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Monistat 3 Related Hypoaesthesia

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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: Pruritus, Burning sensation, Hypoaesthesia, Vaginal discharge, Discomfort

Posted By Anonymous in askapatient.com on February 15, 2014 @ 12:00 am

Side Effects: I purchased the Monistat 3 with the pre filled cream applicator. Soon after I inserted the medicine and laid down, I experienced severe itching and burning and so much discomfort for ab...

Druginformer Identified Side Effects: Burning sensation, Hypoaesthesia

Posted By Anonymous in askapatient.com on November 20, 2009 @ 12:00 am

Side Effects: Wow does this burn! Day 1 and the burning is so intense I needed to look up side effects. Thank you everyone who wrote in because non of my friends ever experienced burning when using t...

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* 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.