Does DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE Cause Product use issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use issue have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE. This represents 19.2% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE.
5
Reports of Product use issue with DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE
19.2%
of all DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE reports
5
Deaths
5
Hospitalizations
How Dangerous Is Product use issue From DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE?
Of the 5 reports, 5 (100.0%) resulted in death, 5 (100.0%) required hospitalization, and 5 (100.0%) 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. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE Cause?
Drug hypersensitivity (17)
Gastrointestinal disorder (17)
Hypertension (17)
Nasopharyngitis (17)
Pemphigus (17)
Pericarditis (17)
Pain (16)
Abdominal discomfort (15)
Alopecia (15)
Anti-cyclic citrullinated peptide antibody positive (15)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)