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Propofol

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

Propofol is a rapid-acting intravenous anesthetic used to induce and maintain general anesthesia during surgical procedures, as well as provide sedation for patients undergoing mechanical ventilation in intensive care settings. It works by enhancing the inhibitory effects of GABA in the brain, producing unconsciousness and amnesia. The drug is administered only by qualified healthcare professionals in controlled settings due to its potent effects on breathing and cardiovascular function.

Quick summary

Propofol is a widely-used intravenous anesthetic and sedative that works by modulating GABA receptors to produce rapid, controllable sedation and unconsciousness during surgery and critical care.

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

Key facts at a glance

ATC
N01AX10
RxNorm
8782
Generic
Propofol
Class
atc-n01
Brands
Propoflo, Propovan, Diprivan, Propoven
Availability
rx
Lactation
unknown
Routes
—
Forms
injection, suspension
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 - significantly above typical anesthetic doses (1.5-2.5 mg/kg induction)
Chronic overdose: Prolonged high-dose infusion may lead to propofol infusion syndrome (PRIS) with metabolic disturbances and organ failure
Immediate actions
Discontinue infusion, maintain airway, provide ventilatory support, intravenous fluids, vasopressors if needed
Antidote
No specific antidote exists - supportive care only(Supportive care is the primary treatment as there is no reversal agent)
Poison Control: 1-800-222-1222

Special Populations

8 groups
✗

pregnancy

first trimester
unsafe
FDA Category
B
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks, particularly in first trimester

Monitor

regular fetal monitoring and uterine activity

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

⚠

pregnancy

third trimester
caution
FDA Category
B
Dose Adjustment

reduce dose

Key Recommendations

use lowest effective dose, may cause neonatal respiratory depression at delivery

Monitor

fetal monitoring, neonatal assessment at birth

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

pump and discard milk for 24 hours

Key Recommendations

temporary interruption of breastfeeding recommended after administration

Monitor

observe infant for sedation

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce dose by 20-40%

Key Recommendations

use lower induction and maintenance doses, slow administration

Monitor

continuous hemodynamic and respiratory monitoring

Use with caution and monitor for adverse effects.

⚠

pediatric_age

neonates
caution
FDA Category
B
Dose Adjustment

reduce dose, use with extreme caution

Key Recommendations

not recommended for ICU sedation in neonates, use only for anesthesia induction

Monitor

continuous cardiovascular and respiratory monitoring

Use with caution and monitor for adverse effects.

⚠

pediatric_age

children 1 12 years
caution
FDA Category
B
Dose Adjustment

adjust weight-based dosing

Key Recommendations

use lower doses, not recommended for prolonged sedation in ICU

Monitor

close hemodynamic and respiratory monitoring

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

may require dose reduction

Key Recommendations

use lower doses, metabolites may accumulate

Monitor

monitor for prolonged sedation, renal function

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

reduce dose due to decreased hepatic clearance

Monitor

monitor liver function and sedation depth

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1989

Initial FDA approval for anesthetic use

drug_classWHO
2023

Drug class

Value:General anesthetic

ATC classification as N01A (general anesthetics)

usageMedical guidelines
2023

Common uses

Value:Induction and maintenance of general anesthesia, sedation for procedures

Primary therapeutic applications

pharmacologyFDA
2023

Mechanism of action

Value:GABA-A receptor agonist

Primary pharmacodynamic mechanism

Propofol is used for induction and maintenance of general anesthesia during surgery, sedation during diagnostic procedures, and prolonged sedation for mechanically ventilated patients in ICUs. It is also commonly used for procedural sedation in outpatient settings such as endoscopy and minor surgeries.

Propofol produces its anesthetic and sedative effects by positively modulating the GABA-A receptor complex in the central nervous system. This enhances the inhibitory signaling of GABA, the brain's primary inhibitory neurotransmitter, leading to decreased neuronal activity, sedation, and loss of consciousness. The drug's mechanism of action involves multiple receptor targets beyond GABA-A, contributing to its rapid onset and smooth recovery profile.

Propofol carries significant risks including respiratory depression, hypotension, and loss of airway reflexes, requiring continuous monitoring by trained personnel. It should only be administered by professionals skilled in anesthesia or critical care with appropriate resuscitation equipment available. The drug is contraindicated in patients with known propofol infusion syndrome risk factors and requires careful dosing adjustments in elderly, debilitated, or hemodynamically unstable patients. Propofol is not an analgesic, so additional pain medication may be needed during surgical procedures.

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 July 26, 2026. · Read our editorial policy