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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 Product storage error? 56 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 56 reports of Product storage error have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.

56
Reports of Product storage error with TOFACITINIB
0.0%
of all TOFACITINIB reports
0
Deaths
7
Hospitalizations

How Dangerous Is Product storage error From TOFACITINIB?

Of the 56 reports, 7 (12.5%) required hospitalization, and 1 (1.8%) were considered life-threatening.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 56 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 Product storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Which TOFACITINIB Alternatives Have Lower Product storage error Risk?

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

Related Pages

TOFACITINIB Full Profile All Product storage error Reports All Drugs Causing Product storage error TOFACITINIB Demographics