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Pro-life advocates oppose new FDA guidelines for RU-486 use

WASHINGTON—Pro-life advocates expressed dismay with new Food and Drug Administration guidelines that effectively ex­pand how pregnant women can use RU-486, a drug that induces abortion.

The new rules, announced March 30, allow a woman to use RU-486 — known generi­cally as mifepristone and by its brand name Mifeprex — later into pregnancy and with fewer visits to a doctor. New York Cardinal Timothy M. Dolan, chairman of the U.S. bishops’ pro-life committee, called the FDA’s decision irresponsible.

“The unofficial, off-label use of RU-486 is now the new normal, paving the way for the destruction of even more inno­cent lives, and putting women and girls at risk for all the life-changing effects of abortion,” he said in an April 1 statement. “Far from wanting abortion to be ‘rare’, abortion advocates are celebrating this expanded use as opening an ever-widen­ing door to abortion,” he said. “They are equally celebrating the FDA’s neglect of women’s health. Women have died from this drug, and many who used it after eight weeks of preg­nancy ended up returning for surgical abortions. This an­guish, too, will now be visited on more women.”

“People need to know this is a very, very serious expansion of the use of RU-486,” Deirdre McQuade, spokeswoman for the U.S. Conference of Catholic Bishops’ Secretariat for Pro Life Activities, told Catholic News Service March 31.

“Clearly the loosening of the FDA guidelines puts more women, girls and unborn chil­dren at risk,” McQuade said, while expressing concern that women and girls will be faced with the possibility of deliver­ing a “recognizably human child” at home with no one in attendance.

McQuade also expressed con­cern that the new guidelines al­low non-physicians to dispense or prescribe the drug. “This raises a huge question. Do we want nurses, physician’s assis­tants, non-MDs overseeing the prescription of a drug that has very serious consequences for women?”

Dr. Grazie Pozo Christie, an advisory board member with the Catholic Association, in a March 31 statement called the extension of time that RU-486 can be used “substantial.”

Christie, a radiologist who said she performs fetal ultra­sound daily, explained that a 10-week-old fetus is “a well-developed and recognizably human creature. Head, hands, feet and vigorous movement are evident even to the un­trained eye.”

“Also at issue is the psycho­logical and physical impact on a woman, sent home to experi­ence the very painful cramps of a chemical abortion of a fetus that size,” she added. “Be­sides the considerable blood loss and pain, there is every chance of a woman recognizing a fully formed fetus amongst the expelled ‘products of con­ception.’”

Randall K. O’Bannon, direc­tor of education and research at National Right to Life, said in a statement March 30 that the new guidelines do not make chemical abortion safer.

“In the end, it is obvious that the FDA’s new protocol serves only the interest of the abortion industry by expand­ing their base of potential customers, increasing their profit margin and reducing the level of staff and amount of resources they have to devote to the patient,” O’Bannon said. “Certainly, none of the modifi­cations is of any benefit to the unborn child.”

The new FDA guidelines for RU-486 brings the regimen for taking the drug in line with what has become standard medical practice:

  • Extending the period when a woman can take the drug to 70 days of pregnancy, from 49.
  • Lowering the dosage to 200 milligrams from 600 milli­grams.
  • Reducing the number of visits to a doctor by a woman to two from three.

RU-486 is used with another drug called misoprostol, a prostaglandin, to induce a chemical abortion by block­ing the hormone progesterone needed to sustain a pregnancy. The FDA said it changed the guidelines governing RU-486 “based on data and informa­tion submitted by the drug manufacturer.”

Some abortion opponents said the announcement was politically motivated in the midst of presidential and con­gressional elections as Repub­lican and Democrat candidates seek support from women.

The FDA said in the an­nouncement that its decision was based on medical science.

“After reviewing the supple­mental application, the agency determined that Mifeprex is safe and effective when used to terminate a pregnancy in accordance with the revised labeling,” the agency said.

Dr. Mark S. DeFranceso, president of the American Congress of Obstetricians and Gynecologists, welcomed the new regimen in a statement, saying it “reflects the current available scientific evidence and best practices and includes many of the recommendations that ACOG had presented to the agency. Extending ap­proved use of mifepristone through 70 days of gestation is proven to be safe and effective, and will give women more time to make the decision that is right for them.”

In his statement, Cardinal Dolan offered the Church’s assistance to “any woman who finds herself pregnant” and needs help. He invited women to “come to Catholic agencies for nonjudgmental, caring as­sistance.”

 

By Dennis Sadowski   |   Catholic News Service

 

Photo from Wikimedia/lunar caustic: This embryo at 9-10 weeks is recognizably human. The new FDA guidelines allow a woman to use RU-486 through 70 days of gestation.






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