Mikafungin Teva 100 mg prašak za koncentrat za otopinu za infuziju Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

mikafungin teva 100 mg prašak za koncentrat za otopinu za infuziju

teva b.v., swensweg 5, haarlem, nizozemska - mikafunginnatrij - prašak za koncentrat za otopinu za infuziju - 100 mg - urbroj: svaka bočica sadrži 100 mg mikafungina (u obliku mikafunginnatrija)

Mikafungin Teva 50 mg prašak za koncentrat za otopinu za infuziju Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

mikafungin teva 50 mg prašak za koncentrat za otopinu za infuziju

teva b.v., swensweg 5, haarlem, nizozemska - mikafunginnatrij - prašak za koncentrat za otopinu za infuziju - 50 mg - urbroj: svaka bočica sadrži 50 mg mikafungina (u obliku mikafunginnatrija)

Mikafungin Sandoz 100 mg prašak za otopinu za infuziju Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

mikafungin sandoz 100 mg prašak za otopinu za infuziju

sandoz d.o.o., maksimirska 120, zagreb, hrvatska - mikafunginnatrij - prašak za otopinu za infuziju - 100 mg - urbroj: svaka bočica sadrži mikafunginnatrij što odgovara 100 mg mikafungina

Mikafungin Sandoz 50 mg prašak za otopinu za infuziju Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

mikafungin sandoz 50 mg prašak za otopinu za infuziju

sandoz d.o.o., maksimirska 120, zagreb, hrvatska - mikafunginnatrij - prašak za otopinu za infuziju - 50 mg - urbroj: svaka bočica sadrži mikafunginnatrij što odgovara 50 mg mikafungina.

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

eurartesim

alfasigma s.p.a. - piperaquine tetraphosphate, artenimol - malarija - antiprotozoals - eurartesim je indiciran za liječenje nekompliciranog plasmodium falciparum malarije kod odraslih, djece i dojenčadi 6 mjeseci i više i težine 5 kg ili više. treba uzeti u obzir formalne preporuke za odgovarajuće korištenje противомалярийных posrednika.

Clopidogrel/Acetylsalicylic acid Teva Europska Unija - hrvatski - EMA (European Medicines Agency)

clopidogrel/acetylsalicylic acid teva

teva pharma b.v. - clopidogrel, acetylsalicylic acid - acute coronary syndrome; myocardial infarction - kombinacije - klopidogrel/acetilsalicilna kiselina teva je indiciran za prevenciju aterotrombotskih događaja u odraslih bolesnika koji već uzimaju klopidogrel i acetilsalicilnu kiselinu (ask). Клопидогрел/Ацетилсалициловая kiselina tewa je fiksna kombinacija doza lijekova za nastavak terapije: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.

Clopidogrel Acino Europska Unija - hrvatski - EMA (European Medicines Agency)

clopidogrel acino

acino ag - klopidogrel - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - antitrombotska sredstva - clopidogrel is indicated in adults for the prevention of atherothrombotic events in: , , , patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease, 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), st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy, patients suffering from acute coronary syndrome. , ,.

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Europska Unija - hrvatski - 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.