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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 Product use issue? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Product use issue have been filed in association with DEUCRAVACITINIB (SOTYKTU). This represents 1.0% of all adverse event reports for DEUCRAVACITINIB.

23
Reports of Product use issue with DEUCRAVACITINIB
1.0%
of all DEUCRAVACITINIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product use issue From DEUCRAVACITINIB?

Of the 23 reports, 1 (4.3%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEUCRAVACITINIB. However, 23 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) Adverse event (74) Mouth ulceration (72) Folliculitis (65)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which DEUCRAVACITINIB Alternatives Have Lower Product use issue 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 Product use issue Reports All Drugs Causing Product use issue DEUCRAVACITINIB Demographics