Urging the Director of the Food and Drug Administration to reevaluate the safety of all chemical abortion drugs in light of recent independent studies, and for other purposes.
This resolution urges the Director of the Food and Drug Administration (FDA) to undertake a comprehensive reevaluation of the safety of all chemical abortion drugs . This call is made in light of recent independent studies that suggest a significantly higher rate of serious complications than currently reported, alongside concerns about expanded access under previous administrations. The resolution highlights that chemical abortions now constitute over half of all abortions in the United States, with expanded access raising issues regarding potential violations of federal law, increased risks of coercion, and intentional misuse. It specifically requests the FDA to publicly release a full safety review of these drugs, incorporating real-world outcomes and complications to address these growing concerns.
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Timeline
Submitted in House
Referred to the House Committee on Energy and Commerce.
Submitted in House
Referred to the House Committee on Energy and Commerce.
Health
Urging the Director of the Food and Drug Administration to reevaluate the safety of all chemical abortion drugs in light of recent independent studies, and for other purposes.
USA119th CongressHRES-803| House
| Updated: 10/10/2025
This resolution urges the Director of the Food and Drug Administration (FDA) to undertake a comprehensive reevaluation of the safety of all chemical abortion drugs . This call is made in light of recent independent studies that suggest a significantly higher rate of serious complications than currently reported, alongside concerns about expanded access under previous administrations. The resolution highlights that chemical abortions now constitute over half of all abortions in the United States, with expanded access raising issues regarding potential violations of federal law, increased risks of coercion, and intentional misuse. It specifically requests the FDA to publicly release a full safety review of these drugs, incorporating real-world outcomes and complications to address these growing concerns.