Does CLOBETASOL Cause Product dose omission issue? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Product dose omission issue have been filed in association with CLOBETASOL (CLOBETASOL PROPIONATE). This represents 0.8% of all adverse event reports for CLOBETASOL.
61
Reports of Product dose omission issue with CLOBETASOL
0.8%
of all CLOBETASOL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From CLOBETASOL?
Of the 61 reports.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOBETASOL. However, 61 reports have been filed with the FAERS database.