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New Rules for Reporting Adverse Events from Abortion Drugs

This act introduces new requirements for healthcare providers and patients to report adverse events related to abortion drugs. The goal is to improve data collection on the safety of these medications, potentially affecting the availability of information on their use and potential health risks for women.
Key points
Healthcare providers must report any deaths or adverse events associated with abortion drugs to the FDA and manufacturers within 15 days.
Online portals will be established for both healthcare practitioners and patients to easily and confidentially report adverse events.
More data on prescribed abortion drugs, their shipment, deaths, and serious adverse events will be collected and published annually, increasing transparency.
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Additional Information
Print number: 117_HR_6702
Sponsor: Rep. Walorski, Jackie [R-IN-2]
Process start date: 2022-02-09