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Prasterone

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

Prasterone (DHEA) is a naturally occurring hormone precursor that is converted in the body to both androgens and estrogens. It is primarily used to treat dyspareunia (painful intercourse) in postmenopausal women and has been studied for hypoactive sexual desire disorder. The medication works by supplementing hormone levels that decline with age and menopause.

Quick summary

Prasterone is a hormone precursor used primarily for sexual symptoms in postmenopausal women.

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

Key facts at a glance

ATC
A14
RxNorm
unknown
Generic
Prasterone
Class
atc-a14
Brands
Intrarosa
Availability
otc
Pregnancy
D
Lactation
caution
Half-life (h)
20
Onset (min)
0
Duration (h)
24
Routes
oral, vaginal
Forms
vaginal insert, oral tablet
Regions
United States, Canada, European Union
Monitoring
endometrial thickness

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 of 10 grams or higher may cause serious toxicity based on extrapolated data from DHEA supplement studies
Chronic overdose: Prolonged use exceeding recommended intravaginal doses may lead to hormonal imbalance and androgen excess symptoms
Immediate actions
Gastric lavage within 1-2 hours of ingestion if oral, monitor vital signs, provide supportive care
Antidote
No specific antidote exists; treatment is supportive and symptomatic(Supportive care is effective when initiated promptly; no specific antagonist available)
Poison Control: 1-800-222-1222

Special Populations

10 groups
✗

pregnancy

first trimester
contraindicated
FDA Category
X
Dose Adjustment

avoid use

Key Recommendations

do not use during pregnancy; contraindicated due to potential fetal harm from hormonal exposure

Monitor

not applicable - avoid use

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

✗

pregnancy

second trimester
contraindicated
FDA Category
X
Dose Adjustment

avoid use

Key Recommendations

do not use during pregnancy; contraindicated due to potential fetal harm

Monitor

not applicable - avoid use

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

✗

pregnancy

third trimester
contraindicated
FDA Category
X
Dose Adjustment

avoid use

Key Recommendations

do not use during pregnancy; contraindicated

Monitor

not applicable - avoid use

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

✗

lactation

breastfeeding
contraindicated
FDA Category
X
Dose Adjustment

avoid use

Key Recommendations

not recommended during breastfeeding; prasterone may transfer into breast milk and could affect infant hormone levels

Monitor

not applicable - avoid use

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

✗

pediatric_age

children adolescents
unsafe
FDA Category
N
Dose Adjustment

not established

Key Recommendations

not indicated for pediatric patients; safety and efficacy not established in patients under 18 years of age

Monitor

not applicable

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

✓

geriatric

elderly
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

appropriate for use in elderly postmenopausal women with vulvar and vaginal atrophy; no dose adjustment required based on age alone

Monitor

routine gynecological monitoring as appropriate

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

no dose adjustment required; minimal systemic absorption with intravaginal administration

Monitor

standard monitoring

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

use with caution; limited data available on severe renal impairment

Monitor

clinical judgment recommended

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

no dose adjustment required; minimal systemic absorption with intravaginal administration

Monitor

standard monitoring

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

use with caution; limited data available on severe hepatic impairment

Monitor

clinical judgment recommended

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classFDA
2023

Drug class

Value:Steroid hormone/DHEA

Prasterone is a bioidentical hormone (dehydroepiandrosterone)

usageFDA
2023

Common uses

Value:Treatment of vulvar and vaginal atrophy in postmenopausal women

Indication for Intrarosa vaginal insert

regulatoryFDA
2023

FDA approval year

Value:2016

FDA approval for Intrarosa (prasterone)

administrationFDA
2023

Route of administration

Value:Vaginal insert

Intravaginal administration

FDA-approved for treating moderate to severe dyspareunia (painful intercourse) due to menopause. Also used off-label for adrenal insufficiency, low libido, and symptoms of lupus.

As a DHEA (dehydroepiandrosterone) precursor, prasterone is converted peripherally to active androgens and estrogens, which act on vaginal and other target tissues to improve mucosal health and reduce pain.

May cause androgenic side effects such as acne and hirsutism. Not recommended during pregnancy or breastfeeding. Should be used with caution in patients with hormone-sensitive conditions. Intravaginal use is associated with vaginal discharge.

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 26, 2026. · Read our editorial policy