Pajjiż: Ingilterra
Lingwa: Ingliż
Sors: MHRA (Medicines & Healthcare Products Regulatory Agency)
Glimepiride
Zentiva Pharma UK Ltd
A10BB12
Glimepiride
4mg
Oral tablet
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 06010201; GTIN: 5013841201784
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 symptoms 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. WHAT IS IN THIS LEAFLET 1. What Amaryl is and what it is used for 2. What you need to know before you take Amaryl 3. How to take Amaryl 4. Possible side effects 5. How to store Amaryl 6. Contents of the pack and other information Amaryl is a medicine taken by mouth to help lower blood sugar. It belongs to a group of medicines called sulfonylureas. Amaryl works by increasing the amount of insulin released from your pancreas. The insulin then lowers your blood sugar levels. WHAT AMARYL IS USED FOR: • Amaryl is used to treat a certain form of diabetes (type 2 diabetes mellitus) when diet, physical exercise and weight reduction alone have not been able to control your blood sugar levels. • You are allergic to: glimepiride or other sulfonylureas (medicines used to lower your blood sugar such as glibenclamide) or sulfonamides (medicines for bacterial infections such as sulfamethoxazole) or any of the other ingredients of this medicine (listed in section 6) • You have insulin dependent diabetes (type 1 diabetes mellitus) • You have diabetic ketoacidosis (a complication of diabetes when your acid level is raised in your body and you may have some of the following signs: fatigue, feeling sick (nausea), frequent urination and muscular stiffness) • You are in a diabetic coma • You have severe kidney disease • You have a severe liver disease Do not take this medicine if any of the above apply to you. If you are not sure, talk to your doctor or pharmacist before taking Amaryl. TALK TO YOUR DOC Aqra d-dokument sħiħ
AMARYL 4MG TABLETS Summary of Product Characteristics Updated 06-Nov-2013 | Zentiva 1. Name of the medicinal product Amaryl 4 mg, tablet 2. Qualitative and quantitative composition [Each tablet contains 4 mg glimepiride.] Excipients: also contains 135.9 mg lactose monohydrate per tablet. For the full list of excipients, see section 6.1. 3. Pharmaceutical form Tablet The tablets are light blue, oblong and scored on both sides. The tablets can be divided into equal doses. 4. Clinical particulars 4.1 Therapeutic indications Amaryl is indicated for the treatment of type 2 diabetes mellitus, when diet, physical exercise and weight reduction alone are not adequate. 4.2 Posology and method of administration For oral administration The basis for successful treatment of diabetes is a good diet, regular physical activity, as well as routine checks of blood and urine. Tablets or insulin cannot compensate if the patient does not keep to the recommended diet. Posology Dose is determined by the results of blood and urinary glucose determinations. The starting dose is 1 mg glimepiride per day. If good control is achieved this dose should be used for maintenance therapy. For the different dose regimens appropriate strengths are available. If control is unsatisfactory the dose should be increased, based on the glycaemic control, in a stepwise manner with an interval of about 1 to 2 weeks between each step, to 2, 3 or 4 mg glimepiride per day. A dose of more than 4 mg glimepiride per day gives better results only in exceptional cases. The maximum recommended dose is 6 mg glimepiride per day. In patients not adequately controlled with the maximum daily dose of metformin, concomitant glimepiride therapy can be initiated. While maintaining the metformin dose, the glimepiride therapy is started with a low dose, and is then titrated up depending on the desired level of metabolic control up to the maximum daily dose. The combination therapy should be initiated under close medical supervision. In patients not adequately controlled with t Aqra d-dokument sħiħ