Does DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE Cause Rheumatoid arthritis? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Rheumatoid arthritis have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE. This represents 75.0% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE.
How Dangerous Is Rheumatoid arthritis From DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE?
Of the 12 reports, 9 (75.0%) resulted in death, 10 (83.3%) required hospitalization, and 10 (83.3%) were considered life-threatening.
Is Rheumatoid arthritis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE\TRIPROLIDINE. However, 12 reports have been filed with the FAERS database.