Skip to content

Isoproterenol

Published: July 26, 2026Updated: July 26, 2026

Isoproterenol is a potent non-selective beta-adrenergic agonist used primarily in cardiac care settings. It stimulates both beta-1 receptors in the heart to increase heart rate and cardiac output, and beta-2 receptors in the bronchi to produce bronchodilation. This medication is typically reserved for acute care situations requiring rapid cardiovascular or respiratory support.

Quick summary

A beta-adrenergic stimulant used for cardiac arrhythmias and bronchospasm in acute care settings.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy

Key facts at a glance

ATC
C01CA02
RxNorm
6054
Generic
Isoproterenol
Class
atc-c01
Brands
Isuprel
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
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)intravenous infusion
Usual dose
2-10 mcg/min
Maximum
consult physician
Frequency
continuous infusion
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)intravenous infusion
Usual dose
0.05-0.5 mcg/kg/min
Maximum
consult physician
Frequency
continuous infusion
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)intravenous infusion
Usual dose
2-10 mcg/min
Maximum
consult physician
Frequency
continuous infusion
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose exceeding 10 mg may cause serious cardiovascular toxicity
Chronic overdose: Prolonged use leading to tolerance and decreased therapeutic response
Immediate actions
Discontinue drug, monitor cardiac rhythm, establish IV access, administer beta-blockers with caution
Antidote
No specific antidote available(Treatment is supportive and symptomatic)
Poison Control: 1-800-222-1222

Special Populations

9 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

use only if clearly needed and benefits outweigh potential risks to fetus

Monitor

regular fetal heart rate monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

avoid if possible close to delivery due to potential uterine relaxation

Monitor

fetal monitoring and uterine activity assessment

Use with caution and monitor for adverse effects.

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

use with caution or avoid due to unknown excretion in breast milk

Monitor

monitor infant for adverse effects

⚠

pediatric_age

children under 12
caution
FDA Category
C
Dose Adjustment

weight-based dosing required

Key Recommendations

use with extreme caution in children due to risk of tachyarrhythmias and bronchospasm

Monitor

continuous cardiac and respiratory monitoring

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly over 65
caution
FDA Category
C
Dose Adjustment

start with lower dose

Key Recommendations

use with caution due to increased sensitivity to beta-adrenergic effects and higher risk of cardiovascular events

Monitor

close monitoring of heart rate blood pressure and cardiac rhythm

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

no major dose adjustment needed

Key Recommendations

use with caution and monitor renal function

Monitor

monitor renal function and for adverse effects

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
C
Dose Adjustment

consider dose reduction

Key Recommendations

use with caution in severe renal impairment

Monitor

monitor renal function and cardiac function closely

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

use lower dose

Key Recommendations

use with caution as drug is extensively metabolized in liver

Monitor

monitor cardiac function and liver function tests

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

severe
caution
FDA Category
C
Dose Adjustment

significant dose reduction

Key Recommendations

use with extreme caution in severe hepatic impairment

Monitor

intensive cardiac monitoring and liver function assessment

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1940s

Original FDA approval date for Isoproterenol

drug_classWHO
2023

Drug class

Value:Non-selective beta-adrenergic agonist

Pharmacological classification based on mechanism of action

usageMedical guidelines
2023

Common uses

Value:Treatment of bradycardia, heart block, bronchial asthma, and COPD

Primary therapeutic applications

mechanismFDA
2023

Mechanism of action

Value:Beta-1 and beta-2 adrenergic receptor agonist

Pharmacodynamic mechanism

Management of symptomatic bradycardia and heart block when atropine and temporary pacing are ineffective or unavailable; bronchospasm during anesthesia; cardiac emergencies requiring increased heart rate or cardiac output.

Acts as a non-selective agonist at beta-adrenergic receptors with minimal alpha-receptor activity. Stimulation of cardiac beta-1 receptors increases heart rate and contractility, while beta-2 receptor activation in bronchial smooth muscle produces bronchodilation.

Requires continuous cardiac monitoring during administration. Use with caution in patients with coronary artery disease, hypertension, hyperthyroidism, or diabetes. May cause tachycardia, arrhythmias, or hypotension. Administered via IV infusion or subcutaneously; dosage is highly individualized based on clinical response.

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

WellAlly may earn a referral fee from linked resources at no extra cost to you. Editorial content is never influenced by commercial relationships.

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 July 26, 2026. · Read our editorial policy