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Defining Drugs - How Government Became the Arbiter of Pharmaceutical Fact (Paperback, 2 New Edition)
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Defining Drugs - How Government Became the Arbiter of Pharmaceutical Fact (Paperback, 2 New Edition)
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Drug-related morbidity and mortality is rampant in contemporary
industrial society, despite or perhaps because, government has
assumed a critical role in the process by which drugs are developed
and approved. Parrish asserts that, as a people, Americans need to
understand how it is that government became the arbiter of
pharmaceutical fact. The consequences of our failure to understand,
he argues, may threaten individual choice and forestall the
development of responsible therapeutics. Moreover, if current
standards and control continues unabated, the next therapeutic
reformation might well make possible the sanctioned commercial
exploitation of patients. In Defining Drugs, Parrish argues that
the federal government became arbiter of pharmaceutical fact
because the professions of pharmacy and medicine, as well as the
pharmaceutical industry, could enforce these definitions and
standards only through police powers reserved to government.
Parrish begins his provocative study by examining the development
of the social system for regulating drug therapy in the United
States. He reviews the standards that were negotiated, and the
tensions of the period between Progressivism and the New Deal that
gave cultural context and historical meaning to drug use in
American society. Parrish describes issues related to the
development of narcotics policy through education and legislation
facilitated by James Beal and Edward Kremers, and documents the
federal government's evolving role as arbiter of market tensions
between pharmaceutical producers, government officials, and private
citizens in professional groups, illustrating the influence of
government in writing enforceable standards for pharmaceutical
therapies. He shows how the expansion of political rights for
practitioners and producers has shifted responsibility for
therapeutic consequences from individual practitioners and patients
to government. This timely and controversial volume is written for
the scholar and the compassionate practitioner alike, and a general
public concerned with pharmacy regulation in a free society.
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