Abortion Pill Kills

Live Action is exposing the shocking history of the abortion pill and the abortion industry’s plan to deregulate the lethal abortion pill drug.

Since the FDA first approved this drug, 5.6 million preborn children have been killed by this pill. The FDA’s website states that “As of June 30, 2022, there were 28 reports of deaths in patients associated with mifepristone since the product was approved in September 2000 (read more here) and the FDA has received over 4,000 reports of adverse events from women experiencing hemorrhage, excruciating abdominal pain, and severe life-threatening infections. FDA claims that “ The adverse events cannot with certainty be causally attributed to mifepristone.”

*Please Note, this report has been written in consultation with the American Association of Pro-life OB/GYNS (AAPLOG). 

What is the abortion pill?

The abortion pill is known under the brand name “Mifeprex” or, generically, mifepristone. For use as an abortion drug, it is administered in a 200 mg dosage. The abortion pill may also often be referred to as “chemical abortion,” “medication abortion,” “medical abortion,” or “RU-486” and was approved by the FDA for use in a drug regimen along with a second drug known generically as misoprostol. Mifepristone kills the child in the womb by blocking the pregnancy hormone progesterone, which is needed to sustain a pregnancy. The action of the drug deprives the developing human being of the nutrients he/she needs to survive. Misoprostol (originally approved for use as an ulcer drug) is taken either hours or days after mifepristone, causing contractions to expel the child from the womb.

This drug regimen has been approved by the FDA for use up to 10 weeks or 70 days of pregnancy, though some practitioners prescribe it far beyond this approved gestational limit.

Further Reading:

Risks

Beyond the millions of children the abortion pill has killed, some women have suffered from its adverse effects. From 2000 through December 31, 2024, 4,252 adverse effects have been reported to the FDA*, including:

  • 1,056 hospitalizations (excluding death) with 97 involving ectopic pregnancies
  • 606 instances of blood loss requiring transfusion
  • 422 infections (79 severe)
  • 36 maternal deaths (through December 31, 2024)

In 2016, the FDA removed the requirement that any adverse event (complication) except death be reported to the abortion pill’s manufacturers. This leaves open the potential for a great number of unreported complications. In addition, some abortion providers now advise women to claim they are experiencing natural miscarriages when presenting to emergency departments.

*The FDA claims that “The adverse events cannot with certainty be causally attributed to mifepristone because of concurrent use of other drugs, other medical or surgical treatments, co-existing medical conditions, and information gaps about patient health status and clinical management of the patient.”

FURTHER READING:

Funders

Over the past two decades, many of the same investors in the brand name and generic abortion pill manufacturers, Danco Laboratories and GenBioPro, have funded other abortion industry groups along with clinical trial location sites and sponsors – which purport to show that the abortion pill is safe and effective.

FURTHER READING:

Abortion Pill Reversal

Some medical practitioners offer a treatment to attempt to counteract the effects of mifepristone. They believe that if administered in time after a woman has taken the first drug in the abortion pill regimen, this treatment could potentially save the life of a preborn child. (The treatment is not likely to be effective if administered after the second drug, misoprostol, is taken.)

This treatment involves the administration of progesterone, a necessary and natural pregnancy hormone required to sustain life, in an attempt to outcompete the progesterone-blocking effects of mifepristone. For decades, medical practitioners have safely prescribed progesterone to women at risk of miscarriage.

According to a 2024 primer from the Charlotte Lozier Institute:

Drs. George Delgado, Matt Harrison, and Mary Davenport have conducted studies providing evidence for the efficacy of abortion pill reversal. The most notable study in 2018 found that when following 754 patients who decided to attempt to reverse a drug-induced abortion, around 66% had continuing pregnancies when using the most effective regimens of intramuscular progesterone and high-dose oral progesterone within 72 hours of taking mifepristone.

In women who had reversals as well as subsequent follow-up after delivery, there were seven reported birth defects. The associated rate, 2.7%, is equal to​ the birth defect rate among the general population, which is approximately 3%. There thus appears to be no increased risk of birth defects, according to Delgado, for babies born after mifepristone reversal.

*Go to abortionpillreversal.com if you are in need of help

FURTHER READING:

Self-Managed Abortion

The abortion industry is rapidly pushing to increase abortion sales and decrease the blood on their hands by promoting self-managed abortions. The abortion industry has heavily promoted self-managed or DIY at-home abortions under the guise of being a more holistic and comfortable way for women to abort in their own homes. In reality, however, telabortion, order-by-mail abortion, and over-the-counter chemical abortion have increased sales and left women to face the reality of potentially seeing their deceased children when they deliver them at home. Many women never consult or see a medical practitioner when taking the abortion pill at home, and if she experiences complications, she is often left to visit an emergency room or urgent care with no help whatsoever from her abortion pill prescriber.

FURTHER READING:

Abortion Pill Stories

Hear the stories of women who have been affected by the abortion pill.

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