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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 Product quality issue? 27 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product quality issue have been filed in association with EZETIMIBE (Ezetimibe). This represents 0.2% of all adverse event reports for EZETIMIBE.

27
Reports of Product quality issue with EZETIMIBE
0.2%
of all EZETIMIBE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Product quality issue From EZETIMIBE?

Of the 27 reports, 2 (7.4%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EZETIMIBE. However, 27 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 quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which EZETIMIBE Alternatives Have Lower Product quality issue 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 Product quality issue Reports All Drugs Causing Product quality issue EZETIMIBE Demographics