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The FDA claimed in 2023 that less than 0.5% of women suffered “serious adverse reactions” to the abortion pill. A recent study, however, found that the pill is over 20 times more dangerous than the FDA initially claimed.
From The Daily Wire. The abortion pill is many times more dangerous than the FDA claimed, with more than one in 10 women suffering serious complications, a new study found.
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About 11.2% of 154,554 women experienced a “serious adverse event” after taking the mifepristone abortion pill in 2023, according to new research commissioned by the Foundation for the Restoration of America and released Monday.
That works out to about 17,310 women who suffered serious adverse events …
This is about 22 times higher than what the FDA put on its label for the brand Mifeprex in 2023 — the FDA cited clinical studies saying less than 0.5% of women suffered “serious adverse reactions” to mifepristone.
The two-pill chemical abortion regimen, mifepristone usually followed by misoprostol, aims to end the life of the unborn baby and expel it from the woman’s uterus. However, the drugs sometimes fail to expel all the fetal tissue, which can cause life-threatening complications. …
“This bombshell report is further evidence that our government uses phony data and politicized science to lie to its people. In this case, those lies further political ideologies rather than the health, safety, and well-being of women and children,” Doug Truax, founder of the Foundation for the Restoration of America, which commissioned the study, told The Daily Wire.
“If you had any other drug that was kind of similar in terms of the magnitude of what this thing does, anywhere north of 2% and they’d shut it down,” Truax said.
“They’re just hell bent on just increasing the amount of abortions.”
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(Excerpt from The Daily Wire. Photo Credit: Liudmila Chernetska/Getty Images via Canva Teams)