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WASHINGTON, DC, (CWNews.com) - The manufacturer of the abortion pill mifepristone, also known by the designation RU-486, has issued a warning letter to doctors that two women have died and six woman developed serious illnesses after taking the drug.
The Food and Drug Administration and Danco Laboratories, which sells the drug under the brand name Mifeprex, said two women experience "serious systemic bacterial infections" and one of the them died. Another suffered a non-fatal heart attack, and three women had ectopic pregnancies that ruptured, killing one. In an ectopic pregnancy the embryo develops outside the womb, often in the fallopian tubes. The FDA warned doctors not to prescribe the abortion drug to abort ectopic pregnancies.
Danco and the FDA both asserted that no causal relationship had been established between the drug and the deaths and illnesses, but pro-life groups immediately assailed the drug and its makers and said their predictions of disaster are coming true.
Wendy Wright of Concerned Women for America said, "The
FDA approved RU-486 under intense political pressure, and now women are
suffering the consequences." She added, "We warned the public that this would
happen when the drug was approved. RU-486 is harmful to women. Abortion
lobbyists should stop putting their political agenda above women's health, and
end their advocacy and distribution of RU-486."
http://www.ewtn.com/vnews/getstory.asp?number=25694
Saint
Charbel for Life
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