AURO-RAMIPRIL TABLETS 5 ramipril 5mg tablet bottle

Valsts: Austrālija

Valoda: angļu

Klimata pārmaiņas: Department of Health (Therapeutic Goods Administration)

Aktīvā sastāvdaļa:

ramipril, Quantity: 5 mg

Pieejams no:

Arrotex Pharmaceuticals Pty Ltd

SNN (starptautisko nepatentēto nosaukumu):

Ramipril

Zāļu forma:

Tablet, uncoated

Kompozīcija:

Excipient Ingredients: pregelatinised maize starch; croscarmellose sodium; sodium stearylfumarate; lactose monohydrate; iron oxide red; sodium bicarbonate

Ievadīšanas:

Oral

Vienības iepakojumā:

30

Receptes veids:

(S4) Prescription Only Medicine

Ārstēšanas norādes:

? Treatment of hypertension. Data are currently not available to support the use of Ramipril in renovascular hypertension. ,? Post MI heart failure ,? Prevention of progressive renal failure in patients with persistent proteinuria in excess of 1 g/day. ,? For reducing the risk of myocardial infarction, stroke, cardiovascular death or the need for revascularisation procedures in patients 55 years of age or more who have clinical evidence of coronary artery disease, stroke, or peripheral vascular disease. ,? For reducing the risk of myocardial infarction, stroke, cardiovascular death or revascularization procedures in diabetic patients 55 years or more with one or more of the following risk factors: systolic blood pressure >160mmHg or diastolic blood pressure >90mmHg (or on antihypertensive treatment); total cholesterol >5.2mmol/L; HDL cholesterol <0.9mmol/L; current smoker; known microalbuminuria; any evidence of previous vascular disease.

Produktu pārskats:

Visual Identification: Light pink coloured mottled, flat faced bevel edged round uncoated tablet debossed with 'H' & '19' separated by score line on one side and plain on other side; Container Type: Bottle; Container Material: HDPE; Container Life Time: 2 Years; Container Temperature: Store below 25 degrees Celsius; Container Closure: Child resistant closure

Autorizācija statuss:

Registered

Autorizācija datums:

2011-10-06