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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

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

Related Pages

TOFACITINIB Full Profile All Underdose Reports All Drugs Causing Underdose TOFACITINIB Demographics