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Neurontin Related Hostility

Official Government Database Reports71
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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: Mood swings, Anger, Anxiety, Hostility, Disturbance in attention, Insomnia, Mania, Thought blocking

Posted By Anonymous in askapatient.com on August 21, 2007 @ 12:00 am

Side Effects: extreme mood swings of hostile/anger/rage variety and very manic when i have always been the opposite; word recall (i am a writer and avid reader so this was bad); worsening of already ...

Druginformer Identified Side Effects: Lethargy, Mood swings, Nervousness, Hostility, Depression, Somnolence, Weight increased

Posted By Anonymous in askapatient.com on July 16, 2004 @ 12:00 am

Side Effects: weight gain, depression, mood swings have only been taking it 2 mos.but saw no difference in pain levels with 300x3/day. Lethargic all the time & feel sleepy but had much diff...

Druginformer Identified Side Effects: Mood swings, Dysarthria, Hostility

Posted By Lionyx in prescriptiondrug-info.com on January 17, 2010 @ 12:00 am

... These included: Mental Confusion Severe drowsiness Dizziness Lack of coordination Numbness in toes Swelling in feet Belligerent Hostility Argumentative Mood Swings Rapid speech,...

* 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.