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Neurontin Related Influenza like illness

Official Government Database Reports430
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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: Tremor, Abdominal distension, Confusional state, Diarrhoea, Influenza like illness

Posted By Anonymous in askapatient.com on November 26, 2011 @ 12:00 am

Side Effects: Severe bloating, shakey, flu like symptoms, fuzzy eyes, extreme diareah

Druginformer Identified Side Effects: Chest pain, Nausea, Pain, Pruritus, Inflammation, Dyspnoea, Influenza like illness, Muscular weakness, Pyrexia, Rash, Somnolence, Weight increased

Posted By Anonymous in askapatient.com on August 1, 2010 @ 12:00 am

... pain, chronic severe nausea almost 24/7, I now feel like sometimes I can't stand to put food in my mouth, I have episodes where I feel like i have the flu and fever, chest pain, shortness of breath, a...

Druginformer Identified Side Effects: Crying, Influenza like illness, Somnolence

Posted By Anonymous in askapatient.com on October 27, 2007 @ 12:00 am

... the medication, I developed flu-like symptoms. As the days when on, they became increasingly worse and eventually so severe I could not get out of bed. I was constantly crying for no reason. I had ...

* 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.