Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

amgen europe bv (8014444) - filgrastim - injektionslösung - teil 1 - injektionslösung; filgrastim (24655) 0,48 milligramm

Europäische Union - Deutsch - EMA (European Medicines Agency)

amgen europe b.v. - blinatumomab - vorläuferzelle lymphoblastische leukämie-lymphom - antineoplastische mittel - blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options. blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b-precursor all as part of the consolidation therapy (see section 4.

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

amgen switzerland ag - panitumumabum - konzentrat zur herstellung einer infusionslösung - panitumumabum 100 mg, natrii acetas trihydricus, natrii chloridum, acidum aceticum glaciale, aqua ad iniectabile q.s. ad solutionem pro 5 ml corresp. natrium 17.25 mg. - metastasierendes kolorektales karzinom - biotechnologika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

amgen switzerland ag - panitumumabum - konzentrat zur herstellung einer infusionslösung - panitumumabum 400 mg, natrii acetas trihydricus, natrii chloridum, acidum aceticum glaciale, aqua ad iniectabile q.s. ad solutionem pro 20 ml corresp. natrium 69 mg. - metastasierendes kolorektales karzinom - biotechnologika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

amgen switzerland ag - romiplostimum - 250 mcg pulver und lösungsmittel zur herstellung einer injektionslösung - praeparatio cryodesiccata: romiplostimum 250 µg, mannitolum, saccharum, histidinum, polysorbatum 20, acidum hydrochloridum dilutum pro vitro. solvens: aqua ad iniectabile 0.72 ml. - chronische (idiopathische) immunthrombozytopenische purpura (itp) - biotechnologika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

amgen switzerland ag - romiplostimum - 500 mcg pulver und lösungsmittel zur herstellung einer injektionslösung - praeparatio cryodesiccata: romiplostimum 500 µg, mannitolum, saccharum, histidinum, polysorbatum 20, acidum hydrochloridum dilutum pro vitro. solvens: aqua ad iniectabile 1.2 ml. - chronische (idiopathische) immunthrombozytopenische purpura (itp) - biotechnologika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

amgen switzerland ag - denosumabum - injektionslösung - denosumabum 120 mg, sorbitolum 78.1 mg, polysorbatum 20, acidum aceticum glaciale aut natrii hydroxidum, aqua ad iniectabile q.s. ad solutionem pro 1.7 ml corresp. natrium 0.7 mg. - knochenmetastasen solider tumoren; riesenzelltumoren des knochens - biotechnologika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

amgen switzerland ag - apremilastum - filmtabletten - apremilastum 30 mg, cellulosum microcristallinum, lactosum monohydricum 180 mg, carmellosum natricum conexum corresp. natrium 1.68 mg, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum, talcum, e 171, e 172 (rubrum), e 172 (flavum), e 172 (nigrum), pro compresso obducto. - aktive psoriasis-arthritis und mittelschwere bis schwere plaque-psoriasis - synthetika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

amgen switzerland ag - apremilastum - 20 mg, 30 mg, filmtabletten - i) 10 mg: apremilastum 10 mg, cellulosum microcristallinum, lactosum monohydricum 60 mg, carmellosum natricum conexum corresp. natrium 0.56 mg, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum, talcum, e 171, e 172 (rubrum), pro compresso obducto. ii) 20 mg: apremilastum 20 mg, cellulosum microcristallinum, lactosum monohydricum 120 mg, carmellosum natricum conexum corresp. natrium 1.12 mg, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum, talcum, e 171, e 172 (rubrum), e 172 (flavum), pro compresso obducto. iii) 30 mg: apremilastum 30 mg, cellulosum microcristallinum, lactosum monohydricum 180 mg, carmellosum natricum conexum, natrium 1.68 mg, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum, talcum, e 171, e 172 (rubrum), e 172 (flavum), e 172 (nigrum), pro compresso obducto. - aktive psoriasis-arthritis und mittelschwere bis schwere plaque-psoriasis - synthetika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

amgen switzerland ag - blinatumomabum - pulver für ein konzentrat zur herstellung einer infusionslösung - praeparatio cryodesiccata: blinatumomabum 38.5 µg, acidum citricum monohydricum, trehalosum dihydricum, lysini hydrochloridum, polysorbatum 80, natrii hydroxidum, pro vitro corresp. natrium 1.5 mg. solvens: acidum citricum monohydricum, lysini hydrochloridum, polysorbatum 80, natrii hydroxidum, aqua ad iniectabile q.s. ad solutionem pro 10 ml corresp. natrium 18.35 mg. - onkologikum - biotechnologika