Rosuvastatin Teva Pharma 40 mg Film-coated Tablets Ai-len - Tiếng Anh - HPRA (Health Products Regulatory Authority)

rosuvastatin teva pharma 40 mg film-coated tablets

teva b.v. - rosuvastatin - film-coated tablet - 40 milligram(s) - hmg coa reductase inhibitors; rosuvastatin - hmg-coa reductase inhibitors - treatment of hypercholesterolaemia adults, adolescents and children aged 6 years or older with primary hypercholesterolaemia (type iia including heterozygous familial hypercholesterolaemia) or mixed dyslipidaemia (type iib) as an adjunct to diet when response to diet and other non-pharmacological treatments (e.g. exercise, weight reduction) is inadequate. homozygous familial hypercholesterolaemia as an adjunct to diet and other lipid lowering treatments (e.g. ldl apheresis) or if such treatments are not appropriate. prevention of cardiovascular events prevention of major cardiovascular events in patients who are estimated to have a high risk for a first cardiovascular even

FOMEPIZOLE EUSA PHARMA Ai-len - Tiếng Anh - HPRA (Health Products Regulatory Authority)

fomepizole eusa pharma

eusa pharma (uk) limited - fomepizole sulphate - concentrate for soln for inf - 5 mg/ml - fomepizole

Clopidogrel Teva Pharma (previously Clopidogrel HCS) Liên Minh Châu Âu - Tiếng Anh - EMA (European Medicines Agency)

clopidogrel teva pharma (previously clopidogrel hcs)

teva b.v.  - clopidogrel (as hydrochloride) - myocardial infarction; peripheral vascular diseases; stroke - antithrombotic agents - 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.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.

Telmisartan Teva Pharma Liên Minh Châu Âu - Tiếng Anh - EMA (European Medicines Agency)

telmisartan teva pharma

teva b.v. - telmisartan - hypertension - agents acting on the renin-angiotensin system - treatment of essential hypertension in adults.

AMISULPRIDE SANDOZ PHARMA amisulpride 100 mg uncoated tablet blister pack Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

amisulpride sandoz pharma amisulpride 100 mg uncoated tablet blister pack

southern cross pharma pty ltd - amisulpride, quantity: 100 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; microcrystalline cellulose; magnesium stearate; sodium starch glycollate type a; hypromellose - amisulpride is indicated for the treatment of acute and chronic schizophrenic disorders, in which positive symptoms (such as delusions, hallucinations, thought disorders) and/or negative symptoms (such as blunted affect, emotional and social withdrawal) are prominent, including patients characterised by predominant negative symptoms.

AMISULPRIDE SANDOZ PHARMA amisulpride 200 mg uncoated tablet blister pack Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

amisulpride sandoz pharma amisulpride 200 mg uncoated tablet blister pack

southern cross pharma pty ltd - amisulpride, quantity: 200 mg - tablet, uncoated - excipient ingredients: hypromellose; lactose monohydrate; microcrystalline cellulose; magnesium stearate; sodium starch glycollate type a - amisulpride is indicated for the treatment of acute and chronic schizophrenic disorders, in which positive symptoms (such as delusions, hallucinations, thought disorders) and/or negative symptoms (such as blunted affect, emotional and social withdrawal) are prominent, including patients characterised by predominant negative symptoms.

AMISULPRIDE SANDOZ PHARMA amisulpride 400 mg uncoated tablet blister pack Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

amisulpride sandoz pharma amisulpride 400 mg uncoated tablet blister pack

southern cross pharma pty ltd - amisulpride, quantity: 400 mg - tablet, uncoated - excipient ingredients: sodium starch glycollate type a; hypromellose; microcrystalline cellulose; magnesium stearate; lactose monohydrate - amisulpride is indicated for the treatment of acute and chronic schizophrenic disorders, in which positive symptoms (such as delusions, hallucinations, thought disorders) and/or negative symptoms (such as blunted affect, emotional and social withdrawal) are prominent, including patients characterised by predominant negative symptoms.

Sodium Nitrite Hope Pharmaceuticals 30 mg/mL Solution for Injection Ai-len - Tiếng Anh - HPRA (Health Products Regulatory Authority)

sodium nitrite hope pharmaceuticals 30 mg/ml solution for injection

hope pharmaceuticals ltd - sodium nitrite - solution for injection - 30 milligram(s)/millilitre - sodium nitrite

Sodium Thiosulfate Hope Pharmaceuticals 250 mg/mL Solution for Injection Ai-len - Tiếng Anh - HPRA (Health Products Regulatory Authority)

sodium thiosulfate hope pharmaceuticals 250 mg/ml solution for injection

hope pharmaceuticals ltd - sodium thiosulfate - solution for injection - 250 milligram(s)/millilitre - antidotes; thiosulfate

CABAZITAXEL EVER PHARMA cabazitaxel 60 mg/6 mL concentrated solution for injection vial Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

cabazitaxel ever pharma cabazitaxel 60 mg/6 ml concentrated solution for injection vial

interpharma pty ltd - cabazitaxel, quantity: 60 mg - injection, concentrated - excipient ingredients: polysorbate 80; ethanol absolute; macrogol 300; citric acid - cabazitaxel ever pharma in combination with prednisone or prednisolone is indicated for the treatment of patients with metastatic castration resistant prostate cancer previously treated with a docetaxel containing regimen.