Does ERENUMAB-AOOE Cause Incorrect product administration duration? 77 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 77 reports of Incorrect product administration duration have been filed in association with ERENUMAB-AOOE. This represents 0.2% of all adverse event reports for ERENUMAB-AOOE.
77
Reports of Incorrect product administration duration with ERENUMAB-AOOE
0.2%
of all ERENUMAB-AOOE reports
58
Deaths
57
Hospitalizations
How Dangerous Is Incorrect product administration duration From ERENUMAB-AOOE?
Of the 77 reports, 58 (75.3%) resulted in death, 57 (74.0%) required hospitalization, and 57 (74.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 77 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ERENUMAB-AOOE Alternatives Have Lower Incorrect product administration duration 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