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Nasonex Related Gastrooesophageal reflux disease

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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: Arthralgia, Headache, Polyuria, Fatigue, Dizziness, Abdominal pain, Nausea, Eye pain, Myalgia, Sinusitis, Anxiety, Arrhythmia, Diarrhoea, Dry mouth, Dyspnoea, Ear infection, Gastrooesophageal reflux disease, Insomnia, Photosensitivity reaction, Vision blurred, Haemorrhage, Oropharyngeal pain

Posted By Anonymous in askapatient.com on June 22, 2014 @ 12:00 am

... dry mouth, throat and sinuses, bleeding nose, persistent left ear infection, left sided throat pain, occassional difficulty breathing, insomnia and muscle and joint pain, headaches, nausea, aggrivated...

Druginformer Identified Side Effects: Pain, Myalgia, Dysgeusia, Gastrooesophageal reflux disease, Insomnia

Posted By Anonymous in askapatient.com on November 6, 2008 @ 12:00 am

Side Effects: major soar throat!!! It hurts so bad I can't sleep. I went out twice in the middle of the night to get stuff from the drug store. My situation may have been exaggerated by acid reflux p...

Druginformer Identified Side Effects: Nausea, Dysgeusia, Gastrooesophageal reflux disease

Posted By Anonymous in askapatient.com on July 12, 2008 @ 12:00 am

Side Effects: bad tast in mouth, nausea, and acid reflux....stopped taking it for four days and nausea continues...anyone else had this problem with nausea and lasting after you stop for days.


* 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.