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

mircera

roche registration gmbh - Метокси polietilen glikol-эпоэтин beta - anemia; kidney failure, chronic - antianemijski pripravci - treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in adult patients (see section 5. treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in paediatric patients from 3 months to less than 18 years of age who are converting from another erythropoiesis stimulating agent (esa) after their haemoglobin level was stabilised with the previous esa (see section 5.

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

scemblix

novartis europharm limited - asciminib hydrochloride - leukemija, mijelogeni, kronični, bcr-abl pozitivan - antineoplastična sredstva - scemblix is indicated for the treatment of adult patients with philadelphia chromosome positive chronic myeloid leukaemia in chronic phase (ph+ cml cp) previously treated with two or more tyrosine kinase inhibitors (see section 5.

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

lytgobi

taiho pharma netherlands b.v. - futibatinib - cholangiocarcinoma - agenti imaju antikancerogena - lytgobi monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (fgfr2) fusion or rearrangement that have progressed after at least one prior line of systemic therapy.

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

zepatier

merck sharp & dohme b.v. - danas tvrtka otvara, razvija, grazoprevir - hepatitis c, kronični - direct acting antivirals, antivirals for systemic use, antivirals for treatment of hcv infections - zepatier is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients 12 years of age and older who weigh at least 30 kg (see sections 4. 2, 4. 4 i 5. virus hepatitisa c (hcv) genotip-specifične aktivnosti vidi 4. 4 i 5.

Uniring 0,120 mg/0,015 mg tijekom 24 sata, sustav za isporuku u rodnicu Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

uniring 0,120 mg/0,015 mg tijekom 24 sata, sustav za isporuku u rodnicu

pharmaswiss Česká republika s.r.o., jankovcova 1569/2c, prag, Češka - etonogestrelum, ethinylestradiolum - sustav za isporuku u rodnicu - 0,120 mg/0,015 mg tijekom 24 sata - urbroj: 1 prsten sadrži 11,0 mg etonogestrela i 3,474 mg etinilestradiola, tijekom razdoblja od 3 tjedna prsten otpušta prosječno 0,120 mg etonogestrela i 0,015 mg etinilestradiola u 24 sata

Perlinring 0,120 mg/0,015 mg tijekom 24 sata, sustav za isporuku u rodnicu Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

perlinring 0,120 mg/0,015 mg tijekom 24 sata, sustav za isporuku u rodnicu

actavis group ptc ehf., reykjavikurvegur 76-78, hafnarfjordur, island - etonogestrelum, ethinylestradiolum - sustav za isporuku u rodnicu - 0,120 mg/0,015 mg tijekom 24 sata - urbroj: jedan prsten sadrži 11,7 mg etonogestrela i 2,7 mg etinilestradiola, tijekom razdoblja od 3 tjedna prsten otpušta prosječno 0,120 mg etonogestrela i 0,015 mg etinilestradiola u 24 sata

Etonogestrel/Etinilestradiol Mithra 0,120 mg/0,015 mg tijekom 24 sata, sustav za isporuku u rodnicu Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

etonogestrel/etinilestradiol mithra 0,120 mg/0,015 mg tijekom 24 sata, sustav za isporuku u rodnicu

novalon s.a., rue saint-georges 5, liege, belgija - etonogestrel etinilestradiol - sustav za isporuku u rodnicu - 0,120 mg + 0,015 mg/24 sata - urbroj: 1 vaginalni prsten sadrži 11,7 mg etonogestrela i 2,7 mg etinilestradiola, tijekom razdoblja od 3 tjedna prsten otpušta prosječno 0,120 mg etonogestrela i 0,015 mg etinilestradiola u 24 sata