Does DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE Cause Product use issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use issue have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE. This represents 43.8% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE.
How Dangerous Is Product use issue From DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE?
Of the 7 reports, 4 (57.1%) resulted in death, 5 (71.4%) required hospitalization, and 5 (71.4%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE. However, 7 reports have been filed with the FAERS database.