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Neurontin Related Agitation

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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: Malaise, Agitation, Memory impairment, Aggression, Amnesia, Cough, Dyspnoea, Respiration abnormal, Somnolence, Abasia, Decreased appetite, Suicidal behaviour, Oropharyngeal pain

Posted By Anonymous in askapatient.com on June 2, 2011 @ 12:00 am

Side Effects: Memory loss, agitation, extreme tiredness, sores on mouth and sore throat thought was getting sick so took longer then got so bad that stopped taking med started coughing up skin from t...

Druginformer Identified Side Effects: Agitation, Cardiac flutter, Illogical thinking, Insomnia, Psychomotor hyperactivity

Posted By Anonymous in askapatient.com on March 19, 2009 @ 12:00 am

Side Effects: My heart raced, I was hyper, agitated, edgy, on a "high", but not a good one. Couldn't sleep. Definitely was not the drug for me. Never felt so "out of sorts" as when I was ...

Druginformer Identified Side Effects: Headache, Pain, Agitation, Sleep disorder, Drug withdrawal syndrome, Walking disability, Confusional state, Disturbance in attention, Insomnia, Mood altered, Balance disorder, Psychotic disorder

Posted By Anonymous in askapatient.com on June 29, 2006 @ 12:00 am

... to take him off after just one week, wow, he fell apart even more for about 5-6 harrowing days. I guess these were withdrawls, after only 1 week? He had sudden severe headaches when coming off. Diso...

Druginformer Identified Side Effects: Agitation, Amnesia, Disturbance in attention, Drug ineffective

Posted By Anonymous in askapatient.com on March 29, 2006 @ 12:00 am

... not find words to express my thoughts. Took forever to finish a sentence sometimes. Three years after stopping, still have side effect such as memory problems, concentration, aggitation. Would not ...

Druginformer Identified Side Effects: Dizziness, Agitation, Crying

Posted By Anonymous in askapatient.com on September 27, 2005 @ 12:00 am

Side Effects: I lost words and was agitated a lot. I got upset easily and cried a lot. I got so dizzy that I had to hold on to walls when I walked. This drug made me absolutely miserable....

Druginformer Identified Side Effects: Constipation, Arthralgia, Chest pain, Fatigue, Hypersomnia, Agitation, Myocardial infarction, Anxiety, Amnesia, Depression, Insomnia, Swelling, Urinary tract infection, Weight increased

Posted By Anonymous in askapatient.com on September 27, 2004 @ 12:00 am

... hands, knee down my leg and foot. swelling, weightgain, Memory loss, aggitation, chest pains feeling like a mini heart attack would feel, depression, anxiety, constipation, carried urinary tract infe...

Druginformer Identified Side Effects: Fatigue, Sedation, Agitation

Posted By ragafin in prescriptiondrug-info.com on January 16, 2012 @ 12:00 am

been taking 400mg neurontin 3x daily ~ only 9 months, because I got tired of the drugged feeling, I cut back to 300mg 2x day and 400mg 1x day, the drugged feeling left, but after a much higher level o...


* 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.