Impacts of Patent Expiry and Regulatory Policies on Daily Cost of Pharmaceutical Treatments in OECD Countries (2004-2010)

Working Paper: CEPR ID: DP9140

Authors: Ernst R. Berndt; Pierre Dubois

Abstract: Cross-country variability in regulatory frameworks, industrial policy, physician/pharmacy autonomy, brand/generic distinctions, and in the practice of medicine contributes to ambiguous interpretations of pharmaceutical cost comparisons. Here we report cross-country comparisons that: (i) focus on 11 therapeutic classes experiencing patent expiration and loss of exclusivity 2004-2010 in eight industrialized countries; (ii) convert revenues and unit sales to cost per day of treatment and number patient days treated using the World Health Organizations? Defined Daily Dosage metrics; (iii) compare patterns in costs per day of treatment with price index measures based on average price per day of treatment for each molecule computed over all molecule versions; (iv) utilizing econometric methods, model and quantify various factors affecting variations in daily treatment price indexes such as national regulatory and reimbursement policy changes, physician/pharmacy autonomy, and other factors; and (v) simulate changes in expenditures by country and therapeutic class had counterfactual policies been implemented.

Keywords: cross-country comparisons; generic drugs; pharmaceutical costs

JEL Codes: D4; I11; I18; L11; L65; O34


Causal Claims Network Graph

Edges that are evidenced by causal inference methods are in orange, and the rest are in light blue.


Causal Claims

CauseEffect
patent expirations (O34)daily treatment costs (H51)
regulatory changes (G18)treatment costs (Q52)
policy changes (J18)price indexes (C43)
patent expirations (O34)daily treatment costs in pharmacy-driven markets (I11)
regulatory changes (G18)daily treatment costs in pharmacy-driven markets (I11)
regulatory changes (G18)daily treatment costs in physician-driven markets (I11)

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