What REALLY happened when the FDA approved the abortion pill?

Obviously, the Food and Drug Administration (FDA) should never have approved a drug intended to kill an innocent preborn child. However, real-world data shows that the abortion pill also poses serious health risks for the mother as well.

Pro-abortion advocates claim to care about women's health. So, how did such a dangerous drug ever receive FDA approval?

Today’s episode dives into a complex and eye-opening investigation into the FDA's approval of the abortion pill combination of mifepristone (RU-486) and misoprostol. Researcher Teresa Marsano joins us to reveal how a web of politics, pharmaceutical deals, and population control strategies converged to push the drug onto the U.S. market—and ultimately around the world.

As you listen, you’ll hear how the abortion pill’s approval involved unusual regulatory shortcuts for RU486, a second drug (misoprostol) used off-label, and real-world data that paints a very different picture than what the public (and abortion-vulnerable women) have been told. Teresa also traces how U.S. government, the Population Council, and the World Health Organization viewed FDA approval as the gateway to distributing the abortion pill globally.

This conversation covers a lot of ground—history, science, law, and ethics—so keep the big picture in mind: how pressure on the FDA led to unusual regulatory practices with profound implications for women’s health and population policy.

As with all guests, Teresa Marsano's views are her own and not necessarily reflective of HLI.

Teresa's first episode on Living a Culture of Life podcast: How Abortion Pill Vendors Violate Public Health Laws | Teresa Marsano

Download your FREE eBook to find out more about the United States' depopulation agenda: Uncover the Global Depopulation Project (Funded With Your Tax Dollars!) | Human Life International

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