Drug Notebook

FDA Alerts

Special Alerts:

[Posted 08/21/2008] FDA informed healthcare professionals that the Agency is investigating a report from the Simvastatin and Ezetimibe in Aortic Stenosis (SEAS) trial of a possible association between the use of ezetimibe with simvastatin (Vytorin) and a potentially increased incidence of cancer. Vytorin is a combination product of simvastatin and ezetimibe used to decrease the production of cholesterol by the liver and inhibit the absorption of cholesterol in the intestine to reduce LDL-cholesterol levels and reduce the risk of cardiovascular events. Recently, FDA obtained preliminary results from the SEAS trial. The clinical trial tested whether lowering LDL-cholesterol with Vytorin would reduce the risk of cardiovascular events in individuals with aortic stenosis. A lower overall cardiovascular risk was not found with Vytorin. However, there was an additional observation that a larger percentage of subjects treated with Vytorin were diagnosed with and died from all types of cancer combined when compared to placebo during the 5-year study.

FDA anticipates receiving a final SEAS study report in about 3 months and the Agency's review and evaluation of the clinical trial data and other relevant information should take approximately 6 months. FDA will communicate its conclusions and recommendations at that time. Healthcare professionals and caregivers should continue to monitor patients taking Vytorin and report side effects from the use of this drug to the Agency. For more information visit the FDA website at: http://www.fda.gov/medwatch/safety/2008/safety08.htm#ezetimibe2 and http://www.fda.gov/cder/drug/early_comm/ezetimibe_simvastatin_SEAS.htm.

[Posted 08/08/2008] FDA notified healthcare professionals of the risk of muscle injury, rhabdomyolysis, which can lead to kidney failure or death, when simvastatin (Zocor) is used with amiodarone (Cordarone, Pacerone ). This risk is dose-related and increases when a dose of simvastatin greater than 20 mg per day is given with amiodarone. Although a revision of the simvastatin labeling in 2002 described an increased risk of rhabdomyolysis when amiodarone is taken with simvastatin doses greater than 20 mg daily, FDA continues to receive reports of rhabdomyolysis in patients treated concurrently with amiodarone and simvastatin. Prescribers should be aware of the increased risk of rhabdomyolysis when simvastatin is prescribed with amiodarone, and they should avoid doses of simvastatin greater than 20 mg per day in patients taking amiodarone. For more information visit the FDA website at: http://www.fda.gov/medwatch/safety/2008/safety08.htm#Simvastatin, http://www.fda.gov/cder/drug/infopage/simvastatin_amiodarone/default.htm, http://www.fda.gov/cder/drug/InfoSheets/HCP/simvastatin_amiodaroneHCP.htm, http://dailymed.nlm.nih.gov/dailymed/search.cfm?startswith=simvastatin and http://dailymed.nlm.nih.gov/dailymed/search.cfm?startswith=amiodarone&x=10&y=11.

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simvastatin
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(SIM va stah tin)

Pharmacokinetics

Absorption

Bioavailability

Rapidly absorbed following oral administration; undergoes extensive first-pass metabolism in the liver. Absolute bioavailability is <5%. Peak plasma concentrations are attained at 4 hours.

Onset

A therapeutic response usually is apparent within 2 weeks; maximal response occurs within 4–6 weeks.

Simvastatin-ezetimibe fixed-combination preparation (Vytorin®) is bioequivalent to corresponding dosages of the individual components.

Distribution

Extent

Distributed mainly to the liver. Crosses the blood-brain barrier.

Plasma Protein Binding

About 95% bound to plasma proteins.

Elimination

Metabolism

Metabolized by CYP3A4 to active metabolites.

Elimination Route

Excreted in urine (13%) and feces (60%).

Half-life

0.5–3 hours.

Special Populations

Patients with moderate to severe renal insufficiency may have decreased clearance of simvastatin and its metabolites.

Stability

Storage

Oral

Tablets

Simvastatin: 5–30°C.

Fixed-combination of simvastatin and ezetimibe (Vytorin®): Well-closed containers at 20–25°C.

Actions

Pending revision, the material in this section should be considered in light of more recently available information in the MEDWATCH notification at the beginning of this monograph.

  • Prodrug requiring hydrolysis in vivo for activity.
  • Inhibits HMG-CoA reductase, causing subsequent reduction in hepatic cholesterol synthesis. Reduces serum concentrations of total cholesterol, LDL-cholesterol, apo B, and triglycerides.
  • Statins may slow progression and/or induce regression of atherosclerosis in coronary and/or carotid arteries, modulate BP in hypercholesterolemic patients with hypertension, and possess anti-inflammatory activity.

Advice to Patients

  • Importance of informing patients about risks, especially rhabdomyolysis, associated with statins alone or combined with other drugs. Importance of patients promptly reporting muscle pain, tenderness, or weakness; brown urine; flu-like symptoms; and malaise.
  • Importance of adhering to nondrug therapies and measures (i.e., therapeutic lifestyle changes, including dietary management, weight control, physical activity, and management of potentially contributory disease [e.g., diabetes mellitus]).
  • Importance of women informing their clinician if they are or plan to become pregnant or plan to breast-feed. Necessity for clinicians to advise women and adolescent girls to avoid pregnancy (i.e., using effective and appropriate contraceptive methods) during therapy and to advise pregnant women of risk to fetus.
  • Importance of informing clinician of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses.
  • Importance of informing patients of other important precautionary information. (See Cautions.)

Preparations

Simvastatin
RoutesDosage FormsStrengthsBrand NamesManufacturer
OralTablets, film-coated5 mgZocor®Merck
10 mgZocor®Merck
20 mgZocor®Merck
40 mgZocor®Merck
80 mgZocor®Merck
Simvastatin and Ezetimibe
RoutesDosage FormsStrengthsBrand NamesManufacturer
OralTablets10 mg with Ezetimibe 10 mgVytorin®Merck/Schering-Plough
20 mg with Ezetimibe 10 mgVytorin®Merck/Schering-Plough
40 mg with Ezetimibe 10 mgVytorin®Merck/Schering-Plough
80 mg with Ezetimibe 10 mgVytorin®Merck/Schering-Plough

Comparative Pricing

Pricing information provided by drugstore.com.

Simvastatin 10MG Tablets TEVA PHARMACEUTICALS USA30/$19.99 or 90/$49.97
Simvastatin 20MG Tablets TEVA PHARMACEUTICALS USA30/$27.99 or 90/$73.97
Simvastatin 40MG Tablets TEVA PHARMACEUTICALS USA30/$27.99 or 90/$75.97
Simvastatin 5MG Tablets TEVA PHARMACEUTICALS USA30/$17.99 or 90/$42.98
Simvastatin 80MG Tablets TEVA PHARMACEUTICALS USA30/$32.99 or 90/$89.97
Vytorin 10-10MG Tablets MERCK/SCHERING-PLOUGH PHARM30/$103.99 or 90/$295.96
Vytorin 10-20MG Tablets MERCK/SCHERING-PLOUGH PHARM30/$100.99 or 90/$289.96
Vytorin 10-40MG Tablets MERCK/SCHERING-PLOUGH PHARM30/$100.99 or 90/$296.96
Vytorin 10-80MG Tablets MERCK/SCHERING-PLOUGH PHARM30/$100.99 or 90/$289.96
Zocor 10MG Tablets MERCK HUMAN HEALTH90/$240.97 or 180/$481.97
Zocor 20MG Tablets MERCK HUMAN HEALTH30/$139.99 or 90/$404.97
Zocor 40MG Tablets MERCK HUMAN HEALTH90/$405.99 or 180/$809.96
Zocor 5MG Tablets MERCK HUMAN HEALTH30/$66.99 or 90/$179.96
Zocor 80MG Tablets MERCK HUMAN HEALTH30/$146.99 or 90/$405

AHFS Drug Information. © Copyright, 1959-2008, Selected Revisions September 2008. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.

† Use is not currently included in the labeling approved by the US Food and Drug Administration.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

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