Does UPADACITINIB Cause Device breakage? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Device breakage have been filed in association with UPADACITINIB (Rinvoq). This represents 0.1% of all adverse event reports for UPADACITINIB.
36
Reports of Device breakage with UPADACITINIB
0.1%
of all UPADACITINIB reports
0
Deaths
12
Hospitalizations
How Dangerous Is Device breakage From UPADACITINIB?
Of the 36 reports, 12 (33.3%) required hospitalization.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 36 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 Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which UPADACITINIB Alternatives Have Lower Device breakage Risk?
UPADACITINIB vs URAPIDIL
UPADACITINIB vs UREA
UPADACITINIB vs URIDINE TRIACETATE
UPADACITINIB vs UROFOLLITROPIN
UPADACITINIB vs URSODIOL