SORAFENIB STADA 200 mg/1 tableta film tableta Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

sorafenib stada 200 mg/1 tableta film tableta

hemofarm proizvodnja farmaceutskih proizvoda d.o.o. banja luka - sorafenib - film tableta - 200 mg/1 tableta - 1 film tableta sadrži: 200 mg sorafeniba u obliku sorafenib tosilata

SORAFENIB STADA 400 mg/1 tableta film tableta Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

sorafenib stada 400 mg/1 tableta film tableta

hemofarm proizvodnja farmaceutskih proizvoda d.o.o. banja luka - sorafenib - film tableta - 400 mg/1 tableta - 1 film tableta sadrži: 400 mg sorafeniba u obliku sorafenib tosilata

Lunsumio Europska Unija - hrvatski - EMA (European Medicines Agency)

lunsumio

roche registration gmbh - mosunetuzumab - limfom, folikularni - antineoplastic agents, monoclonal antibodies - lunsumio as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (fl) who have received at least two prior systemic therapies.

Carvykti Europska Unija - hrvatski - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - multipli mijelom - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Kimmtrak Europska Unija - hrvatski - EMA (European Medicines Agency)

kimmtrak

immunocore ireland limited - tebentafusp - uveal neoplasms - antineoplastična sredstva - kimmtrak is indicated as monotherapy for the treatment of human leukocyte antigen (hla)-a*02:01-positive adult patients with unresectable or metastatic uveal melanoma.