MITHEGAN XL 16 Milligram Prolonged Release Capsules Ireland - English - HPRA (Health Products Regulatory Authority)

mithegan xl 16 milligram prolonged release capsules

pharmathen s.a. - galantamine hydrobromide - prolonged release capsules - 16 milligram

MITHEGAN XL 24 Milligram Prolonged Release Capsules Ireland - English - HPRA (Health Products Regulatory Authority)

mithegan xl 24 milligram prolonged release capsules

pharmathen s.a. - galantamine hydrobromide - prolonged release capsules - 24 milligram

QUODIXOR 150 Base Milligrams Film Coated Tablet Ireland - English - HPRA (Health Products Regulatory Authority)

quodixor 150 base milligrams film coated tablet

pharmathen s.a. - ibandronate sodium monohydrate - film coated tablet - 150 base milligrams - bisphosphonates

REFAZ 250 Milligram Film Coated Tablet Ireland - English - HPRA (Health Products Regulatory Authority)

refaz 250 milligram film coated tablet

pharmathen s.a. - levofloxacin hemihydrate - film coated tablet - 250 milligram - fluoroquinolones

REFAZ 500 Milligram Film Coated Tablet Ireland - English - HPRA (Health Products Regulatory Authority)

refaz 500 milligram film coated tablet

pharmathen s.a. - levofloxacin hemihydrate - film coated tablet - 500 milligram - fluoroquinolones

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.

Grepid European Union - English - EMA (European Medicines Agency)

grepid

pharmathen s.a. - clopidogrel (as besilate) - peripheral vascular diseases; stroke; myocardial infarction - antithrombotic agents - prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six 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.prevention of atherothrombotic and thromboembolic events in atrial fibrillationin adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin-k antagonists and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke.

Sabervel European Union - English - EMA (European Medicines Agency)

sabervel

pharmathen s.a. - irbesartan - hypertension - agents acting on the renin-angiotensin system - sabervel is indicated in adults for the treatment of essential hypertension.it is also indicated for the treatment of renal disease in adult patients with hypertension and type 2 diabetes mellitus as part of an antihypertensive medicinal product regimen.