“But test them all; hold on to what is good.” – 1 Thessalonians 5:21
In 2000, the U.S. Food and Drug Administration (FDA) first approved Mifepristone, the chemical abortion pill, which is directly liable for the killing of 7.5 million preborn babies over the last 25 years. When the abortion pill was first approved, the FDA conferred upon it the Risk Evaluation and Mitigation Strategy (REMS) designation, as it was classified as an extremely dangerous drug.
Unfortunately, during the Obama and Biden years, the two administrations lessened the REMS restrictions on the abortion pill. The relaxed posture on Mifepristone by the administrations has allowed the destructive drug to become easily accessible for women.
A couple of months ago, twenty-two state Attorneys General sent a joint letter to the Trump Administration pleading for the reversal of Biden’s pro-death policies by stopping the selling and mailing of the dangerous abortion pill, and to reinstate safety regulations on it. Recently, the U.S. Health and Human Services Secretary Robert F. Kennedy Jr. and FDA Commissioner Marty Makary have responded to the letter by stating that the FDA will conduct “its own review of the evidence, including real-world outcomes and evidence, relating to the safety and efficacy of the drug.”
There is an overwhelming amount of evidence that reveals the destructive, damaging nature of the abortion pill that will, without a doubt, be found in the FDA review. Hopefully, the FDA will act quickly on its findings and protect women and preborn children from this deadly drug.
LET US PRAY…
Father, we praise You that the FDA is officially launching an investigative review on the abortion pill, Mifepristone. Lord, empower the FDA to use its findings to protect women and preborn children from the dangerous, destructive, and deadly drug. Father, thank You for the bold twenty-two state Attorneys General who sent this request letter to the Trump Administration. In Jesus’ Name, Amen.