Volume 4, Issue 3, Page 10 (March 2008)
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The letter is available at: www.fda.gov/medwatch/safety/2008/safety08.htm#Tysabri. Serious adverse events in natalizumab users should be reported to Biogen Idec at 800-456-2255, or to the FSA at www.fda.gov/medwatch.
PII: S1553-3212(08)70106-7
doi:10.1016/S1553-3212(08)70106-7
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