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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 Dyspepsia? 2,264 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 2,264 reports of Dyspepsia have been filed in association with TOFACITINIB (XELJANZ XR). This represents 1.5% of all adverse event reports for TOFACITINIB.

2,264
Reports of Dyspepsia with TOFACITINIB
1.5%
of all TOFACITINIB reports
683
Deaths
822
Hospitalizations

How Dangerous Is Dyspepsia From TOFACITINIB?

Of the 2,264 reports, 683 (30.2%) resulted in death, 822 (36.3%) required hospitalization, and 792 (35.0%) were considered life-threatening.

Is Dyspepsia Listed in the Official Label?

Yes, Dyspepsia 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 Dyspepsia?

ADALIMUMAB (3,586) METHOTREXATE (2,690) RITUXIMAB (2,289) PREDNISONE (2,224) APREMILAST (2,207) ETANERCEPT (2,100) ESOMEPRAZOLE (2,064) TOCILIZUMAB (2,046) LEFLUNOMIDE (1,981) INFLIXIMAB (1,885)

Which TOFACITINIB Alternatives Have Lower Dyspepsia Risk?

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

Related Pages

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