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Neurontin Related Compulsions

Official Government Database Reports12
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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: Agitation, Discomfort, Drug ineffective, Eye disorder, Compulsions

Posted By Anonymous in askapatient.com on March 15, 2012 @ 12:00 am

Side Effects: A lot of eye issues. Darting back and forth, also couldn't read, and became like I had side blinders on. I only saw what was infront of me. Also early am aggitation. I'm not sure how we...

Druginformer Identified Side Effects: Euphoric mood, Disturbance in attention, Libido increased, Compulsions, Social phobia

Posted By Anonymous in askapatient.com on March 24, 2010 @ 12:00 am

Side Effects: euphoria, increased libido, sometimes brain fog. it is awesome... saved my life. it reduced irritability, obsessions, compulsions and delete almost whole social phobia. it rai...

Druginformer Identified Side Effects: Headache, Sedation, Nightmare, Abnormal dreams, Feeling hot, Thinking abnormal, Weight increased, Compulsions, Appetite disorder

Posted By Anonymous in askapatient.com on May 1, 2007 @ 12:00 am

... hot, seems I am having trouble thinking/focus during day, maybe weight gain/compulsive eating. Waking in the morning I feel drugged up, but then much better. a bit of a headache first 2 nights, but s...


* 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.