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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 Dry eye? 756 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 756 reports of Dry eye have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.5% of all adverse event reports for TOFACITINIB.

756
Reports of Dry eye with TOFACITINIB
0.5%
of all TOFACITINIB reports
19
Deaths
97
Hospitalizations

How Dangerous Is Dry eye From TOFACITINIB?

Of the 756 reports, 19 (2.5%) resulted in death, 97 (12.8%) required hospitalization, and 18 (2.4%) were considered life-threatening.

Is Dry eye Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 756 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 Dry eye?

DUPILUMAB (10,892) CYCLOSPORINE (1,310) ADALIMUMAB (1,253) METHOTREXATE (1,023) LIFITEGRAST (1,013) ETANERCEPT (992) LENALIDOMIDE (649) TOCILIZUMAB (565) CENEGERMIN-BKBJ (537) HYPROMELLOSE 2910 (521)

Which TOFACITINIB Alternatives Have Lower Dry eye Risk?

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

Related Pages

TOFACITINIB Full Profile All Dry eye Reports All Drugs Causing Dry eye TOFACITINIB Demographics