Does UPADACITINIB Cause Condition aggravated? 859 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 859 reports of Condition aggravated have been filed in association with UPADACITINIB (Rinvoq). This represents 1.3% of all adverse event reports for UPADACITINIB.
859
Reports of Condition aggravated with UPADACITINIB
1.3%
of all UPADACITINIB reports
92
Deaths
256
Hospitalizations
How Dangerous Is Condition aggravated From UPADACITINIB?
Of the 859 reports, 92 (10.7%) resulted in death, 256 (29.8%) required hospitalization, and 103 (12.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 859 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which UPADACITINIB Alternatives Have Lower Condition aggravated Risk?
UPADACITINIB vs URAPIDIL
UPADACITINIB vs UREA
UPADACITINIB vs URIDINE TRIACETATE
UPADACITINIB vs UROFOLLITROPIN
UPADACITINIB vs URSODIOL