Страна: Великобритания
Език: английски
Източник: MHRA (Medicines & Healthcare Products Regulatory Agency)
Candesartan cilexetil
Neon Healthcare Ltd
C09CA06
Candesartan cilexetil
16mg
Oral tablet
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 02050502; GTIN: 5035382000411
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. This includes any possible side effects not listed in this leaflet. See section 4. What is in this leaflet: 1. What Amias is and what it is used for 2. What you need to know before you take Amias 3. How to take Amias 4. Possible side effects 5. How to store Amias 6. Contents of the pack and other information 1. WHAT AMIAS IS AND WHAT IT IS USED FOR The name of your medicine is Amias. The active ingredient is candesartan cilexetil. This belongs to a group of medicines called angiotensin II receptor antagonists. It works by making your blood vessels relax and widen. This helps to lower your blood pressure. It also makes it easier for your heart to pump blood to all parts of your body. This medicine is used for: • treating high blood pressure (hypertension) in adult patients and in children and adolescents aged 6 to under 18 years. • treating adult heart failure patients with reduced heart muscle function, when Angiotensin Converting Enzyme (ACE) inhibitors cannot be used or in addition to ACE inhibitors when symptoms persist despite treatment and mineralocorticoid receptor antagonists (MRA) cannot be used (ACE inhibitors and MRAs are medicines used to treat heart failure). 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE AMIAS Do not take Amias • if you are allergic to candesartan cilexetil or any of the other ingredients of this medicine (listed in section 6). • if you are more than 3 months pregnant (it is also better to avoid Amias in early pregnancy – see pregnancy section). • if you have severe liver disease or biliary obstruction (a problem with the drain Прочетете целия документ
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Amias 16 mg Tablets. 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each tablet contains 16 mg candesartan cilexetil. Each tablet contains 81.3 mg lactose monohydrate. For a full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Tablet. Amias 16 mg Tablets are round light pink tablets with one convex side and one scored flat side, embossing 16 on convex side. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Amias is indicated for the: • Treatment of essential hypertension in adults. • Treatment of hypertension in children and adolescents aged 6 to <18 years. • Treatment of adult patients with heart failure and impaired left ventricular systolic function (left ventricular ejection fraction ≤ 40%) when Angiotensin Converting Enzyme (ACE) inhibitors are not tolerated or as add-on therapy to ACE inhibitors in patients with symptomatic heart failure, despite optimal therapy, when mineralocorticoid receptor antagonists are not tolerated (see sections 4.2, 4.4, 4.5, and 5.1). 4.2 POSOLOGY AND METHOD OF ADMINISTRATION Posology in Hypertension The recommended initial dose and usual maintenance dose of Amias is 8 mg once daily. Most of the antihypertensive effect is attained within 4 weeks. In some patients whose blood pressure is not adequately controlled, the dose can be increased to 16 mg once daily and to a maximum of 32 mg once daily. Therapy should be adjusted according to blood pressure response. Amias may also be administered with other antihypertensive agents (see sections 4.3, 4.4, 4.5 and 5.1. Addition of hydrochlorothiazide has been shown to have an additive antihypertensive effect with various doses of Amias. _Older people _ No initial dose adjustment is necessary in elderly patients. _Patients with intravascular volume depletion _ An initial dose of 4 mg may be considered in patients at risk for hypotension, such as patients with possible volume depletion (see section 4.4). _Patients with renal impairment _ The starting dose is Прочетете целия документ