Tamiflu associated with Changes in Behavior

March 20, 2008

Roche and FDA informed healthcare professionals of neuropsychiatric events associated with the use of , in patients with .The label has been revised as follows: can be associated with a variety of neurologic and behavioral symptoms which can include events such as hallucinations, delirium, and , in some cases resulting in fatal outcomes. These events may occur in the setting of encephalitis or encephalopathy but can occur without obvious severe disease. There have been postmarketing reports (mostly from Japan) of delirium and leading to injury, and in some cases resulting in fatal outcomes, in patients with who were receiving . Because these events were reported voluntarily during clinical practice, estimates of frequency cannot be made but they appear to be uncommon based on usage data. These events were reported primarily among pediatric patients and often had an and rapid resolution. The contribution of to these events has not been established. Patients with should be closely monitored for signs of . If neuropsychiatric symptoms occur, the risks and benefits of continuing treatment should be evaluated for each patient.

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