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Sunday, July 17, 2011

RU486 - increase in serious side affects released quietly

New FDA Report: Abortion Drug Kills 14 Women, Injures 2,200
by Steven Ertelt | Washington, DC | LifeNews.com | 7/12/11 3:02 PM

The Food and Drug Administration has quietly released a new report about the deaths of and injuries to women from the dangerous RU 486 abortion drug and the Obama administration has done nothing to make the information available to women.

Following its approval during the Clinton administration, the FDA released a report in 2006 that received widespread attention for showing more than 1,100 women had been subjected to “adverse effects” resulting from their taking the abortion drug mifepristone, commonly known a RU 486. Pro-life advocates have waited five years for the FDA to come out with a new report of problems associated with the drug — despite mounting evidence that the abortion drug continues to kill and injure women across the globe.

The FDA, with no fanfare, has released a new report, dated April 30, 2011. The report indicates 14 women in the United States alone have died from using the mifepristone abortion drug and 2,207 women have been injured by it.

Of the women experiencing medical and physical problems resulting from the abortion drug, 612 women required hospitalizations, 339 experienced blood loss significant enough to require a transfusion, 256 experienced infections and 48 women experienced what the FDA labeled as “severe infections.” Given that the RU 486 abortion drug caused sepsis, a potentially lethal infection that resulted in the deaths of women from around the world, the “serious infections” were very likely life-threatening situations.

“Severe infections generally involve death or hospitalization for at least 2-3 days, intravenous antibiotics for at least 24 hours, total antibiotic usage for at least 3 days, and any other physical or clinical findings, laboratory data or surgery that suggest a severe infection,” the FDA report states. Read full article

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