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Carboprost

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

Carboprost is a synthetic prostaglandin F2α analog used primarily to control postpartum hemorrhage when conventional treatments are ineffective, and to induce termination of pregnancy in the second trimester. It works by stimulating powerful uterine contractions that compress bleeding vessels and facilitate expulsion of uterine contents.

Quick summary

Carboprost is a prostaglandin analog that controls postpartum bleeding and terminates second-trimester pregnancies by inducing strong uterine contractions.

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

Key facts at a glance

ATC
G02AD04
RxNorm
2051
Generic
Carboprost
Class
atc-g02
Brands
Hemabate
Availability
rx
Lactation
unknown
Routes
—
Forms
injection, prefilled syringe
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)injection
Usual dose
250 mcg IM or intramyometrial
Maximum
consult physician
Frequency
may repeat every 15-90 minutes as needed, maximum 8 doses
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (not_applicable)injection
Usual dose
not typically indicated for pediatric patients
Maximum
consult physician
Frequency
not applicable
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)injection
Usual dose
250 mcg IM or intramyometrial
Maximum
consult physician
Frequency
may repeat every 15-90 minutes as needed, maximum 8 doses
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity (approximately 8 times the therapeutic dose)
Chronic overdose: Cumulative dosing exceeding 8 mg total or repeated dosing without appropriate interval
Immediate actions
Discontinue medication, establish IV access, monitor vital signs, provide supportive care, consider gastric decontamination if oral exposure
Antidote
No specific antidote available(Supportive care is primary treatment; no specific antidote proven effective)
Poison Control: 1-800-222-1222

Special Populations

7 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; not indicated for routine use in first trimester

Monitor

regular fetal monitoring if used

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

⚠

pregnancy

second third trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

used for postpartum hemorrhage and pregnancy termination in second trimester when medically necessary

Monitor

intensive maternal and fetal monitoring

Use with caution and monitor for adverse effects.

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

discontinue breastfeeding

Key Recommendations

avoid breastfeeding during treatment and for at least 24 hours after administration

Monitor

monitor infant for adverse effects

✗

pediatric_age

under 12 years
unsafe
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

not indicated for use in children under 12 years of age

Monitor

not applicable

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with caution in elderly patients; start with lower dose and titrate slowly

Monitor

monitor vital signs and renal function closely

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with caution; renal function may affect drug clearance

Monitor

monitor renal function tests closely; adjust dose based on creatinine clearance

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with caution; hepatic metabolism may be impaired

Monitor

monitor liver function tests closely

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classWHO
2023

Drug class

Value:Prostaglandin F2α analog

Prostaglandin analog classification

prescribingFDA
2023

FDA approval year

Value:1992

Original FDA approval date for Hemabate

usageFDA
2023

Primary indications

Value:Postpartum hemorrhage, pregnancy termination

Main therapeutic indications

administrationFDA
2023

Route of administration

Value:Intramuscular injection

Standard route of administration

Treatment of postpartum hemorrhage refractory to conventional measures; induction of mid-trimester pregnancy termination; management of missed abortion or intrauterine fetal death requiring evacuation.

Acts as a prostaglandin F2α receptor agonist in the myometrium, triggering vigorous uterine contractions that compress spiral arteries to achieve hemostasis, while also promoting cervical ripening and softening.

Typically administered intramuscularly; common adverse effects include fever, chills, nausea, vomiting, and diarrhea; contraindicated in patients with active asthma, cardiovascular impairment, or known prostaglandin hypersensitivity; requires careful hemodynamic monitoring during use.

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