The New Pharmaceutical Litigation
What It Is and Where It Is Going
About This Event

During the past two or three years pharmaceutical-related litigation has increased dramatically. It also has shifted its focus to Medicaid and Medicare drug reimbursement rates, the introduction of generic drugs when branded drug patents expire, and marketing practices directed at health care organizations.

Much of this litigation began as actions by individual state and local governments or the federal government, most notably an $800 million settlement of a federal action involving a single product. This success has spurred numerous consumer class action suits, coordinated efforts by state attorneys general, litigation by health care organizations, and vigorous litigation support from AARP.

What does the new litigation environment--and its costs--mean for taxpayers and consumers? Is the pharmaceutical industry facing an onslaught similar to the one launched against the tobacco industry in the 1990s? Discussing these issues are AEI resident scholar John E. Calfee and Michael S. Greve, the John G. Searle Scholar and director of the Federalism Project at AEI.

Agenda
9:45 a.m. Registration
10:00 Panelists: John E. Calfee, AEI
Michael S. Greve, AEI
11:15 Adjournment
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AEI Participants

 

John E.
Calfee
  • Economist John E. Calfee (1941-2011) studied the pharmaceutical industry and the Food and Drug Administration (FDA), along with the economics of tobacco, tort liability, and patents. He previously worked at the Federal Trade Commission's Bureau of Economics. He had also taught marketing and consumer behavior at the business schools of the University of Maryland at College Park and Boston University. While Mr. Calfee's writings are mostly on pharmaceutical markets and FDA regulation, his academic articles and opinion pieces covered a variety of topics, from patent law and tort liability to advertising and consumer information. His books include Prices, Markets, and the Pharmaceutical Revolution (AEI Press, 2000) and Biotechnology and the Patent System (AEI Press, 2007). Mr. Calfee wrote regularly for AEI's Health Policy Outlook series. He testified before Congress and federal agencies on various topics, including alcohol advertising; biodefense vaccine research; international drug prices; and FDA oversight of drug safety.

 

Michael S.
Greve
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