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Pro-Life Leaders Criticize FDA Over Abortion Pill Safety Concerns

Policeman stands guard at the U.S. Supreme Court in Washington

Pro-life leaders have raised concerns over the Food and Drug Administration's (FDA) approach to the controversial abortion pill, mifepristone, which has sparked a high-stakes legal battle. The U.S. Supreme Court recently heard arguments in a case that could impact nationwide access to abortion pills, particularly mifepristone, drawing criticism from pro-life advocates.

The FDA approved mifepristone in 2000 for ending pregnancies up to 10 weeks gestation. In 2021, the FDA made changes to increase accessibility, including eliminating the requirement for in-person doctor visits for prescriptions. However, a federal appeals court in Texas later deemed these changes illegal, leading to the current Supreme Court review.

Pro-life leaders, including March for Life President Jeanne Mancini, have accused the FDA of jeopardizing women's health by relaxing safety measures around mifepristone. They argue that the drug, which carries a black box warning indicating serious risks, should not be prescribed without proper medical oversight.

National Right to Life President Carol Tobias criticized the FDA for yielding to pressure from the abortion industry and allowing mifepristone to be distributed without in-person exams. SBA Pro-Life America President Marjorie Dannenfelser emphasized the importance of upholding safeguards for women and girls, urging the Supreme Court to reinstate previous safety standards.

On the other hand, pro-choice groups maintain that mifepristone is a safe and essential drug in the realm of reproductive health, especially in a post-Roe landscape. The case, FDA v. Alliance for Hippocratic Medicine, remains a focal point of debate between pro-life and pro-choice advocates, with each side emphasizing the importance of women's health and safety.

Erik Baptist of Alliance Defending Freedom highlighted that pro-life groups are advocating for the reinstatement of longstanding safety protocols surrounding mifepristone. The outcome of this case could have significant implications for the regulation of abortion pills and women's healthcare in the United States.

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