Does TOFACITINIB Cause Intentional underdose? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Intentional underdose have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.
43
Reports of Intentional underdose with TOFACITINIB
0.0%
of all TOFACITINIB reports
3
Deaths
10
Hospitalizations
How Dangerous Is Intentional underdose From TOFACITINIB?
Of the 43 reports, 3 (7.0%) resulted in death, 10 (23.3%) required hospitalization.
Is Intentional underdose Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 43 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 underdose?
BUPRENORPHINE\NALOXONE (1,037)
NIRAPARIB (677)
FLUTICASONE\SALMETEROL (605)
DIMETHYL (364)
LEVODOPA (196)
TECFIDERA (180)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (167)
DROXIDOPA (163)
ICOSAPENT ETHYL (145)
FLUTICASONE (144)
Which TOFACITINIB Alternatives Have Lower Intentional underdose Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN