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Prochlorperazine

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

Prochlorperazine is a first-generation antipsychotic medication belonging to the phenothiazine class, primarily used to treat schizophrenia, other psychotic disorders, severe nausea and vomiting, and sometimes anxiety. It works by blocking dopamine D2 receptors in the brain, which helps reduce psychotic symptoms and nausea.

Quick summary

Prochlorperazine is an antipsychotic used to treat schizophrenia, severe nausea, and vomiting by blocking dopamine receptors in the brain.

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

Key facts at a glance

ATC
N05AB04
RxNorm
8704
Generic
Prochlorperazine
Class
atc-n05
Brands
Compazine, Compro
Availability
rx
Lactation
unknown
Routes
oral, rectal
Forms
injection, solution, 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
5-10mg 3-4 times daily
Maximum
consult physician
Frequency
every 6-8 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
2.5mg 1-3 times daily
Maximum
consult physician
Frequency
every 8-12 hours as needed
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
5mg 1-3 times daily
Maximum
consult physician
Frequency
every 8-12 hours as needed
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity
Chronic overdose: Prolonged use at doses exceeding 75-100mg daily may lead to cumulative toxicity including tardive dyskinesia and neuroleptic malignant syndrome
Immediate actions
Gastric lavage within 1-2 hours of ingestion, activated charcoal, airway management, IV fluids for hypotension
Antidote
No specific antidote(Treatment is supportive and symptomatic; no specific antagonist exists)
Poison Control: 1-800-222-1222

Special Populations

10 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh potential risks to fetus

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use near term due to potential effects on newborn

Monitor

monitor newborn for extrapyramidal symptoms

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

excreted in breast milk, use only if absolutely necessary

Monitor

monitor infant for excessive drowsiness

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce dose, start low

Key Recommendations

increased sensitivity to sedation and extrapyramidal effects, use lower initial doses

Monitor

monitor for orthostatic hypotension, sedation, and movement disorders

Use with caution and monitor for adverse effects.

✗

pediatric_age

children under 2
contraindicated
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

not recommended for children under 2 years or weighing less than 10 kg

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, monitor closely for extrapyramidal symptoms

Monitor

close monitoring for adverse reactions

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

no significant adjustment needed

Key Recommendations

use with caution, monitor renal function

Monitor

monitor renal function periodically

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
C
Dose Adjustment

reduce dose

Key Recommendations

dose reduction recommended in severe renal impairment

Monitor

monitor renal function and for adverse effects

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

use lower dose

Key Recommendations

metabolized in liver, use with caution

Monitor

monitor liver function and for adverse effects

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

severe
unsafe
FDA Category
C
Dose Adjustment

avoid or use very low dose

Key Recommendations

avoid in severe hepatic impairment due to significantly impaired metabolism

Monitor

close monitoring required if used

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

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1956

Original FDA approval date for Prochlorperazine

drug_classWHO
2023

Drug class

Value:Phenothiazine antipsychotic/antiemetic

ATC classification N05AB04

usageMedical guidelines
2023

Common uses

Value:Nausea and vomiting, vertigo, migraine, anxiety

Primary therapeutic indications

mechanismFDA
2023

Mechanism of action

Value:Dopamine D2 receptor antagonist

Primary pharmacodynamic action

Treatment of schizophrenia and other psychotic disorders, severe nausea and vomiting (including chemotherapy-induced and post-operative), vertigo, and occasionally anxiety disorders.

Blocks dopamine D2 receptors in the brain's mesolimbic pathway, reducing dopamine-mediated neurotransmission and alleviating psychotic symptoms. Its antiemetic effect is primarily mediated through blockade of dopamine receptors in the chemoreceptor trigger zone.

May cause drowsiness, dizziness, extrapyramidal symptoms (such as tardive dyskinesia and parkinsonism), orthostatic hypotension, and anticholinergic effects. Use with caution in elderly patients with dementia-related psychosis. May interact with other CNS depressants, anticholinergic drugs, and medications that affect QT interval. Avoid use in patients with known hypersensitivity to phenothiazines.

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