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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 Hypersensitivity? 6,172 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6,172 reports of Hypersensitivity have been filed in association with TOFACITINIB (XELJANZ XR). This represents 4.0% of all adverse event reports for TOFACITINIB.

6,172
Reports of Hypersensitivity with TOFACITINIB
4.0%
of all TOFACITINIB reports
1,409
Deaths
2,286
Hospitalizations

How Dangerous Is Hypersensitivity From TOFACITINIB?

Of the 6,172 reports, 1,409 (22.8%) resulted in death, 2,286 (37.0%) required hospitalization, and 1,711 (27.7%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for TOFACITINIB.

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 Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which TOFACITINIB Alternatives Have Lower Hypersensitivity Risk?

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

Related Pages

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