Does ERENUMAB-AOOE Cause Intercepted product administration error? 1,015 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,015 reports of Intercepted product administration error have been filed in association with ERENUMAB-AOOE. This represents 2.0% of all adverse event reports for ERENUMAB-AOOE.
1,015
Reports of Intercepted product administration error with ERENUMAB-AOOE
2.0%
of all ERENUMAB-AOOE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Intercepted product administration error From ERENUMAB-AOOE?
Of the 1,015 reports, 5 (0.5%) required hospitalization.
Is Intercepted product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 1,015 reports have been filed with the FAERS database.
What Other Side Effects Does ERENUMAB-AOOE Cause?
Accidental exposure to product (9,923)
Device difficult to use (9,530)
Wrong technique in product usage process (9,359)
Drug dose omission by device (6,340)
Migraine (4,290)
Drug ineffective (3,813)
Constipation (3,104)
Product storage error (2,958)
Headache (2,787)
Injection site pain (2,715)
What Other Drugs Cause Intercepted product administration error?
EVOLOCUMAB (2,508)
DENOSUMAB (1,209)
ETANERCEPT (574)
DARBEPOETIN ALFA (385)
PEGFILGRASTIM (356)
LEUPROLIDE (307)
ERYTHROPOIETIN (301)
ROMOSOZUMAB-AQQG (115)
BENZYL ALCOHOL\ETANERCEPT (112)
CARFILZOMIB (102)
Which ERENUMAB-AOOE Alternatives Have Lower Intercepted product administration error Risk?
ERENUMAB-AOOE vs ERENUMAB\ERENUMAB-AOOE
ERENUMAB-AOOE vs ERGOCALCIFEROL
ERENUMAB-AOOE vs ERGOCALCIFEROL\PHYTONADIONE\RETINOL\TOCOPHEROL
ERENUMAB-AOOE vs ERIBULIN
ERENUMAB-AOOE vs ERLOTINIB