Does TOFACITINIB Cause Eosinophil count increased? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Eosinophil count increased have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.
11
Reports of Eosinophil count increased with TOFACITINIB
0.0%
of all TOFACITINIB reports
1
Deaths
2
Hospitalizations
How Dangerous Is Eosinophil count increased From TOFACITINIB?
Of the 11 reports, 1 (9.1%) resulted in death, 2 (18.2%) required hospitalization.
Is Eosinophil count increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 11 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 Eosinophil count increased?
ALBUTEROL (1,359)
PREDNISONE (846)
BUDESONIDE\FORMOTEROL (719)
DUPILUMAB (712)
TIOTROPIUM (682)
MEPOLIZUMAB (670)
MONTELUKAST (504)
BUDESONIDE (493)
CLOZAPINE (475)
FLUTICASONE\SALMETEROL (416)
Which TOFACITINIB Alternatives Have Lower Eosinophil count increased Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN