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Antidepressant Medications and Suicide Risk: What Was the Impact of FDA Warning?

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Abstract

Suicide is one of the most relevant public health pathological behavior worldwide and is frequently associated with major depression. Antidepressant (AD) medications are usually considered as a treatment of first choice although evidence that AD drugs may stimulate suicidality especially in children and adolescents has been reported. In 2004, the Food and Drug Administration (FDA) issued a black boxed warning for AD treatment in these populations, but no concluding evidence has been found to date. This chapter aimed to review the current literature concerning the effect of AD medications on suicidality together with discussing the effects of FDA warning on AD prescription volumes and suicidality in the different age groups. Moreover, future perspectives based on recent pharmacogenomic findings and updated clinical management strategies will be discussed in order to provide some further understandings and practical suggestions to better manage this debated topic.

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Serafini, G., Solano, P., Amore, M. (2016). Antidepressant Medications and Suicide Risk: What Was the Impact of FDA Warning?. In: López-Muñoz, F., Srinivasan, V., de Berardis, D., Álamo, C., Kato, T. (eds) Melatonin, Neuroprotective Agents and Antidepressant Therapy. Springer, New Delhi. https://doi.org/10.1007/978-81-322-2803-5_31

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  • Publisher Name: Springer, New Delhi

  • Print ISBN: 978-81-322-2801-1

  • Online ISBN: 978-81-322-2803-5

  • eBook Packages: MedicineMedicine (R0)

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