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Medical Progress Report
No. 3  November 2006


The Human Cost of Federal Price Negotiations:
The Medicare Prescription Drug Benefit and Pharmaceutical Innovation

Benjamin Zycher
Senior Fellow, Manhattan Institute for Policy Research

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Appendix A: Further Observations on the Incentives of Federal Policymakers

Economists may disagree about many things, but absent among them is the role of incentives in the determination of choice behavior. Whether shaping the choices made by individuals in isolation or in groups acting collectively, the nature and power of the relevant incentives can be used to predict decisions and outcomes, at least directionally, in both the private and public sectors. With respect to the latter, the incentives confronting policymakers and agency administrators making decisions under a given set of rules, constraints, and opportunities will yield particular kinds of choices, while a different set of incentives or institutional arrangements will engender different outcomes.

These initial observations are trivial, but seemingly few people apply them to emerging public policy issues as those specific legislative and regulatory choices come to the fore. Such policy choices can significantly affect individuals, firms, industries, and the economy, so the importance of analyzing the incentives of policymakers as a tool with which to predict the implications of policy choices ought not to be ignored.

As discussed in Section II, the incentives of federal policymakers are inherently biased in favor of current budget savings at the expense of greater, rather than lesser, inclusiveness of federal drug formularies, relative to the case for private profit-seeking intermediaries balancing the demand of customers pursuing both price savings and formulary inclusiveness. This has the short-term effect of reducing the number of drugs included in the formularies; because of this relatively weaker incentive to include given drugs in formularies, prices can be predicted to be lower than in the alternative case.[a1]

The narrow long-term effect of these lower prices must be a reduction in the flow of research and development investments in pharmaceuticals, in turn yielding fewer medicines and higher medical costs (and greater suffering) over time.[a2] The pharmaceutical producers — which are entities with infinite lives — have incentives to preserve the flow of efficient research and development investments; those incentives are consistent with the partial incentives of private purchasers to make formularies more, rather than less, inclusive.[a3] In this sense, the profit motive leads the pharmaceutical producers implicitly to represent the interests of future patients, while the large profit-seeking retail buyers implicitly represent the interests of current patients.[a4] It is reasonable to predict that the bargaining process between pharmaceutical producers and the firms serving retail customers will yield current prices and investment flows that are roughly efficient.

A different long-term dynamic emerges in a world in which the incentives of federal policymakers transform pharmaceutical pricing into an implicit tax/transfer mechanism. As noted above, the stream of relatively large price discounts negotiated by the federal government is analogous to a flow of tax revenues distributed to drug consumers (or to the beneficiaries of other budget programs) in the form of ongoing price savings. For any given drug, there is a negotiated price (or price discount), P*, that maximizes the present value of the flow of price savings.[a5] Prices higher than P* (i.e., smaller discounts) would yield a smaller flow of price savings but a higher stream of research and development investment.[a6] Prices lower than P* would yield a smaller flow of price savings because of more stringent formulary exclusions imposed by the drug producers[a7] and clearly engender a lower stream of research and development investment. A price lower than P* may make both consumers and producers worse off and therefore cannot be the optimal price or price discount. The observation to be made here is that the incentives of federal policymakers lead them systematically to demand prices lower than P*.

Consider the decision-making environment confronting a policymaker driven to use tax and expenditure policies to maximize political support.[a8] Additional tax revenues (in this context, price savings on drugs) always serve the interests of policymakers as long as the price discounts in the short run do not create economic effects that over time offset the price-discount stream more than fully during the policymakers’ terms in office.[a9] In other words, as long as industry adjustments to adverse policies take longer than the terms of current policymakers, their net political incentive is to transfer as much wealth as possible from the producers to their constituencies.[a10] In the absence of constraints on the choices made by current policymakers--the extreme case--the federal government would pay only the marginal production cost for drugs, thus maximizing the current flow of price savings while ignoring the obvious adverse effects for future investment in research and development and production capacity.

Such constraints do exist, of course. The longer-term adverse effects of current policy choices should be resisted in some measure by the political parties, which to a degree have longer time horizons than given policymakers, who in turn might have incentives to take such effects into account to the extent that they receive funding and other kinds of support from the parties. Some patient groups and others will oppose actions yielding important expected declines in the future delivery of medical and pharmaceutical services. The pharmaceutical sector is an interest group of nontrivial influence. In addition, to the extent that policymakers can hide their behavior from voters, they might choose to demand smaller drug price discounts than otherwise would be the case.[a11]

Even in the presence of such constraints, policymakers can be predicted to negotiate a price lower (price discounts that are greater) than the price P* that maximizes the present value of the flow of price savings as long as their political time horizons are shorter than the period over which the industry would adjust fully to the implicit tax inherent in the actual negotiated price. Moreover, the short time horizon of the policymakers leads them to favor preservation of the negotiated price below P*, because a lower price yields a larger stream of price savings (implicit tax revenues) immediately, while the longer-term benefits of the larger research and development investments yielded by P* will accrue politically to their successors. In short, negotiation of prices lower than P* yields a political equilibrium (or trap) in which no current policymaker has an incentive to choose policies avoiding or reducing the adverse research and development effects of the negotiated prices.[a12]

Appendix B: Data Tables

Table B1. Historical and Projected Data on Pharmaceutical Research and Development: NSF Data and Investment Growth of 7.967 Percent (millions of year 2005 dollars)

Table B2. Historical and Projected Data on Pharmaceutical Research and Development: NSF Data and Investment Growth of 4 Percent (millions of year 2005 dollars)

Table B3. Historical and Projected Data on Pharmaceutical Research and Development: PhRMA Data and Investment Growth of 4 Percent (millions of year 2005 dollars)

 

Appendix C: Charts

Chart 1. Base Case R & D Investment

Chart 2. Base Case R & D Capital Stocks

Chart 3. First Sensitivity Case R & D Investment

Chart 4. First Sensitivity Case R & D Capital Stocks

Chart 5. Second Sensitivity Case R & D Investment

Chart 6. Second Sensitivity Case R & D Capital Stocks

 

Appendix D: Brief Observations on the Congressional Research Service Report on Federal Price Negotiations for Drugs

The Congressional Research Service (CRS) has prepared a brief analysis of the arguments for and against federal negotiation of drug prices for Medicare beneficiaries.[d1] Summary observations on that paper are as follows.

The paper argues that differential pricing (“price discriminate”) of drugs flows from the monopoly power of the producers attendant upon the issue of patents, as well as the presence of “numerous channels of distribution from manufacturer to consumer.” This argument is poor at best: Differential pricing is fully consistent with competitive conditions[d2] and even in the absence of patent restrictions on entry and the like can yield improved economic efficiency. This is particularly the case with such goods as drugs with low marginal production costs; differential pricing can enable producers to cover large fixed costs while still producing aggregate levels of output that equate marginal cost and marginal value.

The discussion of the VA pricing system is incorrect, in that it fails to distinguish between the mandated minimum 24 percent discount from the AMP (the FCP) and the FSS requirement that the pharmaceutical producers sell drugs to the VA at the “best price” offered to private-sector buyers. These are not “negotiated” prices, particularly given that FSS “best prices” must be offered as well to many health-care programs receiving federal funding; thus does the FSS “best price” requirement allow the federal government and many others to receive the benefits of private-sector negotiations without undertaking any negotiations themselves. The VA is entitled under the law to receive the lower of the FCP and FSS prices.

The discussion of third-party (middlemen) markups is poor: Wholesalers and the like reduce various types of transaction costs. Why else would profit-seeking firms utilize them? The elimination of such layers of market participants by a large government program does not by simple virtue of that fact improve “efficiency.” Instead, it shifts the various transaction costs onto someone else: the taxpayers, the drug producers, the consumers, and so on. While it may be the case that federal involvement would reduce various kinds of transaction costs, that ought not to be assumed; and the experience with other federal procurement programs is not encouraging.

The paper argues that the “plethora of choices” under Medicare Part D “is not universally viewed as a positive outcome.” Even in principle, consumers cannot be made better off with fewer options; cost reductions might be one effect of fewer options, which is why no market has an infinite number of competitors, but a federal takeover of such market functions as price negotiations is not obviously consistent with that goal.

The paper in its discussion of the arguments against federal price negotiations fails to consider the differing incentives of federal policymakers and large private buyers in terms of the tradeoffs between low prices and more inclusive formularies.

Finally, the paper argues that “there is very little evidence that quantifies the degree to which reductions in retail prices would lead to fewer new products being introduced.” That is simply incorrect: Various works by Santerre, Vernon, Lichtenberg, and others referenced above are examples.


 

 


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TABLE OF CONTENTS:

EXECUTIVE SUMMARY

ABOUT THE AUTHOR

INTRODUCTION

Crucial Differences between the Federal Government and the PBMs

Prices under Current Federal Drug Programs

Some Simple Economics of Investment

Quantitative Analysis of Research and Development Investment under a Federal Price Negotiation System

Table 1: Pharmaceutical Research and Development Investment and Capital

Table 2: Federal/Total Government Drug Spending Shares and Implied Compound Tax Rates

Table 3: Total Pharmaceutical Research and Development Investment and Capital with Implicit Federal Price Negotiation Tax

Table 4: Total Pharmaceutical Research and Development Investment and Capital with Implicit Federal Price Negotiation Tax: First Sensitivity Case

Table 5: Total Pharmaceutical Research and Development Investment and Capital with Implicit Federal Price Negotiation Tax: Second Sensitivity Case

Table 6: Projected Declines in Investment and Development of New Medicines, 2007–25

Table 7: FDA New Drug Approvals

Related Research Findings

Table 8: Comparison of Empirical Findings

CONCLUSION

REFERENCES

ENDNOTES

APPENDIX A: Further Observations on the Incentives of Federal PolicyMakers

APPENDIX B: Data Tables

Table B1. Historical and Projected Data on Pharmaceutical Research and Development: NSF Data and Investment Growth of 7.967 Percent (millions of year 2005 dollars)

Table B2. Historical and Projected Data on Pharmaceutical Research and Development: NSF Data and Investment Growth of 4 Percent (millions of year 2005 dollars)

Table B3. Historical and Projected Data on Pharmaceutical Research and Development: PhRMA Data and Investment Growth of 4 Percent (millions of year 2005 dollars)

APPENDIX C: Charts

Chart 1. Base Case R & D Investment

Chart 2. Base Case R & D Capital Stocks

Chart 3. First Sensitivity Case R & D Investment

Chart 4. First Sensitivity Case R & D Capital Stocks

Chart 5. Second Sensitivity Case R & D Investment

Chart 6. Second Sensitivity Case R & D Capital Stocks

APPENDIX D: Brief Observations on the Congressional Research Service Report on Federal Price Negotiations for Drugs

 


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