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Primary Care Companion to The Journal of Clinical Psychiatry logoLink to Primary Care Companion to The Journal of Clinical Psychiatry
letter
. 2010;12(2):PCC.09l00800. doi: 10.4088/PCC.09l00800blu

Addition of Bupropion SR to Varenicline Alleviated Depression and Suicidal Ideation: A Case Report

Maher Karam-Hage 1,, Kairav R Shah 1, Paul M Cinciripini 1
PMCID: PMC2910992  PMID: 20694128

To the Editor: Varenicline, bupropion sustained release (SR), and nicotine replacement therapy are established and US Food and Drug Administration (FDA)–approved treatments for smoking cessation.13 Recently, there has been a surge of postmarketing reports to the FDA associating varenicline with depressive symptoms, fatigue, suicidal ideation, or in some cases death.4

Case report. Ms A, a 49-year-old white woman with non–small cell lung cancer, had been smoking since she was 14 years old an average of 20 cigarettes/d. Her Fagerström Test for Nicotine Dependence5 score was 7 (maximum = 10), indicating high nicotine dependence. She also had experienced past episodes of depression with anxiety that had been treated with paroxetine 30 mg/d for the last 9 years. The patient had previously taken varenicline for 2 weeks but was unable to quit smoking; however, she had felt more depressed and began having thoughts of suicide (driving her car off a bridge).

At our program in June 2008, varenicline treatment (1 mg bid) was restarted, at the patient's request. After 3 weeks, Ms A's smoking decreased to 2 cigarettes/d, but her depression worsened again and she started having thoughts of suicide. We recommended that she discontinue varenicline immediately, continue taking paroxetine 30 mg/d, and start taking bupropion SR 150 mg in the morning for 7 days and then twice per day, along with 5 or 6 sessions of supportive therapy.

Afraid of returning to regular smoking without varenicline, Ms A did not stop taking it but rather added bupropion. Four weeks later, the patient reported no side effects, complete abstinence from tobacco, and few cravings for nicotine. Moreover, she had not experienced disturbing dreams or suicidal ideation. Her Center for Epidemiologic Studies Depression Scale (CES-D)6 score was 2 (normal range, 0–7), which was an improvement relative to her first visit (CES-D score = 25) and her fourth visit before starting bupropion treatment.

To our knowledge, this is the first case report of combined pharmacologic treatment for smoking cessation involving bupropion SR and varenicline. The patient's depressive symptoms improved significantly with the addition of bupropion SR, and the patient remained abstinent from smoking. The combination of these 2 agents merits further investigation in a rigorous and well-controlled clinical trial.

REFERENCES

  • 1.Gonzales D, Rennard SI, Nides M, et al. Varenicline Phase 3 Study Group: Varenicline, an α4β2 nicotinic acetylcholine receptor partial agonist, vs sustained-release bupropion and placebo for smoking cessation: a randomized controlled trial. JAMA. 2006;296:47–55. doi: 10.1001/jama.296.1.47. [DOI] [PubMed] [Google Scholar]
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Articles from Primary Care Companion to The Journal of Clinical Psychiatry are provided here courtesy of Physicians Postgraduate Press, Inc.

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