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Maximum allowable cost: can the government control drug costs?
Journal of Health Politics, Policy and Law
|January 1, 1979
Summary
In 1973, the US government aimed to control drug costs in federal programs by requiring generic drugs unless a therapeutic difference exists. This policy faced industry challenges, potentially undermining its benefits.
Area of Science:
- Health Policy
- Pharmaceutical Economics
- Government Regulation
Background:
- Federal drug reimbursement policies were established in 1973 to control pharmaceutical costs.
- The policy mandated reimbursement at the lowest available drug cost, barring significant therapeutic differences between brands and generics.
Purpose of the Study:
- To analyze the political history and justification behind the 1973 federal drug cost-containment program.
- To explore controversies surrounding government-funded drug benefit programs.
- To anticipate pharmaceutical industry responses to price control measures.
Main Methods:
- Historical analysis of the 1973 drug reimbursement policy.
- Examination of the political and economic rationale for the program.
- Review of ongoing debates on public drug financing.
Main Results:
- The 1973 policy represented an early governmental effort to regulate pharmaceutical prices.
- The program's success was anticipated to provoke counter-strategies from the pharmaceutical industry.
- Potential industry tactics could diminish the intended cost-saving benefits of the program.
Conclusions:
- The 1973 drug cost-control initiative was a significant policy intervention.
- Anticipated pharmaceutical industry responses pose a threat to the program's efficacy.
- The long-term impact of such policies on drug pricing and access remains a critical issue.