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Gabapentin Related Rash

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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: Dizziness, Malaise, Rash

Posted By gabapentin: I was taking 300 m... in drugs.com on November 5, 2013 @ 12:00 am

I was taking 300 mgs 3 x daily. The drunk, dizziness, overall sick feeling was just to much. Took for 3 weeks. The doc then lowered my dose to 100 2x a.m. and noon and 300 5 p.m. I was still getting t...

Druginformer Identified Side Effects: Pain, Pruritus, Fall, Rash

Posted By Anonymous in askapatient.com on August 18, 2013 @ 12:00 am

Side Effects: Still have pain, horrible itchy rash on hands and feet. Feel off balance I will be on this med long-term... I can barely function the pain is so bad if I miss a dose, but the...

Druginformer Identified Side Effects: Rash

Posted By Anonymous in drugs.com on December 23, 2012 @ 12:00 am

I have generalized anxiety disorder and Panic Disorder going on ten years now. I've been on Zoloft the entire time. I had a bad relapse of symptoms this year while on Zoloft. I bumped it up to 200 mg ...

Druginformer Identified Side Effects: Dry mouth, Rash

Posted By Sandy in fdb.rxlist.com on July 4, 2009 @ 12:00 am

Did help with my walking,feet "sleeping", etc. It's easy to use since it's just a pill. The problem with it was a very bad rash on both arm and back of hand; very dry mouth especially in the mornin...

Druginformer Identified Side Effects: Dry mouth, Rash

Posted By Sandy in fdb.rxlist.com on July 4, 2009 @ 12:00 am

Did help with my walking,feet "sleeping", etc. It's easy to use since it's just a pill. The problem with it was a very bad rash on both arm and back of hand; very dry mouth especially in the mornin...


* 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.