Does UPADACITINIB Cause Complication associated with device? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Complication associated with device have been filed in association with UPADACITINIB (Rinvoq). This represents 0.1% of all adverse event reports for UPADACITINIB.
33
Reports of Complication associated with device with UPADACITINIB
0.1%
of all UPADACITINIB reports
0
Deaths
7
Hospitalizations
How Dangerous Is Complication associated with device From UPADACITINIB?
Of the 33 reports, 7 (21.2%) required hospitalization.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 33 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which UPADACITINIB Alternatives Have Lower Complication associated with device Risk?
UPADACITINIB vs URAPIDIL
UPADACITINIB vs UREA
UPADACITINIB vs URIDINE TRIACETATE
UPADACITINIB vs UROFOLLITROPIN
UPADACITINIB vs URSODIOL