Does TOFACITINIB Cause Full blood count abnormal? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Full blood count abnormal have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.
69
Reports of Full blood count abnormal with TOFACITINIB
0.0%
of all TOFACITINIB reports
2
Deaths
11
Hospitalizations
How Dangerous Is Full blood count abnormal From TOFACITINIB?
Of the 69 reports, 2 (2.9%) resulted in death, 11 (15.9%) required hospitalization.
Is Full blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 69 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 Full blood count abnormal?
ALBUTEROL (3,060)
PREDNISONE (2,230)
BUDESONIDE\FORMOTEROL (1,786)
TIOTROPIUM (1,754)
MONTELUKAST (1,529)
MEPOLIZUMAB (1,440)
BUDESONIDE (1,339)
PALBOCICLIB (1,146)
CICLESONIDE (916)
PANTOPRAZOLE (776)
Which TOFACITINIB Alternatives Have Lower Full blood count abnormal Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN