Clopidogrel Viatris (previously Clopidogrel Taw Pharma) European Union - English - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - clopidogrel besilate - peripheral vascular diseases; stroke; myocardial infarction - 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), 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 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 5.1.

Pirfenidone Viatris European Union - English - EMA (European Medicines Agency)

pirfenidone viatris

viatris limited - pirfenidone - idiopathic pulmonary fibrosis; lung diseases; respiratory tract diseases - immunosuppressants - pirfenidone viatris is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

Dapagliflozin Viatris European Union - English - EMA (European Medicines Agency)

dapagliflozin viatris

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - drugs used in diabetes - type 2 diabetes mellitusdapagliflozin viatris is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance.- in addition to other medicinal products for the treatment of type 2 diabetes.for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4.4, 4.5 and 5.1.heart failuredapagliflozin viatris is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction.chronic kidney diseasedapagliflozin viatris is indicated in adults for the treatment of chronic kidney disease.

Aripiprazole Mylan Pharma (previously Aripiprazole Pharmathen) European Union - English - EMA (European Medicines Agency)

aripiprazole mylan pharma (previously aripiprazole pharmathen)

mylan pharmaceuticals limited - aripiprazole - schizophrenia; bipolar disorder - psycholeptics - aripiprazole mylan pharma is indicated for the treatment of schizophrenia in adults and in adolescents aged 15 years and older.aripiprazole mylan pharma is indicated for the treatment of moderate to severe manic episodes in bipolar i disorder and for the prevention of a new manic episode in adults who experienced predominantly manic episodes and whose manic episodes responded to aripiprazole treatment.aripiprazole mylan pharma is indicated for the treatment up to 12 weeks of moderate to severe manic episodes in bipolar i disorder in adolescents aged 13 years and older.

Traumon Gel 10% Malta - English - Medicines Authority

traumon gel 10%

viatris healthcare gmbh lutticher strasse 5 53842 troisdorf, germany - etofenamate - gel - etofenamate 100 mg/g - topical products for joint and muscular pain

Atorvastatin Viatris 10 mg film-coated tablets Malta - English - Medicines Authority

atorvastatin viatris 10 mg film-coated tablets

viatris limited damastown industrial park, mulhuddart, dublin 15, dublin, ireland - film-coated tablet - atorvastatin 10 mg - lipid modifying agents

Atorvastatin Viatris 20 mg film-coated tablets Malta - English - Medicines Authority

atorvastatin viatris 20 mg film-coated tablets

viatris limited damastown industrial park, mulhuddart, dublin 15, dublin, ireland - film-coated tablet - atorvastatin 20 mg - lipid modifying agents

Atorvastatin Viatris 40 mg film-coated tablets Malta - English - Medicines Authority

atorvastatin viatris 40 mg film-coated tablets

viatris limited damastown industrial park, mulhuddart, dublin 15, dublin, ireland - film-coated tablet - atorvastatin 40 mg - lipid modifying agents

Atorvastatin Viatris 80 mg film-coated tablets Malta - English - Medicines Authority

atorvastatin viatris 80 mg film-coated tablets

viatris limited damastown industrial park, mulhuddart, dublin 15, dublin, ireland - film-coated tablet - atorvastatin 80 mg - lipid modifying agents

Quetiapine/VIATRIS 25 mg film-coated tablets Malta - English - Medicines Authority

quetiapine/viatris 25 mg film-coated tablets

viatris limited damastown industrial park, mulhuddart, dublin 15, dublin, ireland - film-coated tablet - quetiapine fumarate 25 mg - psycholeptics