Does CLOBETASOL Cause Condition aggravated? 297 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 297 reports of Condition aggravated have been filed in association with CLOBETASOL (CLOBETASOL PROPIONATE). This represents 3.8% of all adverse event reports for CLOBETASOL.
297
Reports of Condition aggravated with CLOBETASOL
3.8%
of all CLOBETASOL reports
4
Deaths
28
Hospitalizations
How Dangerous Is Condition aggravated From CLOBETASOL?
Of the 297 reports, 4 (1.3%) resulted in death, 28 (9.4%) required hospitalization, and 3 (1.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOBETASOL. However, 297 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CLOBETASOL Alternatives Have Lower Condition aggravated Risk?
CLOBETASOL vs CLOBETASONE
CLOBETASOL vs CLODRONATE
CLOBETASOL vs CLOFARABINE
CLOBETASOL vs CLOFAZIMINE
CLOBETASOL vs CLOMETHIAZOLE