Does TOFACITINIB Cause Intentional product misuse? 2,331 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,331 reports of Intentional product misuse have been filed in association with TOFACITINIB (XELJANZ XR). This represents 1.5% of all adverse event reports for TOFACITINIB.
2,331
Reports of Intentional product misuse with TOFACITINIB
1.5%
of all TOFACITINIB reports
112
Deaths
299
Hospitalizations
How Dangerous Is Intentional product misuse From TOFACITINIB?
Of the 2,331 reports, 112 (4.8%) resulted in death, 299 (12.8%) required hospitalization, and 83 (3.6%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 2,331 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
TERIPARATIDE (1,503)
Which TOFACITINIB Alternatives Have Lower Intentional product misuse Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN