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On November 10, 2005, the Food and Drug Administration (FDA) added a warning to the labeling
of ORTHO EVRA transdermal contraceptive "Patch".
The following links will provide additional information:
At this time, the FDA is not suggesting that women using ORTHO EVRA change to another contraceptive method.
If you have concerns, please talk to your Student Health Services physician or nurse practitioner about
how this information relates to your use of ORTHO EVRA.
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