Does EZETIMIBE Cause Intentional product misuse? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Intentional product misuse have been filed in association with EZETIMIBE (Ezetimibe). This represents 0.4% of all adverse event reports for EZETIMIBE.
50
Reports of Intentional product misuse with EZETIMIBE
0.4%
of all EZETIMIBE reports
22
Deaths
32
Hospitalizations
How Dangerous Is Intentional product misuse From EZETIMIBE?
Of the 50 reports, 22 (44.0%) resulted in death, 32 (64.0%) required hospitalization, and 26 (52.0%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EZETIMIBE. However, 50 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which EZETIMIBE Alternatives Have Lower Intentional product misuse Risk?
EZETIMIBE vs EZETIMIBE\ROSUVASTATIN
EZETIMIBE vs EZETIMIBE\SIMVASTATIN
EZETIMIBE vs EZOGABINE
EZETIMIBE vs FACTOR XIII CONCENTRATE
EZETIMIBE vs FAM-TRASTUZUMAB DERUXTECAN-NXKI