What is the classification of Verapamil (calcium channel blocker)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 6, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Classification of Verapamil

Verapamil is classified as a non-dihydropyridine calcium channel blocker (CCB) that specifically inhibits calcium influx through the high-voltage-activated L-type calcium channel. 1, 2

Pharmacological Classification Details

  • Verapamil belongs to the phenylalkylamine subclass of calcium channel blockers, which is distinct from dihydropyridines (like amlodipine) and benzothiazepines (like diltiazem) 1, 3
  • It functions as a calcium ion influx inhibitor (slow-channel blocker or calcium ion antagonist) that modulates the influx of ionic calcium across cell membranes 2
  • Verapamil inhibits calcium influx through L-type calcium channels located in:
    • Arterial smooth muscle
    • Cardiac myocytes (contractile cells)
    • Cardiac conduction tissue 1, 2

Pharmacological Effects

  • Verapamil has less selectivity for vasculature compared to dihydropyridine CCBs 1
  • It produces more pronounced effects on:
    • Myocardial contractility (negative inotropic effect)
    • Cardiac pacemaker function
    • Atrioventricular conduction (negative chronotropic and dromotropic effects) 1
  • It causes coronary and peripheral arterial vasodilation 2
  • Verapamil has antiarrhythmic properties, particularly for supraventricular tachyarrhythmias 1, 4
  • It has local anesthetic properties approximately 1.6 times that of procaine on an equimolar basis 2

Clinical Applications

  • Treatment of hypertension through decreased systemic vascular resistance 2, 5
  • Management of angina pectoris, including vasospastic (Prinzmetal's) angina 1, 2
  • Treatment of supraventricular tachyarrhythmias 1
  • Used in atrial fibrillation and flutter for rate control 1

Pharmacokinetic Properties

  • Verapamil is metabolized in the liver by cytochrome P450 3A4 1
  • More than 90% of orally administered verapamil is absorbed 2

Important Clinical Considerations

  • Verapamil should not be used in combination with ivabradine due to risk of severe bradycardia 1
  • It is contraindicated in patients with:
    • Significant left ventricular dysfunction
    • Increased risk for cardiogenic shock
    • PR interval greater than 0.24 second
    • Second or third-degree atrioventricular block without a cardiac pacemaker 1
  • Common adverse effects include:
    • Constipation (especially in elderly individuals)
    • Hypotension
    • Bradycardia
    • Leg edema 1, 3

Distinguishing Features from Other Calcium Channel Blockers

  • Unlike dihydropyridine CCBs (amlodipine, nifedipine), verapamil has significant effects on cardiac conduction and contractility 1, 6
  • Verapamil and diltiazem (non-dihydropyridines) are more myocardial-selective, while dihydropyridines are more vascular-selective 6
  • Some research suggests verapamil may also have beta-blocking properties, though this is not its primary mechanism 7

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.