VA Class: HS875
Chemical Name: (5Z,9α,11α,13E,15S)-9,11,15-Trihydroxy-15-methyl-prosta-5,13-dien-1-oic acid
Molecular Formula: C21H36O5•C4H11NO3
CAS Number: 58551-69-2
Medically reviewed on January 1, 2018
Uses for Carboprost Tromethamine
Termination of Pregnancy
Used after failure of another method (e.g., in the event of premature rupture of membranes with loss of hypertonic abortifacients accompanied by inadequate uterine activity, when repeated intra-amniotic drug administration needed to expel fetus); used to induce abortion after membrane rupture.1
Treatment of postpartum hemorrhage in the presence of uterine atony that has not responded to usual therapy (i.e., IV oxytocin, uterine massage, IM ergot alkaloids [unless contraindicated]).1 8 9 10 12 13 20
Carboprost Tromethamine Dosage and Administration
Administer by deep IM injection.1
Available as carboprost tromethamine; dosage is expressed in terms of carboprost.1
Termination of Pregnancy
Subsequently, 250 mcg at 1.5- to 3.5-hour intervals depending on uterine response.1 15 After several 250-mcg doses, may increase dose to 500 mcg if uterine contractility is inadequate.1 15 Maximum total dose is 12 mg.1
Initially, 250 mcg; repeat every 15–90 minutes up to a maximum total dose of 2 mg.1 8 10 Single dose usually adequate.1 13 20 Clinician should determine the need for additional doses and dosing interval based on clinical events.1
Termination of Pregnancy
Maximum total dose is 12 mg; continuous administration for >2 days not recommended.1
Maximum total dose is 2 mg.1
Cautions for Carboprost Tromethamine
Known hypersensitivity to carboprost.1
Acute pelvic inflammatory disease.1
Active cardiac, pulmonary, renal, or hepatic disease.1
Administer by qualified professional personnel in a hospital where intensive care and surgical facilities are immediately available.1
Considerations in Patients Undergoing Termination of Pregnancy
Carboprost does not affect the fetoplacental unit.1 Possibility exists that a previable fetus could exhibit transient signs of life following carboprost-induced abortion; carboprost is not indicated if the fetus has reached the stage of viability.1
If the pregnancy is not terminated with carboprost, complete abortion using another method.1
Benzyl Alcohol in Neonates
Carboprost tromethamine injection contains as a preservative benzyl alcohol, which has been associated with toxicity (fatalities) in neonates.1 (See Pediatric Use under Cautions.)
Proliferation of long bones reported in neonates receiving long-term therapy with alprostadil (prostaglandin E1).1 22 No evidence that short-term administration of carboprost has similar effects on bone.1
Transient fever (i.e., temperature elevations >1.1°C) reported in approximately 12.5% of patients.1 When used for termination of pregnancy, may be difficult to distinguish drug-induced temperature elevations from post-abortion endometritis.1
Caution in patients with hypertension, hypotension, or cardiovascular disease.1
Not indicated in pediatric patients.1
Large amounts of benzyl alcohol (i.e., 100–400 mg/kg daily) have been associated with toxicity (fatal “gasping syndrome”) in neonates;1 2 3 4 5 6 7 each mL of carboprost tromethamine injection contains 9.45 mg of benzyl alcohol.1
Common Adverse Effects
Interactions for Carboprost Tromethamine
May increase activity of other oxytocic agents; concomitant use not recommended.1
Carboprost Tromethamine Pharmacokinetics
When used for postpartum hemorrhage, increase in uterine tone and decreased bleeding noted after about 45 minutes.13
Excreted in urine (83%), mainly as metabolites.19
Increases the amplitude and frequency of uterine contractions throughout pregnancy; uterine response to the drug increases with the duration of pregnancy.23
After delivery, uterine contractions impede uterine blood flow.1
Produces cervical dilation.15
Advice to Patients
Importance of women informing clinicians if they plan to breast-feed.1
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses.1
Importance of informing patients of other important precautionary information.1 (See Cautions.)
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.
250 mcg (of carboprost)/mL
Hemabate (with benzyl alcohol)
AHFS DI Essentials. © Copyright 2018, Selected Revisions January 1, 2008. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814.
1. Pharmacia & Upjohn. Hemabate (carboprost tromethamine) injection prescribing information. New York, NY; 2006 Mar.
2. American Academy of Pediatrics Committee on Fetus and Newborn and Committee on Drugs. Benzyl alcohol: toxic agent in neonatal units. Pediatrics. 1983; 72:356-8. http://www.ncbi.nlm.nih.gov/pubmed/6889041?dopt=AbstractPlus
3. Anon. Benzyl alcohol may be toxic to newborns. FDA Drug Bull. 1982; 12(2):10-11.
4. Centers for Disease Control. Neonatal deaths associated with use of benzyl alcohol. MMWR. 1982; 31:290-1. http://www.ncbi.nlm.nih.gov/pubmed/6810084?dopt=AbstractPlus
5. Gershanik J, Boecler B, Ensley H et al. The gasping syndrome and benzyl alcohol poisoning. N Engl J Med. 1982; 307:1384-8. http://www.ncbi.nlm.nih.gov/pubmed/7133084?dopt=AbstractPlus
6. Menon PA, Thach BT, Smith CH et al. Benzyl alcohol toxicity in a neonatal intensive care unit: incidence, symptomatology, and mortality. Am J Perinatol. 1984; 1:288-92. http://www.ncbi.nlm.nih.gov/pubmed/6440575?dopt=AbstractPlus
7. Anderson CW, Ng KJ, Andresen B et al. Benzyl alcohol poisoning in a premature newborn infant. Am J Obstet Gynecol. 1984; 148:344-6. http://www.ncbi.nlm.nih.gov/pubmed/6695984?dopt=AbstractPlus
8. American College of Obstetricians and Gynecologists (ACOG) Committee on Practice Bulletins. Postpartum hemorrhage. Practice Bulletin No. 76. Obstet Gynecol. 2006; 108:1039-47. http://www.ncbi.nlm.nih.gov/pubmed/17012482?dopt=AbstractPlus
9. Oleen MA, Mariano JP. Controlling refractory atonic postpartum hemorrhage with Hemabate sterile solution. Am J Obstet Gynecol. 1990; 16:205-8.
10. Briggs GG, Wan SR. Drug therapy during labor and delivery, part 2. Am J Health-Syst Pharm. 2006; 63:1131-9. http://www.ncbi.nlm.nih.gov/pubmed/16754739?dopt=AbstractPlus
11. Bygdeman M. Pharmacokinetics of prostaglandins. Best Pract Res Clin Obstet Gynaecol. 2003; 17:707-16. http://www.ncbi.nlm.nih.gov/pubmed/12972009?dopt=AbstractPlus
12. Dildy GA. Postpartum hemorrhage: new management options. Clin Obstet Gynecol. 2002; 45:330-44. http://www.ncbi.nlm.nih.gov/pubmed/12048393?dopt=AbstractPlus
13. Hayashi RH, Castillo MS, Noah ML. Management of severe postpartum hemorrhage with prostaglandin F2α analogue. Obstet Gynecol. 1984; 63:806-8. http://www.ncbi.nlm.nih.gov/pubmed/6610143?dopt=AbstractPlus
14. World Health Organization task force on the use of prostaglandins for regulation of fertility. Prostaglandins and abortion. I. Intramuscular administration of 15-methyl prostaglandin F2αfor induction of abortion in weeks 10 to 20 of pregnancy. Am J Obstet Gynecol. 1977; 129:593-6. http://www.ncbi.nlm.nih.gov/pubmed/920759?dopt=AbstractPlus
15. Schwallie PC, Lamborn KR. Induction of abortion by intramuscular administration of (15S)-15-methyl PGF2α: an overview of 815 cases. J Reprod Med. 1979; 23:289-93. http://www.ncbi.nlm.nih.gov/pubmed/392084?dopt=AbstractPlus
16. Stubblefield PG, Carr-Ellis S, Borgatta L. Methods for induced abortion. Obstet Gynecol. 2004; 104:174-85. http://www.ncbi.nlm.nih.gov/pubmed/15229018?dopt=AbstractPlus
17. Bygdeman M, Swahn ML. Uterine contractility during pregnancy and the effect of abortifacient drugs. Bailliere’s Clin Obstet Gynecol. 1990; 4:249-61.
18. Karim SMM, Sharma SD. Termination of second trimester pregnancy with 15 methyl analogues of prostaglandins E2 and F2α. J Obstet Gynaecol Br Commonw. 1972; 79:737-43. http://www.ncbi.nlm.nih.gov/pubmed/5070889?dopt=AbstractPlus
19. Hansson G, Granström E. Metabolism of 15-methyl-prostaglandin F2α in the cynomologus monkey and the human female. Biochem Med. 1977; 18:420-39. http://www.ncbi.nlm.nih.gov/pubmed/413545?dopt=AbstractPlus
20. Buttino L, Garite TJ. The use of 15 methyl F2α prostaglandin (prostin 15M) for the control of postpartum hemorrhage. Am J Perinatol. 1986; 3:241-3. http://www.ncbi.nlm.nih.gov/pubmed/3487334?dopt=AbstractPlus
21. Bergström S, Greén K, Bygdeman M. Metabolism and pharmaco-kinetics of 15 methyl PGF2α and its ester after administration via various routes. Prostaglandins. 1976; 12 (Suppl):17-26.
22. Pharmacia. Prostin VR Pediatric (alprostadil) injection prescribing information. Kalamazoo, MI; 2002 Sep.
23. AHFS Drug Information 2007. McEvoy GK, ed. Dinoprostone. Bethesda, MD: American Society of Health-System Pharmacists; 2007: 3267-9.
24. Pfizer, Morris Plains, NJ: Personal communication.
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- Drug class: uterotonic agents
Other brands: Hemabate