Does TOFACITINIB Cause Device dislocation? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Device dislocation have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.
15
Reports of Device dislocation with TOFACITINIB
0.0%
of all TOFACITINIB reports
0
Deaths
5
Hospitalizations
How Dangerous Is Device dislocation From TOFACITINIB?
Of the 15 reports, 5 (33.3%) required hospitalization.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does TOFACITINIB Cause?
Drug ineffective (30,382)
Pain (21,659)
Condition aggravated (16,925)
Arthralgia (15,640)
Fatigue (13,551)
Rheumatoid arthritis (12,277)
Off label use (11,736)
Headache (11,061)
Joint swelling (10,686)
Malaise (9,040)
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 TOFACITINIB Alternatives Have Lower Device dislocation Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN