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Promethazine

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

Promethazine is a first-generation antihistamine that provides relief from allergic reactions, itching, and skin conditions like dermatitis. It also possesses antiemetic properties, making it effective for preventing and treating nausea, vomiting, and motion sickness, while its sedative effects make it useful for pre-procedural sedation.

Quick summary

A sedating antihistamine used for allergies, nausea, and motion sickness, with additional sedative properties.

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
D04AA10
RxNorm
8745
Generic
Promethazine
Class
atc-d04
Brands
Phenergan, Promethegan, Phenadoz
Availability
rx
Lactation
unknown
Routes
oral, rectal
Forms
injection, suspension, solution, capsule, 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
25mg every 4-6 hours
Maximum
consult physician
Frequency
as needed, not exceeding 50mg daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
0.5mg per lb
Maximum
consult physician
Frequency
every 4-6 hours as needed
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
25mg 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 exceeding 1 gram may cause serious toxicity in adults
Chronic overdose: Long-term use at supratherapeutic doses can lead to cumulative CNS depression and anticholinergic effects
Immediate actions
call emergency services, administer activated charcoal if within 1 hour of ingestion, monitor vital signs, provide supportive care
Antidote
no specific antidote(treatment is supportive and symptomatic, no specific 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 if benefits outweigh potential risks to fetus

Monitor

regular prenatal checkups

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

avoid prolonged use, use only when needed

Monitor

fetal monitoring if used long-term

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid near term

Key Recommendations

avoid use close to delivery due to potential respiratory depression in newborn

Monitor

monitor newborn for sedation and respiratory depression

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

contraindicated

Key Recommendations

do not use during breastfeeding - drug passes into breast milk

Monitor

N/A

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

✗

pediatric_age

under 2 years
contraindicated
FDA Category
C
Dose Adjustment

do not use

Key Recommendations

contraindicated due to risk of fatal respiratory depression

Monitor

N/A

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

⚠

pediatric_age

2 years and older
caution
FDA Category
C
Dose Adjustment

weight-based dosing, avoid high doses

Key Recommendations

use with extreme caution, not for sedation in children

Monitor

monitor for respiratory depression

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
C
Dose Adjustment

start with lower dose, reduce dose by 25-50%

Key Recommendations

use with caution due to increased sensitivity to anticholinergic effects

Monitor

monitor for confusion, sedation, falls, constipation

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild
caution
FDA Category
C
Dose Adjustment

no significant adjustment needed

Key Recommendations

monitor renal function

Monitor

periodic renal function monitoring

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate to severe
caution
FDA Category
C
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with caution, dose reduction recommended

Monitor

regular monitoring of renal function and drug levels

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with caution, metabolized in liver

Monitor

monitor liver function tests

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

severe
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

contraindicated in severe hepatic impairment

Monitor

N/A

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

Statistics and clinical data

prescribingFDA
2023

Commonly prescribed since

Value:1950s

General prescribing information for Promethazine products including Phenergan, Promethegan, and Phenadoz

drug_classWHO
2023

Drug class

Value:First-generation H1 antihistamine, phenothiazine derivative

ATC classification as antihistamine agent

usageMedical guidelines
2023

Common uses

Value:Nausea/vomiting, motion sickness, allergic rhinitis, sedation, preoperative sedation

Primary therapeutic applications approved for Promethazine

prescribingFDA
2023

Available formulations

Value:Oral tablets, rectal suppositories, injectable solution, oral syrup

Dosage forms available for Promethazine

Treatment of allergic conditions including rhinitis, conjunctivitis, and dermatologic reactions; prevention and treatment of nausea, vomiting, and vertigo associated with motion sickness; pre- and post-operative sedation; as an adjunct to analgesics for enhanced pain relief.

Blocks histamine H1 receptors, reducing allergic symptoms such as itching, sneezing, and runny nose. Its antiemetic effect is attributed to action on the vomiting center in the brainstem, while sedation occurs through central nervous system depression.

May cause significant drowsiness and should be avoided when operating machinery. Contraindicated in children under 2 years due to risk of respiratory depression. Can cause photosensitivity reactions. Avoid concurrent use with alcohol or other CNS depressants. Anticholinergic effects may occur.

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