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New warning issued on Rituxan for lupus

Biogen Idec and Genentech have warned doctors that two patients taking Rituxan for lupus have died of a rare brain infection called progressive multifocal leukoencephalopathy, or PML. Rituxan is approved for non-Hodgkin's lymphoma and rheumatoid arthritis and cancer patients have already been warned about their risk of PML. One analyst noted that the new risk for lupus may make it harder for the companies to gain approval to use Rituxan for lupus and M.S. Biogen Idec has also had to deal with the risk of PML raised by its MS drug Tysabri. That drug was withdrawn until a new safety program was assembled.

- read the FDA's warning on the drug
- here's the report from The New York Times

Related Articles:
Rituxan data encourages researchers. Report
FDA approves Rituxan for rheumatoid arthritis. Report
FDA allows Tysabri back on the market. Report

More stories about FDA   Genentech   multiple sclerosis   Tysabri   Rituxan   non-Hodgkin's lymphoma   lupus   Biogen Idec   PML   Rheumatoid Arthritis   lymphoma  

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