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Pamelor Related Flushing

Official Government Database Reports9
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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: Thought withdrawal, Somnolence, Flushing, Lethargy

Posted By Anonymous in askapatient.com on December 28, 2012 @ 12:00 am

Side Effects: Extreme grogginess in the morning. In a daze and out of it for most of the day.I have checked my temp a few times, but no fever, just feeling flushed. I am supposed to go to 25MG start...

Druginformer Identified Side Effects: Weight decreased, Heart rate abnormal, Fatigue, Mouth breathing, Dizziness, Flushing, Thought withdrawal, Abnormal dreams, Antisocial behaviour, Dry mouth, Hallucination, visual, Hyperhidrosis, Insomnia, Muscle spasms

Posted By Anonymous in askapatient.com on February 19, 2011 @ 12:00 am

Side Effects: Couldn't sleep, felt disconnected, in a daze, no energy, lost weight, dry mouth, then the real problems started, vivid dreams, heart pounding, muscle cramps, couldn't catch my breath, s...

Druginformer Identified Side Effects: Tremor, Flushing, Dry mouth, Photosensitivity reaction, Weight increased

Posted By Anonymous in everydayhealth.com on March 8, 2005 @ 12:00 am

... somewhat embarassing, but not the worst price to pay. The only other another annoying side effect I notice is photosensitivity. All of the other side effects (dry mouth, tremors, weight gain, etc.) ...


* 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.