Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Den Europæiske Union - dansk - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - clopidogrelhydrochlorid - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antitrombotiske midler - , , , , 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. , , ,.

Porcilis Lawsonia Vet. lyofilisat og solvens til injektionsvæske, emulsion Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

porcilis lawsonia vet. lyofilisat og solvens til injektionsvæske, emulsion

intervet international b.v. - lawsonia intracellularis, lyofiliseret - lyofilisat og solvens til injektionsvæske, emulsion

Porcilis Lawsonia ID Vet. lyofilisat og solvens til injektionsvæske, emulsion Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

porcilis lawsonia id vet. lyofilisat og solvens til injektionsvæske, emulsion

intervet international b.v. - lawsonia intracellularis bakterie, stamme ms b3903, (levende, svækket) - lyofilisat og solvens til injektionsvæske, emulsion

Tomahawk 200 EC Emulsionskoncentrat Danmark - dansk - SEGES Landbrug & Fødevarer

tomahawk 200 ec emulsionskoncentrat

adama northern europe b.v. - fluroxypyr - emulsionskoncentrat - 200 g/l fluroxypyr

Tomahawk Danmark - dansk - Adama

tomahawk

adama - 200 g/l fluroxypyr - herbicider

Tomahawk 180 EC Emulsionskoncentrat Danmark - dansk - SEGES Landbrug & Fødevarer

tomahawk 180 ec emulsionskoncentrat

adama northern europe b.v. - fluroxypyr - emulsionskoncentrat - 180 g/l fluroxypyr

Enterisol Ileitis Vet. lyofilisat og solvens til oral suspension Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

enterisol ileitis vet. lyofilisat og solvens til oral suspension

boehringer ingelheim vetmedica gmbh - lawsonia intracellularis bakterie, stamme ms b3903, (levende, svækket) - lyofilisat og solvens til oral suspension - svin

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Den Europæiske Union - dansk - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - clopidogrel besilat - peripheral vascular diseases; stroke; myocardial infarction - antitrombotiske midler - 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-segment elevation akut myokardieinfarkt, i kombination med asa i medicinsk behandlede patienter, der er berettiget til trombolytisk terapi. 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 yderligere oplysninger henvises der til afsnit 5.

Myalepta Den Europæiske Union - dansk - EMA (European Medicines Agency)

myalepta

amryt pharmaceuticals dac - metreleptin - lipodystrofi, familiær delvis - andre alimentary tract and metabolism produkter, - myalepta er indiceret som et supplement til kost som en substitutionsterapi til at behandle de komplikationer af leptin mangel i lipodystrofi (ld) patienter med bekræftet medfødte generelle ld (berardinelli-seip syndrom) eller erhvervet generelle ld (lawrence syndrom) hos voksne og børn på 2 år og abovewith bekræftet familiær delvis ld eller erhvervet, delvis ld (barraquer-simons syndrom), hos voksne og børn på 12 år og derover, for hvem standard-behandlinger har undladt at opnå tilstrækkelig metabolisk kontrol.