Does TOFACITINIB Cause Underdose? 476 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 476 reports of Underdose have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.3% of all adverse event reports for TOFACITINIB.
476
Reports of Underdose with TOFACITINIB
0.3%
of all TOFACITINIB reports
265
Deaths
334
Hospitalizations
How Dangerous Is Underdose From TOFACITINIB?
Of the 476 reports, 265 (55.7%) resulted in death, 334 (70.2%) required hospitalization, and 318 (66.8%) were considered life-threatening.
Is Underdose Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 476 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 Underdose?
ADAPALENE (5,192)
AVOBENZONE\OCTISALATE\OCTOCRYLENE (3,722)
INSULIN LISPRO (3,156)
ETANERCEPT (3,145)
GALCANEZUMAB-GNLM (2,909)
ENZALUTAMIDE (2,017)
FLUTICASONE\SALMETEROL (1,600)
ALBUTEROL (1,593)
EXENATIDE (1,571)
TROFINETIDE (1,540)
Which TOFACITINIB Alternatives Have Lower Underdose Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN