Fifty-three members of the House of Representatives sent a letter to the FDA to argue against Planned Parenthood's request that restrictions be removed from the distribution of the chemical abortion drug mifepristone. The drug has been linked to thousands of complications and 24 deaths in the United States alone, and a generic version of mifepristone, which up to this point had only been sold under the name Mifeprex, has been approved by the FDA.
An excerpt from the representatives' letter states, “We vigorously opposed calls by Planned Parenthood and other pro-abortion advocates to remove the REMS [Risk Evaluation and Mitigation Strategy] for mifepristone. Allowing the drug to be available without medical supervision will have dire consequences for women and children.” Click here for more.