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User Voices for Gabapentin

The following are comments from users that experienced side effects while taking Gabapentin

Respiration Abnormal

... times for syncope; experienced excessive sleepiness during the day and had difficulty driving and staying awake; herniated disk (L4-L5); stenosis; curved spine; problems breathing and weezing that mim...


Source: MIRAPEX: Side effects, ratings, and pa...

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Respiration Abnormal

... off. Took ages to get used to tight band feeling round head, vision problems and weight gain. The worst side effect is constipation and bloating. Sometimes I feel as if I can't breathe because I'm so ...


Source: comments/gabapentin/for-peripheral-neu...

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Respiration Abnormal

... sick so took longer then got so bad that stopped taking med started coughing up skin from throat it hurt worse than tonsel taken out couldn't eat for 4 days breathing problems lungs felt heavyand shor...


Source: NEURONTIN: Side effects, ratings, and ...

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Respiration Abnormal

Side Effects: Difficulties breathing/Dysphnea.

Neurontin helped me for almost a month, but ended up with giving me problems breathing . So I had to drop it, unfortunately. Because it gave me...


Source: NEURONTIN: Side effects, ratings, and ...

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Respiration Abnormal

Side Effects: Helped me fall asleep quickly, but I would have disturbing dreams in which I felt paralyzed and as if I couldn't breathe and would die if I didn't awaken quickly. These dreams would ha...


Source: MIRAPEX: Side effects, ratings, and pa...

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* 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.