flutiform (affilia) innúðalyf, dreifa 250 míkróg/10 míkróg
mundipharma a/s - fluticasonum própíónat; formoterolum fúmarat - innúðalyf, dreifa - 250 míkróg/10 míkróg
flutiform (affilia) innúðalyf, dreifa 50 míkróg/5 míkróg
mundipharma a/s - fluticasonum própíónat; formoterolum fúmarat - innúðalyf, dreifa - 50 míkróg/5 míkróg
madopar hart hylki 100 mg og 25 mg
roche pharmaceuticals a/s - benserazidum hýdróklóríð; levodopum inn - hart hylki - 100 mg og 25 mg
madopar hart hylki 50 mg og 12,5 mg
roche pharmaceuticals a/s - benserazidum hýdróklóríð; levodopum inn - hart hylki - 50 mg og 12,5 mg
madopar tafla 125 mg
roche pharmaceuticals a/s - benserazidum hýdróklóríð; levodopum inn - tafla - 125 mg
madopar depot hart forðahylki 100 mg/25 mg
roche pharmaceuticals a/s - benserazidum hýdróklóríð; levodopum inn - hart forðahylki - 100 mg/25 mg
madopar quick lausnartafla 100 mg/25 mg
roche pharmaceuticals a/s - levodopum inn; benserazidum hýdróklóríð - lausnartafla - 100 mg/25 mg
madopar quick lausnartafla 50 mg/12,5 mg
roche pharmaceuticals a/s - levodopum inn; benserazidum hýdróklóríð - lausnartafla - 50 mg/12,5 mg
oxynorm stungulyfs-/innrennslisþykkni, lausn 10 mg/ml
mundipharma a/s - oxycodonum hýdróklóríð - stungulyfs-/innrennslisþykkni, lausn - 10 mg/ml
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.