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US FDA orders "black box" suicidality warnings and studies for Chantix and Zyban

This article was originally published in SRA

Executive Summary

The US Food and Drug Administration has ordered Pfizer and GlaxoSmithKline to add “black box” label warnings about serious neuropsychiatric effects for the smoking cessation drugs Chantix (varenicline) and Zyban (bupropion)1. The companies also must conduct postmarketing clinical trials to determine the incidence of serious neuropsychiatric symptoms, including depression and suicidality, in patients taking the therapies.

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