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Pamelor Related Syncope

Official Government Database Reports21
Online Conversations3
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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: Chest discomfort, Constipation, Chest pain, Dizziness, Syncope, Agitation, Hypersensitivity, Mood swings, Urticaria, Tinnitus, Nervousness, Anxiety, Dyspnoea, Hallucination, Hallucination, auditory, Irritability, Muscle twitching, Panic attack, Pyrexia, Rash, Restlessness, Somnolence, Swelling, Psychotic disorder, Oropharyngeal pain, Impulsive behaviour

Posted By Anonymous in askapatient.com on June 18, 2012 @ 12:00 am

... be back to normal. This is a scary drug. Here are some of its side effects. Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the ...

Druginformer Identified Side Effects: Syncope, Hostility, Irritability

Posted By Anonymous in askapatient.com on December 23, 2009 @ 12:00 am

... cost: I want from being angry and irritable to being extraordinarily hostile. The hostility persists long after I have stopped taking the drug. Something in my brain was knocked out of balance and n...

Druginformer Identified Side Effects: Constipation, Fatigue, Dizziness, Syncope, Drug ineffective, Dry mouth, Somnolence

Posted By Anonymous in askapatient.com on November 29, 2004 @ 12:00 am

Side Effects: constipation, dry mouth, dizziness, fainting, feel tired all the time hasn't worked yet I've been on it for a year and take 75mg a nigh


* 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.