Does TOCILIZUMAB Cause Device defective? 400 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 400 reports of Device defective have been filed in association with TOCILIZUMAB (Tocilizumab-anoh). This represents 0.4% of all adverse event reports for TOCILIZUMAB.
400
Reports of Device defective with TOCILIZUMAB
0.4%
of all TOCILIZUMAB reports
0
Deaths
16
Hospitalizations
How Dangerous Is Device defective From TOCILIZUMAB?
Of the 400 reports, 16 (4.0%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOCILIZUMAB. However, 400 reports have been filed with the FAERS database.
What Other Side Effects Does TOCILIZUMAB Cause?
Drug ineffective (32,342)
Rheumatoid arthritis (20,652)
Pain (18,384)
Off label use (18,256)
Arthralgia (15,536)
Joint swelling (14,831)
Fatigue (13,802)
Rash (12,327)
Drug intolerance (11,952)
Contraindicated product administered (11,547)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
INSULIN GLARGINE (397)
EXENATIDE (387)
BUDESONIDE\FORMOTEROL (378)
Which TOCILIZUMAB Alternatives Have Lower Device defective Risk?
TOCILIZUMAB vs TOCILIZUMAB-AAZG
TOCILIZUMAB vs TOCOPHEROL
TOCILIZUMAB vs TOFACITINIB
TOCILIZUMAB vs TOFERSEN
TOCILIZUMAB vs TOLNAFTATE