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Wellbutrin Related Borderline personality disorder

Official Government Database Reports7
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Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

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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: Pain, Borderline personality disorder, Drug ineffective

Posted By suski in fdb.rxlist.com on November 5, 2008 @ 12:00 am

... as other meds do. But if your insurance will only pay for a generic, make sure you ask for BUPROPRION, not BUDAPRION. The latter does not work! During my time on it, I started hurting myself again. I ...

Druginformer Identified Side Effects: Borderline personality disorder, Binge eating, Eating disorder, Terminal insomnia, Purging

Posted By Anonymous in everydayhealth.com on February 6, 2006 @ 12:00 am

... However, the bulemia is only mild and ocassional, so my doctor thought this drug was worth a shot. I have major depression with bipolar disease, borderline personality disorder, and the eating disor...

* 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.