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New Rules for Reporting Adverse Events from Abortion Drugs

This act aims to improve data collection on abortion drugs and related adverse events. It mandates healthcare providers and manufacturers to report such events and allows patients to self-report issues. The goal is to ensure more accurate information on the safety of these medications.
Key points
Mandatory reporting of deaths and other adverse events related to abortion drugs to the FDA and manufacturers within 15 days.
Mandatory reporting of prescribing, dispensing, or administering abortion drugs to the FDA and CDC within 15 days.
Creation of online portals for healthcare providers and patients to easily and confidentially report adverse events.
Annual publication of detailed data on the number of abortion drugs prescribed, adverse events, and deaths associated with their use.
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Additional Information
Print number: 118_HR_2570
Sponsor: Rep. Pfluger, August [R-TX-11]
Process start date: 2023-04-10