Does TOFACITINIB Cause Product label issue? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Product label issue have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.
23
Reports of Product label issue with TOFACITINIB
0.0%
of all TOFACITINIB reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product label issue From TOFACITINIB?
Of the 23 reports, 1 (4.3%) resulted in death, 2 (8.7%) required hospitalization.
Is Product label issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 23 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 label issue?
RIVAROXABAN (379)
ACETAMINOPHEN (276)
GUSELKUMAB (177)
USTEKINUMAB (164)
DIMETHICONE\LOPERAMIDE (154)
CETIRIZINE (138)
IBUPROFEN (99)
GOLIMUMAB (76)
POLYETHYLENE GLYCOL 3350 (76)
FENTANYL (72)
Which TOFACITINIB Alternatives Have Lower Product label issue Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN