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Gabapentin Related Anger

Official Government Database Reports150
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.

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Druginformer Identified Side Effects: Agitation, Hypoaesthesia, Anger, Paraesthesia, Restlessness, Suicidal behaviour

Posted By Gabapentin in fdb.rxlist.com on July 23, 2015 @ 12:00 am

... this. Only one 300mg dose made me sleep for over 12 hours, I guess that is how it helps pain. After waking I found myself with an intense feeling of anger, rage, and very agitated mood.I could not cal...

Druginformer Identified Side Effects: Nightmare, Anger, Abnormal dreams

Posted By gus in fdb.rxlist.com on August 22, 2013 @ 12:00 am

ightmares and extreme anger in these dreams

Druginformer Identified Side Effects: Flatulence, Chills, Anger, Drug withdrawal syndrome, Dyspepsia, Hyperhidrosis, Influenza like illness, Muscular weakness, Decreased appetite, Fear

Posted By Usually happy in fdb.rxlist.com on August 15, 2013 @ 12:00 am

... has been two weeks now and the misery is still with me. So angry at my dr for prescribing this med! Don't try it if you've got a tender stomach! Now, I've got miserable nausea, gas pains that wake me ...

Druginformer Identified Side Effects: Anger, Panic attack

Posted By doodlebug in fdb.rxlist.com on April 6, 2013 @ 12:00 am

While this is an easy to use drug within 3 days of starting the medication I began to get uncontrollably angry over very minor things. I stopped taking it and it has gotten even worse. Hope this is ...

* 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.