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Amgen/J&J ESAs get REMS in US
17 February 2010
Malini Guha

The US FDA has approved a long-awaited REMS risk-management programme to inform healthcare providers and patients about the well-known risks of the erythropoiesis-stimulating agents (ESAs) marketed by Amgen and Johnson & Johnson. The REMS includes a training program called APPRISE for...



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