TabletsTablets
Schedule H (Prescription Required)Antihypertensives & BP RegulatorsCode: 2859

S-Metoprolol + Telmisartan Tablet (25/ 20Mg)

Generic Formulation:S-Metoprolol + Telmisartan Tablet (25/ 20Mg)
Pack Size:10's

MRP Under Process

Official PMBI MRP is being updated for catalog code 2859.

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Clinical Overview

Telmisartan and Metoprolol Succinate (Extended-Release) combines an ARB with a cardioselective beta-1 adrenergic blocker. Telmisartan reduces afterload and inhibits vascular remodeling, while extended-release metoprolol attenuates sympathetic nervous activity, reduces resting and exercise heart rates, lowers myocardial oxygen demand, and stabilizes cardiac rhythm. Indicated for hypertension associated with coronary artery disease, stable angina, post-myocardial infarction, or resting tachycardia.

AI-assistedClinical summary synthesized from pharmacopoeial references (CDSCO, WHO EML, IP/BP/USP). Not clinician-reviewed. Drug code 2859.Report inaccuracy

Usage Guidelines

Take orally once daily in the morning with a glass of water, with or immediately after food. Swallow whole; do not crush or chew extended-release tablets. Never discontinue abruptly; taper gradually over 1-2 weeks.

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: Bradycardia (slow heart rate), dizziness, fatigue, cold extremities, hypotension, mild shortness of breath. Rare/Severe: Boxed warning: Exacerbation of angina/myocardial infarction upon abrupt cessation; fetal toxicity, heart block, and bronchospasm in asthmatics.

*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: Abrupt cessation can precipitate severe angina, ventricular arrhythmias, or myocardial infarction. Black box warning for fetal toxicity. Contraindicated in severe bradycardia, second- or third-degree AV block, and cardiogenic shock.

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.