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New Report Shows American Women Enthusiastic About Mifepristone Use
EXTREMIST ATTEMPT TO BLOCK FDA APPROVAL IS
MEDICAL McCARTHYISM, SAYS FEMINIST MAJORITY
ARLINGTON, VA -- The Feminist Majority applauded a new report published in the July/August issue of Archives of Family Medicine which finds that almost all women who have undergone an early medical abortion with mifepristone (formerly called RU 486) in the Population Council's U.S. clinical trials would recommend the procedure to others and would choose it again themselves. At the same time, the Feminist Majority condemned recent Congressional attempts to block FDA approval of mifepristone.
"Mifepristone offers women a method of terminating a pregnancy that is earlier, non-invasive, and more private. The Population Council study documents the tremendous enthusiasm of women and physicians for this method of very early medical abortion. It has been a full decade since this drug became available in France. American women will not tolerate further delays in making this medical breakthrough available here," said Feminist Majority President Eleanor Smeal.
Referring to recent Congressional action that could prohibit FDA approval of mifepristone, Smeal stated, "How ironic it is that as new studies are released showing the safety, efficacy, and acceptability of mifepristone to American women Congress is making a last ditch effort to block its availability in the United States. This outrageous attempt to limit the FDA's ability to review new drugs is nothing short of medical McCarthyism and exposes the extremism of the anti-abortion movement."
On July 14, the U.S. House of Representatives, by a close vote of 223 to 202, passed the Coburn amendment to the agricultural appropriations bill prohibiting FDA funding for testing, development, or approval of drugs that cause abortion. Similar language may be considered in the Senate.
Feminist Majority Director of Policy and Research Jennifer Jackman, Ph.D., added, "Never before has Congress dictated to the FDA what drugs the agency can and cannot approve. This amendment dangerously undermines the ability of the FDA to scientifically evaluate medical advances, threatens scientific research and development, and is an unconstitutional restriction on women's abortion rights. Anti-abortion politics already has caused unconscionable delays in the development of mifepristone's other potential uses such as the treatment of endometriosis, fibroid tumors, meningioma, Cushing's Syndrome, and labor induction. Adoption of the Coburn Amendment would further jeopardize the health and lives of women."
Now available to women in France, Sweden, and Great Britain, mifepristone has been used by over 200,000 women worldwide as a safe and effective method of early abortion. The FDA deemed mifepristone "approvable" in September 1996; final approval is pending. The Feminist Majority Foundation leads the largest public education campaign to bring this medical breakthrough to the United States.