Does KETOCONAZOLE Cause Incorrect product administration duration? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Incorrect product administration duration have been filed in association with KETOCONAZOLE (Ketoconazole). This represents 0.3% of all adverse event reports for KETOCONAZOLE.
14
Reports of Incorrect product administration duration with KETOCONAZOLE
0.3%
of all KETOCONAZOLE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From KETOCONAZOLE?
Of the 14 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOCONAZOLE. However, 14 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which KETOCONAZOLE Alternatives Have Lower Incorrect product administration duration Risk?
KETOCONAZOLE vs KETOPROFEN
KETOCONAZOLE vs KETOPROFEN LYSINE
KETOCONAZOLE vs KETOROLAC TROMETHAMINE
KETOCONAZOLE vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOCONAZOLE vs KETOTIFEN