Zeposia 0.23 mg Capsule rigide সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

zeposia 0.23 mg capsule rigide

bristol-myers squibb sa - ozanimodum - capsule rigide - ozanimodum 0.23 mg ut ozanimodi hydrochloridum 0.25 mg, cellulosum microcristallinum, silica colloidalis anhydrica, carmellosum natricum conexum corresp. natrium max. 0.187 mg, magnesii stearas, kapselhülle: gelatina, e 171, e 172, drucktinte: lacca, propylenglycolum, kalii hydroxidum, e 172, pro capsula. - multiple sklerose, colitis ulcerosa - synthetika

Zeposia 0.46 mg Capsule rigide সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

zeposia 0.46 mg capsule rigide

bristol-myers squibb sa - ozanimodum - capsule rigide - ozanimodum 0.46 mg ut ozanimodi hydrochloridum 0.5 mg, cellulosum microcristallinum, silica colloidalis anhydrica, carmellosum natricum conexum corresp. natrium max. 0.187 mg, magnesii stearas, kapselhülle: gelatina, e 171, e 172, drucktinte: lacca, propylenglycolum, kalii hydroxidum, e 172, pro capsula. - multiple sklerose, colitis ulcerosa - synthetika

Zeposia 0.92 mg Capsule rigide সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

zeposia 0.92 mg capsule rigide

bristol-myers squibb sa - ozanimodum - capsule rigide - ozanimodum 0.92 mg ut ozanimodi hydrochloridum 1, cellulosum microcristallinum, silica colloidalis anhydrica, carmellosum natricum conexum corresp. natrium max. 0.187 mg, magnesii stearas, kapselhülle: gelatina, e 171, e 172, drucktinte: lacca, propylenglycolum, kalii hydroxidum, e 172, pro capsula. - multiple sklerose, colitis ulcerosa - synthetika

Mayzent 0.25 mg Compresse rivestite con film সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

mayzent 0.25 mg compresse rivestite con film

novartis pharma schweiz ag - siponimodum - compresse rivestite con film - siponimodum 0.25 mg ut siponimodi fumaras, excipiens pro compresso obducto. - sekundär progrediente multiple sklerose (spms) bei erwachsenen - synthetika

Mayzent 2.00 mg Compresse rivestite con film সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

mayzent 2.00 mg compresse rivestite con film

novartis pharma schweiz ag - siponimodum - compresse rivestite con film - siponimodum 2.0 mg ut siponimodi fumaras, excipiens pro compresso obducto. - sekundär progrediente multiple sklerose (spms) bei erwachsenen - synthetika

Entyvio subkutan 108 mg Injektionslösung  in einem Fertigpen সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

entyvio subkutan 108 mg injektionslösung in einem fertigpen

takeda pharma ag - vedolizumabum - injektionslösung in einem fertigpen - vedolizumabum 108 mg, acidum citricum monohydricum, natrii citras dihydricus corresp. natrium 1.11 mg, histidinum, histidini hydrochloridum monohydricum, arginini hydrochloridum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 0.68 ml. - colite ulcerosa, morbo di crohn - biotechnologika

Entyvio subkutan 108 mg Injektionslösung  in einer Fertigspritze সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

entyvio subkutan 108 mg injektionslösung in einer fertigspritze

takeda pharma ag - vedolizumabum - injektionslösung in einer fertigspritze - vedolizumabum 108 mg, acidum citricum monohydricum, natrii citras dihydricus corresp. natrium 1.11 mg, histidinum, histidini hydrochloridum monohydricum, arginini hydrochloridum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 0.68 ml. - colite ulcerosa, morbo di crohn - biotechnologika

Gamifant ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

gamifant

swedish orphan biovitrum ab (publ) - emapalumab - immune system diseases - gamifant is indicated for the treatment of paediatric patients aged under 18 years with primary haemophagocytic lymphohistiocytosis (hlh).

Kesimpta ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

kesimpta

novartis ireland ltd - ofatumumab - sclerosi multipla recidivante-remittente - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.

Ultomiris 300 mg/3 ml Concentrato per soluzione per Infusione সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

ultomiris 300 mg/3 ml concentrato per soluzione per infusione

alexion pharma gmbh - ravulizumabum - concentrato per soluzione per infusione - ravulizumabum 300 mg, natrii dihydrogenophosphas, dinatrii phosphas, argininum, saccharum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 3 ml corresp. natrium 4.6 mg. - paroxysmale nächtliche hämoglobinurie (pnh); atypisches hämolytisch-urämisches syndrom (ahus); generalisierte myasthenia gravis, neuromyelitis-optica-spektrum-erkrankungen (nmosd) - biotechnologika