Does DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE Cause Intentional product use issue? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Intentional product use issue have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE. This represents 68.8% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE.
How Dangerous Is Intentional product use issue From DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE?
Of the 11 reports, 8 (72.7%) resulted in death, 9 (81.8%) required hospitalization, and 9 (81.8%) were considered life-threatening.
Is Intentional 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, 11 reports have been filed with the FAERS database.