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)

teva pharma b.v. - clopidogrel (as hydrochloride) - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - antitrombootilised ained - clopidogrel on näidatud täiskasvanute ennetamise atherothrombotic sündmused:kannatavate patsientide müokardiinfarkti (paar päeva kuni vähem kui 35 päeva), ischaemic insult (7 päeva kuni vähem kui 6 kuud) või väljakujunenud perifeersete arterite haigus. 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 segmendi elevatsiooniga ägeda müokardi infarkti korral kombinatsioonis asa on meditsiiniliselt ravitud patsientide abikõlblikud trombolüütiline ravi. täiendava teabe jaoks vt osa 5.

Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi winthrop industrie - klopidogreeli vesiniksulfaat - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - antitrombootilised ained - secondary prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six 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 patients undergoing percutaneous coronary intervention (including patients undergoing a stent replacement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic 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. ennetamine atherothrombotic ja trombembooliliste sündmuste kodade fibrillationin täiskasvanud patsientidel, kellel on kodade virvendus, kes on vähemalt üks riskifaktor veresoonkonna sündmused, ei sobi ravi koos vitamiin-k antagonistid ja kes on vähese verejooksu riski, clopidogrel on näidustatud kombinatsioonis asa ennetamise atherothrombotic ja trombembooliliste sündmuste, sealhulgas insult.

Eesti - eesti - Ravimiamet

sandoz pharmaceuticals d.d. - rivaroksabaan - õhukese polümeerikattega tablett - 15mg 14tk; 15mg 28tk; 15mg 100tk; 15mg 20tk; 15mg 42tk; 15mg 50tk; 15mg 30tk

Eesti - eesti - Ravimiamet

sandoz pharmaceuticals d.d. - rivaroksabaan - õhukese polümeerikattega tablett - 10mg 30tk; 10mg 10tk; 10mg 7tk; 10mg 28tk; 10mg 14tk; 10mg 50tk; 10mg 42tk; 10mg 5tk; 10mg 100tk

Eesti - eesti - Ravimiamet

sandoz pharmaceuticals d.d. - rivaroksabaan - õhukese polümeerikattega tablett - 20mg 28tk; 20mg 14tk; 20mg 98tk; 20mg 100tk; 20mg 5tk; 20mg 20tk; 20mg 30tk; 20mg 42tk; 20mg 50tk

Eesti - eesti - Ravimiamet

krka, d.d., novo mesto - rivaroksabaan - õhukese polümeerikattega tablett - 10mg 56tk; 10mg 28tk; 10mg 15tk; 10mg 90tk; 10mg 14tk; 10mg 30tk; 10mg 100tk; 10mg 60tk; 10mg 98tk

Eesti - eesti - Ravimiamet

krka, d.d., novo mesto - rivaroksabaan - õhukese polümeerikattega tablett - 15mg 28tk; 15mg 98tk; 15mg 30tk; 15mg 90tk; 15mg 14tk; 15mg 60tk; 15mg 42tk; 15mg 100tk

Eesti - eesti - Ravimiamet

krka, d.d., novo mesto - rivaroksabaan - õhukese polümeerikattega tablett - 20mg 56tk; 20mg 42tk; 20mg 15tk; 20mg 28tk; 20mg 98tk; 20mg 30tk; 20mg 60tk; 20mg 90tk; 20mg 10tk

Eesti - eesti - Ravimiamet

krka, d.d., novo mesto - rivaroksabaan - õhukese polümeerikattega tablett - 2,5mg 28tk; 2,5mg 98tk; 2,5mg 56tk; 2,5mg 100tk; 2,5mg 14tk; 2,5mg 10tk; 2,5mg 30tk