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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 Laboratory test abnormal? 395 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 395 reports of Laboratory test abnormal have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.3% of all adverse event reports for TOFACITINIB.

395
Reports of Laboratory test abnormal with TOFACITINIB
0.3%
of all TOFACITINIB reports
105
Deaths
135
Hospitalizations

How Dangerous Is Laboratory test abnormal From TOFACITINIB?

Of the 395 reports, 105 (26.6%) resulted in death, 135 (34.2%) required hospitalization, and 109 (27.6%) were considered life-threatening.

Is Laboratory test abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 395 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 Laboratory test abnormal?

LENALIDOMIDE (4,215) CINACALCET (4,210) POMALIDOMIDE (1,218) ADALIMUMAB (845) ETANERCEPT (753) DALFAMPRIDINE (650) PALBOCICLIB (550) NIRAPARIB (536) METHOTREXATE (507) ECULIZUMAB (441)

Which TOFACITINIB Alternatives Have Lower Laboratory test abnormal Risk?

TOFACITINIB vs TOFERSEN TOFACITINIB vs TOLNAFTATE TOFACITINIB vs TOLODODEKIN ALFA TOFACITINIB vs TOLTERODINE TOFACITINIB vs TOLVAPTAN

Related Pages

TOFACITINIB Full Profile All Laboratory test abnormal Reports All Drugs Causing Laboratory test abnormal TOFACITINIB Demographics