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Pamelor Related Emotional distress

Official Government Database Reports29
Online Conversations4

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: Constipation, Abdominal discomfort, Dry skin, Cystitis, Emotional distress

Posted By Anonymous in askapatient.com on October 25, 2012 @ 12:00 am

... went off of it last year due to increase heart palipitation that began and have since stopped since going off this. I have longterm affects from this drug, although my severe constipation i had during...

Druginformer Identified Side Effects: Insomnia, Emotional distress, Decreased appetite

Posted By Anonymous in askapatient.com on April 4, 2011 @ 12:00 am

Side Effects: hyper-emotional, difficulty falling asleep and staying asleep but did not feel tired as a result, loss of apetite I had had an almost constant tension headache for nearly 3 mo...

Druginformer Identified Side Effects: Agitation, Anger, Arrhythmia, Weight decreased, Emotional distress

Posted By Anonymous in everydayhealth.com on January 1, 2010 @ 12:00 am

... in the fact that they have been used for a long time. I don't trust the newer drugs. We just dont know what they do yet!Tried Lyrica (made me weepy) and Wellbutrin (made me very angry and agitated)....

Druginformer Identified Side Effects: Nausea, Constipation, Palpitations, Diarrhoea, Drug ineffective, Dry mouth, Hallucination, Orthostatic hypotension, Withdrawal syndrome, Emotional distress

Posted By Anonymous in askapatient.com on September 16, 2009 @ 12:00 am

... was severe, laxatives didn't work. Bowel movements became painful and bloody. Developed a fissure. Also, experienced terrible withdrawal while coming off (nausea, vivid/terrifying dreams/ insomnia, h...

* 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.