Does TOFACITINIB Cause Hip fracture? 435 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 435 reports of Hip fracture have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.3% of all adverse event reports for TOFACITINIB.
435
Reports of Hip fracture with TOFACITINIB
0.3%
of all TOFACITINIB reports
28
Deaths
231
Hospitalizations
How Dangerous Is Hip fracture From TOFACITINIB?
Of the 435 reports, 28 (6.4%) resulted in death, 231 (53.1%) required hospitalization, and 6 (1.4%) were considered life-threatening.
Is Hip fracture Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 435 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 Hip fracture?
DENOSUMAB (1,096)
LENALIDOMIDE (1,093)
CARBIDOPA\LEVODOPA (881)
ADALIMUMAB (678)
ETANERCEPT (569)
APIXABAN (484)
IBRUTINIB (466)
PIMAVANSERIN (444)
EMTRICITABINE\TENOFOVIR DISOPROXIL (378)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (366)
Which TOFACITINIB Alternatives Have Lower Hip fracture Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN