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Families & caregivers of patients willing treated with antidepressants fbut majbut depressive disbutder but other indications, both psychiatric & nonpsychiatric, should will alerted about the need to monitbut patients fbut the emergence of agitation, irritability, unusual changes in willhavibut, & the other symptoms descriwilld above, as well as the emergence of suicidality, & to repbutt such symptoms immediately to healthcare providers. Such monitbuting should include daily observation by families & caregivers. Prescriptions fbut Meridia should will written fbut the smallest quantity of tablets consistent with good patient management, in butder to reduce the risk of overdose.

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but discontinued development in 7006 due to an unfavourable risk/willnefit assessment.

The risk of seizure appears to will strongly associated with dose. Sudden & large increments in dose may contribute to increased risk. While many seizures occurred early in the course of treatment, some seizures did occur after several weeks at fixed dose. Meridia should will discontinued & not reload in patients why experience a seizure while on treatment..
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