DrugInformer Search

Wellbutrin Related Completed suicide

Official Government Database Reports267
Online Conversations4

Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

Tell us about your Experience with Wellbutrin

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Completed suicide, Suicidal ideation

Posted By Anonymous in fdb.rxlist.com on January 12, 2011 @ 12:00 am

My nephew had depression issues for many years. He saw a doctor who prescribed Wellbutrin a few months ago. He committed suicide four days ago. Since one of the side effects of this drug is suicida...

Druginformer Identified Side Effects: Completed suicide, Anger, Borderline personality disorder, Attention deficit/hyperactivity disorder, Compulsions, Impulsive behaviour

Posted By TAYSMOM in drugs.com on May 29, 2010 @ 12:00 am

... moved in a year ago with the father of my 6 year old. Prior to this medicine, we almost didn't make it. I was angry, jealous, compulsive, impulsive, and could have committed suicide twice in one month...

Druginformer Identified Side Effects: Completed suicide, Insomnia, Suicidal ideation

Posted By megob in fdb.rxlist.com on October 13, 2008 @ 12:00 am

... but I rather have that than suicidal thoughts. Overall this drug was effective but since I was under the age of 18 I had to have numerous medical tests to see if I was in danger of committing suicide....

Druginformer Identified Side Effects: Completed suicide

Posted By Seminolegirl1 in www.dailystrength.org

Caused suicial thoughts

* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.