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Neurontin Related Depression

Official Government Database Reports2,372
Online Conversations62

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: Suicidal behaviour, Depression, Tinnitus, Dizziness

Effectiveness Rating:     Overall Rating:

Posted By Jan on June 23, 2018 @ 1:56 pm

Druginformer Identified Side Effects: Depression, Dry mouth, Dizziness, Malaise, Nausea

Posted By Anonymous in askapatient.com on April 27, 2015 @ 12:00 am

Side Effects: While taking this drug I felt extremely dizzy, nauseous, a horrible dry mouth, malaise, and depression. It is difficult for me to envision anyone wanting to stay on this medi...

Druginformer Identified Side Effects: Anger, Depression, Insomnia, Suicidal ideation

Posted By Anonymous in askapatient.com on April 13, 2014 @ 12:00 am

... to being pregnant. The next 3 weeks after stopping it were terrible. It caused depression and suicidal thoughts. I had Insomnia for 4 days where I didn't sleep at all. I was abnormally angry for the 3...

Druginformer Identified Side Effects: Flatulence, Memory impairment, Amnesia, Depression, Disturbance in attention, Dyspepsia, Fluid retention, Insomnia, Vision blurred

Posted By Anonymous in askapatient.com on April 10, 2014 @ 12:00 am

Side Effects: Where to start, let's see, gas, memory loss, forgetting everything, depression, water retention, brain fog, and indigestion so bad it kept me up! I was not myself, I tapered down after ...

Druginformer Identified Side Effects: Nightmare, Crying, Anxiety, Depression, Drug ineffective, Herpes zoster, Withdrawal syndrome, Psychotic disorder

Posted By Anonymous in askapatient.com on February 11, 2014 @ 12:00 am

complete nightmare. only realized that it was causing depression & anxiety when i reduced down to 400mg daily. i was having awful swings in mood & crying at the drop of a hat. have also ...

Druginformer Identified Side Effects: Depression, Disturbance in attention, Somnolence

Posted By Anonymous in askapatient.com on December 22, 2013 @ 12:00 am

Side Effects: Drowsiness,"brain fog", worsening depression

Druginformer Identified Side Effects: Arthralgia, Depression, Sciatic nerve injury, Weight increased

Posted By Anonymous in askapatient.com on June 11, 2013 @ 12:00 am

Side Effects: Orgasms not as strong. Some weight gain. I always suspected that my body aches and pains that have been increasing over the last few years and have culminated it seems leading to scia...

Druginformer Identified Side Effects: Mood swings, Anxiety, Aggression, Depression, Irritability

Posted By Anonymous in askapatient.com on July 24, 2012 @ 12:00 am

Side Effects: woorsening of depression, anxiety, irratibility, aggression and wild mood swings. I don't believe it was worth the side effects for the little pain relief I got from the drug....

Druginformer Identified Side Effects: Fatigue, Pain, Depression, Analgesic therapy

Posted By Anonymous in askapatient.com on December 25, 2011 @ 12:00 am

I wake up feeling 50 lbs. heavier. My back feels like a truck ran over me. Tired all day. No enthusiasm. My pain has increased by 100%. I have to take more of my normal pain med.s just t...

Druginformer Identified Side Effects: Depression, Libido increased

Posted By Anonymous in askapatient.com on December 20, 2011 @ 12:00 am

Side Effects: Decrease pain, decrease anxiety/depression,increased libido.

* 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.