Does ERENUMAB-AOOE Cause Device issue? 1,242 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,242 reports of Device issue have been filed in association with ERENUMAB-AOOE. This represents 2.5% of all adverse event reports for ERENUMAB-AOOE.
1,242
Reports of Device issue with ERENUMAB-AOOE
2.5%
of all ERENUMAB-AOOE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Device issue From ERENUMAB-AOOE?
Of the 1,242 reports, 5 (0.4%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 1,242 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ERENUMAB-AOOE Alternatives Have Lower Device issue 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