Eesti - eesti - Ravimiamet

pharmaceutical works polpharma s.a. - atorvastatiin - õhukese polümeerikattega tablett - 20mg 50tk; 20mg 98tk; 20mg 20tk; 20mg 7tk; 20mg 56tk; 20mg 4tk; 20mg 10tk; 20mg 14tk

Eesti - eesti - Ravimiamet

pharmaceutical works polpharma s.a. - atorvastatiin - õhukese polümeerikattega tablett - 10mg 20tk; 10mg 56tk; 10mg 100tk; 10mg 500tk; 10mg 30tk; 10mg 10tk; 10mg 50tk; 10mg 4tk; 10mg 98tk

Eesti - eesti - Ravimiamet

pharmaceutical works polpharma s.a. - atorvastatiin - õhukese polümeerikattega tablett - 40mg 10tk; 40mg 30tk; 40mg 200tk; 40mg 500tk; 40mg 56tk; 40mg 28tk; 40mg 14tk

Eesti - eesti - Ravimiamet

pharmaceutical works polpharma s.a. - esomeprasool - süste-/infusioonilahuse pulber - 40mg 10viaal

Eesti - eesti - Ravimiamet

g.l. pharma gmbh - rivaroksabaan - õhukese polümeerikattega tablett - 20mg 60tk; 20mg 10tk; 20mg 14tk; 20mg 45tk; 20mg 28tk; 20mg 90tk; 20mg 98tk

Eesti - eesti - Ravimiamet

g.l. pharma gmbh - rivaroksabaan - õhukese polümeerikattega tablett - 10mg 45tk; 10mg 30tk; 10mg 90tk; 10mg 100tk; 10mg 5tk; 10mg 42tk; 10mg 60tk; 10mg 10tk

Eesti - eesti - Ravimiamet

g.l. pharma gmbh - rivaroksabaan - õhukese polümeerikattega tablett - 15mg 30tk; 15mg 45tk; 15mg 10tk; 15mg 42tk; 15mg 14tk; 15mg 5tk; 15mg 90tk; 15mg 60tk; 15mg 100tk

Eesti - eesti - Ravimiamet

sopharma ad - askorbiinhape - süste-/infusioonilahus - 100mg 1ml 2ml 10tk; 100mg 1ml 5ml 10tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

taw pharma (ireland) limited - klopidogreelvesinikkloriid - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antitrombootilised ained - , , , , secondary prevention of atherothrombotic events, , clopidogrel is indicated in: , - adult 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. , - 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). ,     - st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy. , , 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. , , for further information please refer to section 5. , , ,.

Euroopa Liit - eesti - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - pramipeksooli divesinikkloriid monohüdraat - restless legs syndrome; parkinson disease - parkinsoni tõve ravimid - mirapexin on näidustatud idiopaatilise parkinsoni tõve nähtude ja sümptomite raviks, üksinda (ilma levodopata) või kombinatsioonis levodopaga, i. jooksul haiguse, läbi hilisstaadiumis levodopa toime möödub või muutub vastuoluline ja ravitoime kõikumised esinevad (annuse lõpu või "on-off" kõikumine). mirapexin on näidustatud sümptomaatiline ravi mõõduka kuni raske idiopaatilise rahutute-jalgade sündroom annustes kuni 0. 54 mg aluse (0. 75 mg soola).