Does ERENUMAB-AOOE Cause Device use error? 711 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 711 reports of Device use error have been filed in association with ERENUMAB-AOOE. This represents 1.4% of all adverse event reports for ERENUMAB-AOOE.
711
Reports of Device use error with ERENUMAB-AOOE
1.4%
of all ERENUMAB-AOOE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device use error From ERENUMAB-AOOE?
Of the 711 reports, 3 (0.4%) required hospitalization.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 711 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 Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ETANERCEPT (665)
TREPROSTINIL (563)
Which ERENUMAB-AOOE Alternatives Have Lower Device use 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