Does DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE Cause Condition aggravated? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Condition aggravated have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE. This represents 56.3% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE.
How Dangerous Is Condition aggravated From DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE?
Of the 9 reports, 6 (66.7%) resulted in death, 7 (77.8%) required hospitalization, and 7 (77.8%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE. However, 9 reports have been filed with the FAERS database.