Epysqli Unione Europea - croato - EMA (European Medicines Agency)

epysqli

samsung bioepis nl b.v. - Экулизумаб - hemoglobinuria, paroxysmal - imunosupresivi - epysqli is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). evidence of clinical benefit is demonstrated in patients with haemolysis with clinical symptom(s) indicative of high disease activity, regardless of transfusion history.

Ultomiris Unione Europea - croato - 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.

ULTOMIRIS 1100 mg/11 mL Koncentrat za otopinu za infuziju Bosnia Erzegovina - croato - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

ultomiris 1100 mg/11 ml koncentrat za otopinu za infuziju

amicus pharma d.o.o. - ravulizumab - koncentrat za otopinu za infuziju - 1100 mg/11 ml - 1 bočica sa 11 ml koncentrata za otopinu za infuziju sadrži 1100 mg ravulizumaba (100 mg/ml)

ULTOMIRIS 300 mg/30 mL Koncentrat za otopinu za infuziju Bosnia Erzegovina - croato - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

ultomiris 300 mg/30 ml koncentrat za otopinu za infuziju

amicus pharma d.o.o. - ravulizumab - koncentrat za otopinu za infuziju - 300 mg/30 ml - 1 bočica sa 30 ml koncentrata za otopinu za infuziju sadrži 300 mg ravulizumaba (10 mg/ml)

CIPRINOL 200 mg/100 mL otopina za infuziju Bosnia Erzegovina - croato - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

ciprinol 200 mg/100 ml otopina za infuziju

krka farma d.o.o. sarajevo - ciprofloksacin - otopina za infuziju - 200 mg/100 ml - 1 ml otopine za infuziju sadrži: 2mg ciprofloksacina (u obliku ciprofloksacin laktata)

Evarrest Unione Europea - croato - EMA (European Medicines Agency)

evarrest

omrix biopharmaceuticals n. v. - ljudskog fibrinogena, ljudskog trombina - hemostaza - lokalni кровоостанавливающие - potporno liječenje u kirurgiji odraslih gdje su standardne kirurške tehnike nedovoljne (vidi odjeljak 5. 1):- za poboljšanje hemostaze.

Piqray Unione Europea - croato - EMA (European Medicines Agency)

piqray

novartis europharm limited  - alpelisib - neoplazme dojki - antineoplastična sredstva - piqray je navedeno u kombinaciji s fulvestrant za liječenje žena nakon menopauze, a muškaraca hormon receptor (op)-pozitivan, людское эпидермическое ako uređaj primatelja 2 faktor rasta (her2 i)-negativan, lokalno-uobičajena ili metastatskih tumora dojke s mutacija pik3ca nakon progresije bolesti nakon hormonske terapije kao monoterapija (vidi odjeljak 5.

Geomycin retard 20% Croazia - croato - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

geomycin retard 20%

genera d.d., svetonedeljska cesta 2, kalinovica, 10436 rakov potok, hrvatska - oksitetraciklin - otopina za injekciju - antibakterijski vmp za sustavne infekcije - goveda, ovaca, svinja

QUINOCOL Croazia - croato - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

quinocol

ceva santé animale,10 avenue de la ballastière, 33500 libourne, francuska - enrofloksacin; kolistin sulfat - otopina za primjenu u vodi za piće - kokoši i purana