Does TOFACITINIB Cause Expired product administered? 93 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 93 reports of Expired product administered have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.1% of all adverse event reports for TOFACITINIB.
93
Reports of Expired product administered with TOFACITINIB
0.1%
of all TOFACITINIB reports
2
Deaths
16
Hospitalizations
How Dangerous Is Expired product administered From TOFACITINIB?
Of the 93 reports, 2 (2.2%) resulted in death, 16 (17.2%) required hospitalization, and 4 (4.3%) were considered life-threatening.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 93 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which TOFACITINIB Alternatives Have Lower Expired product administered Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN