Does KETOCONAZOLE Cause Product dose omission? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product dose omission have been filed in association with KETOCONAZOLE (Ketoconazole). This represents 0.2% of all adverse event reports for KETOCONAZOLE.
9
Reports of Product dose omission with KETOCONAZOLE
0.2%
of all KETOCONAZOLE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission From KETOCONAZOLE?
Of the 9 reports.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOCONAZOLE. However, 9 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which KETOCONAZOLE Alternatives Have Lower Product dose omission Risk?
KETOCONAZOLE vs KETOPROFEN
KETOCONAZOLE vs KETOPROFEN LYSINE
KETOCONAZOLE vs KETOROLAC TROMETHAMINE
KETOCONAZOLE vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOCONAZOLE vs KETOTIFEN