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Secobarbital

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

Secobarbital is a barbiturate medication that acts as a central nervous system depressant, historically used for the short-term treatment of insomnia and as a pre-anesthetic sedative. Due to significant safety concerns including dependence, abuse potential, and overdose risk, it has largely been discontinued in favor of safer alternatives.

Quick summary

A discontinued barbiturate sedative-hypnotic largely replaced by safer medications due to significant safety risks.

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

Key facts at a glance

ATC
N05CA06
RxNorm
9624
Generic
Secobarbital
Class
atc-n05
Brands
—
Availability
rx
Lactation
unknown
Routes
oral
Forms
capsule
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
100mg at bedtime
Maximum
consult physician
Frequency
once daily
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
50mg at bedtime
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, including CNS depression, respiratory failure, and potentially fatal outcomes
Chronic overdose: Prolonged use can lead to tolerance, dependence, and cumulative CNS depression with daily doses exceeding 600mg
Immediate actions
Secure airway and provide ventilatory support, gastric lavage if within 1-2 hours of ingestion, activated charcoal, continuous monitoring
Antidote
No specific antidote exists; treatment is supportive(N/A - supportive care is the mainstay of treatment)
Poison Control: 1-800-222-1222

Special Populations

8 groups
✗

pregnancy

first trimester
unsafe
FDA Category
D
Dose Adjustment

avoid

Key Recommendations

avoid use during pregnancy due to risk of fetal malformations and developmental defects

Monitor

regular fetal monitoring and ultrasound assessments

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

✗

pregnancy

third trimester
unsafe
FDA Category
D
Dose Adjustment

avoid

Key Recommendations

avoid use near term due to risk of neonatal respiratory depression and withdrawal

Monitor

neonatal assessment for respiratory depression and withdrawal symptoms

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

✗

lactation

breastfeeding
unsafe
FDA Category
D
Dose Adjustment

avoid

Key Recommendations

do not breastfeed during secobarbital therapy due to excretion in breast milk

Monitor

monitor infant for excessive sleepiness or difficulty feeding

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use lowest effective dose due to increased sensitivity and decreased metabolism

Monitor

monitor for confusion, sedation, dizziness, and falls

Use with caution and monitor for adverse effects.

✗

pediatric_age

children under 12
unsafe
FDA Category
N
Dose Adjustment

avoid

Key Recommendations

not recommended for use in pediatric populations due to unpredictable response

Monitor

close monitoring for paradoxical reactions and respiratory depression

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

⚠

renal_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use with caution; reduced dosage recommended due to decreased clearance

Monitor

monitor renal function and adjust dose based on clinical response

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use with extreme caution; significant hepatic impairment increases half-life and bioavailability

Monitor

monitor liver function tests and adjust dose based on clinical response

Use with caution and monitor for adverse effects.

✗

alcohol_users

active alcohol use
contraindicated
FDA Category
N
Dose Adjustment

absolute contraindication

Key Recommendations

concurrent use with alcohol is contraindicated due to additive CNS depression

Monitor

monitor for severe respiratory depression, coma, and death

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

Short-acting barbiturate, sedative-hypnotic

usageMedical guidelines
2023

Common uses

Value:Sedative, hypnotic, pre-anesthesia medication

Historical therapeutic applications

regulatoryDEA
2023

Controlled substance schedule

Value:Schedule II (US)

Legal classification due to abuse potential

prescribingFDA
2023

Commonly prescribed since

Value:1930s-1970s (declined)

Historical prescribing period; largely replaced by safer alternatives

Short-term treatment of insomnia and pre-anesthetic sedation. Note: Due to safety concerns, it is rarely prescribed today.

Acts as a GABA-A receptor agonist, enhancing the inhibitory effects of GABA in the central nervous system, resulting in sedation and hypnosis.

Carries high risk of dependence, tolerance, and potentially fatal overdose, especially when combined with other CNS depressants. Largely discontinued due to these risks.

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