ACENOKUMAROL UNION 4 mg/1 tableta tableta 波斯尼亚和黑塞哥维那 - 克罗地亚文 - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

acenokumarol union 4 mg/1 tableta tableta

icm d.o.o. bijeljina - acenokumarol - tableta - 4 mg/1 tableta - 1 tableta sadrži: 4 mg acenokumarola

ERACID 500 mg/1 tableta filmom obložena tableta 波斯尼亚和黑塞哥维那 - 克罗地亚文 - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

eracid 500 mg/1 tableta filmom obložena tableta

farmavita d.o.o. sarajevo - klaritromicin - filmom obložena tableta - 500 mg/1 tableta - 1 filmom obložena tableta sadrži: 500 mg klaritromicin

ERACID 250 mg/1 tableta filmom obložena tableta 波斯尼亚和黑塞哥维那 - 克罗地亚文 - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

eracid 250 mg/1 tableta filmom obložena tableta

farmavita d.o.o. sarajevo - klaritromicin - filmom obložena tableta - 250 mg/1 tableta - 1 filmom obložena tableta sadrži: 250 mg klaritromicin

PRESOLOL 100 mg/1 tableta film tableta 波斯尼亚和黑塞哥维那 - 克罗地亚文 - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

presolol 100 mg/1 tableta film tableta

hemofarm proizvodnja farmaceutskih proizvoda d.o.o. banja luka - метопролол - film tableta - 100 mg/1 tableta - 1 film tableta sadrži: 100 mg metoprololtartarata

PRESOLOL 50 mg/1 tableta film tableta 波斯尼亚和黑塞哥维那 - 克罗地亚文 - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

presolol 50 mg/1 tableta film tableta

hemofarm proizvodnja farmaceutskih proizvoda d.o.o. banja luka - метопролол - film tableta - 50 mg/1 tableta - 1 filmtableta sadrži: 50 mg metoprolol tartarata

PRESOLOL 50 mg/1 tableta film tableta 波斯尼亚和黑塞哥维那 - 克罗地亚文 - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

presolol 50 mg/1 tableta film tableta

hemofarm proizvodnja farmaceutskih proizvoda d.o.o. banja luka - метопролол - film tableta - 50 mg/1 tableta - 1 film tableta sadrži: 50 mg metoprolol tartarata

Stayveer 欧盟 - 克罗地亚文 - EMA (European Medicines Agency)

stayveer

janssen-cilag international nv - bosentan (as monohydrate) - hypertension, pulmonary; scleroderma, systemic - drugi antihipertenzivi sredstva - liječenje plućne arterijske hipertenzije (pah) za poboljšanje sposobnosti vježbanja i simptoma u bolesnika s funkcionalnom klasom svjetske zdravstvene organizacije (who) iii. učinkovitost je prikazan u:primarna (idiopatska i nasljedna) fuj;fuj sekundarne склеродермии bez značajnog интерстициальные bolesti pluća;lag, povezana sa urođenim sistem-na-plućna шунтов i eisenmenger fiziologije. neka poboljšanja su također je prikazano u bolesnika s lag, koji funkcionalna klasa ii. stayveer također je istakao smanjenje broja novih digitalne ulkusa kod pacijenata sa sistemske склеродермией i stalnom digitalni-peptičkog ulkusa.

Clopidogrel Acino 欧盟 - 克罗地亚文 - 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) 欧盟 - 克罗地亚文 - 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 BGR (previously Zylagren) 欧盟 - 克罗地亚文 - EMA (European Medicines Agency)

clopidogrel bgr (previously zylagren)

biogaran - clopidogrel (as hydrogen sulfate) - peripheral vascular diseases; stroke; myocardial infarction - antitrombotska sredstva - sprječavanje атеротромботических događaja klopidogrel prikazan:odrasli pacijenti koji pate инфарктом miokarda (od nekoliko dana do manje od 35 dana), ishemijski moždani udar (od 7 dana prije manje od 6 mjeseci) ili instaliranim bolest perifernih arterija.