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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 DEUCRAVACITINIB Cause Adverse event? 74 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 74 reports of Adverse event have been filed in association with DEUCRAVACITINIB (SOTYKTU). This represents 3.1% of all adverse event reports for DEUCRAVACITINIB.

74
Reports of Adverse event with DEUCRAVACITINIB
3.1%
of all DEUCRAVACITINIB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Adverse event From DEUCRAVACITINIB?

Of the 74 reports.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEUCRAVACITINIB. However, 74 reports have been filed with the FAERS database.

What Other Side Effects Does DEUCRAVACITINIB Cause?

Drug ineffective (228) Acne (225) Pruritus (187) Rash (175) Erythema (124) Psoriasis (122) Off label use (101) Mouth ulceration (72) Folliculitis (65) Headache (65)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which DEUCRAVACITINIB Alternatives Have Lower Adverse event Risk?

DEUCRAVACITINIB vs DEUTETRABENAZINE DEUCRAVACITINIB vs DEUTIVACAFTOR\TEZACAFTOR\VANZACAFTOR DEUCRAVACITINIB vs DEVICE DEUCRAVACITINIB vs DEXAMETHASONE DEUCRAVACITINIB vs DEXAMETHASONE\DEXAMETHASONE

Related Pages

DEUCRAVACITINIB Full Profile All Adverse event Reports All Drugs Causing Adverse event DEUCRAVACITINIB Demographics