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Pamelor Related Hunger

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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: Hunger, Weight increased

Posted By Anonymous in askapatient.com on December 24, 2013 @ 12:00 am

... Rapid weight gain (~10 lbs in about 2 weeks) Haven't experienced any benefit since it has only been 2 weeks. But I am stopping now that I have connected it to insatiable appetite for carbs &...

Druginformer Identified Side Effects: Constipation, Hunger, Blepharospasm, Adverse event, Dry mouth, Hyperhidrosis, Insomnia, Sleep terror, Weight increased, Psychotic disorder

Posted By Anonymous in askapatient.com on November 7, 2011 @ 12:00 am

Side Effects: Dry mouth, trouble sleeping, vivid and I mean vivid nightmares, constipation, lime a brain zapping feeling, weight gain of 10 pounds in one month, Constantly hungry, sweating like crazy...

Druginformer Identified Side Effects: Hunger, Hallucination

Posted By Anonymous in askapatient.com on November 5, 2006 @ 12:00 am

Side Effects: (not taking this drug as an anti-depressant)It has helped chronic pain situation. I am calmer, but a bit thick headed. Need more sleep per night, and I'm hungry more often. Maybe a few ...

Druginformer Identified Side Effects: Hunger, Abdominal discomfort, Nightmare, Discomfort

Posted By Anonymous in everydayhealth.com on August 25, 2005 @ 12:00 am

Nortriptyline Was a nightmare, did very little to help me and made me hungry 24-7. If I didn't eat when the hunger started I felt very sick to my stomach.


* 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.