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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 Anaemia? 1,108 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,108 reports of Anaemia have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.7% of all adverse event reports for TOFACITINIB.

1,108
Reports of Anaemia with TOFACITINIB
0.7%
of all TOFACITINIB reports
21
Deaths
280
Hospitalizations

How Dangerous Is Anaemia From TOFACITINIB?

Of the 1,108 reports, 21 (1.9%) resulted in death, 280 (25.3%) required hospitalization, and 19 (1.7%) were considered life-threatening.

Is Anaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 1,108 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 Anaemia?

LENALIDOMIDE (5,322) CARBOPLATIN (5,312) RIBAVIRIN (5,130) ASPIRIN (4,568) CYCLOPHOSPHAMIDE (4,486) RITUXIMAB (4,399) DEXAMETHASONE (4,352) ADALIMUMAB (3,994) PACLITAXEL (3,949) METHOTREXATE (3,913)

Which TOFACITINIB Alternatives Have Lower Anaemia Risk?

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

Related Pages

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