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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 Therapy non-responder? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Therapy non-responder have been filed in association with DEUCRAVACITINIB (SOTYKTU). This represents 0.6% of all adverse event reports for DEUCRAVACITINIB.

15
Reports of Therapy non-responder with DEUCRAVACITINIB
0.6%
of all DEUCRAVACITINIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Therapy non-responder From DEUCRAVACITINIB?

Of the 15 reports, 1 (6.7%) required hospitalization.

Is Therapy non-responder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEUCRAVACITINIB. However, 15 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 Therapy non-responder?

ETANERCEPT (3,472) APREMILAST (3,360) METHOTREXATE (2,965) RITUXIMAB (2,731) ADALIMUMAB (2,595) PREDNISONE (2,563) TREPROSTINIL (2,289) INFLIXIMAB (2,122) TOCILIZUMAB (1,775) HYDROXYCHLOROQUINE (1,699)

Which DEUCRAVACITINIB Alternatives Have Lower Therapy non-responder 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 Therapy non-responder Reports All Drugs Causing Therapy non-responder DEUCRAVACITINIB Demographics