Does TOCILIZUMAB Cause Product quality issue? 763 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 763 reports of Product quality issue have been filed in association with TOCILIZUMAB (Tocilizumab-anoh). This represents 0.8% of all adverse event reports for TOCILIZUMAB.
763
Reports of Product quality issue with TOCILIZUMAB
0.8%
of all TOCILIZUMAB reports
501
Deaths
451
Hospitalizations
How Dangerous Is Product quality issue From TOCILIZUMAB?
Of the 763 reports, 501 (65.7%) resulted in death, 451 (59.1%) required hospitalization, and 435 (57.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOCILIZUMAB. However, 763 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which TOCILIZUMAB Alternatives Have Lower Product quality issue Risk?
TOCILIZUMAB vs TOCILIZUMAB-AAZG
TOCILIZUMAB vs TOCOPHEROL
TOCILIZUMAB vs TOFACITINIB
TOCILIZUMAB vs TOFERSEN
TOCILIZUMAB vs TOLNAFTATE