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Thiopental

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

Thiopental is a short-acting barbiturate used primarily as an induction agent for general anesthesia. It acts as a central nervous system depressant, producing rapid unconsciousness when administered intravenously. This medication has also been used for sedation and seizure control, though it has largely been replaced by newer agents in many clinical settings.

Quick summary

Thiopental is a barbiturate anesthetic used for rapid induction of general anesthesia and sedation.

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

Key facts at a glance

ATC
N01AF03
RxNorm
10493
Generic
Thiopental
Class
atc-n01
Brands
—
Availability
rx
Lactation
unknown
Routes
—
Forms
prefilled syringe, 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 that may cause serious toxicity or death in adults
Chronic overdose: cumulative CNS depression with repeated administration
Immediate actions
secure airway and provide ventilatory support, consider gastric lavage if within 1-2 hours of ingestion
Antidote
no specific antidote(supportive care is the primary treatment; no antidote available)
Poison Control: 1-800-222-1222

Special Populations

11 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only when benefits clearly outweigh risks; consider alternative anesthetics

Monitor

regular fetal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

use only for essential surgical procedures; regional anesthesia preferred when possible

Monitor

fetal heart rate monitoring during procedure

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

commonly used for cesarean delivery anesthesia; avoid high doses close to delivery

Monitor

fetal monitoring; assess neonatal respiration at birth

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
C
Dose Adjustment

temporarily interrupt breastfeeding

Key Recommendations

thiopental excreted in breast milk; pump and discard milk for 24 hours after administration

Monitor

observe infant for excessive sedation

Use with caution and monitor for adverse effects.

⚠

pediatric_age

neonates
caution
FDA Category
C
Dose Adjustment

significant dose reduction required

Key Recommendations

use reduced doses based on weight; immature hepatic metabolism requires caution

Monitor

close respiratory and cardiovascular monitoring

Use with caution and monitor for adverse effects.

✓

pediatric_age

infants children
safe
FDA Category
C
Dose Adjustment

weight-based dosing

Key Recommendations

commonly used for pediatric anesthesia induction; standard pediatric dosing protocols apply

Monitor

standard pediatric anesthetic monitoring

⚠

geriatric

elderly
caution
FDA Category
C
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use reduced doses due to decreased clearance and increased sensitivity; slower induction and recovery

Monitor

enhanced cardiovascular and respiratory monitoring

Use with caution and monitor for adverse effects.

✓

renal_impairment

mild moderate
safe
FDA Category
C
Dose Adjustment

no significant adjustment needed

Key Recommendations

primarily hepatically metabolized; monitor for accumulation in prolonged use

Monitor

standard monitoring

⚠

renal_impairment

severe
caution
FDA Category
C
Dose Adjustment

use with caution; consider dose reduction

Key Recommendations

accumulation may occur with repeated dosing; extended recovery time possible

Monitor

prolonged monitoring for sedation recovery

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild
caution
FDA Category
C
Dose Adjustment

may require dose reduction

Key Recommendations

primarily metabolized in liver; monitor response carefully

Monitor

close monitoring of sedation depth and recovery

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate severe
caution
FDA Category
C
Dose Adjustment

significant dose reduction required

Key Recommendations

substantial hepatic metabolism impairment; avoid or use very reduced doses; consider alternative agents

Monitor

extended monitoring for recovery; assess liver function

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classWHO
2023

Drug class

Value:Barbiturate

Drug class information

usageMedical guidelines
2023

Common uses

Value:Induction of anesthesia, sedation, seizure control

Common therapeutic uses

prescribingFDA
2023

Commonly prescribed since

Value:1940s

Historical prescribing information

Primarily used for induction of general anesthesia before surgical procedures. Also historically used for sedation in intensive care settings, management of elevated intracranial pressure, and control of certain seizure disorders.

Thiopental enhances the effect of GABA (gamma-aminobutyric acid) at GABA-A receptors in the brain, increasing chloride ion influx into neurons and causing CNS depression. This results in rapid sedation and hypnosis.

Administered exclusively by intravenous injection by qualified healthcare professionals. Causes dose-dependent respiratory depression and hypotension. Contraindicated in patients with porphyria, severe cardiovascular impairment, or known barbiturate allergy. Requires careful monitoring during and after administration.

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