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Procainamide

Published: July 26, 2026Updated: August 24, 2026

Procainamide is a Class IA antiarrhythmic medication used to treat various cardiac rhythm disorders. It works by blocking sodium channels in the heart, which slows electrical conduction and stabilizes irregular heartbeats.

Quick summary

Procainamide is an antiarrhythmic drug used to treat and prevent irregular heartbeats by blocking sodium channels in cardiac tissue.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 2026Editorial policy
BOXED WARNING

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
C01BA02
RxNorm
8700
Generic
Procainamide
Class
atc-c01
Brands
—
Availability
rx
Lactation
unknown
Routes
oral
Forms
prefilled syringe, tablet, capsule, solution
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose of 10 grams or more may cause serious toxicity and potentially fatal outcomes
Chronic overdose: Cumulative daily doses exceeding 2-3 grams or serum levels above 10 mcg/mL can lead to toxicity especially in patients with renal impairment
Immediate actions
Activated charcoal within 1-2 hours of ingestion, gastric lavage for large recent ingestions, continuous cardiac monitoring, intravenous fluids, sodium bicarbonate for QRS widening, advanced cardiac life support as needed
Antidote
No specific antidote exists(Treatment is supportive; early intervention improves outcomes)
Poison Control: 1-800-222-1222

Special Populations

10 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh risks to fetus

Monitor

regular fetal monitoring and uterine activity

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

continue monitoring, consider alternative antiarrhythmics

Monitor

fetal echocardiography and growth monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid near term if possible

Key Recommendations

discuss delivery plan, may affect neonatal transition

Monitor

fetal monitoring, assess for neonatal effects at birth

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

monitor infant closely

Key Recommendations

consider infant side effects including irritability and hypotension

Monitor

observe infant for symptoms

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce dose, start low

Key Recommendations

decreased renal clearance, increased sensitivity to side effects

Monitor

renal function monitoring, ECG, blood pressure

Use with caution and monitor for adverse effects.

⚠

pediatric_age

neonates infants
caution
FDA Category
N
Dose Adjustment

weight-based dosing required

Key Recommendations

use with caution, monitor ECG and blood pressure closely

Monitor

continuous cardiac monitoring

Use with caution and monitor for adverse effects.

✓

pediatric_age

children adolescents
safe
FDA Category
N
Dose Adjustment

weight-based dosing

Key Recommendations

appropriate for supraventricular and ventricular arrhythmias

Monitor

regular ECG and vital sign monitoring

⚠

renal_impairment

mild renal impairment
caution
FDA Category
N
Dose Adjustment

reduce dose by 25%

Key Recommendations

monitor renal function, adjust based on creatinine clearance

Monitor

renal function tests, ECG, drug levels

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe renal impairment
caution
FDA Category
N
Dose Adjustment

reduce dose by 50-75%

Key Recommendations

significant dose reduction required, consider alternative

Monitor

frequent drug level monitoring, renal function

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild hepatic impairment
caution
FDA Category
N
Dose Adjustment

no major adjustment needed

Key Recommendations

minor adjustments may be needed

Monitor

monitor liver function

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classWHO
2023

Drug class

Value:Antiarrhythmic (Class IA)

Classification as Class IA antiarrhythmic agent

usageMedical guidelines
2023

Common uses

Value:Treatment of ventricular arrhythmias and atrial fibrillation

Primary therapeutic indications

prescribingFDA
2023

First FDA approval

Value:1950s

Historical FDA approval information

formulationFDA
2023

Available formulations

Value:Oral tablets and injectable

Available dosage forms

Used to treat and prevent ventricular arrhythmias, including ventricular tachycardia and Wolff-Parkinson-White syndrome, and may be used for certain supraventricular arrhythmias when other treatments are ineffective or contraindicated.

Blocks cardiac sodium channels, which slows the rate of electrical impulse conduction through the heart. It also moderately prolongs the action potential duration and refractoriness, helping to stabilize erratic electrical activity.

Available in IV and oral formulations. Requires careful monitoring due to risks of hypotension, QT prolongation, and potential for drug-induced lupus with prolonged use. May cause blood disorders and should be avoided in patients with complete heart block without a pacemaker. Use requires ECG monitoring and periodic blood level checks.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 24, 2026. · Read our editorial policy