Details
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Marketing Authorization (Malaysia): MAL15065037AZ, indicating approval by the Malaysian National Pharmaceutical Regulatory Agency (NPRA).
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Manufacturer: Merck Sante S.A.S., France; marketed and distributed in Malaysia by Merck Sdn. Bhd.
Content
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Active Ingredient: Each extended-release tablet contains 1000 mg metformin hydrochloride, corresponding to 780 mg metformin base.
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Excipients: For a full list of excipients, please refer to the product's Summary of Product Characteristics.
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Formulation: White to off-white, capsule-shaped, biconvex tablet, debossed on one side with '1000' and on the other side with 'Merck'.
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Pack Size: 60 tablets.
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Manufacturer: Merck Sante S.A.S., France; marketed and distributed in Malaysia by Merck Sdn. Bhd.
Indications
Glucophage XR 1000mg Tablets are indicated for:
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Monotherapy or combination therapy with other oral antidiabetic agents or insulin for the treatment of type 2 diabetes mellitus in adults when dietary management and exercise alone do not result in adequate glycaemic control.
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Reduction of the risk or delay of the onset of type 2 diabetes mellitus in overweight adults with impaired glucose tolerance (IGT), impaired fasting glucose (IFG), and/or increased HbA1c who are at high risk for developing overt type 2 diabetes mellitus and still progressing towards type 2 diabetes mellitus despite implementing intensive lifestyle changes for 3–6 months.
Instructions for Use
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Dosage:
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Adults with normal renal function (GFR ≥90 mL/min):
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The usual starting dose is 500 mg taken once daily with the evening meal.
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After 10 to 15 days, the dose should be adjusted based on blood glucose measurements.
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The maximum recommended dose is 2000 mg daily, taken as a single dose with the evening meal.
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Transfer from other oral antidiabetic agents:
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Discontinue the other agent and initiate Glucophage XR at the same daily dose.
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Combination with insulin:
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Initiate Glucophage XR at 500 mg daily with the evening meal.
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Adjust the insulin dose based on blood glucose measurements.
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Administration:
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Precautions:
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Contraindicated in patients with hypersensitivity to metformin, metabolic acidosis, diabetic coma, or severely impaired renal function (GFR <30 mL/min).
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Use with caution in patients with renal or hepatic impairment.
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Temporarily discontinue use if dehydration occurs or in the presence of conditions that alter renal function.
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Monitor renal function regularly during treatment.
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Avoid alcohol consumption during treatment.
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