Shocking birth control deaths!!

mystifyingeyes · (#1 (**permalink**))

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FDA Criticized On Abortion
WASHINGTON - The father of a teen who died after taking an abortion pill says new safety warnings added by the government aren't enough to protect women. Because a third death now has been linked to RU-486, the Food and Drug Administration should bar sales of the abortion pill, said the grieving father.

"How many more deaths is it going to take before the FDA takes action to remove this drug from the market?" said Monty Patterson, 51, of Livermore, Calif.

His 18-year-old daughter, Holly, died on Sept. 17, 2003, of septic shock caused by inflammation of the uterus. The teen took RU-486 on Sept. 10 to terminate an unplanned pregnancy, Patterson said.

At least two other American women who took the pill in the United States died, although the FDA says it is unclear if their deaths were directly related to the document.

After his daughter's death, Patterson began lobbying for changes to the drug's label to avoid another tragedy. He received a courtesy call Monday from the FDA alerting him to new warnings linking RU-486 to the risk of life-threatening bacterial infections. He didn't learn about the third death until reviewing the agency's Web site.

Anti-abortion activists seized upon Holly Patterson's death in their campaign against Danco Laboratories' product, Mifeprex.

The FDA approved Mifeprex in 2000 to terminate pregnancy up to 49 days after the beginning of the last menstrual cycle. The drug blocks progesterone, a hormone required to sustain a pregnancy. When followed by another medicine, misoprostol, Mifeprex terminates the pregnancy.

Mifeprex already carries a "black box" warning, the agency's most strident alert, to highlight other safety concerns. The FDA said Monday that the drug's black box warning will expand, adding information about such rare but potentially life-threatening complications as serious bacterial infections and bleeding that can follow any abortion, including one induced by Mifeprex.

Since the drug was approved, the agency has received reports of serious bacterial infection, bleeding, ectopic - tubal - pregnancies that have ruptured and death. The fatalities including a death from sepsis, a severe infection, recently reported to FDA and leading to the revised black box.

Serious bacterial infection may silently, without typical signs of infection like fever or tenderness, the label warns. The revised label also cautions health care providers that prolonged, heavy bleeding may warrant surgical intervention.

Women who have taken the drug should contact a doctor immediately if they suffer fever, abdominal pain and heavy bleeding, a medication guiBde aimed at consumers says. And the FDA counsels women to take their medication guide to any health care provider they visit to speed treatment.

In addition, women who take the pill must sign a patient agreement pledging to contact a doctor immediately if they have fever higher than 100.4 degrees that lasts more than four hours or severe abdominal pain. The women are also warned that heavy bleeding that soaks two, thick full-sized sanitary pads per hour for two consecutive hours is cause for contacting a doctor.

According to Danco Laboratories, 360,000 American women have used the pill since it was approved by the FDA. In a letter sent to health care professionals on Nov. 12, the company stood by the safety and efficacy of the drug.

Concerned Women for America blasted the FDA for not pulling RU-486 from the market.

"It is reported that another woman has died after taking the abortion drug RU-486, and the FDA's response is to change the drug's label," said Wendy Wright, the group's senior policy director, in a statement. "This is a dangerous drug that deserves to be pulled off the market immediately."

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