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|Originally, the procedure involved inserting the misoprostol pill into the vagina where the medicine was absorbed. But by the end of 2005, four American women and one Canadian had died of a rare bacterial infection afterward, spurring concern among providers and criticism by abortion opponents.|
|Misoprostol, which is officially approved in the U.S. for preventing stomach ulcers, is sold under the brand name Cytotec and made by Pfizer Inc.|
|Misoprostol (marketed as Cytotec) Information
FDA ALERT – Risks of Use in Labor and Delivery
This Patient Information Sheet is for pregnant women who may receive misoprostol to soften their cervix or induce contractions to begin labor. Misoprostol is sometimes used to decrease blood loss after delivery of a baby. These uses are not approved by the FDA. No company has sent the FDA scientific proof that misoprostol is safe and effective for these uses.
There can be serious side effects, including a torn uterus (womb), when misoprostol is used for labor and delivery. A torn uterus may result in severe bleeding, having the uterus removed (hysterectomy), and death of the mother or baby. These side effects are more likely in women who have had previous uterine surgery, a previous Cesarean delivery (C-section), or several previous births.
This information reflects FDA’s preliminary analysis of data concerning this drug. FDA is considering, but has not reached a final conclusion about, this information. FDA intends to update this sheet when additional information or analyses become available.
Healthcare Professional Information
Prescribing Information (Cytotec Label)
Regulatory History of Misoprostol from [email protected]
Adverse reactions or quality problems experienced with the use of this Product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax, using the contact information at the bottom of this sheet.
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