Eplerenon Bluefish Filmuhúðuð tafla 25 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

eplerenon bluefish filmuhúðuð tafla 25 mg

bluefish pharmaceuticals ab - eplerenonum inn - filmuhúðuð tafla - 25 mg

Eplerenon Bluefish Filmuhúðuð tafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

eplerenon bluefish filmuhúðuð tafla 50 mg

bluefish pharmaceuticals ab - eplerenonum inn - filmuhúðuð tafla - 50 mg

Galantamin STADA Hart forðahylki 16 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

galantamin stada hart forðahylki 16 mg

stada arzneimittel ag - galantaminum brómíð - hart forðahylki - 16 mg

Galantamin STADA Hart forðahylki 24 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

galantamin stada hart forðahylki 24 mg

stada arzneimittel ag - galantaminum brómíð - hart forðahylki - 24 mg

Galantamin STADA Hart forðahylki 8 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

galantamin stada hart forðahylki 8 mg

stada arzneimittel ag - galantaminum brómíð - hart forðahylki - 8 mg

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Evrópusambandið - íslenska - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - clopidogrel besilate - peripheral vascular diseases; stroke; myocardial infarction - blóðþurrðandi lyf - 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). l hækkun, bráð myndun stíflufleygs, ásamt asa í læknisfræðilega sjúklingum rétt fyrir segaleysandi meðferð. 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. nánari upplýsingar er að vísa til kafla 5.