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The Pharmaceutical Journal Vol 265 No 7117 p510
October 07, 2000 Clinical

Safety issues with etanercept

Wyeth is amending the summary of product characteristics for its anti-tumour necrosis factor (TNF) drug etanercept (Enbrel) following reports of blood dyscrasias associated with its use.
The company says that although rare, blood dyscrasias such as pancytopenia and aplastic anaemia, some with a fatal outcome, have been reported during treatment with etanercept in patients with rheumatoid arthritis. Therefore, it is recommending that caution should be exercised when treating patients with a previous history of blood dyscrasias and that, if dyscrasia is confirmed, etanercept should be discontinued. It adds that patients should be told to seek immediate medical advice on developing symptoms suggestive of blood dyscrasia or infection and that these patients should be investigated urgently.