Does KETOCONAZOLE Cause Condition aggravated? 202 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 202 reports of Condition aggravated have been filed in association with KETOCONAZOLE (Ketoconazole). This represents 3.6% of all adverse event reports for KETOCONAZOLE.
202
Reports of Condition aggravated with KETOCONAZOLE
3.6%
of all KETOCONAZOLE reports
13
Deaths
18
Hospitalizations
How Dangerous Is Condition aggravated From KETOCONAZOLE?
Of the 202 reports, 13 (6.4%) resulted in death, 18 (8.9%) required hospitalization, and 10 (5.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOCONAZOLE. However, 202 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which KETOCONAZOLE Alternatives Have Lower Condition aggravated Risk?
KETOCONAZOLE vs KETOPROFEN
KETOCONAZOLE vs KETOPROFEN LYSINE
KETOCONAZOLE vs KETOROLAC TROMETHAMINE
KETOCONAZOLE vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOCONAZOLE vs KETOTIFEN