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

yselty

theramex ireland limited - linzagolix choline - uterusa - hipofiza i hipotalamusni hormoni i analozi - yselty is indicated for the treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age.

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

ultomiris

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.

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

daliresp

astrazeneca ab - roflumilast - plućna bolest, kronična opstruktivna - lijekovi za opstruktivne plućne bolesti dišnih putova, - daliresp je indiciran za terapiju održavanja teške kronične opstruktivne plućne bolesti (kopb) (fev1 manji od 50% predvidjeti) povezane s kroničnim bronhitisom kod odraslih bolesnika s učestalim egzacerbacijama kao dodatak bronhodilatatorima.

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

daxas

astrazeneca ab - roflumilast - plućna bolest, kronična opstruktivna - lijekovi za opstruktivne plućne bolesti dišnih putova, - daxas je indiciran za terapiju održavanja teške kronične opstruktivne plućne bolesti (kopb) (fev1 manji od 50% predvidjeti) povezane s kroničnim bronhitisom kod odraslih bolesnika s učestalim egzacerbacijama u anamnezi kao dodatak bronhodilatacijska terapija.

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

libertek

astrazeneca ab - roflumilast - plućna bolest, kronična opstruktivna - lijekovi za opstruktivne plućne bolesti dišnih putova, - libertek je indiciran za terapiju održavanja teške kronične opstruktivne plućne bolesti (kopb) (fev1 manji od 50% predvidjeti) povezane s kroničnim bronhitisom kod odraslih bolesnika s učestalim egzacerbacijama kao dodatak bronhodilatatorima.

Yasnal 10 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

yasnal 10 mg filmom obložene tablete

krka - farma d.o.o., radnička cesta 48, zagreb - donepezilklorid - filmom obložena tableta - 10 mg - urbroj: svaka filmom obložena tableta sadrži 10 mg donepezilklorida

Yasnal 5 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

yasnal 5 mg filmom obložene tablete

krka - farma d.o.o., radnička cesta 48, zagreb - donepezilklorid - filmom obložena tableta - 5 mg - urbroj: svaka filmom obložena tableta sadrži 5 mg donepezilklorida

ANPROSOL AMINOPAN Hrvatska - hrvatski - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

anprosol aminopan

vet consulting d.o.o., matije gupca 42, 43500 daruvar, hrvatska - vitamin a, d3, e, b1, b2, b6, b12, k3, h, d-pantotenol, kolin klorid, l-alanin, l-arginin, l-cistin, l-glutaminska kiselina, l-histidin, l-izoleucin, l-leucin, l-lizin, dl-metionin, l-fenilalanin, l-prolin, l-serin, l-treonin, l-triptofan, l-tirozin i l-valin - otopina za pripremu peroralne otopine - peradi, konja, goveda, svinja, ovaca i koza