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. Author manuscript; available in PMC: 2010 Nov 1.
Published in final edited form as: Arch Gen Psychiatry. 2009 Nov;66(11):1253–1262. doi: 10.1001/archgenpsychiatry.2009.142

Table 5.

Serious adverse events (SAE’s) reported between 2 weeks pre-quit and 6-months post-quit by treatment condition

Placebo
(n = 189)
Bupropion
(n = 262)
Lozenge
(n = 260)
Patch
(n = 264)
Bupropion
+
Lozenge
(n = 267)
Patch
+
Lozenge
(n = 262)
• Hospitalized for chest pain • Hospitalized after being hit by a car • Hospitalized for breathing difficulty • Hospitalized for treatment of a blood clot in leg • Appendectomy • Hospitalized for cataract surgery
• Hospitalized for cardiac arrhythmia • Hospitalized for chest pain and transient increase in blood pressure • Surgery to place stents • Hospitalized for heart attack • Hospitalized due to breast infection • Inpatient tonsillectomy
• Hospitalized for bronchitis • Medication blind was broken at request of MD; no other info available • Vein transplant surgery related to dialysis • Hospitalized because of auto accident • Hospitalized due to falling • Inpatient hysterectomy because of ovarian tumor
• Hospitalized for pneumonia • Hospitalized for abdominal pain • Hospitalized for CAD and TIA • Hospitalized for mild heart attack • Inpatient carpal tunnel surgery • Hospitalized for pneumonia
• Hospitalized for respiratory infection • Inpatient treatment for alcohol dependence • Death due to COPD and coronary artery disease • Hospitalized for stress-related chest pain
• Hospitalized for pneumonia • Hospitalized for seizures* • Hospitalized for lung infection
• Hospitalized for shortness of breath and heart problems
*

The only SAE labeled as possibly related to study medication. Seizures are an identified potential side effect of bupropion, which the participant was taking at the time of the seizure.