Does KETOCONAZOLE Cause Intentional product use issue? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Intentional product use issue have been filed in association with KETOCONAZOLE (Ketoconazole). This represents 0.8% of all adverse event reports for KETOCONAZOLE.
45
Reports of Intentional product use issue with KETOCONAZOLE
0.8%
of all KETOCONAZOLE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From KETOCONAZOLE?
Of the 45 reports, 1 (2.2%) required hospitalization, and 1 (2.2%) 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 KETOCONAZOLE. However, 45 reports have been filed with the FAERS database.
What Other Side Effects Does KETOCONAZOLE Cause?
Drug ineffective (1,326)
Off label use (657)
Pruritus (559)
Product use issue (428)
Product use in unapproved indication (421)
Alopecia (375)
Therapeutic response unexpected (317)
Psoriasis (312)
Rash (267)
Hair texture abnormal (255)
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 KETOCONAZOLE Alternatives Have Lower Intentional product use issue Risk?
KETOCONAZOLE vs KETOPROFEN
KETOCONAZOLE vs KETOPROFEN LYSINE
KETOCONAZOLE vs KETOROLAC TROMETHAMINE
KETOCONAZOLE vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOCONAZOLE vs KETOTIFEN