Omega-3-acid ethyl esters
Chemical structure of ethyl eicosapentaenoate, an important omega-3-acid ethyl ester | |
| Combination of | |
|---|---|
| Ethyl eicosapentaenoate | Antilipemic agent |
| Ethyl docosahexaenoate | Antilipemic agent |
| Clinical data | |
| Trade names | Lovaza, Omacor, others |
| Other names | Ethyl polyenoate (ChP) |
| AHFS/Drugs.com | Monograph |
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| Routes of administration | By mouth |
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Omega-3-acid ethyl esters are a mixture of ethyl eicosapentaenoate and ethyl docosahexaenoate, which are ethyl esters of the omega−3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) found in fish oil. Together with dietary changes, they are used to treat high blood triglycerides which may reduce the risk of pancreatitis. They are generally less preferred than statins, and use is not recommended by NHS Scotland as the evidence does not support a decreased risk of heart disease. Omega-3-acid ethyl esters are taken by mouth.
Common side effects include burping, nausea, and an upset abdomen. Serious side effects may include liver problems and anaphylaxis. While use in pregnancy has not been well studied, some omega−3 fatty acids appear beneficial. How it works is not entirely clear.
Experts found a dose-dependent increase in the risk for atrial fibrillation in patients with cardiovascular diseases or cardiovascular risk factors who were being treated with omega-3-acid ethyl esters compared with those treated with placebo. The observed risk was at its highest at a dose of 4 g/d.
Omega-3-acid ethyl ester medicines were approved for medical use in the European Union in 2000 and in the United States in 2004. Beyond the branded prescription formulation, it is also available as a generic medication and over the counter. In 2022, it was the 220th most commonly prescribed medication in the United States, with more than 1 million prescriptions.