Monday, October 3, 2016

Zetia Plus Simvastatin (Vytorin) Improves Risk of Cardiovascular Events after an Acute Coronary Syndrome

Zetia plus Simvastatin is a medicine developed by Merck on October 25, 2002 and was even approved by the Food and Drug Administration (FDA). Around two years later, Vytorin was approved by the FDA, which is an accurate dose combination of simvastatin and ezetimibe.

Zetia works in the digestive tract by blocking the absorption of cholesterol from food consumed. If Zetia used in combination with a statin it reduces LDL-C levels by an extra 15 to 20 percent. However, there have been no strong facts or evidence claiming that adding Zetia to a treatment regimen results in reduced patient’s risk of experiencing stroke or heart attack.

Both Vytorin and Zetia indicate as effective therapies to diet for the reducing elevated total cholesterol, non-HDL cholesterol, apolipoprotein B, and LDL cholesterol in patients with primary hyperlipidemia. This medicine comes as 10 mg tablet and Vytorin is a fixed dose combination of ezetimibe (10 mg) with different strengths of simvastatin (10, 20, 40 and 80 mg). A patient can take both medications once daily without or with food.

Common Reactions


Zetia and Vytorin can result in strong reactions such as muscle pain, common cold, joint pain diarrhea, and upper respiratory tract infections. They have varying effects on different patients. Other side-effects include skeletal muscle effects causing myopathy in which the individual feels pain in muscles, or rhabdomyolysis. This is related to the breakdown of muscle that results in increasing the relative dose of statin administered. With 80 mg of simvastatin, a hike in cases of rhabdomyolysis has been observed. But patients, who have been using Vytorin in 10/80 mg over a period of twelve months without any incidents, can continue treatment.

Risk of Cardiovascular Events

There are diverse factors linked with stroke and coronary heart disease. Some of which include age, ethnicity and family history. Other common risks are high cholesterol, unhealthy diets, obesity, excess alcohol and physical inactivity. Hypertension is the most critical risk factor for CVD.
If your blood pressure is too high it can damage supply route dividers, and increase your risk of building up blood coagulation. Blood pressure is measured in millimeters of mercury (mmHg) and is recorded as two figures:
           ·          Systolic weight – the weight of the blood when your heart pulsates to pump blood out.
           ·          Diastolic weight – the weight of the blood when your heart rests in the middle of pulsates, which reflects how firmly your courses are opposing blood stream.


When to avoid Zetia and Vytorin?

Zetia and Vytorin shouldn’t be taken by patients who have a liver impairment. Pregnant women should also avoid the drugs. If you have an allergy to any of the components that are found in these medicines, avoid taking them.
Zetia plus Simvastatin (Vytorin) improves risk of cardiovascular events after an acute coronary syndrome.

Most of the patients with high-risk heart diseases are treated with statins and have decreased LDL-C levels but, still have increased cardiovascular risk. There are various studies to find out whether lowering LDL-C under 70 mg/dL by adding ezetimibe to statin, results in reduced incidence of cardiovascular events including fatal stroke, non-fatal myocardial infarction, and readmission into the hospital for unstable angina, cardiovascular death, and coronary revascularization within a period of 30 days of the initial treatment.

It has been found through various researches that the addition of ezetimibe to a statin can result in a greater decline in cardiovascular events than monotherapy with a statin. It's for the first time that a non-statin cholesterol-lowering medication has directly shown positive results in a study.

With Zetia plus Simvastatin (Vytorin) there has been a significant decrease in the amount of patients who have experienced cardiovascular problems while taking this medicine. Zetia is not implemented for acute coronary syndromes.