Does EZETIMIBE Cause Product substitution issue? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Product substitution issue have been filed in association with EZETIMIBE (Ezetimibe). This represents 0.5% of all adverse event reports for EZETIMIBE.
71
Reports of Product substitution issue with EZETIMIBE
0.5%
of all EZETIMIBE reports
1
Deaths
20
Hospitalizations
How Dangerous Is Product substitution issue From EZETIMIBE?
Of the 71 reports, 1 (1.4%) resulted in death, 20 (28.2%) required hospitalization, and 10 (14.1%) were considered life-threatening.
Is Product substitution issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EZETIMIBE. However, 71 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 Product substitution issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (2,832)
BUPROPION (1,578)
METHYLPHENIDATE (1,408)
CLONAZEPAM (1,288)
LAMOTRIGINE (979)
ALBUTEROL (864)
LEVOTHYROXINE (803)
DULOXETINE (766)
ESTRADIOL (692)
SERTRALINE (636)
Which EZETIMIBE Alternatives Have Lower Product substitution issue Risk?
EZETIMIBE vs EZETIMIBE\ROSUVASTATIN
EZETIMIBE vs EZETIMIBE\SIMVASTATIN
EZETIMIBE vs EZOGABINE
EZETIMIBE vs FACTOR XIII CONCENTRATE
EZETIMIBE vs FAM-TRASTUZUMAB DERUXTECAN-NXKI