Euroopa Liit - eesti - EMA (European Medicines Agency)

amneal pharma europe ltd - levodopa, carbidopa - parkinsoni tõbi - parkinsoni tõve ravimid - parkinsoni tõvega täiskasvanud patsientide sümptomaatiline ravi.

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. , , ,.

Eesti - eesti - Ravimiamet

strides pharma (cyprus) limited - alfakaltsidool - pehmekapsel - 1mcg 30tk; 1mcg 50tk; 1mcg 100tk; 1mcg 90tk

Eesti - eesti - Ravimiamet

strides pharma (cyprus) limited - alfakaltsidool - pehmekapsel - 0,25mcg 100tk; 0,25mcg 50tk; 0,25mcg 90tk

Eesti - eesti - Ravimiamet

strides pharma (cyprus) limited - alfakaltsidool - pehmekapsel - 0,5mcg 30tk; 0,5mcg 100tk; 0,5mcg 50tk; 0,5mcg 90tk

Eesti - eesti - Ravimiamet

seacross pharma (europe) limited - irinotekaan - infusioonilahuse kontsentraat - 20mg 1ml 2ml 1tk; 20mg 1ml 5ml 1tk; 20mg 1ml 25ml 1tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

cangene europe limited - inimese b-hepatiidi immunoglobuliin - immunization, passive; hepatitis b - spetsiifilised immunoglobuliinid - immunoprophylaxis b-hepatiidi - juhusliku kokkupuute mitte-immunised teemasid (sh isikud, kelle vaktsineerimine isincomplete või seisund teadmata). - haemodialysed patsientidel, kuni vaktsineerimine on jõustunud. - vastsündinud on hepatiit b viiruse kandja-ema. - isikutel, kes ei näita immuunsüsteemi reaktsiooni (nr mõõdetav b-hepatiidi antikehade) pärast vaktsineerimist ja kelle pidev profülaktika on vajalik tingitud pidev oht nakatunud b-hepatiidi. tähelepanu tuleks pöörata ka muid ametlikke juhiseid sobiva inim b-hepatiidi immunoglobuliin jaoks intramuskulaarse kasutada.

Eesti - eesti - Ravimiamet

alembic pharmaceuticals europe limited - prasugreel - õhukese polümeerikattega tablett - 10mg 56tk; 10mg 14tk

Eesti - eesti - Ravimiamet

alembic pharmaceuticals europe limited - olmesartaanmedoksomiil - õhukese polümeerikattega tablett - 10mg 28tk; 10mg 14tk; 10mg 98tk; 10mg 20tk; 10mg 56tk; 10mg 90tk

Eesti - eesti - Ravimiamet

alembic pharmaceuticals europe limited - olmesartaanmedoksomiil - õhukese polümeerikattega tablett - 40mg 20tk; 40mg 30tk; 40mg 56tk; 40mg 84tk; 40mg 90tk