Does CODEINE Cause Intentional product use issue? 182 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 182 reports of Intentional product use issue have been filed in association with CODEINE (Codeine-Guaifenesin). This represents 0.8% of all adverse event reports for CODEINE.
182
Reports of Intentional product use issue with CODEINE
0.8%
of all CODEINE reports
101
Deaths
112
Hospitalizations
How Dangerous Is Intentional product use issue From CODEINE?
Of the 182 reports, 101 (55.5%) resulted in death, 112 (61.5%) required hospitalization, and 76 (41.8%) 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. However, 182 reports have been filed with the FAERS database.
What Other Side Effects Does CODEINE Cause?
Drug hypersensitivity (7,479)
Toxicity to various agents (2,951)
Drug ineffective (2,632)
Drug abuse (2,122)
Pain (2,024)
Rash (1,931)
Nausea (1,907)
Rheumatoid arthritis (1,861)
Headache (1,701)
Off label use (1,662)
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)
Which CODEINE Alternatives Have Lower Intentional product use issue Risk?
CODEINE vs CODEINE\GUAIFENESIN
CODEINE vs CODEINE\IBUPROFEN
CODEINE vs CODEINE\PROMETHAZINE
CODEINE vs COLCHICINE
CODEINE vs COLCHICINE\DICYCLOMINE