TabletsTablets
Schedule H (Prescription Required)DiureticsCode: 2137

Telmisartan 40mg + Cilnidipine 10mg + Chlorthalidone 12.5mg Tablets

Generic Formulation:Telmisartan 40mg, Cilnidipine 10mg and Chlorthalidone 12.5mg Tablets
Pack Size:10's
Common Commercial Brand Equivalents:Market reference only
Jan Aushadhi MRP
₹28.13
Brand Estimate*
₹194.45
Estimated Savings:₹166.32 (86% saved)
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*Statutory price across 21,118 listed Kendras
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Clinical Overview

Telmisartan and Chlorthalidone is a potent, long-acting dual antihypertensive combination. Telmisartan delivers selective 24-hour AT1 receptor blockade, while chlorthalidone, a long-acting monosulfonamyl thiazide-like diuretic with a terminal elimination half-life of 40-60 hours, provides sustained intravascular volume and vascular resistance reduction throughout day and night. Indicated for stage 2 hypertension and nocturnal/early morning hypertension surges.

AI-assistedClinical summary synthesized from pharmacopoeial references (CDSCO, WHO EML, IP/BP/USP). Not clinician-reviewed. Drug code 2137.Report inaccuracy

Usage Guidelines

Take orally once daily in the morning with water, with or without meals. Maintain consistent daily hydration. Monitor home blood pressure regularly.

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: Dizziness, fatigue, electrolyte imbalances (hypokalemia, hyponatremia), hyperuricemia (gout flares), orthostatic lightheadedness. Rare/Severe: Boxed warning: Fetal toxicity; acute renal failure, severe hypokalemia, and cardiac arrhythmias.

*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

Black box warning: Fetal toxicity. Contraindicated in pregnancy, anuria, and severe hepatic failure. Baseline and periodic monitoring of serum potassium, sodium, and creatinine is essential. Caution in patients with history of gout.

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 medical practitioner or qualified cardiologist/pharmacist before initiating, altering, or substituting any cardiovascular medication.