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Pro-life groups criticize FDA for abortion drug decision

Regulatory change permits the sale of mifepristone, the first of two drugs used in a chemical abortion, at retail pharmacies

WASHINGTON — The U.S. Food and Drug Administration will allow retail pharmacies to offer abortion pills in the United States for the first time, the agency announced Jan. 3, prompting criticism from Catholic and pro-life groups.

The Biden administration’s rule change comes in the wake of the Supreme Court’s decision last year in Dobbs v. Jackson Women’s Health Organization that struck down the 1973 Roe v. Wade decision, enabling many states to restrict abortion access.

The regulatory change permits the sale of mifepristone, the first of two drugs used in a chemical abortion, at retail pharmacies. The drug could previously only be dispensed by some mail-order pharmacies, or by some doctors or abortion centers.

The rule change ends a previous in-person requirement for its dispersal. The new FDA rules still require a prescription for the drugs, but will permit a wider range of pharmacies to stock and sell them.

Medication abortions are becoming a more common method of abortion, accounting for more than half of the abortions in the United States, according to the Guttmacher Institute, a research center relied on by the abortion industry and advocacy groups.

Some Catholic and other pro-life groups have expressed concern about the safety of the drug. In a document outlining its opposition to expanding access to the drug for abortions, the U.S. Conference of Catholic Bishops argued that the FDA rejects safeguards governing its use that are in place in other countries, noting that in Sweden, for example, a woman undergoing a medication abortion would be “supervised by the midwife for 4 to 6 hours at the outpatient clinic.”

The FDA has called mifepristone “safe when used as indicated and directed.”

In a joint statement to OSV News, Dr. Marie Hilliard, co-chair of the Catholic Medical Association’s ethics committee, and Dr. Lester Ruppersberger, former CMA president, said the FDA has “promulgated a rule allowing for mail-order abortions, via prescribing mifepristone, regardless of the documented risks to women of the use of mifepristone: hemorrhage, infection, and retention of fetal remains (incomplete abortion).”

The new rule, they said, will “put the health of women, and their true informed consent, at risk.”

In a statement, Marjorie Dannenfelser, president of Susan B. Anthony Pro-Life America, said, “Chemical abortion pills can cause dangerous complications including hemorrhage and infection, and complications are more likely when pills are dispensed without medical screening or follow-up care.”

“State lawmakers and Congress must stand as a bulwark against the Biden administration’s pro-abortion extremism,” Dannenfelser said. “We hope to see the FDA do its job to protect the lives of women and put an end to chemical abortions.”

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