Procainamide

Procainamide
PROCAINAMIDE HYDROCHLORIDE® FDA Package Insert
Indications and Usage
Dosage and Administration
Dosage Forms and Strengths
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Overdosage
Description
Clinical Pharmacology
Nonclinical Toxicology
Clinical Studies
How Supplied/Storage and Handling
Patient Counseling Information
Labels and Packages
Clinical Trials on Procainamide
ClinicalTrials.gov

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sheng Shi, M.D. [2]

For patient information about Procainamide, click here.

Synonyms / Brand Names: PROCAINAMIDE HYDROCHLORIDE^®

Overview

Procainamide (proe-KANE-a-mide) (INN, trade names Pronestyl®, Procan®, Procanbid®) is a pharmaceutical antiarrhythmic agent used for the medical treatment of cardiac arrhythmias, classified by the Vaughan Williams classification system as class Ia. Procanbid® will no longer be manufactured.¹

It blocks open sodium (Na⁺) channels and prolongs the cardiac action potential (outward potassium (K⁺) currents may be blocked). This results in slowed conduction, and ultimately the decreased rate of rise of the action potential, which may result in widening of QRS on electrocardiogram (ECG). This drug is used for both supraventricular and ventricular arrhythmias. For example, it can be used to convert new-onset atrial fibrillation, though it is suboptimal for this purpose.

Procainamide is administered intravenously or orally.When administered intravenously, a loading dose should first be given, though care should be taken not to cause hypotension.Procainamide's active metabolite is N-acetyl procainamide, which is excreted by the kidneys and the renal system.

Adverse effects include rash, myalgia, hypersensitivity reactions (fever, agranulocytosis), Drug-Induced Lupus Erythematosus (particularly in slow-acetylators), and proarrhythmic effects (e.g., torsades de pointes). Treatment with procainamide can cause antibody production against cellular components, accounting for the systemic lupus erythematosus-like adverse reactions.

Category

Benzamides;Anilines;Sodium channel blockers;Antiarrhythmic agents;Cardiovascular Drugs

FDA Package Insert

PROCAINAMIDE HYDROCHLORIDE injection, solution

Indications and Usage | Dosage and Administration | Dosage Forms and Strengths | Contraindications | Warnings and Precautions | Adverse Reactions | Drug Interactions | Use in Specific Populations | Overdosage | Description | Clinical Pharmacology | Nonclinical Toxicology | Clinical Studies | How Supplied/Storage and Handling | Patient Counseling Information | Labels and Packages

BOXED WARNING See full prescribing information for complete boxed warning. WARNING: The prolonged administration of procainamide often leads to the development of a positive anti-nuclear antibody (ANA) test, with or without symptoms of a lupus erythematosus-like syndrome. If a positive ANA titer develops, the benefit versus risks of continued procainamide therapy should be assessed.

Taking Alcohol with Procainamide

Alcohol-(Procainamide) interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

References

Template:Antiarrhythmic agents