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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.
User Voices for Sodium Monofluorophosphate
The following are comments from users that experienced side effects while taking Sodium Monofluorophosphate
Dyspnoea
“... Do not avoid them. As uncomfortable as you are, continue with your day "AS IF EVERYTHING IS FINE" even though you might be week, dizzy, have tightness of the chest, short of breath and are sure you ar...”
Source: Anxiety and Stress Forum
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Did the author experience dyspnoea while taking sodium monofluorophosphate?
What is this?Dyspnoea
“... so bad I had to go to the ER. They diagnosed me with diverticulitis, but my GI later dismissed that. Now, I am going through a pretty bad flareup -- shortness of breath , incredibly painful abdominal...”
Source: Lialda
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Did the author experience dyspnoea while taking sodium monofluorophosphate?
What is this?