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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 Therapy interrupted? 1,182 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,182 reports of Therapy interrupted have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.8% of all adverse event reports for TOFACITINIB.

1,182
Reports of Therapy interrupted with TOFACITINIB
0.8%
of all TOFACITINIB reports
0
Deaths
191
Hospitalizations

How Dangerous Is Therapy interrupted From TOFACITINIB?

Of the 1,182 reports, 191 (16.2%) required hospitalization, and 2 (0.2%) were considered life-threatening.

Is Therapy interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 1,182 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 Therapy interrupted?

ADALIMUMAB (5,755) ETANERCEPT (3,397) RELUGOLIX (3,251) CERTOLIZUMAB PEGOL (3,209) LENALIDOMIDE (2,724) UPADACITINIB (1,741) ABATACEPT (1,726) CLOZAPINE (1,722) AMIKACIN (1,283) SECUKINUMAB (1,071)

Which TOFACITINIB Alternatives Have Lower Therapy interrupted Risk?

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

Related Pages

TOFACITINIB Full Profile All Therapy interrupted Reports All Drugs Causing Therapy interrupted TOFACITINIB Demographics