22 Republican lawyers request safety protocols

Exclusive: More than 20 Republican lawyers are demanding the reconstruction of Trump safety protocols to Abortion MivePristone, saying that he raises “serious risks to women.”

In a letter obtained by Fox News Digital, 22 public prosecutors invited the Minister of Health and Humanitarian Services Robert F. Kennedy Junior and head of the Food and Drug Administration Martin Macari to restore guarantees for grains canceled by Obama and Biden departments.

“Modern comprehensive studies of effects in the real world of chemical miscarriage drugs, MEFPPriston mentioned that serious negative events occur more than 22 times more than mentioned on the poster, while the drug is less than half effective as shown. The invitation group.

The EPPA report claims that birth control pills are harmful to women, causing a 1 out of 10 patients with a “dangerous negative event”, including bleeding, emergency room visits and outside the womb.

The head of the FDA does not have “no plans” for changes in the pill policy, but he continues to review safety

The letter, led by the Public Prosecutor in Kansas Chris Kobech, It comes after Kennedy Junior. Makary asked to review the latest data on MIFEPRISTONE and its safety.

“Based on this review, the FDA (FDA) must consider restoring the safety protocols that it identified in 2011 in 2011 in its release to the Risk Assessment and Reduction Management (ReMS) of Mivipriston, but that was removed by Obama and Biden departments,” you read the letters, adding that drugs should come out of the market if Safeguards from Put it in place.

“Instead, in light of the dangerous risks of women who prescribe this drug at the present time without decisive guarantees, and in the event that the FDA is unable In the field of objective diseases.

Senator Josh HolieSend R-MO. , Message to Kennedy Jr. Last month, he urged him to take immediate measures to restore safety degrees in MivePristone after the minister committed to conducting a safety safety review.

Macari previously said that he has no plans to modify the policies surrounding MivePristone, but FDA will work if the data suggests a safety problem.

MivePristone, which was taken with another drug called Mysoprostol to end early pregnancy, was approved for the first time by the FDA (FDA) in 2000 after a “comprehensive and comprehensive review” found that it was safe and effective, according to the agency website, which indicated that periodic reviews since its approval did not specify new safety concerns.

Last year, the Supreme Court rejected a challenge aimed at the availability of medicine. Prosecutors have sought to restrict access to Miviperton throughout the country, including the countries led by Democrats where abortion remains legally. The court did not judge whether the Food and Drug Administration acted legally when it moved during the Obama and Biden departments to ease the rules of the use of the MivePristone that was created during the Clinton administration.

More drug abortion constitute more than half of all miscarriages in the American health care system in 2023, according to a study conducted by the Guttmacher Institute.

Medical groups urging FDA, Kennedy to reconsider a wide approval of the abortion drugs

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“At the present time, women can get MivePristone by participating in one visit with any distance with any approved health care provider (not necessarily a doctor), and requesting medications through a pharmacy from mail request, and self -proof,” the lawyers wrote. “The description is only required to report a harmful event if he realizes that the patient has died.”

“The removal of the decisive safety protocols launched by this FDA in 2016 (and in 2023) only five years before the FDA (FDA), raises the issue of whether removal is driven by other considerations other than the safety of patients … The current FDA’s dedication to the health and welfare of all Americans is encouraging, as well as an exciting review of the contestants.