Does ERENUMAB-AOOE Cause Disorientation? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Disorientation have been filed in association with ERENUMAB-AOOE. This represents 0.1% of all adverse event reports for ERENUMAB-AOOE.
36
Reports of Disorientation with ERENUMAB-AOOE
0.1%
of all ERENUMAB-AOOE reports
1
Deaths
16
Hospitalizations
How Dangerous Is Disorientation From ERENUMAB-AOOE?
Of the 36 reports, 1 (2.8%) resulted in death, 16 (44.4%) required hospitalization, and 2 (5.6%) were considered life-threatening.
Is Disorientation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 36 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 Disorientation?
OLANZAPINE (612)
QUETIAPINE (551)
CARBIDOPA\LEVODOPA (543)
PREGABALIN (521)
TRAMADOL (506)
SERTRALINE (483)
GABAPENTIN (428)
DULOXETINE (427)
LORAZEPAM (404)
SODIUM OXYBATE (393)
Which ERENUMAB-AOOE Alternatives Have Lower Disorientation 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