Fingolimod Mylan Den europeiske union - norsk - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - fingolimod hydrochloride - multippel sklerose, relapsing-remitting - immunsuppressive - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 og 5. 1) or patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Den europeiske union - norsk - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - klopidogrelhydroklorid - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antithrombotic agents - , , , , 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. , , ,.

Abacavir /Lamivudin Mylan 600 mg / 300 mg Norge - norsk - Statens legemiddelverk

abacavir /lamivudin mylan 600 mg / 300 mg

mylan ab - abakavirhydroklorid / lamivudin - tablett, filmdrasjert - 600 mg / 300 mg

Ampicillin Mylan 1 g Norge - norsk - Statens legemiddelverk

ampicillin mylan 1 g

mylan hospital as - ampicillinnatrium - pulver til injeksjons-/infusjonsvæske, oppløsning - 1 g

Ampicillin Mylan 2 g Norge - norsk - Statens legemiddelverk

ampicillin mylan 2 g

mylan hospital as - ampicillinnatrium - pulver til injeksjons-/infusjonsvæske, oppløsning - 2 g

Cetirizin Mylan 10 mg Norge - norsk - Statens legemiddelverk

cetirizin mylan 10 mg

mylan ab - cetirizindihydroklorid - tablett, filmdrasjert - 10 mg

Escitalopram Mylan 10 mg Norge - norsk - Statens legemiddelverk

escitalopram mylan 10 mg

mylan ab - escitalopramoksalat - tablett, filmdrasjert - 10 mg

Escitalopram Mylan 5 mg Norge - norsk - Statens legemiddelverk

escitalopram mylan 5 mg

mylan ab - escitalopramoksalat - tablett, filmdrasjert - 5 mg

Escitalopram Mylan 20 mg Norge - norsk - Statens legemiddelverk

escitalopram mylan 20 mg

mylan ab - escitalopramoksalat - tablett, filmdrasjert - 20 mg