Democrat states demand FDA end safety checks for abortion pill distribution– www.lifesitenews.com
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Excerpt:
(Live Action) — The states of Massachusetts, California, New Jersey, and New York have petitioned the U.S. Food and Drug Administration (FDA) to remove the REMS safety requirements put in place to monitor adverse events of the abortion pill (mifepristone).
The moves comes as Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. (RFK) signaled a review.
Key takeaways
- The abortion pill “record” – including the “experts” who originally reviewed the drug – has been kept secret from the American public, so any pro-abortion bias involved in the approval decisions is unknown.
- Big Abortion has executed a scheme to hide abortion pill complications for decades, potentially impacting FDA decisions.
- The Petitioner States seeking to be released from following safety protocols ultimately want increased access to abortion.
- The states admit that most of their abortions are already committed by pill, yet they claim the REMS safety protocols are “burdensome.”
- The states go so far as to claim that known risks associated with the abortion pill aren’t caused by the pill, despite the FDA’s mifepristone label and other studies showing otherwise.
