Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

ecuphar - hidrokortizon aceponat - kortikosteroidi, dermatološki pripravci - psi - za simptomatsko liječenje upalnih i prurijskih dermatoza kod pasa. for alleviation of clinical signs associated with atopic dermatitis in dogs.

Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinuria, paroxysmal - selektivni imunosupresivi - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.

Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

novo nordisk a/s - turoctocog alfa pegol - hemofilija a - antihemorrhagics - prevencija i liječenje krvarenja kod bolesnika 12 godina s гемофилией a (urođeni deficit faktora viii)u.

Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

juta pharma gmbh - pegfilgrastim - neutropenija - Иммуностимуляторы, - smanjenje duljine trajanja neutropenije i incidencije febrilne neutropenije u odraslih bolesnika liječenih citotoksičnom kemoterapijom zbog zloćudne bolesti (uz iznimku kronične mijeloične leukemije i mijelodisplastičnog sindroma).

Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

celgene europe bv - azacitidin - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastična sredstva - azacitidine celgene is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with:intermediate 2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29 % marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30 % blasts and multi-lineage dysplasia, according to world health organisation (who) classification,aml with >30% marrow blasts according to the who classification.

Croatia - Tiếng Croatia - HALMED (Agencija za lijekove i medicinske proizvode)

elektroničar d.o.o. karlovačka cesta 26/a 10000 zagreb -

Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - рекомбинантный virus везикулярного стоматита (soj indiana) s brisanje koverti glikoprotein, zamijenjen zair ebole (soj киквите 1995) površinski glikoprotein - Геморрагическая groznice ebole - cjepiva - ervebo is indicated for active immunization of individuals 1 year of age or older to protect against ebola virus disease (evd) caused by zaire ebola virus. korištenje ervebo moraju biti u skladu sa službenim preporukama.

Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

santen oy - netarsudil - glaucoma, open-angle; ocular hypertension - ophthalmologicals - smanjenje povećanog od intraokularna pritiska (iop) kod odraslih pacijenata s primarnim otvoren kut glaukoma ili očni hipertenzije.

Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

bayer ag - sulfat larotrectinib - tumori abdomena - antineoplastična sredstva - vitrakvi u monoterapiji namijenjen za liječenje odraslih i pedijatrijska bolesnika s uglednim tumora, koji prikazuju нейротрофический receptor tirozin-kinaze (НТРК) spajanje gena,koji imaju bolest koja je lokalno-najčešće metastaze ili gdje kirurški резекция može dovesti do teških bolesti, i nemaju zadovoljavajući tretman.

Liên Minh Châu Âu - Tiếng Croatia - EMA (European Medicines Agency)

recordati rare diseases - osilodrostat fosfat - cushingov sindrom - kortikosteroidi za sistemsku upotrebu - isturisa propisan za liječenje endogene cushingov sindrom u odraslih.