Europska Unija - hrvatski - EMA (European Medicines Agency)

merck europe b.v. - avelumab - neuroendokrinim tumorima - drugi citostatici, monoklonsko antitijelo - bavencio prikazan kao monoterapija za liječenje odraslih bolesnika s метастатической karcinom iz stanica Меркеля (pmu). bavencio u kombinaciji s акситиниб indiciran za prva linija terapije kod odraslih pacijenata s česta почечно-клеточным raka (pkr). bavencio is indicated as monotherapy for the first‑line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc) who are progression-free following platinum‑based chemotherapy.

Europska Unija - hrvatski - EMA (European Medicines Agency)

gmp-orphan sa - Триентин tetrahydrochloride - hepatolenticularna degeneracija - drugi gastrointestinalni trakt i metabolizam, lijekovi, - cuprior indiciran za liječenje bolesti wilsona kod odraslih, adolescenata i djece ≥ 5 godina s laktoza d-пеницилламин terapija.

Europska Unija - hrvatski - EMA (European Medicines Agency)

vertex pharmaceuticals (ireland) limited - tezacaftor, ivacaftor - cistična fibroza - drugi proizvodi respiratornog sustava - symkevi is indicated in a combination regimen with ivacaftor tablets for the treatment of patients with cystic fibrosis (cf) aged 6 years and older who are homozygous for the f508del mutation or who are heterozygous for the f508del mutation and have one of the following mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene: p67l, r117c, l206w, r352q, a455e, d579g, 711+3a→g, s945l, s977f, r1070w, d1152h, 2789+5g→a, 3272 26a→g, and 3849+10kbc→t.

Europska Unija - hrvatski - EMA (European Medicines Agency)

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - drugi antineoplastični agensi - 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.

Europska Unija - hrvatski - EMA (European Medicines Agency)

akcea therapeutics ireland limited - volanesorsen natrija - hyperlipoproteinemia type i - drugi гиполипидемические modificiranje - waylivra prikazan kao dodatak prehrani kod odraslih pacijenata s genetski potvrdio obiteljska chylomicronemia sindrom (dvs) i visok rizik za razvoj pankreatitis, u kojima je odgovor na prehrane i trigliceridi антигипертензивная terapija je bila neadekvatna.

Europska Unija - hrvatski - EMA (European Medicines Agency)

univar solutions bv - триентин дигидрохлорид - hepatolenticularna degeneracija - drugi gastrointestinalni trakt i metabolizam, lijekovi, - cufence indiciran za liječenje bolesti wilsona u bolesnika s laktoza d-пеницилламин terapije kod odraslih i djece u dobi od 5 i više godina.

Europska Unija - hrvatski - EMA (European Medicines Agency)

evolus pharma b.v. - Ботулотоксин tipa a - starenje kože - drugim opuštanje mišića perifernog radnje posrednika - privremeno poboljšanje izgleda umjerene do teške vertikalne linije između obrva vidio na maksimalnu viku (glabellar linije), kada gravitacije iznad crte lica ima važan psihološki učinak kod odraslih osoba do 65 godina.

Europska Unija - hrvatski - EMA (European Medicines Agency)

blueprint medicines (netherlands) b.v. - avapritinib - tumori gastrointestinalnog stroma - drugi antitumorski lijekovi, inhibitori протеинкиназы - ayvakyt is indicated as monotherapy for the treatment of adult patients with unresectable or metastatic gastrointestinal stromal tumours (gist) harbouring the platelet-derived growth factor receptor alpha (pdgfra) d842v mutation.

Europska Unija - hrvatski - EMA (European Medicines Agency)

vertex pharmaceuticals (ireland) limited - ivacaftor, tezacaftor, elexacaftor - cistična fibroza - drugi proizvodi respiratornog sustava - kaftrio is indicated in a combination regimen with ivacaftor for the treatment of cystic fibrosis (cf) in patients aged 6 years and older who have at least one f508del mutation in the cystic fibrosis transmembrane conductance regulator (cftr) gene.

Europska Unija - hrvatski - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - vrsta ii za skladištenje glikogena - drugi gastrointestinalni trakt i metabolizam, lijekovi, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).