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User Voices for Mometasone Furoate Monohydrate

The following are comments from users that experienced side effects while taking Mometasone Furoate Monohydrate

Drug Tolerance Increased

Side Effects: I did suffer from more sore throats, headaches and nose bleeds while I was using the medication. These were not too severe. I stopped using it when it stopped working as well and bega...


Source: Nasonex (Mometasone Nasal)

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Did the author experience drug tolerance increased while taking nasonex?

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Drug Tolerance Increased

Side Effects: I did suffer from more sore throats, headaches and nose bleeds while I was using the medication. These were not too severe. I stopped using it when it stopped working as well and bega...


Source: Nasonex (Mometasone Nasal)

View full report on related drug tolerance increased

Did the author experience drug tolerance increased while taking mometasone furoate?

What is this?

Drug Tolerance Increased

Side Effects: Shortness of breath, chest tightness, anxiety, weak voice.

I took Nasonex for 1 month and I was pleased. Then it just seemed to stop working for me. I felt like my vocal cords...


Source: NASONEX: Side effects, ratings, and pa...

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Did the author experience drug tolerance increased while taking nasonex?

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* 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.