Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

roche pharma (schweiz) ag - epoetinum beta - les seringues préremplies - epoetinum beta 10000 u.i., ureum, natrii chloridum, polysorbatum 20, natrii dihydrogenophosphas dihydricus, dinatrii phosphas dodecahydricus, calcii chloridum dihydricum, glycinum, leucinum, isoleucinum, threoninum, acidum glutamicum, phenylalaninum 0.3 mg, aqua ad iniectabile q.s. ad solutionem pro 0.6 ml corresp. natrium 0.96 mg. - la stimulation de l'Érythropoïèse - biotechnologika

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

roche pharma (schweiz) ag - epoetinum beta - les seringues préremplies - epoetinum beta 4000 u.i., ureum, natrii chloridum, polysorbatum 20, natrii dihydrogenophosphas dihydricus, dinatrii phosphas dodecahydricus, calcii chloridum dihydricum, glycinum, leucinum, isoleucinum, threoninum, acidum glutamicum, phenylalaninum 0.15 mg, aqua ad iniectabile q.s. ad solutionem pro 0.3 ml corresp. natrium 0.48 mg. - la stimulation de l'Érythropoïèse - biotechnologika

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

roche pharma (schweiz) ag - epoetinum beta - les seringues préremplies - epoetinum beta 6000 u.i., ureum, natrii chloridum, polysorbatum 20, natrii dihydrogenophosphas dihydricus, dinatrii phosphas dodecahydricus, calcii chloridum dihydricum, glycinum, leucinum, isoleucinum, threoninum, acidum glutamicum, phenylalaninum 0.15 mg, aqua ad iniectabile q.s. ad solutionem pro 0.3 ml corresp. natrium 0.48 mg. - la stimulation de l'Érythropoïèse - biotechnologika

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

roche pharma (schweiz) ag - epoetinum beta - les seringues préremplies - epoetinum beta 30000 u.i., ureum, natrii chloridum, polysorbatum 20, natrii dihydrogenophosphas dihydricus, dinatrii phosphas dodecahydricus, calcii chloridum dihydricum, glycinum, leucinum, isoleucinum, threoninum, acidum glutamicum, phenylalaninum 0.3 mg, aqua ad iniectabile q.s. ad solutionem pro 0.6 ml corresp. natrium 1 mg. - la stimulation de l'Érythropoïèse - biotechnologika

France - français - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

sandoz - chlorhydrate de bendamustine - poudre - 25 mg - composition pour un flacon de 20 ml > chlorhydrate de bendamustine : 25 mg - pharmacotherapeutique agents antinéoplasiques, agents alkylants

Union européenne - français - EMA (European Medicines Agency)

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - autres agents antinéoplasiques - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

Union européenne - français - EMA (European Medicines Agency)

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - agents antinéoplasiques - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline biologicals sa - recombinant varicella zoster virus glycoprotein e - l'herpès zoster - vaccins - shingrix is indicated for prevention of herpes zoster (hz) and post-herpetic neuralgia (phn), in:adults 50 years of age or older;adults 18 years of age or older at increased risk of hz. l'utilisation de shingrix doit être en conformité avec les recommandations officielles.

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

novartis pharma schweiz ag - tisagenlecleucelum car-positif, viabilité t-cellules. contient des cellules génétiquement modifiées - zellsuspension zur perfusion - beutel: tisagenlecleucelum car-positive lebensfähige t-zellen. enthält genetisch veränderte zellen 1,2x10e6–6,0x10e8 pro dosi, natrium, chloridum, magnesium, acetas, gluconas, glucosum, 5-hydroxymethylfurfuralum, albuminum, n-acetyltryptophanum natricum, caprylas, aluminium, dextranum 40, dimethylis sulfoxidum, dimethylis sulfonum, q.s. pro 50 ml. - 1) die behandlung von pädiatrischen und jungen erwachsenen patienten im alter bis zu 25 jahren mit akuter lymphatischer b-zell-leukämie (b-zell-all), die refraktär ist, nach einer transplantation rezidiviert ist oder nach zwei therapielinien oder später rezidiviert ist. 2) die behandlung erwachsener patienten mit rezidiviertem oder refraktärem diffus grosszelligem b-zell-lymphom (dlbcl) nach zwei oder mehr linien einer systemischen therapie. 3) behandlung erwachsener patienten mit rezidiviertem oder refraktärem follikulärem lymphom (fl) nach drei oder mehr linien einer systemischen therapie, - greffe: gentherapieprodukt

Belgique - français - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

aspen pharma trading ltd. - melphalan 50 mg - poudre et solvant pour solution pour perfusion - 50 mg - melphalan 50 mg - melphalan