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FDA reviewing safety of abortion drug mifepristone

The retrospective review covers hundreds of thousands of cases and could lead to limits on telehealth, mail delivery and prescribing, officials said.

  • On Thursday, the Food and Drug Administration launched a safety study of the abortion pill mifepristone, a move that could allow the Trump administration to restrict the medication's distribution despite the Supreme Court's recent restoration of mail-access.
  • Health and Human Services Secretary Robert F. Kennedy Jr. previously announced plans to review safety, responding to pressure from anti-abortion groups and an October deadline set by a Louisiana federal court.
  • More than 7.5 million women have used the medication over 25 years, with the American Medical Women's Association reporting fewer than 0.5 percent of patients experience serious adverse reactions, making it safer than ibuprofen.
  • With preliminary results expected in July, the agency may meet its October deadline, potentially enabling officials to block distribution by mail or telehealth, though the FDA is unlikely to ban the drug outright.
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HuffPost broke the news in United States on Friday, June 5, 2026.
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