Does CRISABOROLE Cause Condition aggravated? 613 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 613 reports of Condition aggravated have been filed in association with CRISABOROLE (Eucrisa). This represents 7.9% of all adverse event reports for CRISABOROLE.
613
Reports of Condition aggravated with CRISABOROLE
7.9%
of all CRISABOROLE reports
2
Deaths
12
Hospitalizations
How Dangerous Is Condition aggravated From CRISABOROLE?
Of the 613 reports, 2 (0.3%) resulted in death, 12 (2.0%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CRISABOROLE. However, 613 reports have been filed with the FAERS database.
What Other Side Effects Does CRISABOROLE Cause?
Drug ineffective (1,815)
Application site pain (1,414)
Burning sensation (975)
Off label use (673)
Pain (468)
Pruritus (378)
Rash (342)
Eczema (308)
Erythema (285)
Product use in unapproved indication (242)
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 CRISABOROLE Alternatives Have Lower Condition aggravated Risk?
CRISABOROLE vs CRIZANLIZUMAB
CRISABOROLE vs CRIZANLIZUMAB-TMCA
CRISABOROLE vs CRIZOTINIB
CRISABOROLE vs CROFELEMER
CRISABOROLE vs CROMOLYN