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Neurontin Related Dyspnoea

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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: Malaise, Agitation, Memory impairment, Aggression, Amnesia, Cough, Dyspnoea, Respiration abnormal, Somnolence, Abasia, Decreased appetite, Suicidal behaviour, Oropharyngeal pain

Posted By Anonymous in askapatient.com on June 2, 2011 @ 12:00 am

Side Effects: Memory loss, agitation, extreme tiredness, sores on mouth and sore throat thought was getting sick so took longer then got so bad that stopped taking med started coughing up skin from t...

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: Flatulence, Chest pain, Alopecia, Abdominal distension, Dyspnoea, Heart rate irregular

Posted By Anonymous in askapatient.com on March 9, 2010 @ 12:00 am

Side Effects: Feeling like you are floating, indicision, hair loss, nail damage, gas and bloating, chest pain difficulty breathing and extreme irregular heart beat. symptoms increased in se...

Druginformer Identified Side Effects: Dyspnoea, Respiration abnormal

Posted By Anonymous in askapatient.com on December 14, 2009 @ 12:00 am

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...

Druginformer Identified Side Effects: Dizziness, Hypoaesthesia, Dyspnoea, Somnolence

Posted By Anonymous in askapatient.com on January 14, 2008 @ 12:00 am

Side Effects: dizziness, sleepiness, numbness (which is good in my case), some shortness of breath or fatigue, inability or want to concentrate. pain relief!! I don't take this as prescrib...

Druginformer Identified Side Effects: Tremor, Drug withdrawal syndrome, Depression, Disturbance in attention, Drug ineffective, Dyspnoea, Irritability, Mental impairment, Oedema, Weight increased, Adverse drug reaction

Posted By Anonymous in askapatient.com on August 10, 2004 @ 12:00 am

Side Effects: Weight Gain of 3 sizes-Felt irritable,disoriented, spacey, unable to focus.Tremors to the point of not being able to ride in a car for more than 1/2 an hour, without tremors setting in....

Druginformer Identified Side Effects: Malaise, Nervousness, Depression, Dyspnoea, Psychotic disorder

Posted By Anonymous in askapatient.com on June 2, 2003 @ 12:00 am

... increased my dosage to 500mg daily, spread throughout the day, but I feel worse. I feel labored breathing, a mental foginess but yet edgy and nervous inside. A general malaise and some depression. ...

Druginformer Identified Side Effects: Swelling, Tenderness, Hot flush, Tremor, Chest pain, Headache, Neck pain, Confusional state, Disturbance in attention, Dyspnoea

Posted By Anonymous in askapatient.com on November 11, 2002 @ 12:00 am

Side Effects: Chest pains, hot flashes, shortness of breath, face swelling, worsening of headaches, confusion, inability to focus, trembling, neck pains, soreness in shoulders,

* 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.