Does ERENUMAB-AOOE Cause Maternal exposure timing unspecified? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Maternal exposure timing unspecified have been filed in association with ERENUMAB-AOOE. This represents 0.1% of all adverse event reports for ERENUMAB-AOOE.
27
Reports of Maternal exposure timing unspecified with ERENUMAB-AOOE
0.1%
of all ERENUMAB-AOOE reports
26
Deaths
26
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From ERENUMAB-AOOE?
Of the 27 reports, 26 (96.3%) resulted in death, 26 (96.3%) required hospitalization, and 26 (96.3%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 27 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which ERENUMAB-AOOE Alternatives Have Lower Maternal exposure timing unspecified 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