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Neurontin Related Chills

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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: Photophobia, Chills, Oral pain, Sedation, Burning sensation, Hypotension, Inflammation, Tinnitus, Alopecia, Hepatic congestion, Underweight, Acne, Amnesia, Cough, Dyspepsia, Gastrooesophageal reflux disease, Muscle spasms, Vision blurred, Emotional distress

Posted By Anonymous in askapatient.com on January 8, 2009 @ 12:00 am

... is an initial honeymoon period - you get relief from intolerable nerve pain, you're sleeping, so you continue with the standard dosing protocols (300mg day 1 then up)Caution: if sensitive to drugs or...

Druginformer Identified Side Effects: Tremor, Chills, Anxiety, Poverty of speech, Phobia, Fear

Posted By Anonymous in askapatient.com on September 1, 2005 @ 12:00 am

2-3 hours after intake, especially when coming up from sleep or nap. Started to be afraid to go to sleep, wake-up shivering in bed, stand- up trembling with fast breathing, speech pro...

Druginformer Identified Side Effects: Headache, Pain, Chills, Nightmare, Anxiety, Illogical thinking, Abnormal dreams, Depression, Hyperhidrosis, Insomnia, Decreased appetite

Posted By Anonymous in askapatient.com on July 30, 2005 @ 12:00 am

... I decided it wasn't helping my pain and decided to OFF the neurontin, that's when the real nightmare began. I'm having chills, sweats, anxiety, insomnia, loss of appetite, headache....I just wish I k...


* 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.