The Food and Drug Administration announced Friday that it will overhaul packaging labels for the emergency contraceptive pill, Plan B.
The Food and Drug Administration announced Friday that it will overhaul packaging labels for the emergency contraceptive pill, Plan B, that women can take after having sex to prevent a pregnancy.
The new labels are intended to further distinguish the emergency contraception - also known as the morning after pill - from abortion pills, which end a pregnancy after a fertilized egg has implanted in the lining of a woman's uterus. "Evidence does not support that the drug affects implantation or maintenance of a pregnancy after implantation, therefore it does not terminate a pregnancy," the FDA said in its statement.
About a quarter of women say they've used emergency contraception pills at some point, according to a survey by the Centers for Disease Control released last year.
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FDA changes Plan B label, clarifies it won't cause abortionThe Food and Drug Administration announced Friday that it will overhaul packaging labels for the emergency contraceptive pill, Plan B, that women can take after having sex to prevent a pregnancy
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FDA changes Plan B label, clarifies it won't cause abortionThe Food and Drug Administration announced Friday that it will overhaul packaging labels for the emergency contraceptive pill, Plan B, that women can take after having sex to prevent a pregnancy.
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FDA changes Plan B label, clarifies it won't cause abortionWASHINGTON (AP) — The Food and Drug Administration announced Friday that it will overhaul packaging labels for the emergency contraceptive pill, Plan B, that women can take after having sex to prevent a pregnancy.
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U.S. FDA changes Plan B label to say it does not cause abortionThe consumer information distributed with the emergency contraception now makes clear its mechanism of action does not alter the implantantion of an egg.
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