Europeiska unionen -
svenska -
EMA (European Medicines Agency)
clopidogrel taw pharma (previously clopidogrel mylan)
taw pharma (ireland) limited - klopidogrelhydroklorid - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antitrombotiska medel - , , , , 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. , , ,.
Sverige -
svenska -
Läkemedelsverket (Medical Products Agency)
amlodipin taw pharma 1 mg/ml oral suspension
taw pharma (ireland) ltd - amlodipinbesilat - oral suspension - 1 mg/ml - amlodipinbesilat 1,386 mg aktiv substans
Europeiska unionen -
svenska -
EMA (European Medicines Agency)
clopidogrel viatris (previously clopidogrel taw pharma)
viatris limited - klopidogrelbesilat - peripheral vascular diseases; stroke; myocardial infarction - antitrombotiska medel - 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-segmentet höjd akut hjärtinfarkt, i kombination med asa i medicinskt behandlade patienter berättigade till trombolysbehandling. 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. för ytterligare information hänvisas till avsnitt 5.
Sverige -
svenska -
Läkemedelsverket (Medical Products Agency)
yanatawa 20 mg filmdragerad tablett
stada arzneimittel ag - tadalafil - filmdragerad tablett - 20 mg - tadalafil 20 mg aktiv substans; laktosmonohydrat hjälpämne; natriumlaurilsulfat hjälpämne
Sverige -
svenska -
Läkemedelsverket (Medical Products Agency)
symbicort forte turbuhaler 320 mikrogram/9 mikrogram/inhalation inhalationspulver
pharmachim ab - budesonid; formoterolfumaratdihydrat - inhalationspulver - 320 mikrogram/9 mikrogram/inhalation - laktosmonohydrat hjälpämne; budesonid 320 mikrog aktiv substans; formoterolfumaratdihydrat 9 mikrog aktiv substans - formoterol och budesonid
Sverige -
svenska -
Läkemedelsverket (Medical Products Agency)
symbicort forte turbuhaler 320 mikrogram/9 mikrogram/inhalation inhalationspulver
pharmachim ab - budesonid; formoterolfumaratdihydrat - inhalationspulver - 320 mikrogram/9 mikrogram/inhalation - formoterolfumaratdihydrat 9 mikrog aktiv substans; laktosmonohydrat hjälpämne; budesonid 320 mikrog aktiv substans - formoterol och budesonid