydrated adolescents because there is an increased risk of kidney problems (see paragraph 3 Use in adolescents aged 12 to 18 years).\u003cbr\u003e \u003cbr\u003e Use caution when initiating ibuprofen treatment if you suffer from severe dehydration.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e SPIDIDOL can mask the symptoms of infections such as fever and pain. It is therefore possible that SPIDIDOL may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e Therefore, in case of infection, use ibuprofen therapy with caution.\u003cbr\u003e \u003cbr\u003e NSAIDs can cause an increase in liver function test results.\u003cbr\u003e You should avoid alcohol as it can increase the side effects of NSAIDs, especially those affecting the gastrointestinal tract or central nervous system.\u003cbr\u003e If you experience a hypersensitivity reaction after taking ibuprofen, stop treatment immediately.\u003cbr\u003e Medically assisted measures should be initiated by specialized medical personnel, in line with the symptomatology.\u003cbr\u003e Acid ibuprofen can cause a prolongation of bleeding time because it reversibly inhibits platelet aggregation.\u003cbr\u003e \u003cbr\u003e \u003cem\u003ePay particular attention in the above cases, bearing in mind that any risk is more likely when using this medicine at high doses and in prolonged therapies.\u003c\/em\u003e\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects although not everybody gets them.\u003cbr\u003e \u003cbr\u003e Stop using ibuprofen and consult your doctor immediately if you notice any of the following symptoms:\u003cbr\u003e • reddish, non-raised, target-shaped or circular patches on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes can be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e • widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. The symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e \u003cbr\u003e The following side effects may occur:\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery common\u003c\/b\u003e (may affect more than 1 in 10 people)\u003cbr\u003e - difficulty digesting (dyspepsia);\u003cbr\u003e - diarrhoea.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCommon\u003c\/b\u003e (may affect up to 1 in 10 people)\u003cbr\u003e - abdominal pain or discomfort, burning sensation in the stomach (heartburn), nausea, flatulence;\u003cbr\u003e - headache, dizziness;\u003cbr\u003e - skin disease, skin rash.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon\u003c\/b\u003e (may affect up to 1 in 100 people)\u003cbr\u003e - formation of lesions in the stomach or intestines (peptic ulcers or haemorrhages) sometimes fatal, particularly in the elderly;\u003cbr\u003e - vomiting;\u003cbr\u003e - presence of blood in the stools (melaena);\u003cbr\u003e - inflammation of the stomach (gastritis);\u003cbr\u003e - inflammation of the mouth (stomatitis);\u003cbr\u003e - confusion;\u003cbr\u003e - drowsiness;\u003cbr\u003e - itching, skin irritation (urticaria, exanthema), severe skin problem associated with bleeding (purpura);\u003cbr\u003e - swelling of the face, lips, mouth, tongue or throat that can cause difficulty breathing and swallowing (angioedema);\u003cbr\u003e - allergic reactions;\u003cbr\u003e - difficulty breathing (asthma, worsening of asthma, bronchospasm, dyspnoea).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare\u003c\/b\u003e (may affect up to 1 in 1,000 people)\u003cbr\u003e - formation of lesions in the stomach or intestines (gastrointestinal perforation);\u003cbr\u003e - constipation;\u003cbr\u003e - presence of blood in the vomit (haematemesis);\u003cbr\u003e - inflammation of the mouth associated with the presence of lesions (ulcerative stomatitis);\u003cbr\u003e - worsening of certain chronic inflammatory bowel diseases (colitis and Crohn's disease);\u003cbr\u003e - hearing disorders, perception of ringing in the ear (tinnitus);\u003cbr\u003e - vision disorders (blurred vision, amblyopia and difficulty distinguishing colours);\u003cbr\u003e - alteration of platelet, white blood cell and red blood cell levels (thrombocytopenia, agranulocytosis, aplastic anaemia, haemolytic anaemia, granulocytopenia);\u003cbr\u003e - presence of blood in the urine (haematuria);\u003cbr\u003e - difficulty passing urine (dysuria);\u003cbr\u003e - liver problems (hepatotoxicity);\u003cbr\u003e - alteration of liver function tests (elevated transaminases);\u003cbr\u003e - alteration of diagnostic tests (increased alkaline phosphatase, reduced haematocrit, prolonged bleeding time, decreased blood calcium*, increased uric acid*);\u003cbr\u003e - severe allergic reaction (anaphylaxis);\u003cbr\u003e - cerebrovascular accident*.\u003cbr\u003e * Effect of the NSAID class\u003cbr\u003e \u003cbr\u003e \u003cb\u003eVery rare\u003c\/b\u003e (may affect up to 1 in 10,000 people)\u003cbr\u003e - weakening of sensory and orientation functions (clouding of consciousness);\u003cbr\u003e - severe skin disorders (exfoliative dermatitis, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, allergic vasculitis);\u003cbr\u003e - kidney problems (interstitial nephritis, papillary necrosis, renal failure, including acute form);\u003cbr\u003e - alteration of diagnostic tests (decrease in haemoglobin level in the blood).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNot known\u003c\/b\u003e (frequency cannot be estimated from the available data)\u003cbr\u003e - decreased appetite and body weight (anorexia);\u003cbr\u003e - swelling of a part of the body due to fluid accumulation (oedema);\u003cbr\u003e - fever;\u003cbr\u003e - heart problems (heart failure);\u003cbr\u003e - increased blood pressure (hypertension);\u003cbr\u003e - blood circulation problems (thrombosis);\u003cbr\u003e - decreased blood pressure (hypotension);\u003cbr\u003e - depression and mental problems (psychotic reaction);\u003cbr\u003e - infection of the membranes surrounding the brain without bacterial growth in culture (aseptic meningitis);\u003cbr\u003e - swelling affecting the connection point between the optic nerve and the eye (papilloedema);\u003cbr\u003e - drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swelling of the lymph nodes and an increase in eosinophils (a type of white blood cell);\u003cbr\u003e - worsening of skin rashes;\u003cbr\u003e - unexpected and exaggerated skin manifestations on sun exposure (photosensitivity reaction);\u003cbr\u003e - anaemia;\u003cbr\u003e - muscle stiffness;\u003cbr\u003e - increased uric acid levels in the blood (hyperuricemia);\u003cbr\u003e - poor elimination of sodium and fluids manifested by swelling (oedema);\u003cbr\u003e - menstrual cycle disorders;\u003cbr\u003e - liver inflammation (hepatitis), liver damage, jaundice;\u003cbr\u003e - alteration of kidney function test;\u003cbr\u003e - severe clinical reaction triggered in a sensitized subject on contact with a specific allergen (anaphylactic shock);\u003cbr\u003e - burning and pain in the throat (throat irritation);\u003cbr\u003e - a widespread, red and scaly rash, with the formation of pustules under the skin and blisters located mainly on skin folds, trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using SPIDIDOL if you develop these symptoms and contact your doctor immediately. See also paragraph 2;\u003cbr\u003e - chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome. \u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ZAMBON ITALIA Srl","offers":[{"title":"Default Title","offer_id":46290202493195,"sku":"039600010","price":6.37,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_55cf776a-f18e-4fbf-94e6-c3176cc45b03.png?v=1734081335"},{"product_id":"momentact-analgesico-12bust","title":"MOMENTACT ANALGESIC*12SACHETS","description":"\u003cp\u003e\u003cb\u003eMOMENTACT ANALGESICO 400 mg granules for oral solution\u003c\/b\u003e\u003cbr\u003eIbuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMomentact Analgesico contains ibuprofen, a medicine belonging to the class of analgesic anti-inflammatories, i.e., drugs that combat pain and inflammation.\u003cbr\u003e\u003cbr\u003eMomentact Analgesico is used, in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents aged 12 and over\u003c\/b\u003e, to treat:\u003cbr\u003e- pains of various origins and nature (headaches, toothaches, neuralgia, osteoarticular and muscular pain, menstrual pain).\u003cbr\u003e\u003cbr\u003eConsult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Momentact Analgesico\u003c\/b\u003e\u003cbr\u003e- If you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in section 6).\u003cbr\u003e- If you are allergic to other anti-rheumatic medicines (e.g. acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see section Other medicines and Momentact Analgesico), or allergic to any of the other ingredients of this medicine.\u003cbr\u003e- If the patient is a child under 12 years of age.\u003cbr\u003e- If you are in the last 3 months of pregnancy or are breastfeeding (see section Pregnancy, breastfeeding and fertility).\u003cbr\u003e- If you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer).\u003cbr\u003e- If you have a history of stomach or intestinal bleeding or perforation following the use of medicines.\u003cbr\u003e- If you have a history of two or more separate episodes of stomach ulcer or bleeding.\u003cbr\u003e- In the presence of severe heart disease.\u003cbr\u003e- In the presence of severe liver or kidney disease.\u003cbr\u003e- If you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhoea or insufficient fluid intake.\u003cbr\u003e- If you suffer from phenylketonuria (a congenital error in the metabolism of an amino acid, phenylalanine) (see section Momentact Analgesico contains aspartame).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eWhat you need to know before taking Momentact Analgesico\u003cbr\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck region (angioedema) and chest pain, have been reported with ibuprofen. Stop Momentact Analgesico immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003eSkin reactions:\u003cbr\u003e\u003cbr\u003eSevere skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Momentact Analgesico and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Momentact Analgesico:\u003cbr\u003e- If you have had episodes of breathing difficulties (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs.\u003cbr\u003e- If you suffer from asthma, runny nose (chronic rhinitis), nasal polyps (nasal polyposis) or inflammation of the nasal mucosa (sinusitis) or suffer\/have suffered from allergies, because you could experience breathing difficulties (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs).\u003cbr\u003e- If you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see section Other medicines and Momentact Analgesico).\u003cbr\u003e- If you are elderly or if you have suffered from an ulcer, especially if the ulcer has also manifested with bleeding or perforation (see section Do not take Momentact Analgesico), as the risk of bleeding, ulcer or perforation is higher with high doses of anti-inflammatory drugs. In these cases, you should start treatment with the lowest available dose, and possibly contact your doctor to prescribe a medicine that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you are taking low doses of acetylsalicylic acid or drugs that may increase the risk of stomach and\/or intestinal diseases (see section Other medicines and Momentact Analgesico).\u003cbr\u003e- If you have suffered or suffer from chronic bowel diseases (ulcerative colitis, Crohn's disease) as they may worsen (see section 4 Possible side effects).\u003cbr\u003e- If you have had stomach and intestinal diseases related to the use of drugs, and in particular if you are elderly, you must report any unusual intestinal symptoms (especially bleeding) to your doctor, particularly in the initial stages of treatment.\u003cbr\u003e- If you are taking other medicines that increase the risk of ulcer or stomach and\/or intestinal bleeding, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (serotonin inhibitors), or antiplatelet agents (e.g. acetylsalicylic acid). See also section Other medicines and Momentact Analgesico. If gastrointestinal bleeding or ulceration occurs in patients taking Momentact Analgesico, treatment should be discontinued.\u003cbr\u003e- If you have high blood pressure and the medicines you are taking are unable to lower it and\/or you have heart disease or blood circulation problems in the brain or periphery, or you think you may be at risk for these diseases (for example, if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke).\u003cbr\u003e- If you suffer from high blood pressure and\/or heart disease, as fluid retention, increased blood pressure and swelling have been observed following treatment with NSAIDs. NSAIDs can reduce the action of blood pressure lowering medicines (see section Other medicines and Momentact Analgesico).\u003cbr\u003e- If you have lost a considerable amount of fluids, or if you experience swelling, heart problems or high blood pressure.\u003cbr\u003e- If you have reduced kidney function, heart or liver malfunction, or if you are elderly or on treatment for high blood pressure, as you may be more prone to kidney problems. Furthermore, the usual concomitant use of several painkillers can further increase this risk.\u003cbr\u003e- If you suffer from heart disease.\u003cbr\u003e- If you suffer from liver diseases (hepatic dysfunction).\u003cbr\u003e- If you are elderly, as the risk of bleeding, ulcers and perforations is increased compared to other patients.\u003cbr\u003e- If you suffer from a coagulation disorder or are taking medicines to thin the blood (anticoagulants) (see section Other medicines and Momentact Analgesico).\u003cbr\u003e- If you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, since in rare occasions in patients treated with ibuprofen, symptoms of aseptic meningitis have been observed.\u003cbr\u003eAlthough this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue disorders, it has also been observed in patients who did not manifest concomitant chronic diseases.\u003cbr\u003e- If you are taking medicines to treat pain, heart disease or high blood pressure (see section Other medicines and Momentact Analgesico).\u003cbr\u003e- If you intend to become pregnant (see section Pregnancy, breastfeeding and fertility).\u003cbr\u003e- If you have problems becoming pregnant or are undergoing fertility investigations (see section Pregnancy, breastfeeding and fertility).\u003cbr\u003e- If you have an infection - see section Infections below.\u003cbr\u003e\u003cbr\u003eAnti-inflammatory\/painkiller drugs such as ibuprofen may be associated with a modest increase in the risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003eYou should discuss your therapy with your doctor or pharmacist before taking Momentact Analgesico if you have:\u003cbr\u003e- heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e- high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e\u003cbr\u003eMedicines such as Momentact Analgesico can:\u003cbr\u003e- be associated with the appearance of even serious kidney diseases (such as renal papillary necrosis, analgesic nephropathy and renal failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e- lead to eye disorders, therefore, in case of prolonged treatments, periodic eye examinations are recommended. If visual disturbances occur, stop treatment with Momentact Analgesico.\u003cbr\u003e\u003cbr\u003e\u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003eMomentact Analgesico can mask symptoms of infections such as fever and pain. Therefore, it is possible that Momentact Analgesico may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the infection symptoms persist or worsen, consult your doctor immediately.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003eIf the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Momentact Analgesico can cause side effects, although not everybody gets them. The side effects of the drug can be minimised if you use the lowest recommended dose, and if you use the drug only for the period necessary to control your symptoms.\u003cbr\u003e\u003cbr\u003eIf you develop an ulcer, or stomach and\/or intestinal bleeding, or skin and\/or mucous membrane lesions, you must stop treatment with Momentact Analgesico and consult your doctor. These side effects are usually more frequent in the elderly. The use of Momentact Analgesico can cause side effects that are generally mild or moderate or more serious allergic reactions, even if rarely.\u003cbr\u003e\u003cbr\u003eIf you experience any of the following symptoms, \u003cb\u003eSTOP using\u003c\/b\u003e Momentact Analgesico immediately and consult your doctor or the nearest hospital where you will receive appropriate and specific treatment:\u003cbr\u003e• chest pain, which may be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e• skin rashes or lesions;\u003cbr\u003e• mucosal lesions;\u003cbr\u003e• signs of an allergic reaction, even severe (erythema, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e• peeling skin;\u003cbr\u003e• non-raised reddish spots, target-shaped or circular on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e• widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e• widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e• visual disturbances;\u003cbr\u003e• liver disease (hepatic dysfunction);\u003cbr\u003e• bleeding, ulcer and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e\u003cbr\u003eShould one of the allergic reactions listed above occur, go to the hospital as it is necessary to have immediate availability of equipment, medicines and personnel suitable for emergency treatment, since in rare cases severe side effects, sometimes fatal, have been reported following the use of ibuprofen, even in the absence of known allergy.\u003cbr\u003e\u003cbr\u003eThe risk of these symptoms occurring is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e\u003cbr\u003eFurthermore, you may experience other side effects that have also been reported with other medicines similar to Momentact Analgesico and which are listed below according to frequency:\u003cbr\u003e\u003cbr\u003e\u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e• dizziness\u003cbr\u003e• malaise\u003cbr\u003e• fatigue\u003cbr\u003e\u003cbr\u003e\u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e• stomach inflammation (gastritis)\u003cbr\u003e• insomnia, anxiety\u003cbr\u003e• numbness of limbs or other parts of the body, drowsiness\u003cbr\u003e• nasal congestion (rhinitis) (especially in patients with pre-existing autoimmune disorders, such as systemic lupus erythematosus and mixed connective tissue disease)\u003cbr\u003e• breathing difficulties (bronchospasm, dyspnoea)\u003cbr\u003e• momentary cessation of breathing (apnoea)\u003cbr\u003e• hearing impairment\u003cbr\u003e• ringing in the ears (tinnitus)\u003cbr\u003e• vertigo\u003cbr\u003e• liver disorders (altered liver function)\u003cbr\u003e• liver inflammation (hepatitis)\u003cbr\u003e• yellowing of skin and eyes (jaundice)\u003cbr\u003e• kidney diseases (impairment of renal function and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and renal failure)\u003cbr\u003e• allergic reactions such as rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), asthma, breathing difficulties (bronchospasm or dyspnoea), asthma attacks with lowering of blood pressure\u003cbr\u003e• skin reactions to light (photosensitivity)\u003cbr\u003e• visual disturbances\u003cbr\u003e\u003cbr\u003e\u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e• reduction in the number of blood cells: reduction in white blood cells (leucopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anaemia, aplastic anaemia), platelets (thrombocytopenia)\u003cbr\u003e• depression, confusional state, hallucinations\u003cbr\u003e• inflammation of the optic nerve (optic neuritis)\u003cbr\u003e• inflammation of the meninges, the membranes covering the brain (aseptic meningitis), especially in patients with pre-existing autoimmune disorders (see section Warnings and precautions) with symptoms of nuchal rigidity, headache, nausea, vomiting, fever or disorientation\u003cbr\u003e• eye disorders with visual disturbances and optic nerve disease (toxic optic neuropathy)\u003cbr\u003e• swelling due to fluid accumulation in tissues\u003cbr\u003e• disease that can affect various organs and tissues of the body (lupus erythematosus)\u003cbr\u003e• worsening of inflammation caused by an existing infection (e.g., development of necrotizing fasciitis)\u003cbr\u003e\u003cbr\u003e\u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e• inflammation of the pancreas, a gland involved in digestive processes (pancreatitis)\u003cbr\u003e• sensation of feeling one's own heartbeat (palpitations)*\u003cbr\u003e• heart disease (heart failure)*\u003cbr\u003e• heart attack (myocardial infarction)\u003cbr\u003e• increased fluid around the lungs (acute pulmonary oedema)*\u003cbr\u003e• liver disease (liver failure)*\u003cbr\u003e• hypertension*\u003cbr\u003e• severe allergic reactions, which may include symptoms such as swelling of the face, tongue and throat making it difficult to breathe, rapid heartbeat, severe rapidly occurring allergic reaction which can cause death (anaphylaxis), severe rash or skin exfoliation (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme).\u003cbr\u003eIn exceptional cases, severe skin infections and soft tissue disorders may occur during chickenpox infection\u003cbr\u003e\u003cbr\u003e\u003cb\u003e*these side effects tend to resolve upon discontinuation of treatment\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e\u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e• feeling of heaviness in the stomach\u003cbr\u003e• nausea\u003cbr\u003e• vomiting\u003cbr\u003e• diarrhoea\u003cbr\u003e• gas emission (flatulence)\u003cbr\u003e• constipation\u003cbr\u003e• indigestion\u003cbr\u003e• abdominal pain\u003cbr\u003e• heartburn\u003cbr\u003e• blood in stools\u003cbr\u003e• blood in vomit\u003cbr\u003e• lesions inside the mouth\u003cbr\u003e• worsening of inflammatory diseases of the colon and intestine (colitis, Crohn's disease)\u003cbr\u003e• increased risk of heart attack (myocardial infarction), or lack of blood supply to the brain (stroke)\u003cbr\u003e• high blood pressure\u003cbr\u003e• severe heart disease (heart failure)\u003cbr\u003e• drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell)\u003cbr\u003e• a widespread, red and scaly rash, with pustule formation under the skin and vesicles located mainly on skin folds, trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalised exanthematous pustulosis). Stop using Momentact Analgesico if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.salute.gov.it\/portale\/temi\/soggettoAutorizzatoVenditaOnlineFarmaciMDS.jsp?VOLID=F14409%20\" target=\"_blank\"\u003e\u003cimg src=\"http:\/\/www.farmania.it\/farmaco\/farmaco-promo-farmacia.png\"\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46290208129291,"sku":"037858014","price":8.2,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_2b29830b-9416-4da0-bba8-bb9bfd49afb5.png?v=1734081363"},{"product_id":"aspirina-rapida-10cprmast500mg","title":"ASPIRIN RAPID*10CHEWTAB500MG","description":"\u003cp\u003e\u003cb\u003eAspirina Rapida 500 mg chewable tablets\u003c\/b\u003e\u003cbr\u003e Acetylsalicylic acid\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eAspirina is an analgesic (painkiller: reduces pain), anti-inflammatory and antipyretic (fever reducer: reduces fever).\u003cbr\u003e Aspirina is used for the symptomatic treatment of feverish conditions and flu and cold syndromes, and for the symptomatic treatment of headache, toothache, neuralgia, menstrual pain, rheumatic pain and muscle pain.\u003cbr\u003e The product is for adult patients only.\u003cbr\u003e Consult your doctor if you do not notice an improvement or if your symptoms worsen after 3-5 days.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Aspirina Rapida\u003c\/b\u003e\u003cbr\u003e - if you are allergic to acetylsalicylic acid, other analgesics (painkillers)\/antipyretics (fever reducers)\/non-steroidal anti-inflammatory drugs (NSAIDs) or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you suffer from gastroduodenal ulcer (stomach ulcer or ulcer in the first part of the intestine);\u003cbr\u003e - if you suffer from hemorrhagic diathesis (tendency to bleeding);\u003cbr\u003e - if you suffer from severe kidney (reduced kidney function), liver (hepatic) or heart (cardiac) failure;\u003cbr\u003e - if you suffer from glucose-6-phosphate dehydrogenase deficiency (an enzyme whose genetically determined absence leads to a disease characterized by reduced red blood cell survival);\u003cbr\u003e - if you are already taking \u003cb\u003emethotrexate\u003c\/b\u003e (at doses of 15 mg\/week or more) or \u003cb\u003ewarfarin\u003c\/b\u003e (see Other medicines and Aspirina Rapida);\u003cbr\u003e - if you have previously suffered from asthma induced by the administration of salicylates or similar substances, in particular non-steroidal anti-inflammatory drugs (NSAIDs);\u003cbr\u003e - if you are in the last trimester of pregnancy or are breastfeeding (see Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you are under 16 years of age (see Children and adolescents).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eTalk to your doctor or pharmacist before taking Aspirina Rapida.\u003cbr\u003e \u003cbr\u003e Take the medicine only on a full stomach.\u003cbr\u003e Before administering any medicine, you should take all precautions to prevent unwanted reactions:\u003cbr\u003e • rule out any previous allergic reactions to this or other medicines;\u003cbr\u003e • rule out the existence of other contraindications or conditions that may expose you to the risk of potentially serious undesirable effects. If in doubt, consult your doctor or pharmacist;\u003cbr\u003e • do not use acetylsalicylic acid together with another NSAID or, in any case, do not use more than one NSAID at a time.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAllergic reactions\u003c\/b\u003e\u003cbr\u003e Acetylsalicylic acid and other NSAIDs can cause allergic reactions [including asthma attacks, rhinitis (runny nose), angioedema (swelling of the skin and mucous membranes) or urticaria (small itchy spots on the skin)].\u003cbr\u003e The risk is greater in individuals who have previously experienced an allergic reaction after using this type of medicine (see Do not take Aspirina Rapida) and in individuals who have allergic reactions (e.g., skin reactions, itching, urticaria) to other substances.\u003cbr\u003e In individuals with asthma and\/or rhinitis (with or without nasal polyps) and\/or urticaria, reactions may be more frequent and severe.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eTell your doctor if:\u003c\/b\u003e\u003cbr\u003e - you are to undergo surgery (even minor, such as tooth extraction), as pre-operative use of this medicine may make it more difficult to stop bleeding during surgery (intraoperative hemostasis);\u003cbr\u003e - you need to undergo a fecal occult blood test, as acetylsalicylic acid can cause gastrointestinal bleeding.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIn the following cases, your doctor will only prescribe this medicine after a careful assessment of the risk\/benefit ratio:\u003c\/b\u003e\u003cbr\u003e • if you have an increased risk of allergic reactions, for example if you suffer from asthma and\/or rhinitis (with or without nasal polyps) and\/or urticaria;\u003cbr\u003e • if you have an increased risk of gastrointestinal lesions, as acetylsalicylic acid and other NSAIDs can cause severe gastrointestinal side effects (bleeding, ulcer, perforation); for this reason, these medicines should not be used in individuals who suffer or have suffered in the past from gastrointestinal ulcers or gastrointestinal bleeding (see Do not take Aspirina Rapida) or who consume large quantities of alcohol or higher doses of acetylsalicylic acid (dose-related effect);\u003cbr\u003e • if you have blood coagulation defects or are undergoing treatment with anticoagulant medicines (used to slow down or inhibit the blood coagulation process);\u003cbr\u003e • if you suffer from impaired kidney, heart or liver function;\u003cbr\u003e • if you suffer from asthma;\u003cbr\u003e • if you have hyperuricemia\/gout (increased uric acid level in the blood).\u003cbr\u003e \u003cbr\u003e It is also advisable to consult your doctor if the above-mentioned disorders have occurred in the past.\u003cbr\u003e \u003cbr\u003e • if you are taking medicines not recommended or that require special precautions or dosage adjustment (see Other medicines and Aspirina Rapida);\u003cbr\u003e • if you are over 70 years of age, especially in the presence of concomitant therapies;\u003cbr\u003e • if you are in the first or second trimester of pregnancy (see Pregnancy, breastfeeding and fertility);\u003cbr\u003e • if you are following a low-sodium diet.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e This medicine should not be taken by children and adolescents under 16 years of age.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eElderly\u003c\/b\u003e\u003cbr\u003e The risk of serious side effects is greater in elderly subjects.\u003cbr\u003e If you are over 70 years of age, consult your doctor before taking this medicine.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePatients with impaired kidney and liver function\u003c\/b\u003e\u003cbr\u003e This medicine should be used with caution (see warnings and precautions).\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e The most frequently observed side effects affect the gastrointestinal system.\u003cbr\u003e These disorders can be partially alleviated by taking the medicine on a full stomach. Most side effects are dependent on both the dose and the duration of treatment. The side effects observed with acetylsalicylic acid are generally common to other NSAIDs.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eThe following side effects may occur:\u003cbr\u003e Effects on the blood\u003c\/b\u003e\u003cbr\u003e - prolonged bleeding time,\u003cbr\u003e - gastrointestinal hemorrhage anemia,\u003cbr\u003e - reduction in platelets (thrombocytopenia) in extremely rare cases. Following hemorrhage, hemorrhagic\/iron deficiency anemia (due to iron deficiency) may occur (due, for example, to occult microhemorrhages) with related changes in laboratory parameters and related clinical signs and symptoms such as asthenia (tiredness), pallor and hypoperfusion (reduced blood supply to the tissues).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the nervous system\u003c\/b\u003e\u003cbr\u003e - headache,\u003cbr\u003e - dizziness.\u003cbr\u003e Rarely, the following may occur:\u003cbr\u003e - Reye's syndrome (*), an acute disease affecting the brain and liver, potentially fatal, which almost exclusively affects children.\u003cbr\u003e Rarely to very rarely, the following may occur:\u003cbr\u003e - cerebral hemorrhage, especially in patients with uncontrolled hypertension (high blood pressure) and\/or on anticoagulant therapy (medicines used to slow down or inhibit the blood coagulation process) which, in isolated cases, can be potentially fatal.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the ear\u003c\/b\u003e\u003cbr\u003e - tinnitus (ringing\/hissing\/clanging\/whistling in the ear).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the respiratory system\u003c\/b\u003e\u003cbr\u003e - respiratory disease exacerbated by acetylsalicylic acid,\u003cbr\u003e - asthmatic syndrome\u003cbr\u003e - rhinitis (runny nose)\u003cbr\u003e - nasal congestion (blocked nose) (associated with allergic reactions);\u003cbr\u003e - epistaxis (nosebleed).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the heart\u003c\/b\u003e\u003cbr\u003e - cardiorespiratory distress (severe and acute respiratory failure) (associated with allergic reactions).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the eye\u003c\/b\u003e\u003cbr\u003e - conjunctivitis (associated with allergic reactions).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the gastrointestinal system\u003c\/b\u003e\u003cbr\u003e - gastrointestinal bleeding (occult),\u003cbr\u003e - gastric disturbances,\u003cbr\u003e - heartburn,\u003cbr\u003e - gastrointestinal pain,\u003cbr\u003e - gingival bleeding (bleeding gums),\u003cbr\u003e - vomiting,\u003cbr\u003e - diarrhea,\u003cbr\u003e - nausea,\u003cbr\u003e - crampy abdominal pain (associated with allergic reactions).\u003cbr\u003e Rarely, the following may occur:\u003cbr\u003e - gastrointestinal inflammation,\u003cbr\u003e - gastrointestinal erosion,\u003cbr\u003e - gastrointestinal ulceration,\u003cbr\u003e - hematemesis (vomiting blood or coffee-ground material),\u003cbr\u003e - melena (passing black, tarry stools),\u003cbr\u003e - esophagitis (inflammation of the esophagus).\u003cbr\u003e Very rarely, the following may occur:\u003cbr\u003e - hemorrhagic gastrointestinal ulcer and\/or gastrointestinal perforation with related clinical signs and symptoms and changes in laboratory parameters.\u003cbr\u003e May occur with unknown frequency (especially with long-term treatment):\u003cbr\u003e - intestinal diaphragm disease.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the liver\u003c\/b\u003e\u003cbr\u003e - rarely: hepatotoxicity (hepatocellular injury, generally mild and asymptomatic) which manifests as an increase in transaminases.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the skin\u003c\/b\u003e\u003cbr\u003e - skin rash,\u003cbr\u003e - edema (swelling),\u003cbr\u003e - urticaria,\u003cbr\u003e - itching,\u003cbr\u003e - erythema (redness),\u003cbr\u003e - angioedema (associated with allergic reactions).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the kidneys and urinary tract\u003c\/b\u003e\u003cbr\u003e - impaired kidney function and acute kidney injury (in the presence of altered blood circulation in the kidneys),\u003cbr\u003e - urogenital hemorrhages (of the urinary and genital system).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the body as a whole\u003c\/b\u003e\u003cbr\u003e - procedural hemorrhages (immediately before, during and immediately after surgery),\u003cbr\u003e - hematomas (collections of blood outside the blood vessels).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eEffects on the immune system\u003c\/b\u003e\u003cbr\u003e - rarely: anaphylactic shock (severe allergic reaction, potentially fatal) with related changes in laboratory parameters and clinical manifestations.\u003cbr\u003e \u003cbr\u003e (*) Reye's Syndrome (RS)\u003cbr\u003e RS initially manifests with vomiting (persistent or recurrent) and other signs of varying degrees of brain distress: from sluggishness, drowsiness or personality changes (irritability or aggressiveness) to disorientation, confusion or delirium, up to convulsions or loss of consciousness. It is important to note the variability of the clinical picture: even vomiting may be absent or replaced by diarrhea.\u003cbr\u003e If these symptoms occur in the days immediately following a flu-like episode (or chickenpox or another viral infection) during which acetylsalicylic acid or other medicines containing salicylates have been administered, the doctor's attention must immediately be directed to the possibility of RS.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"\" https: target=\"\" _blank\u003e\u003cimg src=\"\" http:\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"BAYER SpA","offers":[{"title":"Default Title","offer_id":46294555230475,"sku":"004763379","price":7.22,"currency_code":"EUR","in_stock":true}]},{"product_id":"ibuprofene-san-24cpr-riv-200mg","title":"IBUPROFEN SAN*24FC TAB 200MG","description":"\u003cp\u003e\u003cb\u003eIbuprofene Sandoz 200 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003eGeneric medicine\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eThis medicine contains the active ingredient ibuprofen, belonging to a group of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs) which reduce pain (analgesic action) and lower fever.\u003cbr\u003e\u003cbr\u003eIbuprofene Sandoz is indicated for the treatment of various types of pain: menstrual pain, headache, toothache, pain in one or more nerves (neuralgia), bone, joint, and muscle pain (osteoarticular and muscular pain).\u003cbr\u003e\u003cbr\u003eThe medicine is also indicated as an additional therapy in the treatment of fever and flu symptoms.\u003cbr\u003e\u003cbr\u003eConsult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Ibuprofene Sandoz\u003c\/b\u003e\u003cbr\u003e- if you are allergic to the active ingredient, or to any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e- if you are allergic to acetylsalicylic acid or other medicines used to reduce pain (analgesics), fever (antipyretics) such as non-steroidal anti-inflammatory drugs (NSAIDs), especially when the allergy is associated with swelling of the nasal mucosa (nasal polyposis), angioedema and asthma, and presents with an asthmatic reaction (bronchospasm), urticaria, or severe rhinitis (acute rhinitis) (see section Warnings and precautions);\u003cbr\u003e- if you suffer from severe liver or kidney problems;\u003cbr\u003e- if you suffer from severe heart conditions (severe heart failure);\u003cbr\u003e- if you have had stomach and\/or intestinal bleeding (haemorrhage) or perforation after previous treatments with other medicines;\u003cbr\u003e- if you suffer or have suffered from recurrent bleeding or ulcers (two or more distinct episodes of proven ulceration or bleeding);\u003cbr\u003e- if you have had a severe ulcer in the stomach or the first part of the intestine;\u003cbr\u003e- if you have an ongoing ulcer;\u003cbr\u003e- if you have bleeding in the brain (cerebrovascular haemorrhage) or other types of bleeding;\u003cbr\u003e- if you have an alteration in blood cell production, the cause of which is unknown;\u003cbr\u003e- if you are in the last 3 months of pregnancy (See section Pregnancy and breastfeeding);\u003cbr\u003e- if the patient is a child under 12 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking Ibuprofene Sandoz.\u003cbr\u003e\u003cbr\u003eWhat you need to know before taking Ibuprofene Sandoz\u003cbr\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema), and chest pain, have been reported with ibuprofen.\u003cbr\u003eStop Ibuprofene Sandoz immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003ePay particular attention with Ibuprofene Sandoz:\u003cbr\u003eSkin reactions\u003cbr\u003eSevere skin reactions, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalised exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Stop using Ibuprofene Sandoz and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.\u003cbr\u003e\u003cbr\u003eAnti-inflammatory\/pain relief medicines such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially when given in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003eDo not take this medicine if you are already taking other medicines (See section Other medicines and Ibuprofene Sandoz).\u003cbr\u003e\u003cbr\u003eYou should discuss therapy with your doctor or pharmacist before taking Ibuprofene Sandoz if you have:\u003cbr\u003e- heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e- high blood pressure, diabetes, high cholesterol, family history of heart disease or stroke, or if you are a smoker;\u003cbr\u003e- if you have an infection - see section Infections below.\u003cbr\u003e\u003cbr\u003eTake this medicine with caution:\u003cbr\u003e- if you suffer or have suffered in the past from bowel disorders (ulcerative colitis, Crohn's disease);\u003cbr\u003e- if you suffer from heart problems (mild to moderate heart failure, congestive heart failure, confirmed ischemic heart disease, heart decompensation). In this case, your doctor must subject you to frequent checks, especially if you take the medicine for prolonged periods of time;\u003cbr\u003e- if you have hepatic porphyria;\u003cbr\u003e- if you have chronic obstructive pulmonary disease or chronic respiratory tract infections;\u003cbr\u003e- if you are taking medicines that may increase the risk of bleeding, ulceration and perforation such as acetylsalicylic acid (e.g. aspirin) and other NSAIDs, corticosteroids administered orally, by injection or rectally (e.g. cortisone), anticoagulants (e.g. warfarin), selective serotonin reuptake inhibitors (antidepressants) (see section Other medicines and Ibuprofene Sandoz);\u003cbr\u003e- if you have liver, kidney, or heart problems unless you have a severe form of liver, kidney or heart failure, because in these latter cases you must not take Ibuprofene Sandoz (see section 2 Do not take Ibuprofene Sandoz);\u003cbr\u003e- if you have reduced kidney function or if you suffer from liver problems (hepatic dysfunction). In these cases, your doctor must subject you to frequent checks, especially if you take the medicine for prolonged periods of time;\u003cbr\u003e- if you suffer from breathing disorders (asthma), if you have seasonal allergic rhinitis, swelling of the nasal mucosa (e.g. nasal polyps) other allergic diseases or if in the past you have experienced breathing difficulties (bronchospasm), also following the use of other medicines similar to Ibuprofene Sandoz (aspirin or other NSAIDs);\u003cbr\u003e- if the patient is a child or adolescent with dehydration problems, because in this case the medicine can cause kidney problems;\u003cbr\u003e- if you are using medicines that increase urine production (diuretics) or other medicines that may affect kidney function;\u003cbr\u003e- if you have reduced body fluid volume (e.g. before or after major surgery);\u003cbr\u003e- if you are about to undergo or have undergone major surgery;\u003cbr\u003e- if you have stomach or intestinal problems, unless you have one or more conditions for which you must not take Ibuprofene Sandoz (see section Do not take Ibuprofene Sandoz);\u003cbr\u003e- if you are a woman and are planning a pregnancy;\u003cbr\u003e- if you are a woman and have fertility problems or are undergoing fertility investigations, because you should stop treatment with Ibuprofene Sandoz;\u003cbr\u003e- if you have an autoimmune disease e.g. Lupus erythematosus or connective tissue diseases.\u003cbr\u003e\u003cbr\u003eIn these cases, your doctor will keep you under strict control and will periodically re-evaluate the need for treatment with Ibuprofene Sandoz. In addition, your doctor may ask you to undergo periodic examinations (such as monitoring kidney function) to assess your condition during treatment with Ibuprofene Sandoz.\u003cbr\u003e\u003cbr\u003eInfections\u003cbr\u003eIbuprofene Sandoz can mask the symptoms of infections such as fever and pain. Therefore, it is possible that Ibuprofene Sandoz may delay adequate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the infection symptoms persist or worsen, consult your doctor immediately.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eStop treatment and inform your doctor if, during treatment with Ibuprofene Sandoz, you develop:\u003c\/b\u003e\u003cbr\u003e• gastrointestinal bleeding or ulceration\u003cbr\u003e• mucosal lesions or any other sign of an allergic reaction\u003cbr\u003e• fluid retention and swelling due to fluid accumulation (edema)\u003cbr\u003e• signs and symptoms of liver problems or if liver function parameters are not normal (visible from blood tests)\u003cbr\u003e• unusual stomach and intestinal symptoms especially at the beginning of treatment with Ibuprofene Sandoz\u003cbr\u003e• fever, sore throat, superficial mouth ulcers, flu-like symptoms, profound fatigue, unexplained bruising and bleeding because you may have a reduction in white blood cells (agranulocytosis)\u003cbr\u003e• stiffness in the neck, headache, nausea, vomiting, fever, disorientation because you may be suffering from aseptic meningitis. Patients with autoimmune diseases (Systemic Lupus Erythematosus, connective tissue disease) appear to be more predisposed to developing aseptic meningitis\u003cbr\u003e• symptoms of an infection (e.g. headache, fever) or if you notice the worsening of an infection as Ibuprofene Sandoz can mask the signs and symptoms of the infection.\u003cbr\u003e\u003cbr\u003eIn these cases, your doctor will assess whether to continue or discontinue treatment with Ibuprofene Sandoz.\u003cbr\u003e\u003cbr\u003eSevere skin reactions have been reported in association with Ibuprofene Sandoz treatment. Stop taking Ibuprofene Sandoz and consult your doctor immediately if you develop rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very severe skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eOther important information:\u003c\/b\u003e\u003cbr\u003e- During treatment with NSAIDs, including ibuprofen, gastrointestinal bleeding, ulceration or perforation may occur, which can also cause death, and may occur at any time during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events. You should take the lowest effective dose of ibuprofen to reduce the risk of gastrointestinal toxicity and your doctor may prescribe medicines (e.g. misoprostol or proton pump inhibitors) to protect the gastrointestinal mucosa.\u003cbr\u003e- Side effects can be reduced by using the lowest effective dose for the shortest possible time (see section 3 How to take Ibuprofene Sandoz).\u003cbr\u003e- Avoid the use of ibuprofen during treatment with other NSAIDs administered orally, by injection and rectally, including selective cyclooxygenase-2 inhibitors, because it increases the possibility of you having side effects.\u003cbr\u003e\u003cbr\u003eCases of aseptic meningitis have been reported during treatment with ibuprofen, although they are more likely in patients with Lupus erythematosus or connective tissue diseases.\u003cbr\u003e\u003cbr\u003eDuring treatment with this medicine, eye problems (ocular alterations) may occur. Therefore, in case of prolonged treatments, it is recommended to undergo periodic eye (ophthalmological) check-ups.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003eIbuprofene Sandoz is contraindicated in children under 12 years of age.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eElderly patients\u003c\/b\u003e\u003cbr\u003eElderly patients are more likely to experience adverse reactions, especially stomach or intestinal bleeding and perforation which are generally more severe and can be fatal.\u003cbr\u003eIf you are elderly, you should take the lowest dose of Ibuprofene Sandoz. As a precaution, your doctor may have you undergo a kidney function check and prescribe medicines that protect the gastrointestinal mucosa such as misoprostol or proton pump inhibitors.\u003cbr\u003eInform your doctor of any unusual stomach and intestinal symptoms, especially at the beginning of treatment with this medicine.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003eSide effects can be minimized by using the lowest effective dose for the shortest duration of treatment necessary to control symptoms.\u003cbr\u003eSide effects depend on the dose and may vary from patient to patient.\u003cbr\u003e\u003cbr\u003eStop treatment with Ibuprofene Sandoz and consult your doctor immediately if you notice any of the following symptoms:\u003cbr\u003e• chest pain, which may be a sign of a potentially severe allergic reaction called Kounis syndrome;\u003cbr\u003e• reddish, non-elevated, target-shaped or circular spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e• widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e• widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e\u003cbr\u003eThe most commonly observed adverse events affect the stomach and\/or intestines. Stomach or first part of the intestine ulcers (peptic ulcer), perforation or bleeding from the stomach and\/or intestines may occur, which can even be fatal, particularly in the elderly.\u003cbr\u003eIn particular, the risk of bleeding from the stomach and\/or intestines depends on the dose and duration of treatment.\u003cbr\u003e\u003cbr\u003eIn addition to the side effects listed below, dark stools with blood (melena) and vomiting with blood (hematemesis) due to bleeding from the stomach, esophagus, and duodenum have been reported after administration of Ibuprofene Sandoz.\u003cbr\u003e\u003cbr\u003eMedicines such as Ibuprofene Sandoz may be associated with a modest increased risk of heart attack (myocardial infarction) or stroke (see section Warnings and precautions).\u003cbr\u003e\u003cbr\u003eThe following side effects may occur, which generally resolve with discontinuation of treatment:\u003cbr\u003e\u003cbr\u003e\u003cb\u003eCommon side effects (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e- difficulty digesting (dyspepsia)\u003cbr\u003e- abdominal pain\u003cbr\u003e- nausea\u003cbr\u003e- vomiting\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon side effects (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e- allergic reactions including skin rash, hives, itching, and asthmatic attacks\u003cbr\u003e- headache\u003cbr\u003e- dizziness\u003cbr\u003e- insomnia\u003cbr\u003e- agitation\u003cbr\u003e- irritability\u003cbr\u003e- fatigue\u003cbr\u003e- skin rash\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare side effects (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e- ringing and buzzing in the ears (tinnitus)\u003cbr\u003e- hearing impairment\u003cbr\u003e- stomach or first part of the intestine ulcer (peptic ulcer)\u003cbr\u003e- perforation or bleeding from the stomach and\/or intestine\u003cbr\u003e- inflammation of the oral mucosa with ulceration (ulcerative stomatitis)\u003cbr\u003e- inflammation of the stomach (gastritis)\u003cbr\u003e- worsening of colon inflammation (colitis)\u003cbr\u003e- worsening of a chronic inflammatory disease of the digestive system (Crohn's disease)\u003cbr\u003e- kidney failure\u003cbr\u003e- kidney tissue damage (papillary necrosis) (especially in long-term therapy)\u003cbr\u003e- increased uric acid concentration in the blood\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e- worsening of infection-related inflammations (e.g., development of necrotizing fasciitis)\u003cbr\u003e- reduction in the number of platelets in the blood (thrombocytopenia)\u003cbr\u003e- anemia\u003cbr\u003e- reduction in the number of white blood cells in the blood (leukopenia, agranulocytosis)\u003cbr\u003e- reduction in the number of all cells present in the blood (pancytopenia)\u003cbr\u003e- severe allergic reaction (anaphylactic reaction)\u003cbr\u003e- swelling due to fluid accumulation (angioedema)\u003cbr\u003e- aseptic meningitis (infection of the meninges, membranes of the brain)\u003cbr\u003e- alterations in liver function tests\u003cbr\u003e- liver problems, e.g., liver inflammation (hepatitis) and yellowing of the skin, mucous membranes, and eyes (jaundice)\u003cbr\u003e- liver damage, particularly in long-term therapy\u003cbr\u003e- skin and mucous membrane reactions, including severe ones (bullous dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis)\u003cbr\u003e\u003cbr\u003e\u003cb\u003eNot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e- mental alterations (psychotic reactions)\u003cbr\u003e- depression\u003cbr\u003e- vision disorders\u003cbr\u003e- irregular heartbeat (palpitations)\u003cbr\u003e- swelling (edema)\u003cbr\u003e- heart failure\u003cbr\u003e- heart attack\u003cbr\u003e- high blood pressure (hypertension)\u003cbr\u003e- inflammation of the esophagus (esophagitis)\u003cbr\u003e- inflammation of the pancreas (pancreatitis)\u003cbr\u003e- intestinal strictures (diaphragmatic intestinal stenoses)\u003cbr\u003e- gas emission (flatulence)\u003cbr\u003e- diarrhea\u003cbr\u003e- constipation\u003cbr\u003e- edema formation, particularly in patients with high blood pressure or kidney problems (renal insufficiency, nephrotic syndrome, interstitial nephritis) which may be accompanied by acute renal failure\u003cbr\u003e- skin becomes sensitive to light\u003cbr\u003e- a widespread, red, and scaly rash, with pustules forming under the skin and blisters located mainly on skin folds, trunk, and upper limbs, accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003eA severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swelling of lymph nodes, and an increase in eosinophils (a type of white blood cell).\u003cbr\u003eOther side effects reported include: bronchospasm or dyspnea, apnea, epigastric pain, heartburn, rhinitis, anxiety, confusional state, hallucinations, paresthesia, drowsiness, optic neuritis, optic neuropathy, vertigo, photosensitivity reactions, malaise.\u003cbr\u003eStop using Ibuprofene Sandoz if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"\" https: target=\"\" _blank\u003e\u003cimg src=\"\" http:\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"SANDOZ SpA","offers":[{"title":"Default Title","offer_id":46370415345931,"sku":"025636059","price":6.38,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_476f7fa6-d811-4d44-a96a-81d1e8ec1c26.png?v=1735285238"},{"product_id":"moment-12cpr-riv-200mg","title":"MOMENT*12FC TAB 200MG","description":"\u003cp\u003e\u003cb\u003eMOMENT 200 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Ibuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMoment contains ibuprofen, a medicine that belongs to the class of analgesic-anti-inflammatory drugs, i.e., medicines that fight pain and inflammation.\u003cbr\u003e \u003cbr\u003e Moment is used, in \u003cb\u003eadults\u003c\/b\u003e and \u003cb\u003eadolescents from 12 years of age\u003c\/b\u003e, for: - treatment of pain of various origins and natures (headache, toothache, neuralgia, osteo-articular and muscular pain, menstrual pain);\u003cbr\u003e - reduction of symptoms of feverish and flu-like states.\u003cbr\u003e \u003cbr\u003e Contact your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Moment:\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen and\/or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e - if you are allergic to other anti-rheumatic medicines (e.g., acetylsalicylic acid, etc.), medicines used for the treatment of joint or muscle pain (see paragraph Other medicines and Moment);\u003cbr\u003e - if the patient is a child under 12 years of age;\u003cbr\u003e - if you are in the last 3 months of pregnancy or are breastfeeding (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you suffer from stomach and intestinal diseases (e.g., active or severe gastroduodenal ulcer);\u003cbr\u003e - if you have previously had bleeding or perforation of the stomach or intestine after taking medicines;\u003cbr\u003e - if you have previously had two or more distinct episodes of stomach ulcer or bleeding;\u003cbr\u003e - in the presence of severe heart disease (severe heart failure);\u003cbr\u003e - in the presence of severe liver or kidney disease;\u003cbr\u003e - if you have lost a lot of fluids (severe dehydration) due to vomiting, diarrhea or insufficient fluid intake.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine have been reported with ibuprofen, including breathing problems, swelling of the face and neck area (angioedema) and chest pain. Stop Moment immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e \u003cbr\u003e Skin reactions\u003cbr\u003e Severe skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using Moment and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in paragraph 4.\u003cbr\u003e \u003cbr\u003e Talk to your doctor or pharmacist before taking Moment:\u003cbr\u003e - if you have had episodes of breathing difficulties (bronchospasm) after using acetylsalicylic acid (aspirin) or other anti-inflammatory drugs;\u003cbr\u003e - if you suffer from asthma, runny nose (chronic rhinitis), nasal polyps (nasal polyposis) or inflammation of the paranasal sinus mucosa (sinusitis) or suffer\/have suffered from allergies because you may experience breathing difficulties (bronchospasm), skin redness with itching (urticaria) or swelling of the skin and throat (angioedema), especially if you have already had allergic reactions after using other medicines used for the treatment of joint or muscle pain, fever or for the treatment of inflammation (NSAIDs);\u003cbr\u003e - if you are taking other anti-inflammatory medicines, including selective COX-2 inhibitors (an enzyme involved in inflammatory processes), as in these cases the risk of ulcers and bleeding may increase (see paragraph Other medicines and Moment);\u003cbr\u003e - if you are elderly or if you have suffered from an ulcer, especially if the ulcer has also manifested with bleeding or perforation (see paragraph Do not take Moment), as the risk of bleeding, ulcer or perforation is higher, especially with higher doses of anti-inflammatory drugs. In these cases, you must start treatment with the lowest available dose, and possibly consult your doctor to have a medicine prescribed that protects the stomach (misoprostol or proton pump inhibitors). This possibility should also be considered if you are taking low doses of acetylsalicylic acid or drugs that may increase the risk of stomach and\/or intestinal diseases (see paragraph Other medicines and Moment);\u003cbr\u003e - if you have suffered or suffer from chronic bowel diseases (ulcerative colitis, Crohn's disease) as they may worsen (see paragraph 4 Possible side effects);\u003cbr\u003e - if you have had stomach and intestinal diseases related to the use of medicines, and in particular if you are elderly, you must report any unusual intestinal symptoms (especially bleeding) to your doctor, particularly in the initial stages of treatment;\u003cbr\u003e - if you are taking other medicines that increase the risk of stomach and\/or intestinal ulcer or bleeding, such as oral corticosteroids (e.g. cortisone), anticoagulants (e.g. warfarin), antidepressants (selective serotonin reuptake inhibitors), or blood antiplatelets (e.g. acetylsalicylic acid). See also paragraph Other medicines and Moment. If gastrointestinal bleeding or ulceration occurs in patients taking Moment, treatment should be discontinued;\u003cbr\u003e - if you have high blood pressure and the medicines you are taking cannot lower it and\/or you have heart disease or blood circulation problems in the brain or other body parts or you think you may be at risk for these diseases (for example, if you suffer from high blood pressure, diabetes or high cholesterol or if you smoke);\u003cbr\u003e - if you suffer from high blood pressure and\/or have heart disease, as fluid retention, increased blood pressure and swelling have been found after treatment with NSAIDs. NSAIDs can reduce the action of medicines to lower blood pressure (see paragraph Other medicines and Moment);\u003cbr\u003e - if you have lost a considerable amount of fluid, or if swelling, heart problems or high blood pressure appear;\u003cbr\u003e - if you have decreased kidney function, heart or liver malfunction, or if you are elderly or undergoing treatment with medicines for high blood pressure, as you may be more prone to kidney problems. Furthermore, the habitual concomitant use of different painkillers can further increase this risk;\u003cbr\u003e - if you suffer from a clotting disorder or are taking medicines that slow down blood clotting (anticoagulants) (see paragraph Other medicines and Moment);\u003cbr\u003e - if you suffer from a disease that can affect several organs and tissues of the body (diffuse or systemic lupus erythematosus) or a connective tissue disease, present in many parts of the body, such as bones and cartilage, as in rare occasions symptoms of aseptic meningitis have been observed in patients treated with ibuprofen. Although this is more likely to occur in patients with systemic lupus erythematosus and related connective tissue diseases, it has also been observed in patients who did not manifest concomitant chronic diseases;\u003cbr\u003e - if you are taking medicines to treat pain, heart disease or high blood pressure (see paragraph Other medicines and Moment);\u003cbr\u003e - if you intend to become pregnant (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have difficulty becoming pregnant or are undergoing fertility investigations (see paragraph Pregnancy, breastfeeding and fertility);\u003cbr\u003e - if you have an infection - see paragraph Infections below.\u003cbr\u003e \u003cbr\u003e Anti-inflammatory\/painkiller medicines such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if administered in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e \u003cbr\u003e You should discuss therapy with your doctor or pharmacist before taking Moment if you have:\u003cbr\u003e - heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation to the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e - high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker.\u003cbr\u003e \u003cbr\u003e Medicines like Moment can:\u003cbr\u003e - be associated with the appearance of even serious kidney diseases (such as renal papillary necrosis, analgesic nephropathy and kidney failure), therefore your doctor will monitor your kidney function;\u003cbr\u003e - lead to eye disorders, therefore in case of prolonged treatments, periodic eye checks are recommended. If visual disturbances occur, stop treatment with Moment.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInfections\u003c\/u\u003e\u003cbr\u003e Moment can mask symptoms of infections such as fever and pain. It is therefore possible that Moment may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAdolescents\u003c\/b\u003e\u003cbr\u003e If the adolescent is dehydrated, there is a risk of developing kidney disease.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, Moment can cause side effects, although not everyone gets them.\u003cbr\u003e The side effects of the drug can be minimized if you use the lowest dose among those recommended, and if you use the drug only for the period necessary to control your symptoms.\u003cbr\u003e \u003cbr\u003e If you get an ulcer, or stomach and\/or intestinal bleeding, or skin and\/or mucous membrane lesions appear, you must stop treatment with Moment and contact your doctor. These side effects are usually more frequent in the elderly.\u003cbr\u003e \u003cbr\u003e The use of Moment can cause side effects that are generally mild or moderate or more serious reactions, including allergic reactions, albeit rarely.\u003cbr\u003e \u003cbr\u003e If you experience any of the following symptoms, \u003cb\u003eSTOP immediately using\u003c\/b\u003e Moment and contact your doctor or the nearest hospital immediately where you will be given appropriate and specific treatment:\u003cbr\u003e • chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome;\u003cbr\u003e • skin rashes or lesions;\u003cbr\u003e • mucous membrane lesions;\u003cbr\u003e • signs of an allergic reaction, even severe (erythema, itching, urticaria, asthma, swelling of the skin and mucous membranes, anaphylactic shock);\u003cbr\u003e • peeling skin;\u003cbr\u003e • non-raised, target-shaped or circular reddish spots on the trunk, often with central blisters, peeling skin, ulcers of the mouth, throat, nose, genitals and eyes. These severe skin rashes may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis);\u003cbr\u003e • widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome);\u003cbr\u003e • widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • liver disease (hepatic dysfunction);\u003cbr\u003e • bleeding, ulcer and perforation of the stomach and intestine, which can be fatal, particularly in the elderly.\u003cbr\u003e \u003cbr\u003e In the event that one of the allergic reactions listed above occurs, go to the hospital as it is necessary to have immediate availability of equipment, drugs and personnel suitable for emergency treatment, as in rare cases, following the use of ibuprofen, serious side effects, sometimes fatal, have been reported, even in the absence of known allergy.\u003cbr\u003e \u003cbr\u003e The risk of experiencing such symptoms is higher in the early stages of therapy: in most cases the reaction occurs within the first month of treatment.\u003cbr\u003e \u003cbr\u003e Furthermore, you may experience further side effects that have also been reported with other medicines similar to Moment and which are listed below according to frequency:\u003cbr\u003e \u003cbr\u003e \u003cb\u003ecommon (may affect up to 1 in 10 people)\u003c\/b\u003e\u003cbr\u003e • dizziness;\u003cbr\u003e • malaise;\u003cbr\u003e • fatigue;\u003cbr\u003e \u003cbr\u003e \u003cb\u003euncommon (may affect up to 1 in 100 people)\u003c\/b\u003e\u003cbr\u003e • stomach inflammation (gastritis);\u003cbr\u003e • insomnia, anxiety;\u003cbr\u003e • numbness of the limbs or other parts of the body (paresthesia), drowsiness;\u003cbr\u003e • inflammation of the nasal mucosa (rhinitis);\u003cbr\u003e • difficulty breathing (bronchospasm, dyspnea);\u003cbr\u003e • momentary interruption of breathing (apnea);\u003cbr\u003e • visual disturbances;\u003cbr\u003e • hearing impairment;\u003cbr\u003e • ringing in the ears (tinnitus);\u003cbr\u003e • vertigo;\u003cbr\u003e • liver disorders (altered liver function);\u003cbr\u003e • liver inflammation (hepatitis);\u003cbr\u003e • yellowing of the skin and eyes (jaundice);\u003cbr\u003e • kidney diseases (renal function damage and toxic nephropathy in various forms, including interstitial nephritis, nephrotic syndrome and kidney failure);\u003cbr\u003e • hypersensitivity reactions such as rash, urticaria, itching, formation of red spots on the skin (purpura), swelling of the skin and mucous membranes (angioedema), difficulty breathing (bronchospasm or dyspnea), asthma attacks with possible drop in blood pressure;\u003cbr\u003e • skin reactions to light (photosensitivity);\u003cbr\u003e \u003cbr\u003e \u003cb\u003erare (may affect up to 1 in 1,000 people)\u003c\/b\u003e\u003cbr\u003e • reduction in the number of blood cells: reduction in white blood cells (leukopenia, neutropenia, agranulocytosis), red blood cells (hemolytic anemia, aplastic anemia), platelets (thrombocytopenia);\u003cbr\u003e • reduced clotting ability;\u003cbr\u003e • depression, confusional state, hallucinations;\u003cbr\u003e • inflammation of the optic nerve (optic neuritis);\u003cbr\u003e • inflammation of the meninges, the membranes covering the brain (aseptic meningitis, especially in patients with pre-existing autoimmune disorders, see paragraph Warnings and precautions), with symptoms of neck stiffness, headache, nausea, vomiting, fever or disorientation;\u003cbr\u003e • eye disorders with visual disturbances and optic nerve pathology (toxic optic neuropathy);\u003cbr\u003e • swelling due to fluid accumulation in the tissues;\u003cbr\u003e • a disease that can affect several organs and tissues of the body (lupus erythematosus syndrome);\u003cbr\u003e • worsening of inflammations caused by an already existing infection (e.g., development of necrotizing fasciitis);\u003cbr\u003e • high levels of nitrogen in the blood;\u003cbr\u003e • altered liver function tests (increased transaminases, increased alkaline phosphatase);\u003cbr\u003e • abnormal blood tests (reduced hemoglobin, reduced hematocrit, prolonged bleeding time, decreased blood calcium, increased blood uric acid).\u003cbr\u003e \u003cbr\u003e \u003cb\u003every rare (may affect up to 1 in 10,000 people)\u003c\/b\u003e\u003cbr\u003e • inflammation of the pancreas, a gland involved in digestive processes (pancreatitis);\u003cbr\u003e • sensation of feeling one's own heartbeat (palpitations);\u003cbr\u003e • heart disease (heart failure);\u003cbr\u003e • heart attack (myocardial infarction);\u003cbr\u003e • presence of fluid in the lungs (acute pulmonary edema);\u003cbr\u003e • liver disease (hepatic insufficiency);\u003cbr\u003e • hypertension;\u003cbr\u003e • severe allergic reactions, which may include symptoms such as severe asthma, swelling of the face, tongue and throat that make breathing difficult, rapid heartbeat, severe rapidly appearing allergic reaction that can cause death (anaphylaxis), severe skin rash or exfoliation of the skin (toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme);\u003cbr\u003e • severe skin infections and soft tissue disorders may occur during chickenpox infection.\u003cbr\u003e \u003cbr\u003e \u003cb\u003enot known (frequency cannot be estimated from the available data)\u003c\/b\u003e\u003cbr\u003e • feeling of heaviness in the stomach;\u003cbr\u003e • nausea;\u003cbr\u003e • vomiting;\u003cbr\u003e • diarrhea;\u003cbr\u003e • flatulence;\u003cbr\u003e • constipation;\u003cbr\u003e • indigestion;\u003cbr\u003e • abdominal pain;\u003cbr\u003e • heartburn;\u003cbr\u003e • blood in the stools;\u003cbr\u003e • blood in the vomit;\u003cbr\u003e • lesions inside the mouth;\u003cbr\u003e • worsening of inflammatory bowel diseases (colitis, Crohn's disease);\u003cbr\u003e • increased risk of sudden reduction in blood circulation to the brain (stroke);\u003cbr\u003e • allergic reactions, anaphylaxis;\u003cbr\u003e • drug reaction with eosinophilia and systemic symptoms (DRESS syndrome): a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell);\u003cbr\u003e • a widespread, red and scaly rash, with pustules under the skin and vesicles located mainly on skin lesions, on the trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using Moment if you develop these symptoms and contact your doctor immediately. See also paragraph 2.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"\" https: target=\"\" _blank\u003e\u003cimg src=\"\" http:\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":46432147538187,"sku":"025669019","price":7.5,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_2a748cd9-1fc5-49a9-a058-33c5e8721df9.jpg?v=1736408222"},{"product_id":"neooptalidon-8cpr-riv","title":"NEOOPTALIDON*8FC TAB","description":"\u003cp\u003e\u003cb\u003eNEO-OPTALIDON 200 mg + 125 mg + 25 mg film-coated tablets\u003c\/b\u003e\u003cbr\u003e Paracetamol + Propyphenazone + Caffeine\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eNeo-Optalidon is a medicine containing three active ingredients, paracetamol and propyphenazone, which reduce fever and pain, and caffeine, which is a classic component of this type of combination.\u003cbr\u003e \u003cbr\u003e This medicine is used for the symptomatic treatment of pain (e.g. headache, toothache, nerve pain, menstrual pain) and fever.\u003cbr\u003e \u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after 3 days of treatment.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take Neo-Optalidon if:\u003c\/b\u003e\u003cbr\u003e • you are allergic to paracetamol, propyphenazone, caffeine or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e • you are allergic to other chemically similar substances, e.g. other anti-inflammatory drugs belonging to the same class (e.g. para-aminophenols, pyrazolones);\u003cbr\u003e • you are allergic to peanuts or soy;\u003cbr\u003e • you suffer from certain blood disorders such as:\u003cbr\u003e - granulocytopenia (decrease in the number of certain blood cells);\u003cbr\u003e - intermittent porphyria (diseases with alterations of certain enzymes);\u003cbr\u003e - glucose-6-phosphate dehydrogenase deficiency (a disease known as favism or broad bean disease, which causes a decrease in red blood cells);\u003cbr\u003e - severe hemolytic anemia (a disease that destroys red blood cells);\u003cbr\u003e • you suffer from hepatocellular insufficiency (insufficient liver cell function) or kidney failure;\u003cbr\u003e • you are pregnant or breastfeeding (see Pregnancy and breastfeeding).\u003cbr\u003e \u003cbr\u003e Neo-Optalidon should not be administered to children under 12 years of age because it contains caffeine.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eBe CAREFUL not to use Neo-Optalidon in high doses or for a long time, or together with other medicines containing paracetamol, as adverse reactions, including serious ones, may occur, especially affecting the liver, kidneys and blood (see Other medicines and Neo-Optalidon and section 4. Possible side effects).\u003cbr\u003e \u003cbr\u003e Consult your doctor or pharmacist before taking Neo-Optalidon, especially if:\u003cbr\u003e • you have blood disorders or liver or kidney problems;\u003cbr\u003e • you have asthma or nasal inflammation that has lasted for more than 12 weeks (chronic rhinitis);\u003cbr\u003e • you have chronic urticaria (a skin rash characterised by the presence of itchy swellings (wheals) that lasts for 6-12 weeks);\u003cbr\u003e • you are taking other anti-inflammatory drugs (see Other medicines and Neo-Optalidon); in these cases, the use of Neo-Optalidon is not recommended.\u003cbr\u003e \u003cbr\u003e Stop treatment with Neo-Optalidon and consult your doctor:\u003cbr\u003e • if fever appears, as treatment with Neo-Optalidon may not be suitable for your condition;\u003cbr\u003e • if you have chest pain (angina), or notice skin or mucous membrane changes, or any other sign of an allergic reaction (see section 4. Possible side effects).\u003cbr\u003e \u003cbr\u003e This medicine can affect the results of some laboratory tests, such as tests for measuring uric acid (uricemia) and blood glucose (glycemia).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren\u003c\/b\u003e\u003cbr\u003e Neo-Optalidon should not be administered to children under 12 years of age because it contains caffeine.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everyone experiences them.\u003cbr\u003e \u003cbr\u003e Stop taking Neo-Optalidon and contact your doctor if you experience any of the following:\u003cbr\u003e • skin rashes, redness, itching with skin spots (urticaria), swelling of the face, eyes, lips, difficulty breathing (laryngeal edema or asthma), severe allergic reaction (anaphylactic shock);\u003cbr\u003e • severe skin rashes with redness and\/or blistering (e.g. erythema multiforme, Stevens-Johnson Syndrome, toxic epidermal necrolysis).\u003cbr\u003e \u003cbr\u003e Inform your doctor if you experience the following side effects:\u003cbr\u003e • changes in blood cells: thrombocytopenia (decrease in platelets), leucopenia (decrease in white blood cells), agranulocytosis (significant reduction in granulocytes), anemia (decrease in red blood cells);\u003cbr\u003e • liver inflammation (hepatitis) and alterations in its function;\u003cbr\u003e • kidney inflammation (interstitial nephritis), and alterations in its function (kidney failure), blood in the urine (hematuria), absence of diuresis (anuria);\u003cbr\u003e • stomach or intestinal disorders;\u003cbr\u003e • dizziness.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects, you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"\" https: target=\"\" _blank\u003e\u003cimg src=\"\" http:\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"PERRIGO ITALIA Srl","offers":[{"title":"Default Title","offer_id":46458991804683,"sku":"025319043","price":5.02,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_8fd62570-b1c5-4af4-9f6a-29086988ad26.jpg?v=1736926730"},{"product_id":"momenactcompi-10cps-molli25mg","title":"MOMENACTCOMPI'*10 SOFT CAPSULES 25MG","description":"\u003cp\u003e\u003cb\u003eMOMENACTCOMPÌ 25 mg soft capsules\u003c\/b\u003e\u003cbr\u003e Ketoprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eMOMENACTCOMPÌ contains the active ingredient ketoprofen, which belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs) with pain-relieving and anti-inflammatory properties.\u003cbr\u003e MOMENACTCOMPÌ is used in adults and adolescents over 15 years of age for the treatment of pain of various origins or types (headaches, toothaches, neuralgia, menstrual pain, bone and joint (osteoarticular) and muscle pain).\u003cbr\u003e\u003cbr\u003e Consult your doctor if you do not feel better or if you feel worse after three days.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take MOMENACTCOMPÌ\u003c\/b\u003e\u003cbr\u003e - If you are allergic to the active ingredient or any of the components of this medicine, such as peanuts or soy (listed in section 6)\u003cbr\u003e - If you are allergic or have had hypersensitivity reactions in the past (such as asthma, bronchoconstriction, rhinitis, urticaria, etc.) to acetylsalicylic acid or other anti-inflammatory drugs (NSAIDs)\u003cbr\u003e - If you are undergoing intensive diuretic therapy\u003cbr\u003e - If you suffer from a severe form of liver failure (cirrhosis, severe hepatitis)\u003cbr\u003e - If you suffer from certain blood disorders (leukopenia and thrombocytopenia)\u003cbr\u003e - If you have active bleeding\u003cbr\u003e - If you are prone to bleeding (hemorrhagic diathesis)\u003cbr\u003e - If you suffer from blood clotting problems (hemostatic disorders)\u003cbr\u003e - If you have severe heart failure\u003cbr\u003e - If you suffer from a disease characterized by severe stomach lesions called active peptic ulcer, or have suffered in the past from bleeding in the stomach and intestine (gastrointestinal hemorrhage), ulceration or perforation\u003cbr\u003e - If the person who needs to take the medicine is a child under 15 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before taking MOMENACTCOMPÌ.\u003cbr\u003e You can minimize side effects by using the lowest effective dose for the shortest possible duration of treatment needed to control your symptoms.\u003cbr\u003e Tell your doctor or pharmacist if you are taking other anti-inflammatory drugs, as you should avoid concomitant use with other NSAIDs.\u003cbr\u003e Consult your doctor or nurse if you have an infection - see section Infections below.\u003cbr\u003e During treatment with MOMENACTCOMPÌ, cases of gastrointestinal hemorrhage, ulceration and perforation, which can be fatal, may occur at any time, without warning symptoms or a previous history of serious gastrointestinal events. Therefore, if gastrointestinal bleeding (bleeding from the stomach or intestine) occurs, stop treatment with MOMENACTCOMPÌ and contact your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cu\u003ePay particular attention if:\u003c\/u\u003e\u003cbr\u003e • you are elderly or if you are a patient suffering from an ulcer, especially if complicated by hemorrhage or perforation, the risk of gastrointestinal hemorrhage, ulceration or perforation is higher with consistent doses of MOMENACTCOMPÌ;\u003cbr\u003e • you are concomitantly using low doses of aspirin or other drugs that may increase the risk of gastrointestinal events. You may need to take gastroprotective drugs (misoprostol or proton pump inhibitors).\u003cbr\u003e If in doubt, consult your doctor or pharmacist;\u003cbr\u003e • you suffer from stomach or intestinal problems, especially if you are elderly, you must report any abdominal symptoms to your doctor, particularly in the initial stages of your treatment;\u003cbr\u003e • you are simultaneously taking drugs that may increase the risk of ulceration or bleeding, such as oral corticosteroids (cortisone), anticoagulants (blood thinners, such as warfarin), serotonin re-uptake inhibitors (antidepressants) or antiplatelet agents (drugs to reduce blood clotting), you must exercise caution;\u003cbr\u003e • you are a patient with a history of gastrointestinal disease (ulcerative colitis, Crohn's disease), you must take NSAIDs with caution, as these conditions may manifest more severely;\u003cbr\u003e • you suffer from an active stomach ulcer (peptic ulcer);\u003cbr\u003e • you have ever had asthmatic or allergic reactions after taking other types of non-steroidal anti-inflammatory drugs (such as acetylsalicylic acid and its derivatives).\u003cbr\u003e\u003cbr\u003e \u003cbr\u003e \u003cu\u003eYour doctor will carefully monitor you and have you undergo appropriate tests if any of these conditions apply to you:\u003c\/u\u003e\u003cbr\u003e • if you suffer from certain blood disorders (leukopenia and thrombocytopenia);\u003cbr\u003e • if you suffer from severe heart problems (such as hypertension and\/or congestive heart failure);\u003cbr\u003e • if you suffer from severely reduced kidney or liver function;\u003cbr\u003e • if you have a predisposition to bleeding;\u003cbr\u003e • if you suffer from diabetes mellitus;\u003cbr\u003e • if you are being treated concomitantly with agents that promote hyperkalemia (e.g., potassium supplements);\u003cbr\u003e • if you are an elderly person, the possibility of adverse reactions to NSAIDs is greater, especially gastrointestinal bleeding and perforations, which can be fatal.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eThis medicine can cause:\u003c\/u\u003e\u003cbr\u003e • serious heart and blood circulation problems (arterial thrombotic events, heart attack or stroke), especially at high doses and for prolonged treatments;\u003cbr\u003e • fatal skin and mucous membrane diseases, such as exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis, which can manifest with skin and mucous membrane lesions. This can occur especially in the first month of treatment (See section Possible side effects).\u003cbr\u003e • vision problems such as blurred vision (See section Possible side effects).\u003cbr\u003e \u003cbr\u003e You should also consult your doctor if you are a heavy smoker, if you have had previous strokes, if you have diabetes, or if you have high cholesterol levels in your blood.\u003cbr\u003e \u003cbr\u003e If after three days of treatment you do not notice a decrease in pain, you should consult your doctor.\u003cbr\u003e \u003cbr\u003e Infections\u003cbr\u003e MOMENACTCOMPÌ can hide the symptoms of infections such as fever and pain. Therefore, MOMENACTCOMPÌ may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult your doctor immediately.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e This medicine should not be taken by children and adolescents under 15 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e Stop using MOMENACTCOMPÌ and contact your doctor immediately if you experience:\u003cbr\u003e • swelling due to fluid retention (edema)\u003cbr\u003e • severe increase in blood pressure (hypertension) and reduced heart function (heart failure)\u003cbr\u003e • presence of digested blood in stools (as it could be a symptom of intestinal perforation or hemorrhage, potentially fatal if you are an elderly patient)\u003cbr\u003e • severe abdominal pain (which may be a symptom of pancreatitis)\u003cbr\u003e • vomiting mixed with blood (as it could be a symptom of stomach perforation or hemorrhage, potentially fatal, especially if you are an elderly patient)\u003cbr\u003e • worsening of colitis (colon inflammation) and Crohn's disease, sometimes fatal, particularly in the elderly.\u003cbr\u003e MOMENACTCOMPÌ, like other non-steroidal anti-inflammatory drugs (NSAIDs), is associated with a modest increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e \u003cbr\u003e The most commonly observed adverse events with MOMENACTCOMPÌ are:\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCommon\u003c\/b\u003e (may affect up to 1 in 10 people):\u003cbr\u003e • stomach ulcers (peptic)\u003cbr\u003e • stomach and intestinal (gastrointestinal) perforation or hemorrhage, sometimes fatal, particularly in the elderly\u003cbr\u003e • indigestion (dyspepsia)\u003cbr\u003e • abdominal pain\u003cbr\u003e • nausea, vomiting.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eUncommon\u003c\/b\u003e (may affect up to 1 in 100 people):\u003cbr\u003e • diarrhea\u003cbr\u003e • excessive gas production in the intestine (flatulence)\u003cbr\u003e • constipation\u003cbr\u003e • stomach inflammation (gastritis)\u003cbr\u003e • skin rash, itching\u003cbr\u003e • headache, dizziness, light-headedness, drowsiness\u003cbr\u003e • fatigue.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eRare\u003c\/b\u003e (may affect up to 1 in 1000 people):\u003cbr\u003e • inflammation of the mouth with painful lesions (ulcerative stomatitis)\u003cbr\u003e • stomach ulcer\u003cbr\u003e • colon inflammation (colitis)\u003cbr\u003e • asthma attacks\u003cbr\u003e • tingling in the limbs (paresthesia)\u003cbr\u003e • blurred vision\u003cbr\u003e • ringing in the ears (tinnitus)\u003cbr\u003e • liver inflammation (hepatitis), yellowing of the skin and the white part of the eye (jaundice)\u003cbr\u003e • altered liver function tests (increased transaminase levels, increased serum bilirubin)\u003cbr\u003e • reduction in red blood cells (anemia) caused by bleeding\u003cbr\u003e • reduction in certain white blood cells (leukopenia)\u003cbr\u003e • weight gain.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eNot known\u003c\/b\u003e (frequency cannot be estimated from the available data):\u003cbr\u003e • increased sensitivity to light (photosensitivity reactions), rare in cases of systemic administration\u003cbr\u003e • skin problems (skin rash)\u003cbr\u003e • hair loss\u003cbr\u003e • urticaria\u003cbr\u003e • swelling of the face and throat (angioedema)\u003cbr\u003e • erythema, blistering skin reactions (including Stevens-Johnson syndrome) and Toxic Epidermal Necrolysis (severe skin disease with severe peeling, potentially fatal), pustule formation\u003cbr\u003e • feeling of tightness in the chest with difficulty breathing (bronchospasm), particularly in patients with known hypersensitivity to acetylsalicylic acid (ASA and other NSAIDs), rhinitis, difficulty breathing (dyspnea)\u003cbr\u003e • aseptic meningitis (inflammation of the meninges not caused by bacteria)\u003cbr\u003e • convulsions\u003cbr\u003e • taste alteration (dysgeusia)\u003cbr\u003e • abnormal kidney function tests, acute kidney failure, interstitial tubulo-renal nephritis, loss of nutrients for the body (such as proteins) through urine (nephrotic syndrome)\u003cbr\u003e • reduction in the number of granulocytes with consequent increased risk of infections (agranulocytosis), reduction in the number of platelets in the blood (thrombocytopenia), reduced production of blood cells by the bone marrow (aplastic anemia), destruction of red blood cells (hemolytic anemia)\u003cbr\u003e • anaphylactic reactions (including shock)\u003cbr\u003e • depression, hallucinations, confusion, mood alteration\u003cbr\u003e • heart failure, atrial fibrillation, palpitations and tachycardia\u003cbr\u003e • hypertension, vasodilation, inflammation of blood vessels (vasculitis including leukocytoclastic vasculitis)\u003cbr\u003e • hyponatremia (reduction of sodium levels in the blood), hyperkalemia (increase of potassium levels in the blood).\u003cbr\u003e \u003cbr\u003e Clinical studies and epidemiological data suggest that the use of some NSAIDs (especially at high doses and for long-term treatments) may be associated with a modest increased risk of arterial thromboembolic events (e.g., myocardial infarction or stroke).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"\" https: target=\"\" _blank\u003e\u003cimg src=\"\" http:\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ANGELINI PHARMA ITALIA SpA","offers":[{"title":"Default Title","offer_id":49563644723467,"sku":"027366032","price":6.46,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_954a192a-f8fb-45bc-b0b7-afc9b7ff0528.png?v=1740209770"},{"product_id":"algofen-12cpr-riv-200mg","title":"ALGOFEN*12FILMTABS 200MG","description":"\u003cp\u003e\u003cb\u003eALGOFEN 200 mg coated tablets\u003c\/b\u003e\u003cbr\u003eIbuprofen\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003eALGOFEN contains the active ingredient ibuprofen, which belongs to the class of medicines called Non-Steroidal Anti-Inflammatory Drugs (or NSAIDs) that act by reducing pain and inflammation.\u003cbr\u003e\u003cbr\u003eThis medicine is used to treat various types of pain such as: headache, toothache, nerve pain (neuralgia), bone and joint pain (osteoarticular), muscle pain and menstrual pain.\u003cbr\u003e\u003cbr\u003eContact your doctor if you do not feel better or if you feel worse after 3 days.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not use ALGOFEN\u003c\/b\u003e\u003cbr\u003e- if you are allergic to ibuprofen or any of the other ingredients of this medicine (listed in paragraph 6);\u003cbr\u003e- if you are allergic to acetylsalicylic acid or other medicines used to reduce pain (analgesics) and fever (antipyretics) or non-steroidal anti-inflammatory drugs (NSAIDs), particularly when the allergy is associated with swelling of the nasal mucous membrane (nasal polyposis) or asthma, and presents with an asthmatic reaction (bronchospasm), urticaria or severe rhinitis (acute rhinitis) (see Warnings and precautions section);\u003cbr\u003e- if you have suffered from stomach or intestinal ulcers or bleeding after taking other medicines;\u003cbr\u003e- if you suffer from stomach or small intestine (duodenum) ulcers or bleeding;\u003cbr\u003e- if you have suffered two or more such episodes in the past;\u003cbr\u003e- if you have an unknown disorder in blood cell production;\u003cbr\u003e- if you have bleeding in the brain (cerebrovascular hemorrhage) or other types of bleeding;\u003cbr\u003e- if you suffer from a disease that may lead to an increased bleeding tendency;\u003cbr\u003e- if you have severe liver or kidney problems;\u003cbr\u003e- if you are very dehydrated (this condition may be due to vomiting, diarrhea or insufficient fluid intake);\u003cbr\u003e- if you are in the last three months of pregnancy (see Pregnancy, breastfeeding and fertility section);\u003cbr\u003e- if you suffer from severe heart problems (severe heart failure);\u003cbr\u003e- in children under 12 years of age.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003eConsult your doctor or pharmacist before using ALGOFEN.\u003cbr\u003e\u003cbr\u003eAnti-inflammatory\/pain relief medicines such as ibuprofen may be associated with a modest increased risk of heart attack or stroke, especially if taken in high doses. Do not exceed the recommended dose or duration of treatment.\u003cbr\u003e\u003cbr\u003eSigns of an allergic reaction to this medicine, including breathing problems, swelling of the face and neck area (angioedema) and chest pain, have been reported with ibuprofen. Stop ALGOFEN immediately and contact your doctor or emergency medical service immediately if you notice any of these signs.\u003cbr\u003e\u003cbr\u003eSevere skin reactions including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ibuprofen treatment. Stop using ALGOFEN and contact your doctor immediately if you notice any of the symptoms related to these severe skin reactions described in paragraph 4.\u003cbr\u003e\u003cbr\u003eYou should discuss your therapy with your doctor or pharmacist before taking ALGOFEN if:\u003cbr\u003e- you have heart problems including heart attack, angina (chest pain) or if you have a history of heart attack, coronary bypass surgery, peripheral arterial disease (poor circulation in the legs or feet due to narrowing or obstruction of the arteries) or any type of stroke (including mini-stroke or TIA, transient ischemic attack);\u003cbr\u003e- you have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or if you are a smoker;\u003cbr\u003e- you suffer from asthma (difficulty breathing) or other allergies;\u003cbr\u003e- you have seasonal allergic rhinitis, swelling of the nasal mucous membrane (e.g. nasal polyps);\u003cbr\u003e- you have chronic obstructive pulmonary disease or chronic infections of the respiratory tract;\u003cbr\u003e- you have liver or kidney problems, unless you have a severe form of liver or kidney insufficiency, in which case you should not take ALGOFEN (see paragraph 2 Do not use ALGOFEN). If in doubt, consult your doctor;\u003cbr\u003e- you have hepatic porphyria;\u003cbr\u003e- you are using medicines that increase urine production (diuretics) or other medicines that may affect kidney function;\u003cbr\u003e- you have a reduced volume of body fluids (e.g. before or after major surgery);\u003cbr\u003e- you need to undergo or have undergone major surgery;\u003cbr\u003e- you are taking other NSAIDs, including the specific type of NSAIDs called COX-2 inhibitors. In this case, taking ALGOFEN should be avoided;\u003cbr\u003e- you are taking other anti-inflammatory medicines belonging to the corticosteroid family, or medicines used to prevent blood clotting (such as warfarin), or aspirin or antidepressant drugs called selective serotonin reuptake inhibitors or SSRIs;\u003cbr\u003e- you suffer from chronic inflammatory bowel diseases such as colon inflammation with ulcers (ulcerative colitis), inflammation of the digestive tract (Crohn's disease);\u003cbr\u003e- you are elderly, because you may be more susceptible to side effects, which can also be serious or life-threatening (see Elderly and Ulcers, perforations and bleeding in the stomach or intestines);\u003cbr\u003e- if you have stomach or intestinal problems, unless you have one or more conditions for which you should not take ALGOFEN (see Do not use ALGOFEN section);\u003cbr\u003e- you are in the first six months of pregnancy (see Pregnancy, breastfeeding and fertility);\u003cbr\u003e- the patient is an adolescent with dehydration problems, because in this case the medicine may cause kidney problems;\u003cbr\u003e- you have an autoimmune disease e.g. Lupus erythematosus or connective tissue diseases;\u003cbr\u003e- you have an infection (see Infections section below).\u003cbr\u003e\u003cbr\u003e\u003cem\u003eEffects on the heart and brain\u003c\/em\u003e\u003cbr\u003eMedicines containing ibuprofen, such as ALGOFEN, are associated with a slightly higher risk of heart attack (myocardial infarction) or stroke. The risk is higher if you take high doses of ibuprofen and long-term treatments. Do not exceed the recommended doses or the indicated duration of treatment.\u003cbr\u003e\u003cbr\u003e\u003cem\u003eElderly\u003c\/em\u003e\u003cbr\u003eElderly people may be more susceptible to side effects, particularly bleeding and perforation of the digestive tract, which can be fatal.\u003cbr\u003eUlcers, perforations and bleeding in the stomach or intestines\u003cbr\u003eIf you have had a stomach or intestinal ulcer, especially if it was complicated by perforation or accompanied by bleeding, you should pay attention to any unusual abdominal symptoms and report them immediately to your doctor, particularly if these symptoms occur at the beginning of treatment. In fact, the risk of bleeding or ulceration of the digestive tract is greater in this case, particularly in elderly patients. If bleeding or ulceration of the digestive tract occurs, treatment should be discontinued.\u003cbr\u003e\u003cbr\u003eBleeding, ulceration or perforation in the stomach or intestines can occur without any warning signs, even in patients who have never had these problems before. They can also be fatal.\u003cbr\u003e\u003cbr\u003eThe risk of ulcers, perforations or bleeding in the stomach or intestines generally increases with higher doses of ibuprofen. The risk also increases if some other medicines are taken simultaneously with ibuprofen (see Other medicines and ALGOFEN).\u003cbr\u003e\u003cbr\u003e\u003cem\u003eSkin reactions\u003c\/em\u003e\u003cbr\u003eSevere skin reactions have been reported in association with ALGOFEN treatment.\u003cbr\u003eStop taking ALGOFEN and consult your doctor immediately if you experience a rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very severe skin reaction. See paragraph 4.\u003cbr\u003e\u003cbr\u003e\u003cem\u003eInfections\u003c\/em\u003e\u003cbr\u003eALGOFEN can mask the symptoms of infections such as fever and pain. Therefore, ALGOFEN may delay appropriate treatment of the infection, which could increase the risk of complications. This has been observed in pneumonia caused by bacteria and in bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, contact your doctor immediately.\u003cbr\u003e\u003cbr\u003eALGOFEN may decrease the chances of becoming pregnant. Tell your doctor if you are planning a pregnancy or have fertility problems (see Pregnancy, breastfeeding and fertility).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003eThis medicine should not be used in children under 12 years of age (see paragraph 2 Do not use ALGOFEN).\u003cbr\u003eIn dehydrated adolescents, there is a risk of impaired kidney function.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003eLike all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003eSide effects depend on the dose and can vary from patient to patient.\u003cbr\u003e\u003cbr\u003eStop using ibuprofen and consult your doctor immediately if you notice any of the following symptoms:\u003cbr\u003e• reddish, non-raised, target-shaped or circular patches on the trunk, often with central blisters, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes. These severe rashes may be preceded by fever and flu-like symptoms [exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis];\u003cbr\u003e• widespread rash, high body temperature and swollen lymph nodes and increased eosinophils (a type of white blood cell) (DRESS syndrome);\u003cbr\u003e• widespread, red and scaly rash, with bumps under the skin and blisters, accompanied by fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis).\u003cbr\u003e\u003cbr\u003eMedicines containing ibuprofen for long-term treatments may be associated with a slightly higher risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003eIn association with NSAIDs, fluid retention (edema), high blood pressure and heart problems (heart failure) have been reported.\u003cbr\u003e\u003cbr\u003eThe most commonly observed adverse events affect the stomach and\/or intestines. Stomach or first part of the intestine ulcers (peptic ulcer), perforation or bleeding from the stomach and\/or intestines can occur, which can also be fatal, particularly in the elderly. In particular, the risk of bleeding from the stomach and\/or intestines depends on the dose and duration of treatment.\u003cbr\u003e\u003cbr\u003eIn addition to the side effects listed below, after administration of ALGOFEN, the following have been reported: black stools (melena), presence of blood in vomit (digestive tract ulcer with bleeding).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery common side effects (may affect more than 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e- nausea, flatulence, diarrhea, constipation, vomiting;\u003cbr\u003e- indigestion (dyspepsia);\u003cbr\u003e- abdominal pain;\u003cbr\u003e- heartburn.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eCommon side effects (may affect up to 1 in 10 people):\u003c\/b\u003e\u003cbr\u003e- rash;\u003cbr\u003e- headache, drowsiness, dizziness, lightheadedness, fatigue, agitation, insomnia, irritability;\u003cbr\u003e- gastric and duodenal ulcers, sometimes with bleeding and perforation, occult blood loss that can lead to anemia, tar-like black stools, bloody vomit, mouth ulcers, colon inflammation, worsening of inflammatory bowel disease, intestinal wall inflammation;\u003cbr\u003e- vision disturbances.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon side effects (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e- allergic reactions including skin rash, urticaria, itching and asthma attacks;\u003cbr\u003e- skin irritation associated with bleeding (purpura);\u003cbr\u003e- sensitivity of the skin to light;\u003cbr\u003e- altered sensation in some parts of the body (paresthesia);\u003cbr\u003e- difficulty breathing (bronchospasm);\u003cbr\u003e- sneezing, stuffy nose or runny nose (rhinitis);\u003cbr\u003e- stomach inflammation (gastritis);\u003cbr\u003e- liver problems, liver inflammation (hepatitis) and yellowing of the skin, mucous membranes and eyes (jaundice);\u003cbr\u003e- edema formation particularly in patients with high blood pressure or kidney problems (kidney failure, nephrotic syndrome, interstitial nephritis) which may be accompanied by acute kidney failure.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare side effects (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e- cerebrovascular accident (stroke, cerebral hemorrhage);\u003cbr\u003e- whistling and ringing in the ears (tinnitus);\u003cbr\u003e- hearing impairment;\u003cbr\u003e- worsening of colon inflammation (colitis);\u003cbr\u003e- worsening of a chronic inflammatory disease of the digestive system (Crohn's disease);\u003cbr\u003e- kidney failure;\u003cbr\u003e- kidney tissue damage (papillary necrosis) (especially in long-term therapy);\u003cbr\u003e- increased blood uric acid concentration;\u003cbr\u003e- aseptic meningitis (infection of the meninges, membranes of the brain);\u003cbr\u003e- a disease affecting the skin, joints and kidneys (lupus erythematosus syndrome);\u003cbr\u003e- depression, confusion, hallucinations, mental alterations (psychotic reactions);\u003cbr\u003e- increased urea nitrogen, transaminases and alkaline phosphatase, decreased hemoglobin and hematocrit values, inhibition of platelet aggregation, prolonged bleeding time, decreased serum calcium, increased serum uric acid, all observed with a blood test;\u003cbr\u003e- decreased visual acuity.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare side effects (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e- worsening of infections associated with infection (e.g. development of necrotizing fasciitis);\u003cbr\u003e- reduction in the number of platelets in the blood (thrombocytopenia);\u003cbr\u003e- anemia;\u003cbr\u003e- reduction in the number of white blood cells in the blood (leukopenia, agranulocytosis);\u003cbr\u003e- reduction in the number of all cells present in the blood (pancytopenia);\u003cbr\u003e- presence of blood in the urine (hematuria);\u003cbr\u003e- severe allergic reaction (anaphylactic reaction);\u003cbr\u003e- swelling of the face, lips, mouth, tongue or throat, which may cause difficulty swallowing or breathing (angioedema);\u003cbr\u003e- alterations in liver function tests;\u003cbr\u003e- acute hepatitis;\u003cbr\u003e- liver damage, particularly in long-term therapy and liver failure;\u003cbr\u003e- skin and mucous membrane reactions, including severe ones (erythema multiforme, exfoliative dermatitis, bullous reactions including Stevens-Johnson syndrome and toxic epidermal necrolysis);\u003cbr\u003e- fast or irregular heartbeat (palpitations);\u003cbr\u003e- inflammation of the esophagus, narrowing of the intestine;\u003cbr\u003e- severe skin infections, with soft tissue complications, may occur if you have chickenpox;\u003cbr\u003e- fluid accumulation in the lungs, symptoms include shortness of breath, which can be very severe and usually worsens when lying down (pulmonary edema);\u003cbr\u003e- swelling (edema);\u003cbr\u003e- heart attack;\u003cbr\u003e- high blood pressure (hypertension);\u003cbr\u003e- heart failure;\u003cbr\u003e- inflammation of the pancreas;\u003cbr\u003e- unusual hair loss (alopecia);\u003cbr\u003e- menstrual disorders.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eSide effects of unknown frequency (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e- a widespread, red and scaly rash, with the formation of pustules under the skin and blisters located mainly on the skin folds, on the trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalized exanthematous pustulosis). Stop using ALGOFEN if you develop these symptoms and contact your doctor immediately. See also paragraph 2;\u003cbr\u003e- muscle stiffness (musculoskeletal stiffness);\u003cbr\u003e- chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting of side effects\u003c\/b\u003e\u003cbr\u003eIf you get any side effects, including any not listed in this leaflet, talk to your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003eBy reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"\" https: target=\"\" _blank\u003e\u003cimg src=\"\" http:\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"SIT LABORATORIO FARMAC. Srl","offers":[{"title":"Default Title","offer_id":49588683505931,"sku":"023766025","price":3.42,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_d0df41d3-46f6-4381-92b4-a0af78808354.jpg?v=1740561183"},{"product_id":"ibuprofene-zen-20cps-400mg","title":"IBUPROFEN ZEN*20CAPS 400MG","description":"\u003cp\u003e\u003cb\u003eIBUPROFENE ZENTIVA 200 mg soft capsules\u003cbr\u003e IBUPROFENE ZENTIVA 400 mg soft capsules\u003cbr\u003e\u003c\/b\u003e Equivalent medicine\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat it is and what it is used for\u003c\/b\u003e\u003cbr\u003e The name of the medicine is IBUPROFENE ZENTIVA 200 mg or IBUPROFENE ZENTIVA 400 mg.\u003cbr\u003e\u003cbr\u003e The active ingredient (which makes the medicine effective) is ibuprofen. It belongs to a group of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs). NSAIDs relieve pain by modifying the body's response to pain, swelling and high temperature.\u003cbr\u003e\u003cbr\u003e IBUPROFENE ZENTIVA in the form of soft capsules with liquid content dissolves easily in the body, the active ingredient is absorbed more quickly into the bloodstream and therefore rapidly reaches the site of pain.\u003cbr\u003e\u003cbr\u003e IBUPROFENE ZENTIVA is used to relieve headaches, migraines, toothaches, backaches, menstrual pain, muscle pain, fever and cold and flu symptoms.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eIn addition, on medical prescription\u003c\/u\u003e, IBUPROFENE ZENTIVA is also used to relieve pain experienced along the nerves (neuralgia), joint swelling and pain (rheumatic pain) and non-severe joint inflammation (non-severe arthritis).\u003cbr\u003e\u003cbr\u003e IBUPROFENE ZENTIVA 400 mg is recommended for adults and adolescents over 12 years of age (body weight of at least 40 kg).\u003cbr\u003e\u003cbr\u003e Given the amount of active ingredient contained in one capsule, IBUPROFENE ZENTIVA 200 mg is recommended for adults and children over 6 years of age (body weight of at least 20 kg).\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWhat you need to know before taking the medicine\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eDo not take IBUPROFENE ZENTIVA\u003c\/b\u003e\u003cbr\u003e - if you are allergic to ibuprofen (the active ingredient of IBUPROFENE ZENTIVA) or any of the other ingredients of this medicine (listed in section 6);\u003cbr\u003e - if you are hypersensitive to non-steroidal anti-inflammatory drugs and experience shortness of breath, asthma, runny nose, swelling or hives;\u003cbr\u003e - if you have an active or recurrent stomach or duodenal ulcer or bleeding or have ever had this problem repeatedly (i.e. at least twice) in the past;\u003cbr\u003e - if you have ever had gastrointestinal bleeding or perforation related to previous NSAID therapy;\u003cbr\u003e - if you suffer from a blood formation disorder or a blood clotting disorder;\u003cbr\u003e - if you suffer from severe heart, liver or kidney failure;\u003cbr\u003e - if you are a woman in the third trimester of pregnancy.\u003c\/p\u003e\u003cp\u003e\u003cb\u003eWarnings and precautions\u003c\/b\u003e\u003cbr\u003e You should discuss your treatment with your doctor or pharmacist before taking IBUPROFENE ZENTIVA if:\u003cbr\u003e - you suffer from kidney or liver disease;\u003cbr\u003e - you suffer from bronchial asthma;\u003cbr\u003e - you suffer from allergic rhinitis, nasal polyps or chronic obstructive respiratory disorders, due to the increased risk of allergic reactions;\u003cbr\u003e - you are also taking medicines that could increase the risk of gastric toxicity or bleeding (see below);\u003cbr\u003e - you suffer from systemic lupus erythematosus (an immune system disease) or mixed connective tissue disease (risk of aseptic meningitis);\u003cbr\u003e - you suffer from an inflammatory ulcer disease of the digestive tract such as Crohn's disease or ulcerative colitis;\u003cbr\u003e - you have heart problems, including heart failure, angina (chest pain), or if you have had a heart attack, bypass surgery, peripheral artery disease (poor circulation in the legs and feet due to narrowed or blocked arteries), or any type of stroke (including mini-stroke or transient ischemic attack TIA);\u003cbr\u003e - you have high blood pressure, diabetes or high cholesterol, or have a family history of heart disease or stroke, or if you are a smoker;\u003cbr\u003e - you have an infection - see the Infections section below.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eInfections\u003c\/b\u003e\u003cbr\u003e Ibuprofen can mask signs of infections such as fever and pain. It is therefore possible that ibuprofen may delay appropriate treatment of the infection, which can lead to an increased risk of complications. This has been observed in pneumonia caused by bacteria and bacterial skin infections related to chickenpox. If you take this medicine while you have an infection and the symptoms of the infection persist or worsen, consult a doctor immediately.\u003cbr\u003e\u003cbr\u003e Anti-inflammatory\/pain relief medicines such as ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when used at high doses. Do not exceed the recommended dose or duration of treatment. Any risks are more likely in case of high dosages or prolonged treatment. Gastrointestinal bleeding, ulceration or perforation can occur at any time during treatment, with or without warning symptoms or a previous history of severe gastrointestinal events. With increasing dosages, the risk of gastrointestinal bleeding, ulceration or perforation is higher in patients with a history of ulcer and in the elderly. Some concomitant medicines may increase the risk of gastric toxicity or bleeding (other non-steroidal anti-inflammatory drugs, corticosteroids, anticoagulants such as warfarin, selective serotonin reuptake inhibitors (SSRIs) or antiplatelet agents such as acetylsalicylic acid).\u003cbr\u003e\u003cbr\u003e In patients at higher risk of gastrointestinal toxicity, the concomitant use of protective agents (e.g. misoprostol or proton pump inhibitors) should be considered.\u003cbr\u003e\u003cbr\u003e Prolonged use of any type of analgesic for headache can worsen the disorder. If you suffer from frequent or daily headaches despite (or as a result of) regular use of headache medicines, consult your doctor before taking another analgesic. Treatment should be stopped if headache caused by overuse of medicines is diagnosed.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSkin reactions\u003c\/u\u003e\u003cbr\u003e Severe skin reactions have been reported in association with IBUPROFENE ZENTIVA treatment. Stop taking IBUPROFENE ZENTIVA and consult your doctor immediately if you experience rash, mucosal lesions, blisters or other signs of allergy, as these may be the first signs of a very severe skin reaction. See section 4.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eChildren and adolescents\u003c\/b\u003e\u003cbr\u003e There is a risk of kidney impairment in dehydrated children and adolescents.\u003c\/p\u003e\u003cp\u003e\u003cb\u003ePossible side effects\u003c\/b\u003e\u003cbr\u003e Like all medicines, this medicine can cause side effects, although not everybody gets them.\u003cbr\u003e\u003cbr\u003e Stop using the medicine and seek immediate medical attention if any hypersensitivity reactions occur such as skin rashes, mucosal lesions, hives, appearance of purple spots on the skin, sudden swelling around the eyes, feeling of tightness in the chest with difficulty breathing or swallowing, epigastric pain or bleeding from the digestive tract (vomiting blood or black stools).\u003cbr\u003e\u003cbr\u003e The side effects that may occur are listed below according to frequency:\u003cbr\u003e\u003cbr\u003e\u003cb\u003eUncommon (may affect up to 1 in 100 people):\u003c\/b\u003e\u003cbr\u003e • headache;\u003cbr\u003e • abdominal pain, discomfort (nausea), indigestion;\u003cbr\u003e • various skin rashes, hypersensitivity reactions (such as hives and itching).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eRare (may affect up to 1 in 1,000 people):\u003c\/b\u003e\u003cbr\u003e • discomfort (vomiting), diarrhea, constipation, flatulence.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eVery rare (may affect up to 1 in 10,000 people):\u003c\/b\u003e\u003cbr\u003e • problems in the production of blood cells (the first signs are: fever, sore throat, superficial ulcers in the mouth, flu-like symptoms, exhaustion, nosebleeds and skin bleeding);\u003cbr\u003e • sterile inflammation of the meninges (particularly in patients with connective tissue diseases or systemic lupus erythematosus);\u003cbr\u003e • inflammation, ulceration or perforation of the mucous membrane of the digestive tract (black stools and vomiting blood), inflammation of the mouth;\u003cbr\u003e • inability of the kidneys to eliminate waste products (acute kidney failure), blood in the urine and fever may be signs of kidney damage (papillary necrosis);\u003cbr\u003e • disorders of liver function;\u003cbr\u003e • severe forms of skin reactions, including rashes with redness and blisters;\u003cbr\u003e severe hypersensitivity reactions (edema of the face, tongue and larynx, dyspnea, tachycardia, hypotension, severe shock).\u003cbr\u003e\u003cbr\u003e\u003cb\u003eNot known (frequency cannot be estimated from the available data):\u003c\/b\u003e\u003cbr\u003e • hearing disorders;\u003cbr\u003e • heart failure, edema, arterial hypertension;\u003cbr\u003e • worsening of an existing intestinal disease (colitis or Crohn's disease);\u003cbr\u003e • kidney failure;\u003cbr\u003e • difficulty breathing (mainly in patients with bronchial asthma), worsening of asthma;\u003cbr\u003e • a severe skin reaction known as DRESS syndrome may occur. Symptoms of DRESS include: rash, fever, swollen lymph nodes and increased eosinophils (a type of white blood cell);\u003cbr\u003e • increased skin sensitivity to the sun;\u003cbr\u003e • a widespread, red, scaly rash, with pus-filled bumps under the skin and blisters located mainly on the skin folds, trunk and upper limbs accompanied by fever at the beginning of treatment (acute generalised exanthematous pustulosis). Stop using IBUPROFENE ZENTIVA if you develop these symptoms and contact your doctor immediately. See also section 2.\u003cbr\u003e\u003cbr\u003e Medicines containing ibuprofen (or some other NSAIDs), such as ibuprofen, may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eReporting side effects\u003c\/b\u003e\u003cbr\u003e If you get any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. You can also report side effects directly via the national reporting system at: \u003cu\u003ehttps:\/\/www.aifa.gov.it\/content\/segnalazionireazioni-avverse\u003c\/u\u003e.\u003cbr\u003e By reporting side effects you can help provide more information on the safety of this medicine.\u003c\/p\u003e\u003cp\u003e\u003ca href=\"\" https: target=\"\" _blank\u003e\u003cimg src=\"\" http:\u003e\u003c\/a\u003e\u003c\/p\u003e","brand":"ZENTIVA ITALIA Srl","offers":[{"title":"Default Title","offer_id":49588692353291,"sku":"043555059","price":9.53,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_ddee22e6-7cd8-48b4-91ba-2ebc05a2c2a2.jpg?v=1740561263"}],"url":"https:\/\/farmaonline24.it\/en\/collections\/mal-di-testa.oembed?page=6","provider":"FarmaOnline24","version":"1.0","type":"link"}