A shocking new study finds that an abortion drug – long-touted by the FDA as “safe and effective – is in fact “far more dangerous” and puts women at significant risk of contracting sepsis, infections, hemorrhaging, and even hospitalization.
The Ethics and Public Policy Center has released a new analysis of data from more than 800,000 women who were prescribed mifepristone and found that many of the participants had serious adverse side effects from the drug.
Mifepristone is the drug most commonly used in chemical abortions, and it is now reportedly being used in more than six in 10 abortions in the United States.
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The findings were published in a study called “The Abortion Pill Harms Women: Insurance Data Reveals One in Ten Patients Experiences a Serious Adverse Event.” The data was compiled from HIPAA-compliant analysis through an all-payer insurance claims database that includes 865,727 prescribed mifepristone abortions from 2017 to 2023.
In nearly 11% of the cases, women experienced sepsis, infection, hemorrhaging, or other serious adverse events within 45 days of taking the drug.
That figure is 22 times higher than the original summary figure of “less than 0.5%” in clinical trials as reported on the drug label.
“In light of this research, we urge the FDA to reinstate earlier, stronger patient safety protocols and reconsider its approval of mifepristone altogether. Women deserve better than the abortion pill,” urged the study’s authors Ryan Anderson and Jamie Bryan Hall.
“Simply stated, mifepristone, as used in real-world conditions, is not ‘safe and effective,'” they added.
American United for Life, which launched the study in collaboration with EPPC, cites that the FDA’s trial data on the drug is inaccurate and outdated.
“Danco Laboratories markets Mifeprex as ‘the safe and effective abortion pill,’ but our research shows that mifepristone abortion, as currently practiced in the U.S., is not safe and effective. The manufacturer and the FDA rely on the results of 10 clinical trials with a total of 30,966 participants, less than 0.5% of whom reportedly experienced serious adverse reactions,” the study outlines.
The researchers contend the latest findings suggest the FDA should go back to its previous guidelines which stipulated that mifepristone should be administered only in a clinic, medical office, or hospital, and under the supervision of a physician who can assess the gestational age of an embryo and diagnose ectopic pregnancies. Furthermore, it suggests that the drug only be prescribed to a woman who is confirmed by a physician to be in the first seven weeks of pregnancy.
This is certainly not the guideline by which women can receive the drug today. Many women can obtain mifepristone in the mail after completing a virtual (telehealth) visit with a doctor. In some cases, the drugs are mailed to states that actually ban abortion.
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Reprinted with permission from cbn.com. Copyright © 2025 The Christian Broadcasting Network Inc. All rights reserved.
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