Does TOFACITINIB Cause Extra dose administered? 67 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Extra dose administered have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.
67
Reports of Extra dose administered with TOFACITINIB
0.0%
of all TOFACITINIB reports
2
Deaths
6
Hospitalizations
How Dangerous Is Extra dose administered From TOFACITINIB?
Of the 67 reports, 2 (3.0%) resulted in death, 6 (9.0%) required hospitalization.
Is Extra dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 67 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 Extra dose administered?
TIRZEPATIDE (6,774)
DULAGLUTIDE (3,047)
LORATADINE (1,556)
DUPILUMAB (1,422)
FEXOFENADINE (1,413)
NAPROXEN (908)
POLYETHYLENE GLYCOL 3350 (589)
ACETAMINOPHEN (552)
DALFAMPRIDINE (519)
FLUTICASONE\SALMETEROL (499)
Which TOFACITINIB Alternatives Have Lower Extra dose administered Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN