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  • A single-pill combination of amlodipine besylate and atorvastatin calcium (update).

A single-pill combination of amlodipine besylate and atorvastatin calcium (update).

Drugs of today (Barcelona, Spain : 1998) (2007-03-24)
Roy Blank, F D Richard Hobbs, Jose Zamorano, Xavier Girerd
ABSTRACT

This review describes the clinical profile and rationale for the development of a single-pill formulation of the calcium channel blocker amlodipine besylate, a blood-pressure--lowering agent, and atorvastatin calcium, a statin with lipid-lowering antiatherosclerotic properties. Amlodipine and atorvastatin have been demonstrated in numerous clinical trials to be highly effective in lowering blood pressure and low-density lipoprotein cholesterol. Furthermore, both amlodipine and atorvastatin have been demonstrated to reduce cardiovascular events in a broad range of patients' in hypertensive patients with three concomitant cardiovascular risk factors but normal to mildly elevated cholesterol levels, amlodipine combined with atorvastatin demonstrated a reduction in cardiovascular events. The amlodipine/atorvastatin single pill has been shown to improve patients; achievement of national-guideline-recommended blood pressure and lipid target levels and exhibits a safety profile consistent with its parent compounds. The combination pill is now available in parts of Europe in formulations containing either 5 or 10 mg amlodipine and 10 mg atorvastatin. Amlodipine combined with atorvastatin has been demonstrated to reduce cardiovascular events in hypertensive patients at high cardiovascular risk, and the single-pill formulation has the potential to improve adherence and decrease prescription costs. These potential benefits are associated with important implications because hypertensive patients with additional risk factors represent a large proportion of those at risk for cardiovascular events.

MATERIALS
Product Number
Brand
Product Description

USP
Amlodipine besylate, United States Pharmacopeia (USP) Reference Standard
Amlodipine for peak identification, European Pharmacopoeia (EP) Reference Standard
Amlodipine besylate, European Pharmacopoeia (EP) Reference Standard
Supelco
Amlodipine besylate, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Amlodipine besylate, ≥98% (HPLC)