Does EZETIMIBE Cause International normalised ratio increased? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of International normalised ratio increased have been filed in association with EZETIMIBE (Ezetimibe). This represents 0.4% of all adverse event reports for EZETIMIBE.
57
Reports of International normalised ratio increased with EZETIMIBE
0.4%
of all EZETIMIBE reports
4
Deaths
13
Hospitalizations
How Dangerous Is International normalised ratio increased From EZETIMIBE?
Of the 57 reports, 4 (7.0%) resulted in death, 13 (22.8%) required hospitalization, and 3 (5.3%) were considered life-threatening.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EZETIMIBE. However, 57 reports have been filed with the FAERS database.
What Other Side Effects Does EZETIMIBE Cause?
Myalgia (2,066)
Fatigue (876)
Drug ineffective (812)
Arthralgia (766)
Dyspnoea (766)
Nausea (742)
Dizziness (717)
Diarrhoea (688)
Headache (626)
Malaise (591)
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 EZETIMIBE Alternatives Have Lower International normalised ratio increased Risk?
EZETIMIBE vs EZETIMIBE\ROSUVASTATIN
EZETIMIBE vs EZETIMIBE\SIMVASTATIN
EZETIMIBE vs EZOGABINE
EZETIMIBE vs FACTOR XIII CONCENTRATE
EZETIMIBE vs FAM-TRASTUZUMAB DERUXTECAN-NXKI