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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TOCILIZUMAB Cause Intercepted product storage error? 381 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 381 reports of Intercepted product storage error have been filed in association with TOCILIZUMAB (Tocilizumab-anoh). This represents 0.4% of all adverse event reports for TOCILIZUMAB.

381
Reports of Intercepted product storage error with TOCILIZUMAB
0.4%
of all TOCILIZUMAB reports
1
Deaths
14
Hospitalizations

How Dangerous Is Intercepted product storage error From TOCILIZUMAB?

Of the 381 reports, 1 (0.3%) resulted in death, 14 (3.7%) required hospitalization.

Is Intercepted product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOCILIZUMAB. However, 381 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 Intercepted product storage error?

DUPILUMAB (325) OMALIZUMAB (256) ALTEPLASE (227) INSULIN GLARGINE (129) DORNASE ALFA (115) BEVACIZUMAB (113) RITUXIMAB (105) OCRELIZUMAB (88) PERTUZUMAB (84) TRASTUZUMAB (75)

Which TOCILIZUMAB Alternatives Have Lower Intercepted product storage error Risk?

TOCILIZUMAB vs TOCILIZUMAB-AAZG TOCILIZUMAB vs TOCOPHEROL TOCILIZUMAB vs TOFACITINIB TOCILIZUMAB vs TOFERSEN TOCILIZUMAB vs TOLNAFTATE

Related Pages

TOCILIZUMAB Full Profile All Intercepted product storage error Reports All Drugs Causing Intercepted product storage error TOCILIZUMAB Demographics