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Amgen and Wyeth Pharmaceuticals, a division of Wyeth, issued a statement in response to the Food and Drug Administration announcement regarding the results of a safety review of Tumor Necrosis Factor blockers. This safety review was the subject of an FDA Early Communication in June 2008 pertaining to cases of malignancy in pediatric patients exposed to a TNF blocker. As a result of this review, the FDA has required strengthened warnings about the occurrence of lymphoma and other cancers in children and young adults using these medicines.

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