| Subject: | FDA Notifies of Risk of PML with Increased Duration of Exposure to Tysabri |
| Category: | Food and Drug Administration (FDA)
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| Published: | Fri, 5 Feb 2010 - 02:00 pm |
| Audience: Neurological healthcare professionals, patients The Food and Drug Administration (FDA) has notified healthcare professionals and patients that the risk of developing progressive multifocal leukoencephalopathy (PML) increases with the number of Tysabri infusions received. This new safety information, based on reports of 31 confirmed cases of PML received by the FDA as of January 21, 2010, will now be included in the Tysabri drug label and patient Medication Guide. Information about the... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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