Does TOFACITINIB Cause Prescribed underdose? 806 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 806 reports of Prescribed underdose have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.5% of all adverse event reports for TOFACITINIB.
806
Reports of Prescribed underdose with TOFACITINIB
0.5%
of all TOFACITINIB reports
348
Deaths
431
Hospitalizations
How Dangerous Is Prescribed underdose From TOFACITINIB?
Of the 806 reports, 348 (43.2%) resulted in death, 431 (53.5%) required hospitalization, and 367 (45.5%) were considered life-threatening.
Is Prescribed underdose Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 806 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 Prescribed underdose?
NATALIZUMAB (2,162)
SACUBITRIL\VALSARTAN (1,864)
APIXABAN (1,469)
ABATACEPT (1,192)
PIMAVANSERIN (1,165)
FINGOLIMOD (1,114)
RITUXIMAB (1,067)
METHOTREXATE (1,066)
ADALIMUMAB (1,010)
TOCILIZUMAB (1,002)
Which TOFACITINIB Alternatives Have Lower Prescribed underdose Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN