Does DEXTROMETHORPHAN HYDROBROMIDE Cause Dyspnoea? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Dyspnoea have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE (Quality Choice Mucus Relief DM DM). This represents 2.1% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE.
52
Reports of Dyspnoea with DEXTROMETHORPHAN HYDROBROMIDE
2.1%
of all DEXTROMETHORPHAN HYDROBROMIDE reports
26
Deaths
36
Hospitalizations
How Dangerous Is Dyspnoea From DEXTROMETHORPHAN HYDROBROMIDE?
Of the 52 reports, 26 (50.0%) resulted in death, 36 (69.2%) required hospitalization, and 30 (57.7%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN HYDROBROMIDE. However, 52 reports have been filed with the FAERS database.