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Why Are Certain Drugs Having Their Safety Reports Presented To The Pediatric Advisory Committee On November 18, 2005?

The eight products being reviewed are presently due for a public discussion of their adverse events as required by Section 17 of the Best Pharmaceuticals for Children Act (BPCA). BPCA mandates the review of the adverse event reports received during the one­year after a drug has been granted pediatric exclusivity. The FDA's Office of Pediatric Therapeutics (OPT) is authorized to carry out this mandate and is directed by law to refer such adverse event reports to the Pediatric Advisory Committee (PAC) for their review and recommendations regarding any regulatory actions.

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