Does DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE Cause Intentional product use issue? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Intentional product use issue have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE. This represents 53.9% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE.
14
Reports of Intentional product use issue with DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE
53.9%
of all DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE reports
14
Deaths
14
Hospitalizations
How Dangerous Is Intentional product use issue From DEXTROMETHORPHAN HYDROBROMIDE\PSEUDOEPHEDRINE?
Of the 14 reports, 14 (100.0%) resulted in death, 14 (100.0%) required hospitalization, and 14 (100.0%) 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. However, 14 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)