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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 White matter lesion? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of White matter lesion have been filed in association with UPADACITINIB (Rinvoq). This represents 0.0% of all adverse event reports for UPADACITINIB.

9
Reports of White matter lesion with UPADACITINIB
0.0%
of all UPADACITINIB reports
0
Deaths
4
Hospitalizations

How Dangerous Is White matter lesion From UPADACITINIB?

Of the 9 reports, 4 (44.4%) required hospitalization.

Is White matter lesion Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 9 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 White matter lesion?

ADALIMUMAB (84) METHOTREXATE (83) FINGOLIMOD (71) CYTARABINE (57) PREDNISONE (42) METRONIDAZOLE (41) LEVETIRACETAM (38) RITUXIMAB (37) AMPHOTERICIN B (34) DAUNORUBICIN (33)

Which UPADACITINIB Alternatives Have Lower White matter lesion Risk?

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

Related Pages

UPADACITINIB Full Profile All White matter lesion Reports All Drugs Causing White matter lesion UPADACITINIB Demographics