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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does EZETIMIBE Cause Haemoglobin decreased? 47 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Haemoglobin decreased have been filed in association with EZETIMIBE (Ezetimibe). This represents 0.4% of all adverse event reports for EZETIMIBE.

47
Reports of Haemoglobin decreased with EZETIMIBE
0.4%
of all EZETIMIBE reports
2
Deaths
23
Hospitalizations

How Dangerous Is Haemoglobin decreased From EZETIMIBE?

Of the 47 reports, 2 (4.3%) resulted in death, 23 (48.9%) required hospitalization, and 2 (4.3%) were considered life-threatening.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EZETIMIBE. However, 47 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 Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which EZETIMIBE Alternatives Have Lower Haemoglobin decreased Risk?

EZETIMIBE vs EZETIMIBE\ROSUVASTATIN EZETIMIBE vs EZETIMIBE\SIMVASTATIN EZETIMIBE vs EZOGABINE EZETIMIBE vs FACTOR XIII CONCENTRATE EZETIMIBE vs FAM-TRASTUZUMAB DERUXTECAN-NXKI

Related Pages

EZETIMIBE Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased EZETIMIBE Demographics