Flebogamma DIF (previously Flebogammadif) Den Europæiske Union - kroatisk - EMA (European Medicines Agency)

flebogamma dif (previously flebogammadif)

instituto grifols s.a. - imunoglobulina osoba normalan - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - imuni serumi i homologna, - replacement therapy in adults, children and adolescents (0-18 years) in: , primary immunodeficiency syndromes with impaired antibody production;, hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic luekaemia, in whom prophylactic antibiotics have failed;, hypogammaglobulinaemia and recurrent bacterial infections in plateau-phase-multiple-myeloma patients who failed to respond to pneumococcal immunisation;, hypogammaglobulinaemia in patients after allogenic haematopoietic-stem-cell transplantation (hsct);, congenital aids with recurrent bacterial infections. , immunomodulation in adults, children and adolescents (0-18 years) in: , primary immune thrombocytopenia (itp), in patients at high risk of bleeding or prior to surgery to correct the platelet count;, guillain barré syndrome;, kawasaki disease.

Intratect 100 g/l otopina za infuziju Kroatien - kroatisk - HALMED (Agencija za lijekove i medicinske proizvode)

intratect 100 g/l otopina za infuziju

biotest pharma gmbh, landsteinerstr. 5, dreieich, njemačka - imunoglobulin normalni, ljudski, intravenski - otopina za infuziju - 100 g/l - urbroj: 1 ml otopine sadrži 100 mg imunoglobulina normalnog, ljudskog

Intratect 50 g/l otopina za infuziju Kroatien - kroatisk - HALMED (Agencija za lijekove i medicinske proizvode)

intratect 50 g/l otopina za infuziju

biotest pharma gmbh, landsteinerstr. 5, dreieich, njemačka - imunoglobulin normalni, ljudski, intravenski - otopina za infuziju - 50 g/l - urbroj: 1 ml otopine sadrži 50 mg imunoglobulina normalnog, ljudskog

Vectormune FP ILT + AE Den Europæiske Union - kroatisk - EMA (European Medicines Agency)

vectormune fp ilt + ae

ceva-phylaxia co. ltd. - live recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus (rfp-lt) and avian encephalomyelitis virus, strain calnek 1143 (ae) - immunologicals for aves, live viral vaccines, domestic fowl - piletina - for active immunisation of chickens of 8 to 13 weeks of age in order to reduce the skin lesions due to fowlpox, to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis and to prevent egg production losses due to avian encephalomyelitis.

Nobivac DP Plus Den Europæiske Union - kroatisk - EMA (European Medicines Agency)

nobivac dp plus

intervet international b.v. - live attenuated canine distemper virus strain onderstepoort: 105.1 – 106.5 tcid50, live recombinant canine parvovirus strain 630a: 105.1 – 106.7 tcid50 - imunomodulatori za псовые - dogs (small) - for the active immunisation of puppies from 4 weeks of age onwards to prevent clinical signs and mortality of canine distemper virus infection and canine parvovirus infection and to prevent viral excretion following canine distemper virus infection and following canine parvovirus infection.

RHESONATIV 625 i.j./1 mL rastvor  za injekciju Bosnien-Hercegovina - kroatisk - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

rhesonativ 625 i.j./1 ml rastvor za injekciju

remedia d.o.o. sarajevo - antidiarrheal i mokraći (rho) imunoglobulin, humanističke znanosti - rastvor za injekciju - 625 i.j./1 ml - 1 ml sadrži: 625 i.j. imunoglobulin antid, humani

RHESONATIV 625 i.j./1 mL rastvor  za injekciju Bosnien-Hercegovina - kroatisk - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

rhesonativ 625 i.j./1 ml rastvor za injekciju

remedia d.o.o. sarajevo - antidiarrheal i mokraći (rho) imunoglobulin, humanističke znanosti - rastvor za injekciju - 625 i.j./1 ml - 1 ml rastvora za injekciju sadrži: 625 i.j. imunoglobulin antid, humani

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Den Europæiske Union - kroatisk - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - klopidogrel besilat - peripheral vascular diseases; stroke; myocardial infarction - antitrombotska sredstva - secondary prevention of atherothrombotic events clopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. adult patients suffering from acute coronary syndrome. non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa). porastom segmenta st akutni infarkt miokarda, u kombinaciji s ask u liječenju pacijenata koji imaju pravo na thrombolytic terapije. in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic stroke (is) clopidogrel in combination with asa is indicated in:adult patients with moderate to high-risk tia (abcd2 score ≥4) or minor is (nihss ≤3) within 24 hours of either the tia or is event. prevention of atherothrombotic and thromboembolic events in atrial fibrillation:in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. za više informacija, molimo pogledajte odjeljak 5.

Clopidogrel / Acetylsalicylic acid Mylan Den Europæiske Union - kroatisk - EMA (European Medicines Agency)

clopidogrel / acetylsalicylic acid mylan

mylan pharmaceuticals limited - acetylsalicylic acid, clopidogrel hydrogen sulfate - acute coronary syndrome; myocardial infarction - antitrombotska sredstva - Клопидогрел/Ацетилсалициловая kiselina mylan u indiciran za sekundarnu prevenciju атеротромботических događaja kod odraslih pacijenata već prihvatiti kao клопидогрела i ацетилсалициловой kiseline (ask). Клопидогрел/Ацетилсалициловая kiselina mylan u fiksne doze kombiniranog medicinskih proizvoda za nastavak liječenja:ne porast segmenta st akutna koronarna sindrom (nestabilna angina, ili ne-q-infarkt miokarda), uključujući i bolesnike koji su patili стентирование nakon чрескожных koronarnih interventionst porast u segmentu akutnog infarkta miokarda u liječenju pacijenata koji imaju pravo na thrombolytic terapije.

Xofluza Den Europæiske Union - kroatisk - EMA (European Medicines Agency)

xofluza

roche registration gmbh - baloxavir marboxil - gripa, ljudska - antivirusni lijekovi za sustavnu uporabu - treatment of influenzaxofluza is indicated for the treatment of uncomplicated influenza in patients aged 1 year and above. post exposure prophylaxis of influenzaxofluza is indicated for post-exposure prophylaxis of influenza in individuals aged 1 year and above. xofluza should be used in accordance with official recommendations.