| 2005N-0345 | Drug Approvals: Circumstances under which an active ingredient may be simultaneously marketed in both a prescription drug product and an over-the-counter drug product | |||||||||||||||||||||||
| FDA Comment Number : | EC748 | |||||||||||||||||||||||
| Submitter : | Dr. Bridget Bly | Date & Time: | 10/13/2005 08:10:17 | |||||||||||||||||||||
| Organization : | Dr. Bridget Bly | |||||||||||||||||||||||
| Category : | Individual Consumer | |||||||||||||||||||||||
| Issue Areas/Comments | ||||||||||||||||||||||||
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| I am outraged that the FDA has failed to follow the recommendation of its own advisory panel to release the "morning after pill" (Plan B) to consumers. It's blatant political nonsense, and it makes the FDA look like a pawn of politicians. Women need this drug, they have a right to it, and to withhold it violates a woman's right to choose. | ||||||||||||||||||||||||