| Subject: | FDA Provides Safety Information for Rituxan (rituximab) |
| Category: | Food and Drug Administration (FDA)
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| Published: | Tue, 27 Oct 2009 - 06:00 am |
| Audience: Rheumatological healthcare professionals The Food and Drug Administration (FDA) and Genentech have notified healthcare professionals about a third case of progressive multifocal leukoencephalopathy [PML], the first case of PML in a patient with rheumatoid arthritis [RA] treated with Rituxan who has not previously received treatment with a TNF antagonist. Information to date suggests that patients with RA who receive Rituxan have an increased risk of PML. Physicians should... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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