Does TERBINAFINE Cause Incorrect product administration duration? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Incorrect product administration duration have been filed in association with TERBINAFINE (Terbinafine Hydrochloride). This represents 0.4% of all adverse event reports for TERBINAFINE.
29
Reports of Incorrect product administration duration with TERBINAFINE
0.4%
of all TERBINAFINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From TERBINAFINE?
Of the 29 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 TERBINAFINE. However, 29 reports have been filed with the FAERS database.
What Other Side Effects Does TERBINAFINE Cause?
Drug ineffective (905)
Rash (440)
Pruritus (404)
Ageusia (397)
Dysgeusia (265)
Nausea (251)
Fatigue (244)
Erythema (235)
Product use in unapproved indication (232)
Off label use (222)
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 TERBINAFINE Alternatives Have Lower Incorrect product administration duration Risk?
TERBINAFINE vs TERBINAFINE\TERBINAFINE
TERBINAFINE vs TERBUTALINE
TERBINAFINE vs TERCONAZOLE
TERBINAFINE vs TERIFLUNOMIDE
TERBINAFINE vs TERIPARATIDE