ABIRATERONE G.L. PHARMA õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

abiraterone g.l. pharma õhukese polümeerikattega tablett

g.l. pharma gmbh - abirateroon - õhukese polümeerikattega tablett - 500mg 56tk

BUPRENORPHINE G.L. PHARMA keelealune tablett Eesti - eesti - Ravimiamet

buprenorphine g.l. pharma keelealune tablett

g.l. pharma gmbh - buprenorfiin - keelealune tablett - 8mg 7tk; 8mg 10tk; 8mg 28tk; 8mg 30tk; 8mg 49tk

BUPRENORPHINE G.L. PHARMA keelealune tablett Eesti - eesti - Ravimiamet

buprenorphine g.l. pharma keelealune tablett

g.l. pharma gmbh - buprenorfiin - keelealune tablett - 2mg 7tk; 2mg 28tk; 2mg 30tk; 2mg 10tk

BUPRENORPHINE G.L. PHARMA keelealune tablett Eesti - eesti - Ravimiamet

buprenorphine g.l. pharma keelealune tablett

g.l. pharma gmbh - buprenorfiin - keelealune tablett - 4mg 10tk; 4mg 28tk; 4mg 49tk; 4mg 30tk; 4mg 7tk

LEVOMETHADONE G.L.PHARMA suukaudse lahuse kontsentraat Eesti - eesti - Ravimiamet

levomethadone g.l.pharma suukaudse lahuse kontsentraat

g.l. pharma gmbh - levometadoon - suukaudse lahuse kontsentraat - 5mg 1ml 100ml 1tk; 5mg 1ml 150ml 1tk; 5mg 1ml 300ml 1tk; 5mg 1ml 500ml 1tk

METHADONE G.L.PHARMA suukaudse lahuse kontsentraat Eesti - eesti - Ravimiamet

methadone g.l.pharma suukaudse lahuse kontsentraat

g.l. pharma gmbh - metadoon - suukaudse lahuse kontsentraat - 10mg 1ml 300ml 1tk; 10mg 1ml 500ml 1tk; 10mg 1ml 1000ml 1tk; 10mg 1ml 150ml 1tk; 10mg 1ml 100ml 1tk

IMIPENEM/CILASTATIN VENUS PHARMA infusioonilahuse pulber Eesti - eesti - Ravimiamet

imipenem/cilastatin venus pharma infusioonilahuse pulber

venus pharma gmbh - imipeneem+tsilastatiin - infusioonilahuse pulber - 500mg+500mg 10tk; 500mg+500mg 5tk

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

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - klopidogreel-besilaat - peripheral vascular diseases; stroke; myocardial infarction - 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), 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). st segmendi elevatsiooniga ägeda müokardi infarkti korral kombinatsioonis asa on meditsiiniliselt ravitud patsientide abikõlblikud trombolüütiline ravi. 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. täiendava teabe jaoks vt osa 5.

LODOTRA toimeainet modifitseeritult vabastav tablett Eesti - eesti - Ravimiamet

lodotra toimeainet modifitseeritult vabastav tablett

mundipharma gesellschaft m.b.h. - prednisoon - toimeainet modifitseeritult vabastav tablett - 1mg 100tk; 1mg 30tk; 1mg 500tk

LODOTRA toimeainet modifitseeritult vabastav tablett Eesti - eesti - Ravimiamet

lodotra toimeainet modifitseeritult vabastav tablett

mundipharma gesellschaft m.b.h. - prednisoon - toimeainet modifitseeritult vabastav tablett - 2mg 500tk; 2mg 30tk; 2mg 100tk