Does TOFACITINIB Cause Poor quality product administered? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Poor quality product administered have been filed in association with TOFACITINIB (XELJANZ XR). This represents 0.0% of all adverse event reports for TOFACITINIB.
43
Reports of Poor quality product administered with TOFACITINIB
0.0%
of all TOFACITINIB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Poor quality product administered From TOFACITINIB?
Of the 43 reports, 4 (9.3%) required hospitalization, and 1 (2.3%) were considered life-threatening.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOFACITINIB. However, 43 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which TOFACITINIB Alternatives Have Lower Poor quality product administered Risk?
TOFACITINIB vs TOFERSEN
TOFACITINIB vs TOLNAFTATE
TOFACITINIB vs TOLODODEKIN ALFA
TOFACITINIB vs TOLTERODINE
TOFACITINIB vs TOLVAPTAN