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FDA Commissioner Pledges to Investigate Mifepristone

  • On June 4, 2025, FDA Commissioner Marty Makary announced plans to reassess the safety profile of the abortion drug mifepristone in response to new concerns highlighted by a recent study.
  • This review was initiated following a study referenced by Senator Josh Hawley, conducted by a policy research organization, which reported that nearly 11% of women experienced serious complications such as sepsis, infection, or hemorrhaging after using the medication.
  • Drawing from an analysis of nearly 866,000 mifepristone abortions recorded between 2017 and 2023, the study reported rates of side effects such as sepsis, infection, and hemorrhaging that greatly surpass the risks indicated on the FDA label; however, the findings have not undergone peer review.
  • Makary expressed his dedication to thoroughly reviewing the data on mifepristone alongside FDA career scientists, emphasizing that the agency maintains ongoing surveillance of the drug’s safety after its approval, even as critics question the study’s methods and conclusions.
  • The review could influence future regulatory decisions amid ongoing legal challenges and political debate, but its impact on drug access remains unclear at this time.
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RFK Jr. Calls for a Review of Abortion Pill Mifepristone

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LifeNews.com broke the news in New York, United States on Tuesday, June 3, 2025.
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