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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 Haemarthrosis? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Haemarthrosis have been filed in association with EZETIMIBE (Ezetimibe). This represents 0.1% of all adverse event reports for EZETIMIBE.

7
Reports of Haemarthrosis with EZETIMIBE
0.1%
of all EZETIMIBE reports
0
Deaths
7
Hospitalizations

How Dangerous Is Haemarthrosis From EZETIMIBE?

Of the 7 reports, 7 (100.0%) required hospitalization.

Is Haemarthrosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EZETIMIBE. However, 7 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 Haemarthrosis?

ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (3,360) EMICIZUMAB-KXWH (487) RIVAROXABAN (429) COAGULATION FACTOR IX RECOMBINANT HUMAN (318) DAMOCTOCOG ALFA PEGOL (299) --BLOOD-COAGULATION FACTOR VIII FUSION PROTEIN WITH IMMUNOGLOBULIN G1 , ,-BIS WITH IMMUNOGLOBULIN G1 (220) ASPIRIN (208) EFTRENONACOG ALFA (196) COAGULATION FACTOR IX RECOMBINANT HUMAN\ISOPROPYL ALCOHOL (190) APIXABAN (169)

Which EZETIMIBE Alternatives Have Lower Haemarthrosis 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 Haemarthrosis Reports All Drugs Causing Haemarthrosis EZETIMIBE Demographics