Pajjiż: Ingilterra
Lingwa: Ingliż
Sors: MHRA (Medicines & Healthcare Products Regulatory Agency)
Ramipril
Sandoz Ltd
C09AA05
Ramipril
5mg
Oral capsule
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 02050501
PACKAGE LEAFLET: INFORMATION FOR THE USER RAMIPRIL 1.25MG, 2.5MG, 5MG AND 10MG CAPSULES READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS MEDICINE BECAUSE IT CONTAINS IMPORTANT INFORMATION FOR YOU. • Keep this leaflet. You may need to read it again. • If you have any further questions, ask your doctor or pharmacist. • This medicine has been prescribed for you only. Do not pass it on to others. It may harm them even if their signs of illness are the same as yours. • If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET: 1. WHAT RAMIPRIL CAPSULES ARE AND WHAT THEY ARE USED FOR 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE RAMIPRIL CAPSULES 3. HOW TO TAKE RAMIPRIL CAPSULES 4. POSSIBLE SIDE EFFECTS 5. HOW TO STORE RAMIPRIL CAPSULES 6. CONTENTS OF THE PACK AND OTHER INFORMATION 1. WHAT RAMIPRIL CAPSULES ARE AND WHAT THEY ARE USED FOR Ramipril capsules contain a medicine called ramipril. This belongs to a group of medicines called ACE inhibitors (Angiotensin Converting Enzyme Inhibitors). RAMIPRIL CAPSULES WORK BY: decreasing your body’s production of substances that could raise your blood pressure making your blood vessels relax and widen making it easier for your heart to pump blood around your body. RAMIPRIL CAPSULES CAN BE USED: to treat high blood pressure (hypertension) to reduce the risk or delay the worsening of kidney problems (whether or not you have diabetes) to treat your heart when it cannot pump enough blood to the rest of your body (heart failure) as treatment following heart attack (myocardial infarction) complicated with heart failure. 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE RAMIPRIL CAPSULES DO NOT TAKE Ramipril capsules and TELL your doctor if: you are ALLERGIC to the active substance or any other ingredients of this medicine (listed in section 6). you are allergic to any other ACE inhibitor medicine. Signs of an allergic reaction Aqra d-dokument sħiħ
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Ramipril 5mg Capsules 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each capsule contains 5.0mg ramipril. For the full list of excipients, see section 6.1 3 PHARMACEUTICAL FORM Capsule, hard Hard gelatin capsule (size 4), light grey body and green cap. Marked R on the cap and 5 on the body. The capsule contains white or almost white powder. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS - Treatment of hypertension. - Treatment of renal disease. o Incipient glomerular diabetic nephropathy as defined by the presence of microalbuminuria, o Manifest glomerular diabetic nephropathy as defined by macroproteinuria in patients with at least one cardiovascular risk factor (see section 5.1), o Manifest glomerular non diabetic nephropathy as defined by macroproteinuria ≥ 3g/day (see section 5.1). - Treatment of symptomatic heart failure. - Secondary prevention after acute myocardial infarction: reduction of mortality from the acute phase of myocardial infarction in patients with clinical signs of heart failure when started > 48 hours following acute myocardial infarction. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION _Posology _ It is recommended that Ramipril Capsules are taken each day at the same time of the day. Ramipril Capsules can be taken before, with or after meals, because food intake does not modify its bioavailability (see section 5.2). Ramipril Capsules have to be swallowed with liquid. It must not be chewed or crushed._ _ _ _ _Adults _ _Diuretic-Treated patients: _Hypotension may occur following initiation of therapy with Ramipril Capsules; this is more likely in patients who are being treated concurrently with diuretics (see sections 4.3, 4.4, 4.5, and 5.1). Caution is therefore recommended since these patients may be volume and/or salt depleted. If possible, the diuretic should be discontinued 2 to 3 days before beginning therapy with Ramipril Capsules (see section 4.4). In hypertensive patients in whom the diuretic is not discontinued, therap Aqra d-dokument sħiħ