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Personal Injury Law

: A Georgia Lawyer

Exjade and the FDA

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The US Food and Drug Administration (FDA) is reviewing adverse event information for Exjade from a database that tracks all patients who are prescribed deferasirox (Exjade). This information suggests there may be a greater risk for adverse events such as kidney failure, gastrointestinal haemorrhage, and deaths in patients with myelodysplastic syndrome (MDS) compared with patients without these conditions.

Source here.

Full post as published by A Georgia Lawyer on September 26, 2009 (boomark / email).

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