Medically reviewed on March 6, 2018.
Applies to the following strengths: 250 mcg/mL
Usual Adult Dose for:
Additional dosage information:
Usual Adult Dose for Abortion
Initial dose: 250 mcg (1 mL) once by deep IM injection, with a tuberculin syringe
Subsequent doses of 250 mcg (1 mL) may be administered at 1.5 to 3.5 hour intervals depending on uterine response.
An optional test dose of 100 mcg (0.4 mL) may be administered initially. The dose may be increased to 500 mcg (2 mL) if uterine contractility is judged to be inadequate after several doses of 250 mcg (1 mL).
Maximum total dose: 12 mg
Duration of therapy: No more than 2 continuous days
-Aborting pregnancy between the 13 th and 20 th weeks of gestation (calculated from the first day of the last normal menstrual period)
-Failure of expulsion of the fetus during the course of treatment by another method
-Premature rupture of membranes in intrauterine methods with loss of drug and insufficient or absent uterine activity
-Requirement of a repeat intrauterine instillation of drug for expulsion of the fetus
-Inadvertent or spontaneous rupture of membranes in the presence of a previable fetus and absence of adequate activity for expulsion
Usual Adult Dose for Postpartum Bleeding
Initial dose: 250 mcg (1 mL) once by deep IM injection
Additional doses can be administered at intervals of 15 to 90 minutes, if necessary.
Maximum total dose: 2 mg (8 doses)
Comments: The need for additional injections and the administration interval should be determined by the attending physician as dictated by the course of clinical events.
Uses: Refractory postpartum hemorrhage due to uterine atony that has not responded to conventional methods of management.
Renal Dose Adjustments
Liver Dose Adjustments
-Carboprost tromethamine, like other potent oxytocic agents, should be used only with strict adherence to recommended dosages.
-It should be used by medically trained personnel in a hospital which can provide immediate intensive care and acute surgical facilities.
Safety and efficacy have not been established in patients younger than 18 years.
Consult WARNINGS section for additional precautions.
Data not available
-This drug should not be given intravenously.
-Consider pretreatment or coadministration of antiemetic and antidiarrheal drugs to decrease the incidence of gastrointestinal effects.
Storage requirements: Refrigerate at 2C to 8C (36F to 46F)
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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- Drug class: uterotonic agents
Other brands: Hemabate