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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.

Intercepted product storage error: Which Medications Cause It? (2,947 Reports Across 71 Drugs)

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Intercepted product storage error has been reported as an adverse event with 71 different drugs in the FDA's FAERS database, with 2,947 total reports. 6 of these reports resulted in death.The drugs most commonly associated with Intercepted product storage error are TOCILIZUMAB, DUPILUMAB, and OMALIZUMAB.

2,947
Total Reports
71
Drugs Involved
6
Deaths
81
Hospitalizations
51.4 yrs
Average Patient Age
58.4% / 41.6%
Female / Male

Which Drugs Cause Intercepted product storage error Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
TOCILIZUMAB 381 0.4% 1 14 0
DUPILUMAB 325 0.1% 1 14 0
OMALIZUMAB 256 0.4% 0 1 0
ALTEPLASE 227 1.8% 0 0 0
INSULIN GLARGINE 129 0.1% 0 8 0
DORNASE ALFA 115 2.1% 0 0 0
BEVACIZUMAB 113 0.1% 0 0 0
RITUXIMAB 105 0.1% 0 0 0
OCRELIZUMAB 88 0.2% 0 1 0
PERTUZUMAB 84 0.4% 0 0 0
TRASTUZUMAB 75 0.2% 0 0 0
ATEZOLIZUMAB 60 0.2% 0 0 0
LEUPROLIDE 59 0.1% 0 0 0
FARICIMAB\FARICIMAB-SVOA 54 1.6% 0 0 0
SOMATROPIN 52 0.1% 0 2 0
CASIRIVIMAB\IMDEVIMAB 44 1.0% 0 0 0
HYALURONIDASE-ZZXF\PERTUZUMAB\TRASTUZUMAB 43 1.1% 0 0 0
RANIBIZUMAB 41 0.3% 0 0 0
EVOLOCUMAB 40 0.0% 0 4 0
VALGANCICLOVIR 37 0.5% 0 0 0

View all 71 drugs →

Top 3 Drugs Associated With Intercepted product storage error

381 reports
325 reports
256 reports

Related Side Effects

Drug ineffective (1,049,718) Off label use (762,782) Death (660,423) Fatigue (599,248) Nausea (562,301) Diarrhoea (491,550) Pain (471,975) Headache (460,069) Dyspnoea (409,496) Dizziness (352,922)