Does TOFACITINIB Cause Product prescribing error? 805 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 805 reports of Product prescribing error have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.5% of all adverse event reports for TOFACITINIB.
805
Reports of Product prescribing error with TOFACITINIB
0.5%
of all TOFACITINIB reports
19
Deaths
64
Hospitalizations
How Dangerous Is Product prescribing error From TOFACITINIB?
Of the 805 reports, 19 (2.4%) resulted in death, 64 (8.0%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 805 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
RAMIPRIL (322)
Which TOFACITINIB Alternatives Have Lower Product prescribing error Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN