Plavix Euroopa Liit - eesti - EMA (European Medicines Agency)

plavix

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.

NOLITERAX 8MG/2,5MG tablett Eesti - eesti - Ravimiamet

noliterax 8mg/2,5mg tablett

les laboratoires servier - perindopriil+indapamiid - tablett - 8mg+2,5mg 50tk; 8mg+2,5mg 60tk; 8mg+2,5mg 56tk; 8mg+2,5mg 90tk; 8mg+2,5mg 100tk; 8mg+2,5mg 30tk

NOLIPREL ARGININE õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

noliprel arginine õhukese polümeerikattega tablett

les laboratoires servier - perindopriil+indapamiid - õhukese polümeerikattega tablett - 2,5mg+0,625mg 20tk; 2,5mg+0,625mg 14tk; 2,5mg+0,625mg 30tk; 2,5mg+0,625mg 90tk; 2,5mg+0,625mg 500tk; 2,5mg+0,625mg 56tk; 2,5mg+0,625mg 60tk; 2,5mg+0,625mg 100tk

Bondronat Euroopa Liit - eesti - EMA (European Medicines Agency)

bondronat

atnahs pharma netherlands b.v. - ibandroonhape - hypercalcemia; breast neoplasms; neoplasm metastasis; fractures, bone - narkootikumid luuhaiguste raviks - bondronat on näidustatud:ennetamine kardiovaskulaarsed sündmused (patoloogilised luumurrud, luude tüsistused nõuavad kiiritusravi või operatsioon) patsientidel, kellel on rinnavähi ja luu metastases;ravi kasvaja põhjustatud hypercalcaemia koos või ilma metastases.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Euroopa Liit - eesti - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

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. , , ,.

Clopidogrel TAD Euroopa Liit - eesti - EMA (European Medicines Agency)

clopidogrel tad

tad pharma gmbh - clopidogrel (as hydrochloride) - peripheral vascular diseases; stroke; myocardial infarction - antitrombootilised ained - 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.

Ibandronic acid Accord Euroopa Liit - eesti - EMA (European Medicines Agency)

ibandronic acid accord

accord healthcare s.l.u. - ibandroonhape - wounds and injuries; breast diseases; neoplastic processes; calcium metabolism disorders; water-electrolyte imbalance - narkootikumid luuhaiguste raviks - ibandronic acid on näidatud täiskasvanute forprevention, kardiovaskulaarsed sündmused (patoloogilised luumurrud, luude tüsistused nõuavad kiiritusravi või operatsioon) patsientidel, kellel on rinnavähi ja luu metastases. ravi kasvaja põhjustatud hypercalcaemia koos või ilma metastases. ravi osteoporoosi puhul postmenopausis naistel suurenenud risk luumurdude (vt lõik 5. vähendada riski lülisamba murrud on tõendatud meditsiinilise efektiivsuse kohta d) reieluu kaela murdude ei ole tuvastatud.

Raplixa Euroopa Liit - eesti - EMA (European Medicines Agency)

raplixa

mallinckrodt pharmaceuticals ireland limited - inimese fibrinogeen, inimese trombiin - hemostaas, kirurgiline - antihemorraagilised ained - toetusravi juhul, kui tavalised kirurgilised meetodid ei ole hemostaasi paranemiseks piisavad. raplixa tuleb kasutada koos heakskiidetud želatiin sponge. raplixa on näidatud täiskasvanute üle 18-aastane.

EPIRUBICIN EBEWE süste-/infusioonilahuse kontsentraat Eesti - eesti - Ravimiamet

epirubicin ebewe süste-/infusioonilahuse kontsentraat

sandoz pharmaceuticals d.d. - epirubitsiin - süste-/infusioonilahuse kontsentraat - 2mg 1ml 50ml 1tk; 2mg 1ml 100ml 1tk; 2mg 1ml 5ml 1tk

Ketink süstelahus Eesti - eesti - Ravimiamet

ketink süstelahus

industrial veterinaria s.a. - ketoprofeen - süstelahus - 100mg 1ml 250ml 1tk; 100mg 1ml 250ml 10tk; 100mg 1ml 100ml 6tk; 100mg 1ml 250ml 6tk