Fri Feb 18, 2022 – 7:45 pm EST
(LifeSiteNews) – A watchdog group summary of spontaneously reported adverse reactions from the so-called “gold standard” abortion pill regimen shows numerous reports of serious events resulting in hospitalization.
Four total reports of life-threatening sepsis, numerous reports of hemorrhaging, and numerous failed abortions were among the findings of a report on the abortion pill regimen Mifegymiso, released in January by The Canada Vigilance Program, “a spontaneous reporting system” designed to detect “potential health product safety issues.”
The summary shared 43 reports of “adverse reactions” from Mifegymiso, the name in Canada for the combined use of Mifepristone and Misoprostol. The regimen is on the World Health Organization’s (WHO) list of essential drugs and is considered the “gold standard” for early medical abortion, according to the WHO.
A caveat on the first page of the report highlights the fact that these adverse reactions have been reported on a voluntary basis, and they cannot be used to determine the incidence of a particular reaction, or to estimate the risk of a product, since the total number of reactions and number of users of the abortion pill regimen is unknown.
In addition, it
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