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Merck

Misoprostol for the prevention and treatment of postpartum hemorrhage.

Expert opinion on investigational drugs (2012-01-12)
Wendy R Sheldon, Jennifer Blum, Jill Durocher, Beverly Winikoff
ABSTRACT

Uterotonic drugs are recommended for the prevention and treatment of postpartum hemorrhage (PPH), and oxytocin is considered the gold standard for both indications due to its established efficacy and safety. Unfortunately, access to oxytocin is still limited in many low-resource settings due to the need for cool storage, sterile equipment and administration by skilled personnel. Misoprostol , an E1 prostaglandin analog, has therefore been explored as an alternative for such settings due to its proven ability to induce uterine contractions, low cost, stability at room temperature and ease of administration. This review covers evidence from 51 randomized controlled trials for both prevention and treatment of PPH. It discusses efficacy and side effects in the context of the various doses that have been studied using oral, sublingual or rectal routes of administration for both indications. There is now a solid body of evidence to justify the use of misoprostol for postpartum hemorrhage indications in many settings. The evidence supports use of 600 μg orally for the prevention of PPH and 800 μg sublingually for the treatment of PPH. There is no evidence to support the adjunct use of misoprostol following administration of conventional uterotonics for prevention or treatment purposes.

MATERIALS
Product Number
Brand
Product Description

Misoprostol for system suitability, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Misoprostol, ≥99% (HPLC)
Misoprostol, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Misoprostol free acid, ≥90%