Does ERENUMAB-AOOE Cause Product quality issue? 503 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 503 reports of Product quality issue have been filed in association with ERENUMAB-AOOE. This represents 1.0% of all adverse event reports for ERENUMAB-AOOE.
503
Reports of Product quality issue with ERENUMAB-AOOE
1.0%
of all ERENUMAB-AOOE reports
472
Deaths
400
Hospitalizations
How Dangerous Is Product quality issue From ERENUMAB-AOOE?
Of the 503 reports, 472 (93.8%) resulted in death, 400 (79.5%) required hospitalization, and 413 (82.1%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 503 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ERENUMAB-AOOE Alternatives Have Lower Product quality 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