Exposed: Abortion Pill, RU 486, Mifepristone, Mifeprex — Whatever They Call it, it Harms Women & Kills Babies

In a stunningly reckless move, President Obama’s Food and Drug Administration (FDA) recently relaxed standards for the abortion pill [originally called] RU-486. The new guidelines expand its use to abort babies who are even more developed in the womb, and require even less physician supervision of a drug that has hospitalized —and even killed— women. The abortion industry has been increasingly pushing abortion pills, telling women that RU-486 isn’t a REAL abortion. They’ve convinced women that “just taking a pill” early in the pregnancy when the baby is “just a clump of cells” isn’t really killing a child. With these new FDA guidelines, we’re seeing them push that lie even further. Today, Live Action launches its latest video to expose these abortion industry lies and the recklessness of the FDA’s decision — https://www.facebook.com/liveaction/videos/10154118219668728/ In this new video, Dr. Anthony Levatino, an OB/GYN who performed over 1200 abortions, uses medically accurate animations inside the womb to show how RU-486 abortion slowly starves a baby to death over a period of days. He also details how amazingly developed the baby is at this early stage and the pill’s potentially dangerous effects on the mother. These laxer FDA rules will bring huge financial benefits to the abortion industry. While the FDA’s expansion of RU-486’s use from seven weeks of pregnancy to 10 weeks is sure to increase the abortion industry’s clientele, according to the FDA’s own numbers, it also means TRIPLE the drug’s failure rate of the old seven-week limit. This will inevitably lead to more women — and their babies — being subjected to two abortions, as abortionists must then perform...

Exposed: REAL Reason FDA Chemical Abortion Guidelines Changed

Visit https://www.physiciansforlife.org/exposed-abortion-pill-ru-486-mifepristone-mifeprex-whatever-they-call-it-it-harms-women-kills-babies/ to learn about the consequences of these recently ‘relaxed but reckless’ FDA Guidelines for Abortion Pill Use Main Article On March 30th, 2016, the FDA, under the guidance of the Obama administration, made big changes to the rules regarding the use of chemical abortions. Many on the pro-choice side are claiming this move was to expand women’s abortion access. However, in a new video series by Life Dynamics called The Real Story, President Mark Crutcher states that abortion clinics have been providing chemical abortions at one-third dosages for pregnancies that were well past the cut-off date since day one. He reveals that the real reason for the FDA’s decision was to protect abortion industry profits. FDA Smoke and Mirrors – the decision to protect abortion industry profits. (FDA chemical abortion) Mark Crutcher gives the real story behind the decision to change FDA chemical abortion guidelines in the video, The Real Story: FDA’s Strategy to Protect the Abortion Industry’s Profits   (see link  below) Crutcher adds that the abortion industry realized that smaller doses and performing them at much later stages of pregnancy is “a gold mine.” “One-third dosages increase profits, and using it past the specified cut off date grows the customer base.” But with such measures come increased risks and complications. Life Dynamics knows this perhaps better than anybody. For the past 20 years, the pro-life organization has been providing litigation support services to attorneys who sue on behalf of women who have been killed, injured or sexually assaulted while having abortions. Traditionally, incomplete abortions accounted for a small number of cases that they assisted with. But...