Sveits - tysk - Swissmedic (Swiss Agency for Therapeutic Products)

ibsa institut biochimique sa - diclofenacum epolaminum - putz - diclofenacum epolaminum 181 mg corresp. diclofenacum natricum, gelatina, povidonum k 90, sorbitolum liquidum non cristallisabile, kaolinum ponderosum, propylenglycolum 420 mg, dinatrii edetas, acidum tartaricum, carmellosum natricum, natrii polyacrylas, aluminii glycinas, 1,3-butandiolum, polysorbatum 80, titanii dioxidum, aromatica cum benzylis salicylas q.s. amylis cinnamaldehydum q.s. hydroxycitronellalum q.s. alcohol cinnamylicus q.s. isoeugenolum q.s. citronellolum q.s. eugenolum q.s., propylis parahydroxybenzoas 7 mg, e 218 14 mg, aqua purificata, q.s. ad gelatum pro 14000 mg, materiale di supporto: polyesterum, polypropylenum, ad praeparationem pro 140 cm². - antiflogistico - synthetika

Sveits - fransk - Swissmedic (Swiss Agency for Therapeutic Products)

ibsa institut biochimique sa - diclofenacum epolaminum - plâtre - diclofenacum epolaminum 181 mg corresp. diclofenacum natricum, gelatina, povidonum k 90, sorbitolum liquidum non cristallisabile, kaolinum ponderosum, propylenglycolum 420 mg, dinatrii edetas, acidum tartaricum, carmellosum natricum, natrii polyacrylas, aluminii glycinas, 1,3-butandiolum, polysorbatum 80, titanii dioxidum, aromatica cum benzylis salicylas q.s. amylis cinnamaldehydum q.s. hydroxycitronellalum q.s. alcohol cinnamylicus q.s. isoeugenolum q.s. citronellolum q.s. eugenolum q.s., propylis parahydroxybenzoas 7 mg, e 218 14 mg, aqua purificata, q.s. ad gelatum pro 14000 mg, materiale di supporto: polyesterum, polypropylenum, ad praeparationem pro 140 cm². - antiflogistico - synthetika

Tsjekkia - tsjekkisk - SUKL (Státní ústav pro kontrolu léčiv)

ibsa slovakia s.r.o., bratislava array - 14630 diklofenak-epolamin - léčivá náplast - 180mg - diklofenak

Sveits - italiensk - Swissmedic (Swiss Agency for Therapeutic Products)

ibsa institut biochimique sa - diclofenacum epolaminum - gesso - diclofenacum epolaminum 181 mg corresp. diclofenacum natricum, gelatina, povidonum k 90, sorbitolum liquidum non cristallisabile, kaolinum ponderosum, propylenglycolum 420 mg, dinatrii edetas, acidum tartaricum, carmellosum natricum, natrii polyacrylas, aluminii glycinas, 1,3-butandiolum, polysorbatum 80, titanii dioxidum, aromatica cum benzylis salicylas q.s. amylis cinnamaldehydum q.s. hydroxycitronellalum q.s. alcohol cinnamylicus q.s. isoeugenolum q.s. citronellolum q.s. eugenolum q.s., propylis parahydroxybenzoas 7 mg, e 218 14 mg, aqua purificata, q.s. ad gelatum pro 14000 mg, materiale di supporto: polyesterum, polypropylenum, ad praeparationem pro 140 cm². - antiflogistico - synthetika

Saudi-Arabia - engelsk - SFDA (Saudi Food and Drug Authority)- الهيئة العامة للغذاء والدواء

ibsa institute biochimique s.a, switzerland - diclofenac epolamine - medicated plaster - 13-10 mg

USA - engelsk - NLM (National Library of Medicine)

quality care products, llc - diclofenac epolamine (unii: x5f8ekl9zg) (diclofenac - unii:144o8ql0l1) - diclofenac epolamine 180 mg in 14 g - flector® patch is indicated for the topical treatment of acute pain due to minor strains, sprains, and contusions. flector patch is contraindicated in the following patients: - known hypersensitivity (e.g., anaphylactic reactions and serious skin reactions) to diclofenac or any components of the drug product [see warnings and precautions (5.7, 5.9) ] - history of asthma, urticaria, or other allergic-type reactions after taking aspirin or other nsaids. severe, sometimes fatal, anaphylactic reactions to nsaids have been reported in such patients [see warnings and precautions (5.7, 5.8) ] - in the setting of coronary artery bypass graft (cabg) surgery [see warnings and precautions (5.1) ] - flector patch is contraindicated for use on non-intact or damaged skin resulting from any etiology, including exudative dermatitis, eczema, infection lesions, burns or wounds. risk summary published literature reports that use of nsaids, including flector patch, after 30 weeks' gestation increases the risk of premature closu

USA - engelsk - NLM (National Library of Medicine)

preferred pharmaceucitalc inc. - diclofenac epolamine (unii: x5f8ekl9zg) (diclofenac - unii:144o8ql0l1) - diclofenac epolamine 180 mg - flector® patch is indicated for the topical treatment of acute pain due to minor strains, sprains, and contusions. flector patch is contraindicated in the following patients: risk summary published literature reports that use of nsaids, including flector patch, after 30 weeks' gestation increases the risk of premature closure of the fetal ductus arteriosus. data from observational studies regarding potential embryofetal risks of nsaid use, including diclofenac, in women in the first or second trimester of pregnancy are inconclusive. avoid use of nsaids, including flector patch, in pregnant women starting at 30 weeks of gestation (third trimester) (see clinical considerations and data) . in animal reproduction studies, diclofenac epolamine administered orally to pregnant rats and rabbits during the period of organogenesis produced embryotoxicity at approximately 3 and 7 times, respectively, the topical exposure from the maximum recommended human dose (mrhd) of flector patch. in rats, increased incidences of

USA - engelsk - NLM (National Library of Medicine)

rebel distributors corp - diclofenac epolamine (unii: x5f8ekl9zg) (diclofenac - unii:144o8ql0l1) - flector® patch is indicated for the topical treatment of acute pain due to minor strains, sprains, and contusions. - flector patch is contraindicated in patients with a known hypersensitivity to diclofenac. - flector patch is contraindicated in patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients [see warnings and precautions (5.7, 5.13)]. - flector patch is contraindicated for the treatment of perioperative pain in the setting of coronary artery bypass graft (cabg) surgery [see warnings and precautions (5.1)]. - flector patch is contraindicated for use on non-intact or damaged skin resulting from any etiology, including exudative dermatitis, eczema, infection lesions, burns or wounds. teratogenic effects pregnancy category c prior to 30 weeks gestation; category d starting 30 weeks gestation. starting at 30 weeks gestation, avoid use of flector patch, an

USA - engelsk - NLM (National Library of Medicine)

h.j. harkins company, inc. - diclofenac epolamine (unii: x5f8ekl9zg) (diclofenac - unii:144o8ql0l1) - diclofenac epolamine 180 mg - - flector patch is contraindicated in patients with a known hypersensitivity to diclofenac. - flector patch is contraindicated in patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients [see warnings and precautions (5.7, 5.13)]. - flector patch is contraindicated for the treatment of perioperative pain in the setting of coronary artery bypass graft (cabg) surgery [see warnings and precautions (5.1)]. - flector patch is contraindicated for use on non-intact or damaged skin resulting from any etiology, including exudative dermatitis, eczema, infection lesions, burns or wounds. teratogenic effects pregnancy category c prior to 30 weeks gestation; category d starting 30 weeks gestation. starting at 30 weeks gestation, avoid use of flector patch, and other nsaids, in pregnant women as premature closure of the ductus arteriosus in the fetus may occur, flector pat

USA - engelsk - NLM (National Library of Medicine)

pfizer, inc. - diclofenac epolamine (unii: x5f8ekl9zg) (diclofenac - unii:144o8ql0l1) - diclofenac epolamine 180 mg - flector® patch is indicated for the topical treatment of acute pain due to minor strains, sprains, and contusions. flector patch is contraindicated in the following patients: - known hypersensitivity (e.g., anaphylactic reactions and serious skin reactions) to diclofenac or any components of the drug product [see warnings and precautions (5.7, 5.9) ] - history of asthma, urticaria, or other allergic-type reactions after taking aspirin or other nsaids. severe, sometimes fatal, anaphylactic reactions to nsaids have been reported in such patients [see warnings and precautions (5.7, 5.8) ] - in the setting of coronary artery bypass graft (cabg) surgery [see warnings and precautions (5.1) ] - flector patch is contraindicated for use on non-intact or damaged skin resulting from any etiology, including exudative dermatitis, eczema, infection lesions, burns or wounds. risk summary published literature reports that use of nsaids, including flector patch, after 30 weeks' gestation increases the risk of premature closu