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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 Blood glucose increased? 430 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 430 reports of Blood glucose increased have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.3% of all adverse event reports for TOFACITINIB.

430
Reports of Blood glucose increased with TOFACITINIB
0.3%
of all TOFACITINIB reports
3
Deaths
84
Hospitalizations

How Dangerous Is Blood glucose increased From TOFACITINIB?

Of the 430 reports, 3 (0.7%) resulted in death, 84 (19.5%) required hospitalization, and 7 (1.6%) were considered life-threatening.

Is Blood glucose increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 430 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 Blood glucose increased?

INSULIN LISPRO (31,969) INSULIN GLARGINE (19,234) DULAGLUTIDE (9,119) INSULIN HUMAN (8,704) INSULIN ASPART (4,743) METFORMIN (4,038) EXENATIDE (3,363) INSULIN DEGLUDEC (2,644) SEMAGLUTIDE (2,240) TIRZEPATIDE (2,240)

Which TOFACITINIB Alternatives Have Lower Blood glucose increased Risk?

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

Related Pages

TOFACITINIB Full Profile All Blood glucose increased Reports All Drugs Causing Blood glucose increased TOFACITINIB Demographics