DROGEN DEFINIEREN: WIE DIE REGIERUNG ZUM SCHIEDSRICHTER PHARMAZEUTISCHER FAKTEN WURDE-

Ursprünglicher Text
DEFINING DRUGS: HOW GOVERNMENT BECAME THE ARBITER OF PHARMACEUTICAL FACT
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Hinweise des Verkäufers
“Good Condition”
Book Title
defining drugs
Narrative Type
Nonfiction
Educational Level
Adult & Further Education
Personalized
No
Level
Intermediate
Genre
History
Topic
Drugs
Country/Region of Manufacture
United States
California Prop 65 Warning
NA
ISBN
9780765801890
Kategorie

Über dieses Produkt

Product Identifiers

Publisher
Routledge
ISBN-10
0765801892
ISBN-13
9780765801890
eBay Product ID (ePID)
2316162

Product Key Features

Number of Pages
214 Pages
Publication Name
Defining Drugs : How Government Became the Arbiter of Pharmaceutical Fact
Language
English
Subject
Sociology / General, General
Publication Year
2003
Type
Textbook
Subject Area
Social Science
Author
Richard Henry Parrish II
Format
Hardcover

Dimensions

Item Weight
13.6 Oz
Item Length
9 in
Item Width
6 in

Additional Product Features

Intended Audience
College Audience
LCCN
2002-075086
Reviews
"Defining Drugs documents the evolution of social thought and action about pharmaceuticals in the United States in the 20th century. Written from a free-market perspective, Richard Parrish demonstrates how industry, goverment, and profressional leaders used science to justify the expansion of goverment power over standards and people. The Politicized definition of pharmaceutical fact cemented the foundation of pharmacotherapy in the modern pharmacratic state. Parrish's thesis will affect the current debates on federal power concerning the proper role of pharmacists, physicians, prescription laws, and Medicare prescription benefits; dietary supplements and herbal remedies; and nanotechnologies and pharmacgenomics. Scholary in documentation and persuasive in tone, Defining Drugs is an indispensable contribution to our understanding of the debate about drugs and drug policy." --Dr. Thomas Szasz, State University of New York "Parrish provides an invaluable analysis of the transformation of pharmaceutical regulation over the past millennium."--Peter Barton Hutt, Esq., Covington and Burling "Defining Drugs is an essential key for the medical profession and any who would understand the drug industry's regulation processes." --The Midwest Book Review
Illustrated
Yes
Synopsis
This work asserts that, as a people, Americans need to understand how it is that government became the arbiter of pharmaceutical fact. It states that the consequences of our failure to understand may threaten individual choice and forestall the development of responsible therapeutics., 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., 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.
LC Classification Number
RA401.A3P376 2003

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