2013
DOI: 10.5639/gabij.2013.0204.051
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Understanding the components of pharmaceutical expenditure—overview of pharmaceutical policies influencing expenditure across European countries

Abstract: Aim:To explain the components of pharmaceutical expenditure and illustrate the strengths and limitations of this indicator. In particular, we explore policies applied in European countries that aff ect the price and volume of medicines.

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Cited by 15 publications
(11 citation statements)
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“…The medicine price is the retail price that a patient pays to purchase that medicine. The volume is expressed in sales units such as defined daily doses (DDD) or prescribed daily doses (PDD) . Prescribed daily dose (PDD) is the average dose recommended based on studies, pharmacy or medical reports.…”
Section: Methodsmentioning
confidence: 99%
“…The medicine price is the retail price that a patient pays to purchase that medicine. The volume is expressed in sales units such as defined daily doses (DDD) or prescribed daily doses (PDD) . Prescribed daily dose (PDD) is the average dose recommended based on studies, pharmacy or medical reports.…”
Section: Methodsmentioning
confidence: 99%
“…HPV vaccine prices in national vaccination programmes can be substantially lower than their respective list prices. To control the continuously rising pharmaceutical expenditure, governments across countries look for effective mechanisms to yield savings to the health care budgets [ 29 , 30 ]. For vaccination expenditure, a commonly used cost-containment mechanism is tendering: health authorities use their purchasing power and the competition in the market of the vaccines to perform procurement procedures.…”
Section: Introductionmentioning
confidence: 99%
“…This is driven by well-known factors including changing demographics and new premium priced drugs [ 2 , 3 ]. This has resulted in a number of measures and initiatives across countries to moderate growth rates, including initiatives for both new and established medicines [ 4 - 7 ]. Reforms and initiatives for established drugs principally aim to enhance the utilisation of low cost generics versus originators and single sourced (patented) products in a class or related class where all products are seen as essentially therapeutically similar.…”
Section: Introductionmentioning
confidence: 99%