Does ERENUMAB-AOOE Cause Device malfunction? 499 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 499 reports of Device malfunction have been filed in association with ERENUMAB-AOOE. This represents 1.0% of all adverse event reports for ERENUMAB-AOOE.
499
Reports of Device malfunction with ERENUMAB-AOOE
1.0%
of all ERENUMAB-AOOE reports
0
Deaths
9
Hospitalizations
How Dangerous Is Device malfunction From ERENUMAB-AOOE?
Of the 499 reports, 9 (1.8%) required hospitalization, and 2 (0.4%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 499 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 malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which ERENUMAB-AOOE Alternatives Have Lower Device malfunction 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