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Droperidol

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

Droperidol is an antipsychotic medication belonging to the butyrophenone class, primarily used for the prevention and treatment of postoperative nausea and vomiting. It acts as a dopamine D2 receptor antagonist and is also employed for sedation and management of acute agitation in hospital settings.

Quick summary

Droperidol is an antipsychotic/antiemetic medication used to prevent nausea, vomiting, and agitation.

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

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
N05AD08
RxNorm
3648
Generic
Droperidol
Class
atc-n05
Brands
—
Availability
rx
Pregnancy
C
Lactation
caution
Routes
—
Forms
injection
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 including severe CNS depression, hypotension, and cardiac effects
Chronic overdose: Cumulative toxicity may occur with repeated supratherapeutic dosing leading to persistent extrapyramidal symptoms and cardiac toxicity
Immediate actions
Supportive care, airway management, intravenous fluids, continuous cardiac monitoring, consider gastric lavage if within 1 hour of ingestion
Antidote
No specific antidote exists; treatment is supportive(Supportive care is the primary treatment; effectiveness depends on early intervention and severity of toxicity)
Poison Control: 1-800-222-1222

Special Populations

10 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

avoid use during first trimester unless benefits outweigh risks

Monitor

regular fetal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid close to delivery due to potential neonatal effects

Monitor

monitor newborn for extrapyramidal symptoms

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
C
Dose Adjustment

avoid or discontinue breastfeeding

Key Recommendations

droperidol passes into breast milk, consider alternative or suspend breastfeeding

Monitor

monitor infant for sedation and feeding issues

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
C
Dose Adjustment

reduce initial dose by 50%

Key Recommendations

use lowest effective dose, increased sensitivity to adverse effects

Monitor

monitor for sedation, hypotension, and extrapyramidal symptoms

Use with caution and monitor for adverse effects.

✗

pediatric_age

children under 2
unsafe
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

safety and efficacy not established in children under 2 years

Monitor

not applicable

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

⚠

pediatric_age

children 2 12
caution
FDA Category
C
Dose Adjustment

weight-based dosing required

Key Recommendations

use with caution, reserve for severe cases where benefits outweigh risks

Monitor

closely monitor for adverse effects

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild
caution
FDA Category
C
Dose Adjustment

no adjustment needed for mild impairment

Key Recommendations

use standard dosing with monitoring

Monitor

monitor renal function

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
C
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use with caution, monitor for accumulation

Monitor

monitor drug levels and renal function

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild moderate
caution
FDA Category
C
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use with caution due to hepatic metabolism

Monitor

monitor liver function tests

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

severe
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh risks

Monitor

close monitoring required

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classWHO
2023

Drug class

Value:Butyrophenone antipsychotic

Classification as typical antipsychotic and antiemetic

prescribingFDA
2023

FDA approval year

Value:1970

Original FDA approval date for Droperidol

usageMedical guidelines
2023

Common uses

Value:Prevention and treatment of postoperative nausea and vomiting, antipsychotic

Primary therapeutic indications

pharmacologyFDA
2023

Mechanism of action

Value:Dopamine D2 receptor antagonist

Primary pharmacodynamic mechanism

Prevention and treatment of postoperative and chemotherapy-induced nausea and vomiting; sedation and neuroleptanalgesia during surgical procedures; management of acute agitation and behavioral emergencies.

Droperidol blocks dopamine D2 receptors in the chemoreceptor trigger zone and cerebrum, producing antiemetic, antipsychotic, and sedative effects.

May cause QT prolongation and cardiac arrhythmias; use with caution in patients with electrolyte imbalances or cardiac disease; avoid in patients with known hypersensitivity to butyrophenones; use during pregnancy only if benefits justify 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