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Published Online: 1 December 2013

Varenicline, Smoking Cessation, and Neuropsychiatric Adverse Events

Abstract

In contrast to indications that prompted a 2009 black box warning, varenicline-which can more than double the chances of successfully quitting smoking-was not associated with serious risk of depression, suicidal ideation, or aggression across well-controlled trials.

Abstract

Objective

In 2009, the U.S. Food and Drug Administration issued a black box warning for varenicline regarding neuropsychiatric events. The authors used data from randomized controlled trials and from a large Department of Defense (DOD) observational study to assess the efficacy and safety of varenicline.

Method

The authors reanalyzed data from the 17 placebo-controlled randomized controlled trials (N=8,027) of varenicline conducted by Pfizer, using complete intent-to-treat person-level longitudinal data to assess smoking abstinence and reports of suicidal thoughts and behavior, depression, aggression/agitation, and nausea and to compare effects in patients with (N=1,004) and without (N=7,023) psychiatric disorders. The authors also analyzed a large DOD data set to compare acute (30-day and 60-day) rates of neuropsychiatric adverse events in patients receiving varenicline or nicotine replacement therapy (N=35,800) and to assess reports of anxiety, mood, and psychotic symptoms and disorders, other mental disorders, and suicide attempt.

Results

In the randomized controlled trials, varenicline increased the risk of nausea (odds ratio=3.69, 95% CI=3.03–4.48) but not rates of suicidal events, depression, or aggression/agitation. It significantly increased the abstinence rate, by 124% compared with placebo and 22% compared with bupropion. Having a current or past psychiatric illness increased the risk of neuropsychiatric events equally in treated and placebo patients. In the DOD study, after propensity score matching, the overall rate of neuropsychiatric disorders was significantly lower for varenicline than for nicotine replacement therapy (2.28% compared with 3.16%).

Conclusions

This analysis revealed no evidence that varenicline is associated with adverse neuropsychiatric events. The evidence supports the superior efficacy of varenicline relative to both placebo and bupropion, indicating considerable benefit without evidence of risk of serious neuropsychiatric adverse events, in individuals with and without a recent history of a psychiatric disorder.

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Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 1460 - 1467
PubMed: 24030388

History

Received: 20 December 2012
Revision received: 9 April 2013
Accepted: 29 May 2013
Published online: 1 December 2013
Published in print: December 2013

Authors

Details

Robert D. Gibbons, Ph.D.
From the Center for Health Statistics and the Departments of Medicine, Health Studies, and Psychiatry, University of Chicago, Chicago; the Department of Molecular Imaging and Neuropathology, New York State Psychiatric Institute; and the Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York.
J. John Mann, M.D.
From the Center for Health Statistics and the Departments of Medicine, Health Studies, and Psychiatry, University of Chicago, Chicago; the Department of Molecular Imaging and Neuropathology, New York State Psychiatric Institute; and the Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York.

Notes

Address correspondence to Dr. Gibbons ([email protected]).

Funding Information

Supported by NIMH grants MH062185 (to Dr. Mann) and MH8012201 (to Dr. Gibbons).

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