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Verapamil Injection

Nishtar Medical University · FDA-approved active Small molecule

Verapamil blocks L-type calcium channels in cardiac and vascular smooth muscle, reducing calcium influx and slowing electrical conduction.

Verapamil blocks L-type calcium channels in cardiac and vascular smooth muscle, reducing calcium influx and slowing electrical conduction. Used for Supraventricular tachycardia (acute termination and rate control), Atrial fibrillation with rapid ventricular response, Hypertension.

At a glance

Generic nameVerapamil Injection
Also known asVerapamil, Calan, Isoptin
SponsorNishtar Medical University
Drug classCalcium channel blocker (non-dihydropyridine)
TargetL-type calcium channel
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Verapamil is a non-dihydropyridine calcium channel blocker that inhibits the inward movement of calcium ions through L-type calcium channels in the heart and blood vessels. This action decreases myocardial contractility, slows atrioventricular (AV) node conduction, and causes vasodilation, resulting in reduced heart rate, blood pressure, and cardiac workload.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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