Does ERENUMAB-AOOE Cause Product storage error? 2,958 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,958 reports of Product storage error have been filed in association with ERENUMAB-AOOE. This represents 5.9% of all adverse event reports for ERENUMAB-AOOE.
2,958
Reports of Product storage error with ERENUMAB-AOOE
5.9%
of all ERENUMAB-AOOE reports
0
Deaths
23
Hospitalizations
How Dangerous Is Product storage error From ERENUMAB-AOOE?
Of the 2,958 reports, 23 (0.8%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 2,958 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)
Headache (2,787)
Injection site pain (2,715)
Off label use (2,227)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
USTEKINUMAB (1,338)
Which ERENUMAB-AOOE Alternatives Have Lower Product storage 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