Does CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE Cause Intentional product use issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Intentional product use issue have been filed in association with CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE. This represents 25.0% of all adverse event reports for CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE.
5
Reports of Intentional product use issue with CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE
25.0%
of all CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Intentional product use issue From CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE?
Of the 5 reports, 5 (100.0%) required hospitalization, and 5 (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 CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE Cause?
Off label use (8)
Product use issue (8)
Drug ineffective (7)
Headache (7)
Joint swelling (7)
Musculoskeletal stiffness (7)
Pain (7)
Product use in unapproved indication (7)
Pruritus (7)
Drug dependence (5)
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)