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FDA Issues Public Warning Re Elidel and Protopic

On February 15, 2005 the US Food and Drug Administration (FDA) Pediatric Advisory Committee recommended a "black box" warning be placed on topical calcineurin inhibitor (ElidelŪ - pimecrolimus and ProtopicŪ - tacrolimus), followed by the FDA issuing a Public Health Advisory on March 10, 2005 regarding the safety concerns.

Click on one of the titles below to read statements regarding the FDA's black box warning:

American Academy of Dermatology (AAD)

Canadian Dermatology Association (CDA)

National Eczema Association for Science and Education (NEASE)

Inflammatory Skin Disease Institute