Does CLOBETASOL Cause Incorrect product administration duration? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Incorrect product administration duration have been filed in association with CLOBETASOL (CLOBETASOL PROPIONATE). This represents 0.6% of all adverse event reports for CLOBETASOL.
47
Reports of Incorrect product administration duration with CLOBETASOL
0.6%
of all CLOBETASOL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From CLOBETASOL?
Of the 47 reports, 2 (4.3%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOBETASOL. However, 47 reports have been filed with the FAERS database.
What Other Side Effects Does CLOBETASOL Cause?
Drug ineffective (3,217)
Psoriasis (1,317)
Product use in unapproved indication (706)
Pruritus (697)
Therapeutic product effect incomplete (643)
Skin exfoliation (550)
Off label use (540)
Treatment failure (535)
Erythema (464)
Arthralgia (417)
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 CLOBETASOL Alternatives Have Lower Incorrect product administration duration Risk?
CLOBETASOL vs CLOBETASONE
CLOBETASOL vs CLODRONATE
CLOBETASOL vs CLOFARABINE
CLOBETASOL vs CLOFAZIMINE
CLOBETASOL vs CLOMETHIAZOLE