Does EZETIMIBE Cause Wrong technique in product usage process? 30 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Wrong technique in product usage process have been filed in association with EZETIMIBE (Ezetimibe). This represents 0.2% of all adverse event reports for EZETIMIBE.
30
Reports of Wrong technique in product usage process with EZETIMIBE
0.2%
of all EZETIMIBE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Wrong technique in product usage process From EZETIMIBE?
Of the 30 reports, 4 (13.3%) required hospitalization, and 1 (3.3%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EZETIMIBE. However, 30 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which EZETIMIBE Alternatives Have Lower Wrong technique in product usage process Risk?
EZETIMIBE vs EZETIMIBE\ROSUVASTATIN
EZETIMIBE vs EZETIMIBE\SIMVASTATIN
EZETIMIBE vs EZOGABINE
EZETIMIBE vs FACTOR XIII CONCENTRATE
EZETIMIBE vs FAM-TRASTUZUMAB DERUXTECAN-NXKI