A greater understanding of value associated with new pharmaceutical pr
oducts should lead to better decision-making. Most commonly cost-effec
tiveness ratios (CERs) are used to indicate value; however, researcher
s have recently shown that CER estimates are rarely used by decision-m
akers in making formulary decisions. In this article, a cost-consequen
ce approach to estimating the value for money of a new treatment for a
specific disease is described. Using a cost-consequence approach, the
impact of the new treatment on lifetime resource use and costs (inclu
ding specific healthcare service use and costs, and productivity losse
s) and health outcomes (including disease symptoms, life expectancy an
d quality of life) for an individual or group of individuals is estima
ted and presented in a tabular format. The cost-consequence format is
more likely to be approachable, readily understandable and applied by
healthcare decision-makers than a simple CER. The decision-maker may u
se selected items from the cost-consequence analysis to compute compos
ite measures of drug value, such as cost per life-year gained or cost
per quality adjusted life-year (QALY) gained. In general, the cost-con
sequence approach, by making the impact of the new treatment as compre
hensive and transparent as possible, will enable decisionmakers to sel
ect the components most relevant to their perspective and will also gi
ve them confidence that the data are credible to use as the basis for
resource allocation decisions.