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Atenolol

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

Atenolol is a cardioselective beta-blocker used to treat hypertension (high blood pressure), angina (chest pain), and certain heart rhythm disorders. It works by blocking the effects of adrenaline on beta-1 receptors in the heart, which slows the heart rate and reduces the force of contraction, thereby lowering blood pressure. This medication is typically taken as a once-daily oral dose and is commonly prescribed as a first-line treatment for various cardiovascular conditions.

Quick summary

Atenolol is a beta-blocker that lowers blood pressure and heart rate to treat hypertension, angina, and heart rhythm problems.

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

Key facts at a glance

ATC
C07AB03
RxNorm
1202
Generic
Atenolol
Class
atc-c07
Brands
Tenormin, Tenoretic
Availability
rx
Lactation
unknown
Routes
oral
Forms
capsule, solution, tablet
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
50-100mg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
0.5-1 mg/kg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
25-50mg once 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 1 gram or more may cause serious toxicity and potentially fatal outcomes
Chronic overdose: Repeated supratherapeutic doses exceeding 200mg daily may lead to cumulative cardiovascular toxicity including bradycardia, hypotension, and heart failure
Immediate actions
Gastric lavage within 1-2 hours if large dose ingested, activated charcoal, continuous cardiac monitoring, IV fluids
Antidote
Glucagon (no true antidote exists but glucagon is used to reverse beta-blocker effects)(Glucagon is used to increase heart rate and blood pressure by bypassing beta-adrenergic receptors; effectiveness varies by case severity)
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 potential risks to fetus

Monitor

regular fetal monitoring including growth assessments

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

continue only if essential, consider alternative antihypertensives

Monitor

regular fetal monitoring and growth assessments

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid near delivery

Key Recommendations

discontinue 24-48 hours before delivery if possible

Monitor

fetal monitoring and assessment for neonatal bradycardia

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

use lowest effective dose

Key Recommendations

monitor infant for signs of beta-blockade including bradycardia and hypotension

Monitor

observe infant for lethargy, poor feeding, bradycardia

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

start at half usual adult dose

Key Recommendations

use lower initial dose and titrate slowly, monitor renal function

Monitor

regular blood pressure monitoring and renal function tests

Use with caution and monitor for adverse effects.

✗

pediatric_age

children adolescents
unsafe
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

not approved for use in children under 18 years

Monitor

not applicable

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

renal_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

monitor renal function and adjust dose based on creatinine clearance

Monitor

regular renal function monitoring, serum creatinine and BUN

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

reduce dose to 25-50mg daily

Key Recommendations

use with caution, consider alternative therapy

Monitor

close monitoring of renal function and drug levels

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

no significant dose adjustment required as drug is not extensively metabolized

Monitor

standard monitoring

⚠

alcohol_users

chronic alcohol consumption
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

avoid excessive alcohol consumption as it may exacerbate hypotension

Monitor

monitor blood pressure when consuming alcohol

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1981

FDA approval timeline for Atenolol (Tenormin)

drug_classWHO
2023

Drug class

Value:Beta-blocker (Cardioselective)

ATC classification - Beta blocking agents, plain

usageMedical guidelines
2023

Primary indications

Value:Hypertension, angina, arrhythmia, heart attack prevention

Main therapeutic applications

pharmacologyFDA
2023

Mechanism of action

Value:Beta-1 adrenergic receptor blockade

Primary pharmacodynamic mechanism

Atenolol is used to treat high blood pressure (hypertension), angina pectoris (chest pain caused by reduced blood flow to the heart), and certain types of arrhythmias (irregular heartbeat). It may also be prescribed after a heart attack to improve survival rates and reduce the risk of future cardiovascular events.

Atenolol belongs to a class of drugs called beta-1 selective adrenergic blockers. It works by selectively blocking beta-adrenergic receptors in the heart, preventing the action of adrenaline and noradrenaline. This results in reduced heart rate, decreased force of heart contractions, and lowered blood pressure, reducing the heart's workload and oxygen demand.

Do not stop taking Atenolol abruptly, as this may worsen chest pain or cause a heart attack. Common side effects include fatigue, cold extremities, and dizziness. Inform your doctor if you have asthma, severe bradycardia, or heart failure before starting this medication. Alcohol may enhance the blood pressure-lowering effects and should be used cautiously.

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