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Mifepristone: Expanding Women's Options for Early Abortion

Mifepristone, formerly known as RU-486, is an antiprogesterone drug that blocks receptors of progesterone, a key hormone in the establishment and maintenance of human pregnancy. Used in combination with a prostaglandin such as misoprostol, mifepristone induces abortion when administered in early pregnancy, providing women with a medical alternative to aspiration (suction) abortion.

Mifepristone was approved by the U.S. Food and Drug Administration (FDA) on September 28, 2000, for use as an abortifacient despite anti-choice lobbying efforts to prevent its approval. In the United States, the brand name for mifepristone is Mifeprex®, which is manufactured by Danco Laboratories, LLC (Danco, 2000).

Effectiveness And Safety

Since its approval in France in 1988, mifepristone has proven to be a safe, effective, and acceptable option for women seeking abortion during the first several weeks of pregnancy.

  • By the time the FDA approved mifepristone for use in the U.S., more than 600,000 women in Europe had medication abortions using mifepristone (FDA, 2000).
  • Between 1994 and 1995, 2,121 women in Planned Parenthood and other U.S. health centers participated in clinical trials of mifepristone sponsored by the Population Council (Spitz, et al., 1998).
  • In the five years following FDA approval, approximately 575,000 U.S. women have used Mifeprex ("Abortion Pill...", 2006). Planned Parenthood has provided more than 200,000 women with this option (PPFA, 2006).
  • Using the FDA-approved regimen up to 49 days' gestation (measured from the first day of the last menstrual period), about 92 percent of women will complete their abortion without the need for a vacuum aspiration (ACOG, 2005; Spitz, et al., 1998).
  • Evidence-based alternative regimens use a lower dose of mifepristone and a higher dose of misoprostol than the FDA-approved regimen. Some of these alternative regimens have been found to be effective for longer than 49 days' gestation. Planned Parenthood currently provides medication abortion up to 56 days' gestation. Evidence-based alternative regimens have a success rate of about 95 percent (Middleton, et al., 2005; Schaff, et al., 2002).
  • Some women may begin bleeding after taking the mifepristone, before taking misoprostol. For most, the bleeding and cramping begins after taking misoprostol. More than 50 percent of women who use mifepristone abort within four to five hours after taking the misoprostol (Newhall & Winikoff, 2000; Peyron, et al., 1993).
  • An overwhelming majority of women who choose mifepristone for medication abortion are satisfied with the method. One study found that 97 percent of women would recommend the method to a friend. Additionally, 91 percent of the women reported that they would choose the mifepristone regimen again if they had to have another abortion (Hollander, 2000; Jensen, et al., 2000).
  • The most common side effects reported by women using mifepristone plus prostaglandin for early abortion are similar to those of a spontaneous miscarriage: abdominal pain, bleeding, dizziness, fatigue, nausea, and vomiting. Changes in body temperature are also common (ACOG, 2005; Creinin & Aubény, 1999; Stewart, et al., 2005).
  • Because it is a noninvasive procedure, successful medication abortion eliminates certain risks associated with manual vacuum aspiration and dilation and suction curettage (D&C;) such as perforation or risks related to anesthesia (Aguillaume & Tyrer, 1995).
  • Since mifepristone's FDA approval in 2000, there have been six infection-related deaths following mifepristone-induced medication abortion in North America — five in the United States and one in Canada. An additional death was caused by an undiagnosed, untreated ectopic pregnancy — a dangerous condition that mifepristone does not cause or treat ("Abortion Pill...", 2006; Creinin & Aubény, 1999; Danco, 2003; FDA, 2006; Hausknecht, 2003; Laliberté, 2005; Manzer, 2001).
  • On the basis of data currently available, it is believed that the risk of death from medication abortion through 63 days' gestation is about one per 100,000 procedures (Grimes, 2005). The risk of death with surgical abortion is thought to be about one per 1,000,000 through 63 days' gestation (Bartlett, et al., 2004). The risk of death from miscarriage is about one per 100,000 (Saraiya, et al., 1999). But the risk of death associated with childbirth is about 10 times as high as that associated with all abortion (Christiansen & Collins, 2006).

Who Provides Patient With Mifepristone

Mifepristone has been found to be most effective when administered in combination with a prostaglandin such as misoprostol. Elements of the procedures, such as who may prescribe, the type of prostaglandin, the method of administration, the dosage, and the number of days of pregnancy which mifepristone is an option, vary worldwide.

In the United States, medication abortion using mifepristone and misoprostol may be provided by a physician or other clinician under the supervision of a physician who is

  • capable of providing vacuum aspiration or is capable of referring for vacuum aspiration
  • able to diagnose ectopic pregnancy
  • able to assess gestational age

How Mifepristone Is Used

In the U.S., the approved FDA regimen involves three steps: 1) a visit to a clinician to discuss the procedure and its alternatives and to receive a 600 mg dose of mifepristone, 2) a second visit two days later for an oral dose of 400 mcg of misoprostol, a prostaglandin used to treat ulcers that the FDA approved for off-label use to induce contractions for abortion and 3) a third visit on day 14 for a follow up visit. The FDA approved mifepristone for use up to 49 days after the first day of the last menstrual period.

It is generally common for a large majority of clinicians in the U.S. to follow evidence-based alternatives to FDA regimens when they have been shown by published scientific evidence to have notable benefits, including a higher rate of effectiveness, cause fewer side effects, and allow patients more flexibility. Ways in which the mifepristone regimen is often adapted include

  • changing the dosage of the medications — It has been found that 200 mg of mifepristone and 800 mcg of misoprostol is equally or more effective as using 600 mg of mifepristone and 400 mcg of misoprostol.

  • eliminating the second visit — At-home administration of the second drug — the prostaglandin — allows a woman to control the timing and location of the cramping and bleeding associated with the medication abortion process. Studies have shown at-home administration to be both safe and effective (Fiala, et al., 2004).

  • extending the time period for using mifepristone — Studies have found that mifepristone can be effective up to 63 days after the first day of the last menstrual period, dependent upon the regimen used (vaginal administration of the prostaglandin allows the 63-day limit)
    (Boonstra, 2002; Creinin, et al., 2006; Middleton, et al., 2005; Schaff, et al., 2001).

Implications For The Future

As mifepristone becomes widely available, more women may elect to choose this option. Among the expected effects of such a change are these:

  • In France, Great Britain, and Sweden, where mifepristone has been available for at least 12 years, the proportion of abortions that are performed early in pregnancy increased significantly in the years following its approval for medication abortion (Boonstra, 2002).
  • More providers may be willing to offer the medication regimen than currently offer vacuum aspiration services.
  • Mifepristone may offer women more privacy in the abortion decision, along with greater personal control over the process of pregnancy termination.

There is no evidence that the availability of mifepristone for medication abortions increases a nation's rate of abortion. In France, England, and Wales, the abortion rate remained stable from the year prior to mifepristone's approval to 2000. The abortion rate in Sweden fell following mifepristone approval (Jones & Henshaw, 2002).

Other Uses

Medical uses for mifepristone are likely to expand in the future.

Researchers have identified a number of potential uses for mifepristone beyond pregnancy termination, including the treatment of breast cancer, Cushing's syndrome, endometriosis, glaucoma, meningioma, ovarian cancer, prostate cancer, severe depression, and uterine fibroids (DeBattista & Belanoff, 2006; Institute of Medicine, 1993).

Although not currently available in the United States for this use, mifepristone may be used in very low doses to prevent pregnancy as a method of emergency contraception within five days of unprotected intercourse (WHO, 1999). In higher doses, of course, it can be used to terminate pregnancy. Other medications currently used for emergency contraception in the U.S. cannot be used to terminate pregnancy because they are not abortifacients.

History

In spite of its demonstrated effectiveness, safety, and acceptability, mifepristone was continuously targeted by anti-choice activists, causing numerous and lengthy delays in the efforts to make the drug legal and available to the many Americans it might benefit.

Mifepristone/RU-486 was first approved for use in September 1988 in France, where it was developed by the pharmaceutical firm Roussel-Uclaf. In October 1988, Roussel-Uclaf, the sole manufacturer of the drug and holder of the patents, took the unprecedented action of suspending its distribution, citing protests by anti-abortion groups in the U.S., France, and West Germany. Two days later, the French Minister of Health ordered the company to resume distribution in the interests of public health (Aguillaume & Tyrer, 1995).

In 1991, mifepristone was approved by the United Kingdom Licensing Authority for use in Great Britain, and in 1992, it was approved for use in Sweden (Aguillaume & Tyrer, 1995).

Even while the use of mifepristone was expanded to the U.K. and Sweden, however, Roussel-Uclaf announced that it had no intention of marketing the drug in the U.S. or any other country where the company perceived that political and social conditions were unreceptive to the drug. The George H. W. Bush administration, with its overall hostility to abortion, took the additional step of placing mifepristone on a list of drugs banned by the FDA from importation into the U.S. for personal use (Aguillaume & Tyrer, 1995).

In July 1992, Leona Benten attempted to bring mifepristone into the U.S. for personal use — the drug was seized and, in spite of a lower court ruling in Benten's favor, the confiscation was upheld by the U.S. Supreme Court (Talbot, 1999).

The Clinton administration, in one of its first administrative actions in January 1993, asked the FDA to reexamine the import ban. Subsequently, an FDA deputy commissioner indicated that the agency might consider clinical trials in Europe as evidence in determining the drug's safety, an important step for expediting the process of approval.

In May 1994, Department of Health and Human Services Secretary Donna Shalala announced that as a result of encouragement by the Clinton administration, Roussel-Uclaf had donated the U.S. rights for mifepristone to the Population Council, a New York-based nonprofit research institution. The Population Council conducted U.S. clinical trials from 1994-1995. Results of the Population Council clinical trials, showing mifepristone to be highly effective, safe, and acceptable for early abortion, were published in the New England Journal of Medicine and the Archives of Family Medicine in 1998.

Following public hearings on the subject, the FDA Advisory Committee for Reproductive Health Drugs recommended approval of mifepristone in the summer of 1996. The FDA issued an approvable letter for mifepristone in September 1996, indicating that the drug was safe and effective, but that the Population Council and the manufacturer needed to provide additional manufacturing, labeling, and other information in order to obtain final approval (Talbot, 1999).

The Population Council granted the Danco Group, a new women's health pharmaceutical company, an exclusive license to manufacture, market, and distribute mifepristone in the United States. Danco entered into a series of agreements with a manufacturer to produce mifepristone. However, the manufacturer backed out of the project in early 1997. This further delayed the availability of mifepristone in the U.S. Danco has since identified manufacturers willing to produce mifepristone, worked with them towards production, and provided the FDA with the information it needed to make a final review of the application (Talbot, 1999).

Anti-choice legislators continued their efforts to deny women access to this safe, convenient method of abortion. In June 1998, Representative Tom Coburn (R-OK) attempted to prevent the possibility of FDA approval by offering an amendment to a spending bill that would have prohibited the FDA from spending any money to test, develop, or approve any drug for the chemical inducement of abortion. This measure was approved by the House, but it did not make it into the final version of the spending bill. In June 1999, Coburn again introduced — and the House passed — the amendment (Talbot, 1999). In July 2000, a similar amendment was again introduced, but this time rejected by the House (Zimmerman & Lueck, 2000).

Despite anti-choice lobbying efforts that began in 1988 to prevent its approval, mifepristone was finally approved for use as an abortifacient by the FDA on September 28, 2000. In the U.S., the brand name for mifepristone is Mifeprex®, which is manufactured by Danco Laboratories, LLC (Danco, 2000).

Additional Resources

Mifeprex® The Early Option — http://www.earlyoptionpill.com/

U.S. Food and Drug Administration Mifepristone Information — http://www.fda.gov/cder/drug/infopage/mifepristone/default.htm

Cited References

"Abortion Pill Ruled Out in One Woman's Death: FDA Investigating Second Death from Rare Infection." (2006, April 10). The Associated Press.

ACOG — American College of Obstetricians and Gynecologists. (2001, April). "Medical Management of Abortion." ACOG Practice Bulletin, 26, 1-13.

_____. (2005, October). "Medical Management of Abortion." ACOG Practice Bulletin, 67, 1-12.

Aguillaume, Claude J. & Louise B. Tyrer. (1995). "Current Status and Future Projections on Use of RU-486." Contemporary OB/GYN®, 40(6), 23-40.

Bartlett, L.A., et al. (2004). "Risk Factors for Legal Induced Abortion-Related Mortality in the United States." Obstetrics and Gynecology, 103, 729-37.

Boonstra, Heather. (2002). "Mifepristone in the United States: Status and Future." The Guttmacher Report on Public Policy, 5(3), 4-7.

Christiansen, L.R., and K.A. Collins. (2006). "Pregnancy-Associated Deaths: A 15-Year Retrospective Study and Overall Review of Maternal Pathophysiology." American Journal of Forensic Medicine and Pathology, 27, 11-9.

Creinin, Mitchell D. & Elizabeth Aubény. (1999). "Medical Abortion in Early Pregnancy." Pp. 91-106 in Maureen Paul, et al., eds., A Clinician's Guide to Medical and Surgical Abortion. New York: Churchill Livingstone.

Creinin, Mitchell, et al. (2006). "Mifepristone-Misoprostol Medical Abortion Mortality." Medscape General Medicine, 8(2), 26.

Danco Laboratories, LLC. (2000, September 28). Press Release.

_____. (2003, December 1). Statement.

DeBattista, Charles, and Joseph Belanoff. (2006). "The Use of Mifepristone in the Treatment of Neuropsychiatric Disorders." Trends in Endocrinology and Metabolism, 17(30), 117-21.

FDA — U.S. Food and Drug Administration. (2000, September 28). Press Release: FDA Approves Mifepristone for the Termination of Early Pregnancy.

_____. (2006, March 17). FDA Public Health Advisory: Sepsis and Medical Abortion Update.

Fiala, Christian, et al. (2004). "Acceptability of Home-Use of Misoprostol in Medical Abortion." Contraception, 70(5), 387-92.

Grimes, D.A. (2005). "Risks of Mifepristone Abortion in Context." Contraception, 71, 161.

Hausknecht, Richard. (2003). "Mifepristone and Misoprostol for Early Medical Abortion: 18 Months Experience in the United States." Contraception, 67, 463-465.

Hollander, Dore. (2000). "Most Abortion Patients View Their Experience Favorably, But Medical Abortion Gets a Higher Rating than Surgical." Family Planning Perspectives, 32(5), 264.

Institute of Medicine. (1993). Clinical Applications of Mifepristone (RU-486) and Other Antiprogestins: Assessing the Science and Recommending a Research Agenda. Washington, DC: National Academy Press.

Jensen, J.T., et al. (2000). "Acceptability of Suction Curettage and Mifepristone Abortion in the United States: A Prospective Comparison Study." American Journal of Obstetrics & Gynecology, 182(6), 1292-9.

Jones, Rachel & Stanley Henshaw. (2002). "Mifepristone for Early Medical Abortion: Experiences in France, Great Britain and Sweden." Perspectives on Sexual and Reproductive Health, 34(3), 154-161.

Laliberté, Jennifer. (2005, September 30). "Still No Mifepristone for Canada: Is it Safe?" National Review of Medicine, 2(16).

Manzer, Jenny. (2001, September 25). "Death Halts 'Abortion Pill' Trial: Fatality May be Used to Block Drug's Approval in Canada." Medical Post, 37(32), 1.

Middleton, Tamer, et al. (2005). "Randomized Trial of Mifepristone and Buccal or Vaginal Misoprostol for Abortion Through 56 Days of Last Menstrual Period." Contraception, 72, 328-32.

Newhall, Elizabeth Pirruccello & Beverly Winikoff. (2000). "Abortion with Mifepristone and Misoprostol: Regimens, Efficacy, Acceptability and Future Directions." American Journal of Obstetrics and Gynecology, 183(2), S44-53.

Peyron, Rémi, et al. (1993). "Early Termination of Pregnancy with Mifepristone (RU 486) and Orally Active Prostaglandin Misoprostol." New England Journal of Medicine, 328(21), 1509-13.

PPFA — Planned Parenthood Federation of America. (2006). Unpublished tabulations.

Saraiya, M., et al. (1999). "Spontaneous Abortion-Related Deaths Among Women in the United States, 1981-1991." Obstetrics and Gynecology, 94(2), 172-6.

Schaff, Eric, et al. (2001). "Randomized Trial of Oral Versus Vaginal Misoprostol at One Day After Mifepristone for Early Medical Abortion." Contraception, 64, 81-5.

Schaff, Eric, et al. (2002). "Randomized Trial of Oral Versus Vaginal Misoprostol 2 Days After Mifepristone 200 mg for Abortion Up to 63 Days of Pregnancy." Contraception, 66, 247-50.

"Sites Providing Abortions." (2005, Summer). Mifematters, 12, p. 4.

Spitz, Irving M., et al. (1998). "Early Pregnancy Termination with Mifepristone and Misoprostol in the United States." New England Journal of Medicine, 338(18), 1241-7.

Stewart, Felicia H., et al. (2005). "Abortion." Pp. 673-700 in Robert A. Hatcher, et al., eds., Contraceptive Technology, 18th Revised Edition. New York, NY: Ardent Media, Inc.

Talbot, Margaret. (1999, July 11). "The Little White Bombshell." New York Times Magazine, 39-43.

WHO — World Health Organization. Task Force on Postovulatory Methods of Fertility Regulation. (1999). "Comparison of Three Single Doses of Mifepristone as Emergency Contraception: A Randomized Trial." Lancet, 353 (February 27), 697-702.

Zimmerman, Rachel & Sarah Lueck. (2000, September 28). "FDA Expected to Approve Abortion Drug." Wall Street Journal, p. A3.


Lead Author — Susanne Pichler
Revised by — Deborah Friedman, MPH

Current as of May 2006

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