Does ERENUMAB-AOOE Cause Condition aggravated? 822 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 822 reports of Condition aggravated have been filed in association with ERENUMAB-AOOE. This represents 1.6% of all adverse event reports for ERENUMAB-AOOE.
822
Reports of Condition aggravated with ERENUMAB-AOOE
1.6%
of all ERENUMAB-AOOE reports
638
Deaths
592
Hospitalizations
How Dangerous Is Condition aggravated From ERENUMAB-AOOE?
Of the 822 reports, 638 (77.6%) resulted in death, 592 (72.0%) required hospitalization, and 589 (71.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 822 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ERENUMAB-AOOE Alternatives Have Lower Condition aggravated 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