By Institute of Medicine, Board on Health Sciences Policy, Forum on Neuroscience and Nervous System Disorders, Bruce Altevogt, Miriam Davis, Sarah Hanson
The nutrients and Drug management (FDA) now calls for that every one scientific trials for medicines that have an effect on the principal apprehensive system--including psychiatric drugs--are assessed for even if that drug may well reason suicidal ideation or habit. The Institute of Medicine's (IOM) discussion board on Neuroscience and frightened process problems hosted a gathering on June 26, 2009, to debate the FDA's new coverage and the way to investigate top no matter if suicidal techniques expect real suicidal habit within the close to destiny.
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Extra info for CNS Clinical Trials: Suicidality and Data Collection: Workshop Summary
Example text
Caine. 2003. Risk of suicide and related adverse outcomes after exposure to a suicide prevention programme in the US Air Force: Cohort study. BMJ 327(7428):1376. , D. Goldston, and C. Gatsonis. 1993. Suicidal behaviors and childhood-onset depressive disorders: A longitudinal investigation. J Am Acad Child Adolesc Psychiatry 32(1):8–20. Laughren, T. 2009. Development of Division of Psychiatry Products policy on prospective suicidality assessment in studies conducted under INDs. Presentation at the IOM Workshop on CNS Clinical Trials: Suicidality and Data Collection, Washington, DC, June 16.
C. Feig, and E. D. Caine. 2003. Risk of suicide and related adverse outcomes after exposure to a suicide prevention programme in the US Air Force: Cohort study. BMJ 327(7428):1376. , D. Goldston, and C. Gatsonis. 1993. Suicidal behaviors and childhood-onset depressive disorders: A longitudinal investigation. J Am Acad Child Adolesc Psychiatry 32(1):8–20. Laughren, T. 2009. Development of Division of Psychiatry Products policy on prospective suicidality assessment in studies conducted under INDs.
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