TabletsTablets
Schedule H (Prescription Required)Sulfonylureas & SecretagoguesCode: 2813

Gliclazide + Pioglitazone + Metformin Tablet (60/15/500 Mg)

Generic Formulation:Gliclazide + Pioglitazone + Metformin Tablet (60/15/500 Mg)
Pack Size:10's
Common Commercial Brand Equivalents:Market reference only

MRP Under Process

Official PMBI MRP is being updated for catalog code 2813.

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Clinical Overview

Metformin Hydrochloride and Gliclazide (Modified Release) combines an insulin sensitizer with a selectively reversible sulfonylurea. Gliclazide selectively binds to pancreatic beta-cell SUR1 receptors with fast on-off association kinetics, restoring the physiological first-phase insulin secretory burst and offering lower hypoglycemia risk than glibenclamide, while metformin reduces hepatic glucose output. Indicated for type 2 diabetes mellitus when monotherapy provides insufficient glycemic control.

AI-assistedClinical summary synthesized from pharmacopoeial references (CDSCO, WHO EML, IP/BP/USP). Not clinician-reviewed. Drug code 2813.Report inaccuracy

Usage Guidelines

Take orally once daily with breakfast with water. Swallow whole; do not crush or chew modified-release tablets. Do not skip breakfast.

General Administration Advice: Adhere strictly to the prescribed dosage, frequency, and treatment course. For oral medications, swallow with sufficient water. Never stop antibiotics, psychiatric medications, or antihypertensives abruptly without clinical direction.

Possible Side Effects

Common: Hypoglycemia, dyspepsia, nausea, diarrhea, abdominal pain, headache. Rare/Severe: Lactic acidosis, prolonged hypoglycemia, and transient transaminitis.

*Note: Individual physiological responses vary. While many patients experience few or no side effects, notify your treating physician if adverse reactions persist or if hypersensitivity (angioedema, skin rash, dyspnea) occurs.

Precautions & Warnings

Boxed warning for lactic acidosis. Contraindicated in severe renal failure (eGFR < 30 mL/min) and severe hepatic failure. Caution with alcohol consumption.

Schedule H (Prescription Required)

This medication is scheduled under statutory drug regulatory frameworks (CDSCO / Drugs & Cosmetics Rules). Dispensing requires a valid medical prescription from a registered medical practitioner. Self-medication or unsupervised dosage adjustment carries significant clinical risks.

Medical Disclaimer: Statutory Clinical Disclaimer: The information provided is for educational and price-transparency purposes only and does not constitute medical advice, clinical diagnosis, or treatment recommendations. Always consult a registered endocrinologist, diabetologist, or qualified physician before initiating, adjusting dosages of, or substituting any antidiabetic or hormonal medication.