Vibose 0.2 mg Tablet is an oral antidiabetic medicine containing Voglibose, an alpha-glucosidase inhibitor. It is primarily used to control post-prandial hyperglycaemia (PPHG) in patients with diabetes mellitus when diet, exercise, lifestyle modification, or other antidiabetic therapies alone do not provide adequate glycaemic control. Vibose works locally in the gastrointestinal tract to delay carbohydrate digestion and glucose absorption, thereby reducing post-meal blood glucose spikes.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Alpha-Glucosidase Inhibitor
Vibose 0.2 mg is indicated for:
Reduction of post-prandial hyperglycaemia in diabetes mellitus
Non-insulin-dependent diabetes mellitus (NIDDM) as monotherapy
Use in combination with other oral hypoglycaemic agents
Adjunct therapy with insulin in diabetes mellitus patients
Prevention of progression to type 2 diabetes mellitus in patients with impaired glucose tolerance (when diet and exercise alone are insufficient)
Elderly patients and those with hepatic dysfunction or mild to moderate renal impairment where other OHAs are contraindicated or require caution
Prevention of hypoglycaemia in patients with glycogen storage disease type Ib
Management of non-diabetic hyperinsulinaemia to prevent hypoglycaemic episodes
Steroid-induced diabetes mellitus (clinical data limited)
Voglibose inhibits intestinal alpha-glucosidase enzymes located in the brush border of the small intestine. These enzymes are responsible for breaking down complex carbohydrates into absorbable monosaccharides. By inhibiting these enzymes, Vibose delays carbohydrate digestion, resulting in reduced glucose absorption after meals. This leads to lower post-prandial blood glucose levels and a modest long-term reduction in HbA1c.
Adults:
Usual dose: 0.2 mg orally, three times daily, taken immediately before each main meal
Dose may be increased to 0.3 mg three times daily if required
Geriatric Patients:
Recommended to start at a lower dose (e.g. 0.1 mg three times daily)
Careful monitoring of blood glucose and gastrointestinal symptoms is advised
Pediatric Use:
Safety and efficacy in children have not been established
Use Vibose with caution when administered with:
Other antidiabetic drugs such as sulfonylureas, biguanides, insulin, and insulin resistance-improving agents
Drugs that enhance hypoglycaemic effect: beta-blockers, salicylates, MAO inhibitors, fibrates, warfarin
Drugs that reduce hypoglycaemic effect: adrenaline, corticosteroids, thyroid hormones
Vibose 0.2 mg is contraindicated in patients with:
Known hypersensitivity to voglibose or any excipients
Diabetic ketoacidosis or diabetic pre-coma
Severe infections, major trauma, or peri-operative conditions
Gastrointestinal obstruction or conditions predisposing to obstruction
Common adverse effects include:
Diarrhoea, loose stools, abdominal pain, constipation
Flatulence, nausea, vomiting, heartburn
Loss of appetite
Rare but serious effects may include:
Hypoglycaemia (when combined with other OHAs)
Liver dysfunction, hepatitis, jaundice
Anaemia, edema, blurred vision, weakness, hyperkalaemia
Pregnancy: Safety not established; use only if clearly needed
Lactation: Not recommended due to limited safety data
Monitor blood glucose closely when used with other antidiabetic agents
Use with caution in patients with gastrointestinal disorders, hepatic or renal impairment
Special care is required in elderly patients
Overdose does not usually cause hypoglycaemia. Symptoms may include transient gastrointestinal discomfort such as flatulence, diarrhoea, and abdominal pain. Serious systemic effects are unlikely.
Store in a cool and dry place.
Protect from light and keep out of reach of children.
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