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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.

MOEXIPRIL: 23 Adverse Event Reports & Safety Profile

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23
Total FAERS Reports
5 (21.7%)
Deaths Reported
12
Hospitalizations
23
As Primary/Secondary Suspect
Apr 19, 1995
FDA Approved
Chartwell RX, LLC
Manufacturer
Discontinued
Status
Yes
Generic Available

Active Ingredient: MOEXIPRIL HYDROCHLORIDE · Drug Class: Angiotensin Converting Enzyme Inhibitor [EPC] · Route: ORAL · Manufacturer: Chartwell RX, LLC · FDA Application: 020312 · HUMAN PRESCRIPTION DRUG · FDA Label: Available

First Report: 20020106 · Latest Report: 20191029

What Are the Most Common MOEXIPRIL Side Effects?

#1 Most Reported
Drug hypersensitivity
5 reports (21.7%)