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Pamelor Related Feeling jittery

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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 jittery, Confusional state, Drug ineffective, Dry mouth, Somnolence

Posted By Anonymous in askapatient.com on September 29, 2008 @ 12:00 am

... to 3600 mgs daily of Neurontin & 75 mgs nightly of Nortriptyline... The side effects are: very drowsy during the day (don't drive). Easily confused. Dry mouth. Often feel jittery (like too much cof...

Druginformer Identified Side Effects: Constipation, Feeling jittery, Palpitations, Anxiety, Illogical thinking, Abdominal distension, Asthma, Disturbance in attention, Dry mouth, Dyspnoea, Heart rate increased, Hyperhidrosis, Hypopnoea, Muscular weakness, Somnolence, Weight increased, Hot flush

Posted By Anonymous in askapatient.com on September 23, 2008 @ 12:00 am

Side Effects: Dry mouth, fast heart rate, sleepiness, spaciness, some jitters, constipation, trouble concentrating and trouble with word retrieval, fatigue and weakness esp. in legs, LOTS of sweating...

Druginformer Identified Side Effects: Tremor, Feeling jittery, Thought withdrawal, Dry mouth

Posted By Anonymous in askapatient.com on November 21, 2006 @ 12:00 am

Side Effects: Tremors/ shaking (especially in hands), dry mouth, zoned out, jittery, slower responses. Started off on 25mg along with 2mg of Lunesta. The first week I took it I felt majorly...

* 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.