Roctavian Unión Europea - húngaro - EMA (European Medicines Agency)

roctavian

biomarin international limited - valoctocogene roxaparvovec - antihaemorrhagiás - treatment of severe haemophilia a (congenital factor viii deficiency) in adult patients without a history of factor viii inhibitors and without detectable antibodies to adeno-associated virus serotype 5 (aav5).

Thalidomide Lipomed Unión Europea - húngaro - EMA (European Medicines Agency)

thalidomide lipomed

lipomed gmbh - a thalidomide - myeloma multiplex - immunszuppresszánsok - thalidomide lipomed in combination with melphalan and prednisone is indicated as first line treatment of patients with untreated multiple myeloma, aged ≥ 65 years or ineligible for high dose chemotherapy. thalidomide lipomed is prescribed and dispensed in accordance with the thalidomide lipomed pregnancy prevention programme (see section 4.

Pirfenidone Viatris Unión Europea - húngaro - EMA (European Medicines Agency)

pirfenidone viatris

viatris limited - pirfenidone - idiopathic pulmonary fibrosis; lung diseases; respiratory tract diseases - immunszuppresszánsok - pirfenidone viatris is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

Sugammadex Amomed Unión Europea - húngaro - EMA (European Medicines Agency)

sugammadex amomed

aop orphan pharmaceuticals gmbh - sugammadex sodium - neuromuszkuláris blokád - minden más terápiás készítmény - a rokuronium vagy a vekuronium által indukált neuromuszkuláris blokád visszafordítása. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Dimethyl fumarate Teva Unión Europea - húngaro - EMA (European Medicines Agency)

dimethyl fumarate teva

teva gmbh - dimetil-fumarát - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunszuppresszánsok - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Dimethyl fumarate Accord Unión Europea - húngaro - EMA (European Medicines Agency)

dimethyl fumarate accord

accord healthcare s.l.u. - dimetil-fumarát - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunszuppresszánsok - dimethyl fumarate accord is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Sugammadex Piramal Unión Europea - húngaro - EMA (European Medicines Agency)

sugammadex piramal

piramal critical care b.v. - sugammadex sodium - neuromuszkuláris blokád - sugammadexet - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.

Sugammadex Adroiq Unión Europea - húngaro - EMA (European Medicines Agency)

sugammadex adroiq

extrovis eu ltd. - sugammadex sodium - neuromuszkuláris blokád - minden más terápiás készítmény - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Herwenda Unión Europea - húngaro - EMA (European Medicines Agency)

herwenda

sandoz gmbh - trastuzumab - breast neoplasms; stomach neoplasms - daganatellenes szerek - treatment of metastatic and early breast cancer and metastatic gastric cancer (mgc).