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Hexobarbital

Published: July 26, 2026Updated: August 20, 2026

Hexobarbital is a barbiturate derivative historically used as a sedative-hypnotic and intravenous anesthetic agent. It acts as a central nervous system depressant, producing sedation and anesthesia by enhancing GABA receptor activity. While largely replaced by safer alternatives, it was previously employed for induction of anesthesia and short-term sedation.

Quick summary

Hexobarbital is a barbiturate-type sedative and anesthetic that works by depressing the central nervous system.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ATC
N01AF02
RxNorm
5302
Generic
Hexobarbital
Class
atc-n01
Brands
—
Availability
rx
Lactation
unknown
Routes
oral
Forms
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
250-500mg
Maximum
consult physician
Frequency
once daily at bedtime
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
Not recommended
Maximum
consult physician
Frequency
N/A
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
125-250mg
Maximum
consult physician
Frequency
once daily at bedtime
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity, though individual susceptibility varies
Chronic overdose: Prolonged use leading to accumulation and CNS depression
Immediate actions
Secure airway and breathing, support circulation, consider gastric lavage if within 1-2 hours of ingestion, activated charcoal may be considered
Antidote
No specific antidote exists(Supportive care is the mainstay of treatment; hemodialysis may be considered in severe cases)
Poison Control: 1-800-222-1222

Special Populations

9 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid

Key Recommendations

avoid use near delivery due to risk of respiratory depression in newborn

Monitor

fetal heart rate monitoring and neonatal assessment

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

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

avoid

Key Recommendations

discontinue breastfeeding or avoid drug due to excretion in breast milk

Monitor

monitor infant for excessive sedation

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

⚠

geriatric

elderly
caution
FDA Category
C
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use lower initial doses and titrate slowly due to increased sensitivity

Monitor

monitor respiratory status, blood pressure, and cognitive function

Use with caution and monitor for adverse effects.

⚠

pediatric_age

children 2-12 years
caution
FDA Category
C
Dose Adjustment

weight-based dosing with careful titration

Key Recommendations

use only in controlled hospital settings for anesthesia induction

Monitor

continuous vital sign monitoring including respiratory and cardiac status

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

no significant adjustment needed but monitor

Key Recommendations

use with caution and monitor for accumulation

Monitor

monitor renal function and drug levels if available

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
C
Dose Adjustment

reduce dose and extend dosing interval

Key Recommendations

use reduced doses with extended intervals between administrations

Monitor

close monitoring of renal function and clinical response

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild
caution
FDA Category
C
Dose Adjustment

reduce dose by 25%

Key Recommendations

use reduced dose and monitor response carefully

Monitor

monitor liver function tests and clinical sedation levels

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

moderate to severe
unsafe
FDA Category
C
Dose Adjustment

avoid or use extreme caution with significant dose reduction

Key Recommendations

avoid if possible due to severely impaired metabolism

Monitor

intensive monitoring of sedation and respiratory status

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

Statistics and clinical data

drug_classWHO
2023

Drug class

Value:Barbiturate

Hexobarbital belongs to the barbiturate class of central nervous system depressants

usageMedical guidelines
2023

Common uses

Value:Sedation, anesthesia induction

Historical therapeutic uses of Hexobarbital as a sedative-hypnotic agent

prescribingFDA
2023

Prescribing status

Value:Rarely prescribed

Current prescribing status due to safety concerns and availability of safer alternatives

safetyClinical guidelines
2023

Safety profile

Value:Narrow therapeutic index

Risk-benefit considerations for barbiturate use

Previously used for induction of general anesthesia, as a sedative for preoperative medication, and for short-term treatment of insomnia. Its clinical use has significantly declined due to the availability of safer anesthetic and sedative agents.

Acts on GABA-A receptors to enhance inhibitory neurotransmission, increasing chloride ion conductance and neuronal hyperpolarization. This results in sedation, hypnosis, and anesthesia depending on the dose administered.

Barbiturates carry risks of dependence, respiratory depression, and narrow therapeutic index. Require careful dosing and monitoring. Often replaced by benzodiazepines and newer anesthetic agents due to their superior safety profiles.

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 20, 2026. · Read our editorial policy