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. , , ,.

Rivastigmine 1 A Pharma Euroopa Liit - eesti - EMA (European Medicines Agency)

rivastigmine 1 a pharma

1 a pharma gmbh - rivastigmiin - alzheimer disease; dementia; parkinson disease - psychoanaleptics, - kerge kuni mõõdukalt raskekujulise alzheimeri tõve sümptomaatiline ravi. sümptomaatiline ravi kerge kuni mõõdukalt raske dementsuse patsientidel, kellel on idiopaatiline parkinsoni tõbi.

AMLODIPINE SOPHARMA tablett Eesti - eesti - Ravimiamet

amlodipine sopharma tablett

sopharma ad - amlodipiin - tablett - 5mg 14tk; 5mg 30tk; 5mg 28tk; 5mg 56tk; 5mg 90tk; 5mg 60tk; 5mg 50tk; 5mg 98tk

VANCOMYCIN PHARMASWISS infusioonilahuse pulber Eesti - eesti - Ravimiamet

vancomycin pharmaswiss infusioonilahuse pulber

pharmaswiss ceska republika s.r.o. - vankomütsiin - infusioonilahuse pulber - 1000mg 1tk; 1000mg 10tk

AMLODIPINE SOPHARMA tablett Eesti - eesti - Ravimiamet

amlodipine sopharma tablett

sopharma ad - amlodipiin - tablett - 10mg 20tk; 10mg 98tk; 10mg 56tk; 10mg 28tk; 10mg 300tk; 10mg 60tk; 10mg 14tk; 10mg 21tk

VANCOMYCIN PHARMASWISS infusioonilahuse pulber Eesti - eesti - Ravimiamet

vancomycin pharmaswiss infusioonilahuse pulber

pharmaswiss ceska republika s.r.o. - vankomütsiin - infusioonilahuse pulber - 500mg 10tk

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

qinlock

deciphera pharmaceuticals (netherlands) b.v. - ripretinib - seedetraktist esinevad stromaal-kasvajad - antineoplastilised ained - qinlock is indicated for the treatment of adult patients with advanced gastrointestinal stromal tumour (gist) who have received prior treatment with three or more kinase inhibitors, including imatinib.

BENDAMUSTINE BOSTON BIOPHARMA infusioonilahuse kontsentraadi pulber Eesti - eesti - Ravimiamet

bendamustine boston biopharma infusioonilahuse kontsentraadi pulber

boston biopharma lt uab - bendamustiin - infusioonilahuse kontsentraadi pulber - 2,5mg 1ml 100mg 1tk; 2,5mg 1ml 25mg 1tk

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

hetlioz

vanda pharmaceuticals netherlands b.v. - tasimelteon - unehäired, tsirkadiaalne rütm - psühhoeptikumid - hetlioz on näidustatud mitte-24-tunnise unehäirega (mitte-24-tunnise) häire raviks täiskasvanud pimedas.

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

rxulti

otsuka pharmaceutical netherlands b.v. - brexpiprazole - skisofreenia - psühhoeptikumid - skisofreenia ravi.