Does TOFACITINIB Cause Dislocation of vertebra? 600 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 600 reports of Dislocation of vertebra have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.4% of all adverse event reports for TOFACITINIB.
600
Reports of Dislocation of vertebra with TOFACITINIB
0.4%
of all TOFACITINIB reports
464
Deaths
516
Hospitalizations
How Dangerous Is Dislocation of vertebra From TOFACITINIB?
Of the 600 reports, 464 (77.3%) resulted in death, 516 (86.0%) required hospitalization, and 510 (85.0%) were considered life-threatening.
Is Dislocation of vertebra Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 600 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 Dislocation of vertebra?
ADALIMUMAB (942)
METHOTREXATE (900)
ABATACEPT (859)
DICLOFENAC (838)
RITUXIMAB (832)
TOCILIZUMAB (825)
LEFLUNOMIDE (810)
HYDROXYCHLOROQUINE (792)
FOLIC ACID (768)
ALENDRONATE (767)
Which TOFACITINIB Alternatives Have Lower Dislocation of vertebra Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN