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Mirtazapine Related Ear Infection

Official FDA Reports24
Social Media Events2
Active Ingredients
  • Mirtazapine
Additional Drug Brands and Names
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Additional Terms for Ear Infection
  • No additional name found

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Mirtazapine.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride

Mirtazapine

... depersonalization, panic attacks & anxiety (never used to be an issue), nausea, vomiting, apathy, suicidal thoughts, irritability, weakness, no energy at all, ear infections , dizziness, anaemia, sun s...


Source:" REMERON: Side effects, ratings, and pa...

View full report on drug related ear infection

Did the author experience ear infection while taking mirtazapine?

What is this?

Mirtazapine

... got a sore throat and mouth ulcers, but waited a week until my appointment with my regular GP was due before seeking medical attention. By that time I had a middle-ear infection , sickness and diarrhea...


Source:" Remeron

View full report on drug related ear infection

Did the author experience ear infection while taking mirtazapine?

What is this?

Tell us about your Experience with Mirtazapine Related Ear Infection

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Fatigue, Dizziness, Abdominal pain, Nausea, Pruritus, Burning sensation, Vomiting, Anaemia, Sinusitis, Alopecia, Anxiety, Acne, Apathy, Depersonalisation, Diarrhoea, Drug effect increased, Dry eye, Ear infection, Irritability, Muscular weakness, Panic attack, Photosensitivity reaction, Rash, Suicidal ideation, Weight decreased, Adverse drug reaction, Crohn's disease

Posted By Anonymous in askapatient.com on October 13, 2013 @ 12:00 am

... rashes, acne, loss of co ordination, depersonalization, panic attacks & anxiety (never used to be an issue), nausea, vomiting, apathy, suicidal thoughts, irritability, weakness, no energy at all, ear ...

Druginformer Identified Side Effects: Sinus headache, Diarrhoea, Discomfort, Ear infection, Fluid retention, Mouth ulceration, Weight increased

Posted By Anonymous in everydayhealth.com on May 9, 2003 @ 12:00 am

... but waited a week until my appointment with my regular GP was due before seeking medical attention. By that time I had a middle-ear infection, sickness and diarrhea and sinus problems. My GP told me t...



* 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.