Does TOFACITINIB Cause Foot fracture? 379 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 379 reports of Foot fracture have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.2% of all adverse event reports for TOFACITINIB.
379
Reports of Foot fracture with TOFACITINIB
0.2%
of all TOFACITINIB reports
8
Deaths
91
Hospitalizations
How Dangerous Is Foot fracture From TOFACITINIB?
Of the 379 reports, 8 (2.1%) resulted in death, 91 (24.0%) required hospitalization, and 2 (0.5%) were considered life-threatening.
Is Foot fracture Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 379 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 Foot fracture?
ADALIMUMAB (799)
EMTRICITABINE\TENOFOVIR DISOPROXIL (728)
ETANERCEPT (582)
DENOSUMAB (578)
ALENDRONATE (531)
METHOTREXATE (511)
EFAVIRENZ\EMTRICITABINE\TENOFOVIR DISOPROXIL (500)
TENOFOVIR DISOPROXIL (426)
TERIPARATIDE (367)
TOCILIZUMAB (362)
Which TOFACITINIB Alternatives Have Lower Foot fracture Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN