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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 preparation error: Which Medications Cause It? (11,325 Reports Across 42 Drugs)

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Intercepted product preparation error has been reported as an adverse event with 42 different drugs in the FDA's FAERS database, with 11,325 total reports. 9 of these reports resulted in death.The drugs most commonly associated with Intercepted product preparation error are LEUPROLIDE, PEGFILGRASTIM, and DEVICE.

11,325
Total Reports
42
Drugs Involved
9
Deaths
14
Hospitalizations
69.7 yrs
Average Patient Age
15.7% / 84.3%
Female / Male

Which Drugs Cause Intercepted product preparation error Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
LEUPROLIDE 8,621 12.2% 5 6 0
PEGFILGRASTIM 1,514 1.9% 1 1 0
DEVICE 1,033 8.1% 1 1 0
CARFILZOMIB 367 1.7% 0 0 0
BLINATUMOMAB 110 1.2% 0 1 0
BEVACIZUMAB-AWWB 54 1.3% 0 0 0
ROMIPLOSTIM 48 0.6% 1 0 0
TRASTUZUMAB-ANNS 42 3.1% 0 0 0
AFLIBERCEPT 39 0.2% 0 0 0
TOCILIZUMAB 26 0.0% 0 0 0
AVACINCAPTAD PEGOL 20 9.9% 0 0 0
INFLIXIMAB 20 0.0% 0 0 0
ABATACEPT 19 0.0% 0 0 0
OCRELIZUMAB 17 0.0% 0 0 0
BELIMUMAB 16 0.1% 0 0 0
PANITUMUMAB 16 0.2% 0 0 0
RITUXIMAB-ARRX 16 4.6% 0 0 0
ALTEPLASE 15 0.1% 0 0 0
ERYTHROPOIETIN 15 0.2% 0 0 0
MEPOLIZUMAB 14 0.0% 0 0 0

View all 42 drugs →

Top 3 Drugs Associated With Intercepted product preparation error

8,621 reports
1,514 reports
1,033 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)