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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CLOBETASOL Cause Application site dryness? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Application site dryness have been filed in association with CLOBETASOL (CLOBETASOL PROPIONATE). This represents 0.2% of all adverse event reports for CLOBETASOL.

14
Reports of Application site dryness with CLOBETASOL
0.2%
of all CLOBETASOL reports
0
Deaths
0
Hospitalizations

How Dangerous Is Application site dryness From CLOBETASOL?

Of the 14 reports, and 1 (7.1%) were considered life-threatening.

Is Application site dryness Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CLOBETASOL. However, 14 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 Application site dryness?

MINOXIDIL (1,027) INGENOL MEBUTATE (365) SUMATRIPTAN (208) BUPRENORPHINE (100) TESTOSTERONE (63) ADAPALENE (60) DICLOFENAC (55) ESTRADIOL (52) ESTRADIOL\NORETHINDRONE (49) NICOTINE (48)

Which CLOBETASOL Alternatives Have Lower Application site dryness Risk?

CLOBETASOL vs CLOBETASONE CLOBETASOL vs CLODRONATE CLOBETASOL vs CLOFARABINE CLOBETASOL vs CLOFAZIMINE CLOBETASOL vs CLOMETHIAZOLE

Related Pages

CLOBETASOL Full Profile All Application site dryness Reports All Drugs Causing Application site dryness CLOBETASOL Demographics