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

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - klópídógrel hýdróklóríð - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - 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), 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. , , ,.

Aripiprazole Mylan Pharma (previously Aripiprazole Pharmathen) Den Europæiske Union - islandsk - EMA (European Medicines Agency)

aripiprazole mylan pharma (previously aripiprazole pharmathen)

mylan pharmaceuticals limited - aripíprazól - schizophrenia; bipolar disorder - psycholeptics - aripiprazol mylan pharma er ætlað til meðferðar á geðklofa hjá fullorðnum og unglingum 15 ára og eldri. sjúklingum mylan pharma er ætlað fyrir meðferð í meðallagi til alvarlega oflæti þáttur í geðhvarfasýki ég ringulreið og til að fyrirbyggja nýja oflæti þáttur í fullorðnir sem upplifað aðallega oflæti þætti og sem oflæti þáttur brugðist við sjúklingum meðferð. sjúklingum mylan pharma er ætlað fyrir meðferð upp til 12 vikur í meðallagi að alvarlega oflæti þáttur í geðhvarfasýki ég röskun á unglingar eru 13 ára og eldri.

Nuedexta Den Europæiske Union - islandsk - EMA (European Medicines Agency)

nuedexta

jenson pharmaceutical services limited - dextromethorphan, kínidín - neurobehavioral manifestations - Önnur lyf í taugakerfinu - nuedexta er ætlað til einkenna meðferðar á pseudobulbar áhrifum (pba) hjá fullorðnum. verkun hefur aðeins verið rannsökuð hjá sjúklingum með undirliggjandi amyotrophic lateral sclerosis eða mænusigg.

Trandate Filmuhúðuð tafla 200 mg Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

trandate filmuhúðuð tafla 200 mg

aspen pharma trading limited - labetalolum hýdróklóríð - filmuhúðuð tafla - 200 mg

Budesonide/Formoterol Teva Pharma B.V. Den Europæiske Union - islandsk - EMA (European Medicines Agency)

budesonide/formoterol teva pharma b.v.

teva pharma b.v. - budesonide, formoterol - astma - lyf til veikindi öndunarvegi sjúkdómum, - budesonid / formoterol teva pharma b. er ætlað fullorðnum 18 ára og eldri. asthmabudesonide/formóteróli sjá pharma b. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β2 adrenoceptor agonist) is appropriate: orin patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β2 adrenoceptor agonists. in patients already adequately controlled on both inhaled corticosteroids and long-acting β2 adrenoceptor agonists.

Trandate Filmuhúðuð tafla 100 mg Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

trandate filmuhúðuð tafla 100 mg

aspen pharma trading limited - labetalolum hýdróklóríð - filmuhúðuð tafla - 100 mg

Xylocain Smyrsli 50 mg/g Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

xylocain smyrsli 50 mg/g

aspen pharma trading limited - lidocainum inn - smyrsli - 50 mg/g

Marcain Stungulyf, lausn 2,5 mg/ml Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain stungulyf, lausn 2,5 mg/ml

aspen pharma trading limited - bupivacainum hýdróklóríð - stungulyf, lausn - 2,5 mg/ml

Marcain Stungulyf, lausn 5 mg/ml Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain stungulyf, lausn 5 mg/ml

aspen pharma trading limited - bupivacainum hýdróklóríð - stungulyf, lausn - 5 mg/ml

Marcain adrenalin Stungulyf, lausn 2,5 mg/ml+5 míkróg/m Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain adrenalin stungulyf, lausn 2,5 mg/ml+5 míkróg/m

aspen pharma trading limited - bupivacainum hýdróklóríð; adrenalinum bítartrat (epinephrinum bítartrat) - stungulyf, lausn - 2,5 mg/ml+5 míkróg/m