Does UPADACITINIB Cause Device dislocation? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Device dislocation have been filed in association with UPADACITINIB (Rinvoq). This represents 0.1% of all adverse event reports for UPADACITINIB.
49
Reports of Device dislocation with UPADACITINIB
0.1%
of all UPADACITINIB reports
1
Deaths
17
Hospitalizations
How Dangerous Is Device dislocation From UPADACITINIB?
Of the 49 reports, 1 (2.0%) resulted in death, 17 (34.7%) required hospitalization.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 49 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 dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which UPADACITINIB Alternatives Have Lower Device dislocation Risk?
UPADACITINIB vs URAPIDIL
UPADACITINIB vs UREA
UPADACITINIB vs URIDINE TRIACETATE
UPADACITINIB vs UROFOLLITROPIN
UPADACITINIB vs URSODIOL