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Mirtazapine Related Influenza like illness

Official Government Database Reports92
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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: Cough, Hyperhidrosis, Influenza like illness, Pyrexia

Posted By Chuck in fdb.rxlist.com on March 30, 2013 @ 12:00 am

... so vivd and life life, infact they was too life like they carried over into my life after I would wake up I had hallucinations that was so real I also had flue like symptoms cough fever, sweats just l...

Druginformer Identified Side Effects: Throat irritation, Headache, Feeling cold, Hunger, Malaise, Chills, Dry skin, Sinusitis, Influenza like illness, Weight increased

Posted By Clogger Jayne in fdb.rxlist.com on July 13, 2011 @ 12:00 am

... (temps outside were 100 degrees, 80 inside), always felt like I had overeaten even when I had eaten nothing; sinuses stuffed up like I had a head cold, dry scratchy throat; general feeling of malaise....

Druginformer Identified Side Effects: Headache, Dizziness, Nausea, Body temperature increased, Influenza like illness

Posted By wookiewoo in ehealthforum.com on March 17, 2010 @ 12:00 am

... blamed for my severe contrareaction. So I am now totally without antidepressants for the first time in a long while. I still feel tearful,nauseous, dizzy, feverish, and my head throbs but ... every d...


* 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.