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Mirtazapine Related Hypoaesthesia

Official Government Database Reports185
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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: Hypoaesthesia, Abnormal dreams, Muscle spasms, Paraesthesia, Menstruation irregular

Posted By Anonymous in everydayhealth.com on May 9, 2012 @ 12:00 am

... effects listed. Only been taking for less than a week but, as the days go on the symptoms worsen. Very vivid dreams, hot spots under my skin, shaking, palpations, anxious, numbness and tingeling on li...

Druginformer Identified Side Effects: Headache, Hypoaesthesia, Increased appetite, Dry mouth, Mood altered, Somnolence, Vision blurred, Decreased appetite

Posted By Anonymous in drugs.com on February 17, 2012 @ 12:00 am

een taking mirtazapine for 7 weeks - definitely sleep (out like a light) but feel groggy/cloudy head in the morning. I have a constant dull headache and my vision is blurred sometimes - the glasses ...

Druginformer Identified Side Effects: Sedation, Hypoaesthesia, Somnolence

Posted By mslil in mdjunction.com on October 10, 2011 @ 12:00 am

... that this is normal, especially the first week or two. He also seems to only want sugary stuff to eat this morning (another well known side effect)I'm curious if the extreme sedation will wear off and...


* 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.