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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 UPADACITINIB Cause Hyperkeratosis? 18 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Hyperkeratosis have been filed in association with UPADACITINIB (Rinvoq). This represents 0.0% of all adverse event reports for UPADACITINIB.

18
Reports of Hyperkeratosis with UPADACITINIB
0.0%
of all UPADACITINIB reports
0
Deaths
3
Hospitalizations

How Dangerous Is Hyperkeratosis From UPADACITINIB?

Of the 18 reports, 3 (16.7%) required hospitalization.

Is Hyperkeratosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 18 reports have been filed with the FAERS database.

What Other Side Effects Does UPADACITINIB Cause?

Pain (4,444) Arthralgia (3,815) Drug ineffective (3,384) Covid-19 (2,978) Rheumatoid arthritis (2,730) Pain in extremity (2,353) Fatigue (2,153) Fall (2,081) Surgery (2,037) Therapy interrupted (1,741)

What Other Drugs Cause Hyperkeratosis?

CABOZANTINIB S-MALATE (411) ADALIMUMAB (332) SUNITINIB MALATE (170) ETANERCEPT (168) SORAFENIB (150) METHOTREXATE (149) VEMURAFENIB (145) REGORAFENIB (136) RIPRETINIB (124) RITUXIMAB (121)

Which UPADACITINIB Alternatives Have Lower Hyperkeratosis Risk?

UPADACITINIB vs URAPIDIL UPADACITINIB vs UREA UPADACITINIB vs URIDINE TRIACETATE UPADACITINIB vs UROFOLLITROPIN UPADACITINIB vs URSODIOL

Related Pages

UPADACITINIB Full Profile All Hyperkeratosis Reports All Drugs Causing Hyperkeratosis UPADACITINIB Demographics