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Mirtazapine Related Diarrhoea

Official Government Database Reports465
Online Conversations3

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, Nausea, Increased appetite, Diarrhoea, Drug ineffective, Somnolence

Posted By DannyDunn in fdb.rxlist.com on January 31, 2014 @ 12:00 am

... at the 15 mg. level. While sleep improved, the price I paid was feeling like a zombie during the day. There has also been nausea (3 days), diarrhea (1 day), severe headaches (2 days)and increased ap...

Druginformer Identified Side Effects: Restlessness, Polyuria, Fatigue, Diarrhoea, Muscular weakness, Respiration abnormal, Energy increased, Abnormal sleep-related event

Posted By suMarieB in fdb.rxlist.com on June 10, 2013 @ 12:00 am

... Diarrhea is frequent in the morning. Since taking these, I get out of breath just walking 4-5 steps; my bones have been aching, ESP during the nite, and to the point of restless tossing and turning. ...

Druginformer Identified Side Effects: Abdominal discomfort, Diarrhoea, Discomfort, Gingival pain, Somnolence

Posted By Anonymous in drugs.com on March 27, 2010 @ 12:00 am

... to wake up and when I had days off I slept all day and night only getting up for toilet and drinks. After not taking them for a few days had very sore gums, sore stomach, sickness and diarrhea but in ...

* 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.