Does TOFACITINIB Cause Intentional dose omission? 845 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 845 reports of Intentional dose omission have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.5% of all adverse event reports for TOFACITINIB.
845
Reports of Intentional dose omission with TOFACITINIB
0.5%
of all TOFACITINIB reports
5
Deaths
86
Hospitalizations
How Dangerous Is Intentional dose omission From TOFACITINIB?
Of the 845 reports, 5 (0.6%) resulted in death, 86 (10.2%) required hospitalization, and 6 (0.7%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 845 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 dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
SOFOSBUVIR\VELPATASVIR (474)
Which TOFACITINIB Alternatives Have Lower Intentional dose omission Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN