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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 Drug dose omission? 712 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 712 reports of Drug dose omission have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.5% of all adverse event reports for TOFACITINIB.

712
Reports of Drug dose omission with TOFACITINIB
0.5%
of all TOFACITINIB reports
4
Deaths
108
Hospitalizations

How Dangerous Is Drug dose omission From TOFACITINIB?

Of the 712 reports, 4 (0.6%) resulted in death, 108 (15.2%) required hospitalization.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 712 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 Drug dose omission?

ETANERCEPT (10,871) CINACALCET (8,683) EVOLOCUMAB (4,914) ADALIMUMAB (3,993) INSULIN LISPRO (3,063) GOLIMUMAB (2,652) TERIPARATIDE (2,616) APREMILAST (2,466) ALBUTEROL (2,309) FLUTICASONE\SALMETEROL (2,153)

Which TOFACITINIB Alternatives Have Lower Drug dose omission Risk?

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

Related Pages

TOFACITINIB Full Profile All Drug dose omission Reports All Drugs Causing Drug dose omission TOFACITINIB Demographics