Does ERENUMAB-AOOE Cause International normalised ratio increased? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of International normalised ratio increased have been filed in association with ERENUMAB-AOOE. This represents 0.0% of all adverse event reports for ERENUMAB-AOOE.
5
Reports of International normalised ratio increased with ERENUMAB-AOOE
0.0%
of all ERENUMAB-AOOE reports
1
Deaths
2
Hospitalizations
How Dangerous Is International normalised ratio increased From ERENUMAB-AOOE?
Of the 5 reports, 1 (20.0%) resulted in death, 2 (40.0%) required hospitalization.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERENUMAB-AOOE. However, 5 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 International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which ERENUMAB-AOOE Alternatives Have Lower International normalised ratio increased 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