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Gabapentin Related Feeling cold

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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: Feeling cold, Fatigue, Malaise, Chills, Anxiety, Drug ineffective, Influenza like illness

Posted By AMKaloha in fdb.rxlist.com on March 24, 2015 @ 12:00 am

egan taking 300 mg 2x a day. After 4 days I felt like I had the flu -- cold feeling/chills, inner anxious feeling, extreme fatigue and general malaise. Stopped taking it. Went to doctor a week l...

Druginformer Identified Side Effects: Feeling cold, Dry mouth, Weight increased

Posted By greentree lady in fdb.rxlist.com on March 18, 2010 @ 12:00 am

Take 300mg every 8hours. Has helped somewhat with the coldness in my feet due to neuropathy. However, I have dry mouth, weight gain and back pain.

Druginformer Identified Side Effects: Weight increased, Feeling cold, Dry mouth

Posted By greentree lady in fdb.rxlist.com on March 18, 2010 @ 12:00 am

Take 300mg every 8hours. Has helped somewhat with the coldness in my feet due to neuropathy. However, I have dry mouth, weight gain and back pain.

Druginformer Identified Side Effects: Feeling cold, Fatigue, Somnolence

Posted By Anonymous in drugs.com on September 23, 2009 @ 12:00 am

I used this last night for migraines. I took two pills and felt like I was drunk, even when I woke up. It knocked me out cold for 10 hours and I still felt like that when I woke up. I have been exhaus...


* 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.