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DRUG RECORD

 

PROPRANOLOL

OVERVIEW
Propranolol

 

Introduction

Propranolol is a nonselective beta adrenergic receptor blocker (beta blocker) that is widely used for the therapy of hypertension, cardiac arrhythmias, angina pectoris and hyperthyroidism. Propranolol has yet to be convincingly associated with clinically apparent liver injury and is often used in patients with liver disease and cirrhosis.

 

Background

Propranolol (proe pran' oh lol) was the prototype beta-blocker developed for therapy of hypertension and is considered nonselective, acting on both the beta-1 and beta-2 adrenergic receptors. Beta-1 adrenergic blockade reduces the heart rate and myocardial contractility by slowing AV conduction and suppressing automaticity. Beta-2 blockade also affects peripheral vascular resistance and can cause bronchospasm and hypoglycemia. The beta-2 blockade is responsible for the majority of adverse effects associated with propranolol. Propranolol was approved for use in the United States in 1967 and is still commonly used, with more than 6 million prescriptions filled yearly. Propranolol is indicated for the management of hypertension, angina pectoris, idiopathic hypertrophic subaortic stenosis and prevention of migraine and vascular headaches. Propranolol is used off-label for essential tremor, decreasing the heart rate in patients with hyperthyroidism, and prevention of recurrent variceal hemorrhage. Propranolol is available in multiple generic forms and under the trade name of Inderal in tablets of 10, 20, 40, 60, 80 and 90 mg, as well as extended- or sustained-release capsules of 60, 80, 120 and 160 mg. Liquid formulations for oral and parenteral administration are also available. The typical dose of propranolol in adults is 60 to 240 mg daily in 2 divided doses (one with extended release formulations), with subsequent dose modification based upon efficacy and tolerance. Common side effects of propranolol include bradycardia, hypotension, fatigue, dizziness, depression, memory loss, impotence, cold limbs and less commonly severe hypotension, heart failure and bronchospasm. Sudden withdrawal can trigger rebound hypertension. Beta blockers are contraindicated in patients with asthma, bradycardia and heart failure and should be used cautiously in the elderly and in patients with diabetes.

 

Hepatotoxicity

Mild to moderate elevations in serum aminotransferase levels occur in less than 2% of patients on propranolol and are usually transient and asymptomatic, resolving even with continuation of therapy. Despite its widespread use, propranolol has not been convincingly linked to instances of clinically apparent liver injury; the few cases reported have generally occurred in patients who were receiving other well known hepatotoxic agents or where associated with serum enzyme elevations only.

 

Mechanism of Injury

Propranolol undergoes rapid first-pass metabolism by the liver but has little or no effect on P450 activity. The reason why it rarely causes liver injury is unknown; other beta-blockers with similar chemical structures have been linked to cases of clinically apparent, idiosyncratic liver injury.

[References are provided in the overview on Beta-Adrenergic Blocking Agents.]

 

Drug Class:Beta-Adrenergic Blocking Agents

 

 

 

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PRODUCT INFORMATION
Propranolol

 

REPRESENTATIVE TRADE NAMES
Propranolol – Generic, Inderal®

 

DRUG CLASS
Beta-Adrenergic Blocking Agents

 

COMPLETE LABELING

Product labeling at DailyMed, National Library of Medicine, NIH

 

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DRUG CAS REGISTRY NUMBER MOLECULAR FORMULA STRUCTURE
Propranolol 525-66-6 C16-H21-N-O2 Propranolol Chemical Structure

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OTHER REFERENCE LINKS
Propranolol

 

  1. PubMed logoRecent References on Propranolol

  2. Clinical Trials logoTrials on Propranolol

  3. TOXLINE logoTOXLINE Citations on Propranolol

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