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Phenylpropanolamine

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

Phenylpropanolamine is a sympathomimetic decongestant that works by constricting blood vessels in the nasal passages, reducing swelling and congestion. It was historically used to relieve nasal stuffiness from colds, allergies, and sinusitis, though it has been withdrawn from many markets due to safety concerns.

Quick summary

A nasal decongestant that shrinks nasal blood vessels to relieve congestion, now largely withdrawn from the market due to stroke risk.

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

Key facts at a glance

ATC
R01BA01
RxNorm
8175
Generic
Phenylpropanolamine
Class
atc-r01
Brands
Proin, Phenylpro, Uripropamine
Availability
rx
Lactation
unknown
Routes
oral
Forms
tablet, solution
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Toxic dose: Single dose exceeding 10000 mg may cause serious toxicity; however, phenylpropanolamine was withdrawn from the US market in 2000 due to stroke risk
Chronic overdose: Prolonged use or cumulative dosing may lead to cardiovascular complications including hypertension and stroke
Immediate actions
Activated charcoal within 1-2 hours if presentation is early, supportive care including IV fluids, benzodiazepines for agitation, antihypertensives for severe hypertension
Antidote
No specific antidote exists; treatment is supportive(Supportive care is the mainstay of treatment; early intervention improves outcomes)
Poison Control: 1-800-222-1222

Special Populations

10 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring

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

✗

pregnancy

second trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring and blood pressure checks

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use close to delivery due to uterine contractions risk

Monitor

regular fetal monitoring and uterine activity

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

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

discontinue or avoid

Key Recommendations

phenylpropanolamine is excreted in breast milk; avoid use while breastfeeding

Monitor

monitor infant for irritability and feeding changes

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

✗

pediatric_age

children under 12
contraindicated
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

avoid use in children due to increased risk of adverse cardiovascular events

Monitor

not applicable - contraindicated

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

⚠

geriatric

elderly over 65
caution
FDA Category
C
Dose Adjustment

use with caution and reduced dose

Key Recommendations

use with extreme caution in elderly patients; start at lowest effective dose

Monitor

monitor blood pressure and heart rate regularly

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild
caution
FDA Category
C
Dose Adjustment

adjust dose downward

Key Recommendations

use with caution; monitor renal function

Monitor

monitor renal function and blood pressure

Use with caution and monitor for adverse effects.

✗

renal_impairment

moderate to severe
unsafe
FDA Category
C
Dose Adjustment

avoid or significantly reduce dose

Key Recommendations

avoid use in patients with moderate to severe renal impairment

Monitor

closely monitor renal function if use is absolutely necessary

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

⚠

hepatic_impairment

mild
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

use with caution in mild hepatic impairment

Monitor

monitor liver function tests

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

moderate to severe
unsafe
FDA Category
C
Dose Adjustment

avoid

Key Recommendations

avoid use in patients with moderate to severe hepatic impairment

Monitor

not applicable - avoid use

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

Statistics and clinical data

drug_classWHO
2023

Drug class

Value:Sympathomimetic amine

Alpha-adrenergic agonist used primarily as a vasoconstrictor

usageFDA
2023

Common uses

Value:Veterinary urinary incontinence (dogs)

Currently approved for canine urinary sphincter mechanism incontinence

safetyFDA
2023

Market status

Value:Withdrawn from human use

Withdrawn in 2000 due to increased risk of hemorrhagic stroke

prescribingFDA
2023

Historical human use

Value:1970s-2000

Previously used in cold medications and appetite suppressants

Treatment of nasal congestion associated with the common cold, allergic rhinitis, and sinusitis. Previously available in oral and nasal spray formulations.

Acts as an alpha-adrenergic agonist that causes vasoconstriction of the mucosal blood vessels in the nasal passages, reducing swelling and mucus production to improve airflow.

Withdrawn from the US market and many other countries due to associated risk of hemorrhagic stroke, particularly in women. Can increase blood pressure and heart rate. Should not be used by patients with cardiovascular disease, hypertension, or thyroid disorders. Other side effects include insomnia, anxiety, and headache.

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