Does TOFACITINIB Cause Contraindicated product administered? 5,841 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,841 reports of Contraindicated product administered have been filed in association with TOFACITINIB (XELJANZ XR). This represents 3.8% of all adverse event reports for TOFACITINIB.
5,841
Reports of Contraindicated product administered with TOFACITINIB
3.8%
of all TOFACITINIB reports
1,049
Deaths
2,046
Hospitalizations
How Dangerous Is Contraindicated product administered From TOFACITINIB?
Of the 5,841 reports, 1,049 (18.0%) resulted in death, 2,046 (35.0%) required hospitalization, and 1,421 (24.3%) were considered life-threatening.
Is Contraindicated product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 5,841 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 Contraindicated product administered?
ABATACEPT (13,559)
METHOTREXATE (13,121)
ETANERCEPT (12,062)
TOCILIZUMAB (11,547)
ADALIMUMAB (11,270)
LEFLUNOMIDE (11,206)
HYDROXYCHLOROQUINE (10,557)
RITUXIMAB (10,479)
INFLIXIMAB (9,618)
SULFASALAZINE (8,698)
Which TOFACITINIB Alternatives Have Lower Contraindicated product administered Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN