Does BUTENAFINE 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 BUTENAFINE (Butenafine Hydrochloride Athletes Foot). This represents 1.8% of all adverse event reports for BUTENAFINE.
14
Reports of Incorrect product administration duration with BUTENAFINE
1.8%
of all BUTENAFINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From BUTENAFINE?
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 BUTENAFINE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does BUTENAFINE Cause?
Drug ineffective (235)
Product use issue (120)
Product use in unapproved indication (98)
Off label use (97)
Pruritus (35)
Burning sensation (29)
Drug effective for unapproved indication (29)
Rash (28)
Therapeutic response unexpected (27)
Product administered at inappropriate site (26)
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 BUTENAFINE Alternatives Have Lower Incorrect product administration duration Risk?
BUTENAFINE vs BUTORPHANOL
BUTENAFINE vs BUTRANS
BUTENAFINE vs BUTYLSCOPOLAMINE
BUTENAFINE vs BYETTA
BUTENAFINE vs BYETTA PEN DISPOSABLE