The FDA itself admits that a staggering 1 in 25 women WILL wind up in the emergency room after taking the abortion pill.

More than 2/3 of those women will require emergency surgery to save the mother’s life and future fertility. That’s why — for 20 years — the FDA only allowed the drug to be dispensed in person by a licensed physician to help prevent such deadly complications.

The government’s own data shows that in just one recent 18-month period, the drug injured or killed 3,197 women. The most common cause of death to the mother was sepsis, followed by drug toxicity/overdose, ruptured ectopic tubes, hemorrhage, and finally suicide. ALL of these are known side effects, highlighted by the FDA itself in the “Black Box Warning,” the strongest warning the FDA offers.

The patent for this deadly drug just happens to be owned by the Population Council, a eugenics group founded by John D. Rockefeller III with the help of Planned Parenthood founder Margaret Sanger to “reduce human population.” As of 2023, 63% of all abortions are a result of the Population Council’s population reduction drug.

Printed in each box of mifepristone is the FDA alert: “WARNING: SERIOUS AND SOMETIMES FATAL INFECTIONS OR BLEEDING,” before detailing the other numerous and deadly side effects of this abortifacient drug.

But in the quest to keep appeasing their Planned Parenthood donors, the Biden-Harris administration lifted the requirement for a doctor to physically examine the patient. Now out-of-state abortionists are mailing this drug into states with pro-life laws to ensure the abortion-killing machine keeps running at full speed. As a result, women’s lives are in nearly as much danger as their unborn children.

Missouri, Kansas, and Idaho have filed suit in federal court against the Biden-Harris FDA’s illegal actions. Liberty Counsel is on the case, and we are preparing our briefs now.

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The Biden-Harris FDA’s approval for mail-order delivery of this deadly drug not only violates the safety requirements of the Pediatric Research and Equity Act and the Federal Food, Drug, and Cosmetic Act due to potential harms for pregnant women and girls, as well as the Comstock Act, but also disregards state abortion laws and “enable and encourage” people to do what state pro-life laws expressly prohibit. Out-of-state abortionists are even mailing these abortifacients into pro-life states that have banned abortion, breaking state laws and putting their patients (who are often hundreds, if not thousands of miles away) in extreme physical danger.

The FDA lacked legal authority to make these decisions and acted arbitrarily and capriciously, committing an “an abuse of discretion,” and acted “otherwise not in accordance with law,” according to the lawsuit.

“[The] FDA permitted and sometimes even encouraged these illegal activities. But a federal agency cannot authorize unlawful actions,” wrote Missouri, Kansas, and Idaho. “In rolling back safeguard after safeguard, the FDA has turned a blind eye to the known harms of abortion drugs to the detriment of women and girls.”

The FDA needs to be held accountable for its unlawful actions. The FDA should no longer be allowed to circumvent safety laws to allow a eugenic drug to destroy innocent children and harm women. Abortion drugs have never been safe. They harm women while killing children.

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