TORLIPTIN VM 500

Torliptin VM 500 contains Vildagliptin, a member of the islet enhancer class, is a potent and selective DPP-4 inhibitor and Metformin, a biguanide with antihyperglycaemic effects, lowering both basal and postprandial plasma glucose.

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Product Description

Description: Torliptin VM 500 contains Vildagliptin, a member of the islet enhancer class, is a potent and selective DPP-4 inhibitor and Metformin, a biguanide with antihyperglycaemic effects, lowering both basal and postprandial plasma glucose.

Pharmaceutical Dosage Form: Tablet

Route of Administration: Oral

Composition: Each film coated tablet contains:

Vildagliptin      IP                                        50 mg

Metformin Hydrochloride IP                        500 mg

Excipients                                       q.s.

Mechanism of Action: Vildagliptin results in a rapid and complete inhibition of DPP-4 activity, resulting in increased fasting and postprandial endogenous levels of the incretin hormones GLP1 (glucagon-like peptide 1) and GIP (glucose-dependent insulinotropic polypeptide). Metformin decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization.

Indications: Torliptin VM 500 is indicated for the treatment of patients with type II diabetes mellitus when diet, exercise and single agent does not result in adequate glycemic control.

Dosage: As directed by the physician.

Storage: Store protected from moisture, at a temperature not exceeding 30ºC.

Presentation: 10 x 15

Side effects: The following adverse reactions may occur:

Hypoglycaemia

Tremor

Headache

dizziness

Nausea

Contraindications: Torliptin VM 500 is contraindicated in patients with:

Known hypersensitivity to Vildaglitin, Metformin or any of the components of this product.

Any type of acute metabolic acidosis (such as lactic acidosis, diabetic ketoacidosis)

Diabetic pre-coma

Severe renal failure (GFR < 30 ml/min)

Acute conditions with the potential to alter renal function, such as:

dehydration

severe infection

shock

intravascular administration of iodinated contrast agents.

Acute or chronic disease which may cause tissue hypoxia, such as:

cardiac or respiratory failure,

recent myocardial infarction,

shock

Hepatic impairment

Acute alcohol intoxication, alcoholism

Breast-feeding

Drug Interactions:

Alcohol

NSAIDs

ACE Inhibitors

Angiotensin II Receptor Antagonists

Diuretics