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Mirtazapine Related Vision blurred

Official Government Database Reports173
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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: 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: Increased appetite, Vision blurred, Weight increased

Posted By Anonymous in drugs.com on October 2, 2011 @ 12:00 am

Woke up with very blurry vision for 3 hours....was scary! It made me sleep well, but the appetite increase was horrific. I literally thought about food the whole day. Did not take again. I have a spin...

Druginformer Identified Side Effects: Vision blurred

Posted By tikiboom in fdb.rxlist.com on October 16, 2009 @ 12:00 am

Take 30 mg at 6 pm bedtime. (I go to work at 4 am) Upon closing eyes, kaliedoscopic visions appear. Colorful phenomina. Fullness in head during day.

Druginformer Identified Side Effects: Vision blurred, Dizziness, Nausea

Posted By Verwon in prescriptiondrug-info.com on July 13, 2011 @ 12:00 am

Mirtazapine is actually a tetracyclic antidepressant, so it is unrelated to narcotics. Side effects can include: nausea, dizziness, sedation and blurred vision. Learn more: http://www.p...

* 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.