Doctor's Dependency on Big Pharma Larissa Tiller
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Big Pharma Takes It
A Public Eye Report – March 2021 Big Pharma takes it all How pharmaceutical corporations profiteer from their privileges – even in a global health crisis like COVID-19 1 COVID-19, SHOWCASE OF A PERVERTED BUSINESS MODEL 3 2 BIG PHARMA’S 10 STRATEGIES FOR CASHING IN 7 2.1 – Determine R & D priorities by potential profits alone 9 2.2 – Abuse patents to lock up knowledge, inflate prices and limit supply 10 2.3 – Direct the system towards the needs of high-income countries 13 2.4 – Avoid public accountability 16 2.5 – Design clinical trials for self-interest 18 2.6 – Socialise risks, privatise profits 20 2.7 – Embrace public investment, reject public returns 22 2.8 – Impose unjustifiable, unchallengeable prices 24 2.9 – Financialise innovation 29 2.10 – Lobby pervasively 31 3 SWITZERLAND IS ‘PHARMALAND’ 33 4 CONCLUSION: WHAT COVID-19 SHOWS US 37 5 TIME TO ACT: OUR DEMANDS 39 Endnotes 42 IMPRINT Big Pharma takes it all: How pharmaceutical corporations profiteer from their privileges – even in a global health crisis like COVID-19. A Public Eye Report, March 2021, 52 pages. | Authors Patrick Durisch, Gabriela Hertig | Contributors Christa Luginbühl, Oliver Classen | Edition Mary Louise Rapaud | Publishers Romeo Regenass, Ariane Bahri | Layout Karin Hutter, karinhutter.com | Icons opak.cc | Cover picture © Tang Ming Tung/Getty Images PUBLIC EYE Dienerstrasse 12, Postfach, CH-8021 Zurich | +41 (0)44 2 777 999 | [email protected] Avenue Charles-Dickens 4, CH-1006 Lausanne | +41 (0)21 620 03 03 | [email protected] Donations IBAN CH64 0900 0000 1001 0813 5, Public Eye | publiceye.ch 1 ��-19, showcase of a perverted business model Monty Rakusen/Keystone © 4 BIG PHARMA TAKES IT ALL “No one is safe until everybody is safe”, “leave no one behind” are mantras that have been oft repeated by state leaders and the World Health Organization (WHO) since the coronavirus pandemic turned our world upside down in spring, 2020. -
Combating the Funding Effect in Science: What's
KRIMSKY_POSTGALLEY_FINAL.DOC 5/23/10 12:33 PM COMBATING THE FUNDING EFFECT IN SCIENCE: WHAT’S BEYOND TRANSPARENCY? Sheldon Krimsky* INTRODUCTION Professional ethics in government and in fields such as law, engineering, and accounting have evolved to protect the public from employee abuses and misconduct. Among those protections are rules that define, manage, or proscribe conflicts of interest. The term “conflict of interest” has been defined by Thompson as “a set of conditions in which professional judgment concerning a primary interest (such as a patient’s welfare or the validity of research) tends to be unduly influenced by a secondary interest (such as financial gain).”1 Before 1980, little if any attention was given to conflicts of interest in science and medicine. Beginning around that time, a major shift was taking place in sector boundaries affecting the media, finance, banking, medicine, and academia. The missions of distinctive sectors of our society were blended or superimposed onto one another. This has led to a fusion of sector goals and the creation of hybridized institutions. As examples, the entertainment and news sectors have, at times, become indistinguishable; banks and investment houses have begun adopting each other’s roles. And, more to the point of this Article, universities have been investing in for-profit enterprises started by their faculty. The new partnership between academia and business was reinforced by the passage of the Bayh-Dole Act of 1980.2 Under the new law, universities were accorded intellectual property rights from any discoveries that were made under government grants. Business and academia * Sheldon Krimsky is a Professor of Urban & Environmental Policy & Planning in the School of Arts & Sciences and an Adjunct Professor in Public Health and Family Medicine in the School of Medicine at Tufts University. -
BOOKTIVISM: the Power of Words
BOOKTIVISM: The Power of Words Book•ti•vi•sm(noun). 1. The mobilization of groups of concerned citizens produced by reading books offering powerful analyses of social or political issues. 2. A call to action based on the sharing of knowledge through books. 3. Books + activism = “booktivism.” 4. A term first used at the SellingSickness, 2013: People Before Profits conference in Washington, DC, see www.sellingsickness.com. Read. Discuss. Be thoughtful. Be committed. Here are some more suggestions to get you started: 1) Set up a reading group on disease-mongering among interested friends and colleagues. If you do The books included in BOOKTIVISM celebrate recent contributions to the broad topic of disease- not already have a group of interested readers, post a notice in your workplace, library, community mongering, especially as they examine the growing prevalence and consequences of overtreatment, center, apartment building, etc. Once you have a group, decide where to meet. Book clubs can overscreening, overmarketing, and overdiagnosis (see Lynn Payer’s 1992 classic, Disease-Mongers: How meet anywhere – at homes, in dorms, in pubs, in coffeehouses, at libraries, even online! Decide on Doctors, Drug Companies, and Insurers Are Making You Feel Sick, for an introduction to timing and format. Will you meet monthly/bimonthly? You’ll need time to prepare for the sessions, disease-mongering). but not so much time that you lose touch. Circulate the reading guide. It is usually best if one person leads each discussion, to have some questions at the ready and get things rolling. Although the challenge to disease-mongering is not unprecedented (the women’s health movement of the 1970s was another key historical moment), these books represent an impressive groundswell OR, maybe you’d like to of amazing, powerful, brilliant, and often deeply unsettling investigations by physicians, health scientists, 2) Set up a lecture/discussion group. -
The Pharma Barons: Corporate Law's Dangerous New Race to the Bottom in the Pharmaceutical Industry
Michigan Business & Entrepreneurial Law Review Volume 8 Issue 1 2018 The Pharma Barons: Corporate Law's Dangerous New Race to the Bottom in the Pharmaceutical Industry Eugene McCarthy University of Illinois Follow this and additional works at: https://repository.law.umich.edu/mbelr Part of the Business Organizations Law Commons, Consumer Protection Law Commons, Food and Drug Law Commons, and the Rule of Law Commons Recommended Citation Eugene McCarthy, The Pharma Barons: Corporate Law's Dangerous New Race to the Bottom in the Pharmaceutical Industry, 8 MICH. BUS. & ENTREPRENEURIAL L. REV. 29 (2018). Available at: https://repository.law.umich.edu/mbelr/vol8/iss1/3 This Article is brought to you for free and open access by the Journals at University of Michigan Law School Scholarship Repository. It has been accepted for inclusion in Michigan Business & Entrepreneurial Law Review by an authorized editor of University of Michigan Law School Scholarship Repository. For more information, please contact [email protected]. THE PHARMA BARONS: CORPORATE LAW’S DANGEROUS NEW RACE TO THE BOTTOM IN THE PHARMACEUTICAL INDUSTRY Eugene McCarthy* INTRODUCTION......................................................................................... 29 I. THE RACE TO THE BOTTOM AND THE RISE OF THE ROBBER BARONS ..................................................................................... 32 A. Revising the Corporate Codes............................................ 32 B. The Emergence of Nineteenth-Century Lobbying ............. 37 C. The Robber -
JEMH Vol4 No1 Sept
ARTICLE SPECIAL THEME ISSUE ARTICLE Privatization of Knowledge and the Creation of Biomedical Conflicts of Interest Leemon B. McHenry Department of Philosophy, California State University, Northridge Jon N. Jureidini Discipline of Psychiatry, University of Adelaide, South Australia rather than to what is meaningful, so that fi ndings that are Abstract likely to be clinical and meaningful are rejected because they fail to reach statistical signifi cance whereas others that appear Scientifi c and ethical misconduct have increased at an clinically trivial are accepted (Ziliak and McCloskey, 2007). Th e alarming rate as a result of the privatization of knowledge. disenchantment with the psychoanalytic paradigm of psychiatry What began as an eff ort to stimulate entrepreneurship led to a massive investment in psychopharmacology and other and increase discovery in biomedical research by physical interventions. A concession now to the limited benefi t strengthening the ties between industry and academics that psychopharmacology off ers would come at great cost to the has led to an erosion of confi dence in the reporting of profession. A vested interest in protecting the new paradigm of research results. Inherent tensions between profi t-directed neurological models of psychiatric disorders reaches beyond the inquiry and knowledge-directed inquiry are instantiated quest for a secure scientifi c foundation. in psychopharmacology, especially in the co-option of academic activity to corporate objectives. The eff ects of To the vulnerability created by personal bias and questionable these tensions are visible in research agendas, publication methodology we must add the dangers of pervasive fi nancial practices, postgraduate education, academic-industry confl icts of interest, of which we investigate the root cause in this partnerships and product promotion. -
Pharmaceutical Price Regulation
Pharmaceutical Price Regulation Pharmaceutical Price Regulation Public Perceptions, Economic Realities, and Empirical Evidence John A. Vernon and Joseph H. Golec The AEI Press Publisher for the American Enterprise Institute WASHINGTON, D.C. Distributed to the Trade by National Book Network, 15200 NBN Way, Blue Ridge Summit, PA 17214. To order call toll free 1-800-462-6420 or 1-717-794-3800. For all other inquiries please contact the AEI Press, 1150 Seventeenth Street, N.W., Washington, D.C. 20036 or call 1-800-862-5801. Library of Congress Cataloging-in-Publication Data Vernon, John A. Pharmaceutical price regulation : public perceptions, economic realities, and empirical evidence / John A. Vernon and Joseph H. Golec. p. ; cm. Includes bibliographical references. ISBN-13: 978-0-8447-4277-9 ISBN-10: 0-8447-4277-5 1. Pharmaceutical industry—Government policy—United States. 2. Drugs—Prices—Law and legislation—United States. I. Golec, Joseph. II. Title. HD9666.6.V47 2008 338.4'361510973--dc22 2008049681 12 11 10 09 1 2 3 4 5 © 2008 by the American Enterprise Institute for Public Policy Research, Washington, D.C. All rights reserved. No part of this publication may be used or reproduced in any manner whatsoever without permission in writing from the American Enterprise Institute except in the case of brief quotations embodied in news articles, critical articles, or reviews. The views expressed in the publications of the American Enterprise Institute are those of the authors and do not necessarily reflect the views of the staff, advisory panels, officers, or trustees of AEI. Printed in the United States of America Contents LIST OF ILLUSTRATIONS vii INTRODUCTION 1 1. -
Making Medicines Affordable: a National Imperative
THE NATIONAL ACADEMIES PRESS This PDF is available at http://nap.edu/24946 SHARE Making Medicines Affordable: A National Imperative DETAILS 234 pages | 6 x 9 | PAPERBACK ISBN 978-0-309-46805-3 | DOI 10.17226/24946 CONTRIBUTORS GET THIS BOOK Norman R. Augustine, Guru Madhavan, and Sharyl J. Nass, Editors; Committee on Ensuring Patient Access to Affordable Drug Therapies; Board on Health Care Services; Health and Medicine Division; National Academies of Sciences, FIND RELATED TITLES Engineering, and Medicine Visit the National Academies Press at NAP.edu and login or register to get: – Access to free PDF downloads of thousands of scientific reports – 10% off the price of print titles – Email or social media notifications of new titles related to your interests – Special offers and discounts Distribution, posting, or copying of this PDF is strictly prohibited without written permission of the National Academies Press. (Request Permission) Unless otherwise indicated, all materials in this PDF are copyrighted by the National Academy of Sciences. Copyright © National Academy of Sciences. All rights reserved. Making Medicines Affordable: A National Imperative Norman R. Augustine, Guru Madhavan, and Sharyl J. Nass, Editors Committee on Ensuring Patient Access to Affordable Drug Therapies Board on Health Care Services Health and Medicine Division A Consensus Study Report of Copyright National Academy of Sciences. All rights reserved. Making Medicines Affordable: A National Imperative THE NATIONAL ACADEMIES PRESS 500 Fifth Street, NW Washington, DC 20001 This activity was supported by grants from the American College of Physicians, Breast Cancer Research Foundation, Burroughs Wellcome Fund, California Health Care Foundation, The Commonwealth Fund, Laura and John Arnold Foundation, Milbank Memorial Fund, and the Presidents’ Committee of the National Academies of Sciences, Engineering, and Medicine. -
Privatizing Biomedical Citizenship: Risk, Duty, and Potential in the Circle of Pharmaceutical Life
Privatizing Biomedical Citizenship: Risk, Duty, and Potential in the Circle of Pharmaceutical Life Jonathan Kahn* Introduction .............................................................................. 791 I. Getting Bodies ................................................................ 796 II. GINA: Law as an Adjunct to Recruitment .................... 815 III. Citizenship: Duty as an Adjunct to Recruitment .......... 825 IV. Citizens, Good Citizens, and Bio-Citizens ..................... 832 V. Constructing Citizenship in a Post-Genomic Age ......... 837 VI. Privatizing Citizenship................................................... 843 VII. Call of Duty: The Million Veteran Program .................. 849 VIII. The Problem of Consent: Revising the Common Rule .. 853 IX. NCATS: From Populations to Corporations .................. 867 A. Delineating the Precompetitive Space .................... 873 B. The Alchemy of Precompetitive Space .................... 878 X. Conclusion: Cui Bono? Risk, Duty, and Potential in the Circle of Pharmaceutical Life .................................. 888 A. Asymmetries of Risk ................................................ 890 B. Duties Without Rights ............................................. 894 INTRODUCTION Genomic research is at an impasse. In the decade since the completion of the first draft of the human genome, progress has been made, but few of the grandest promises of genomics have materialized. Biomedical researchers largely agree that one critical thing is essential to propel genomics -
Autonomy, Disinterest, and Entrepreneurial Science
AUTONOMY, DISINTEREST, AND ENTREPRENEURIAL SCIENCE Sheldon Krimsky here is general agreement among a wide spectrum comprises the elite universities that award doctoral de- Tof informed observers that, beginning in the late grees. To be classified a category I institution in the 1970s and early 1980s, American research universities AAUP database, a university must grant a minimum of underwent changes that brought them greater commer- 30 doctoral-level degrees annually, awarded by three or cialization. The changes involved: more unrelated disciplines. Category II institutions ei- ther do not grant doctoral degrees or they grant too few z Greater emphasis on intellectual property to qualify as Category I. The lowest rung of the classi- z Stronger ties between academia and the private fication consists of two-year colleges whose faculty has sector, including research and development part- no ranks. Between the first and second ranked schools nerships (Categories I and II) the average full professor salaries differ by $25,000 (Academe, March/April 2005). z Greater emphasis on research over teaching and Out of 3,773 institutions AAUP surveyed in 2004- service 05, about 8 percent (299) were classified as Category I. However, Category I institutions have 48 percent of the z Less concern about protecting traditional academic values such as free and open exchange of ideas, total faculty in the entire system of universities: 176,000 and sharing of biological materials such as cell out of 368,000. Moreover, the top 200 research institu- lines tions accounted for 95 percent of all the Research and Development (R&D) expenditures in 1997 (National z More emphasis in new income streams whatever Science Foundation, Science & Engineering Indicators, their source. -
When Science Falls from Grace
BOOK REVIEW When science falls from grace is rather a relatively small matter which is generated in and is normally effectively managed by that smaller segment of the larger society which The Great Betrayal: Fraud in Science is the scientific community” (p. 112). Judson is justifiably skeptical of Handler’s assessment. Horace Freeland Judson Yet, there is insufficient data to verify or debunk the myth about fraud in Harcourt, Inc., 2004 science or to confirm whether it has risen in recent years. One of the prob- lems of measuring the frequency of scientific fraud is in knowing how to 480 pp., hardcover, $28.00 define it. Judson explores how our scientific agencies arrived at a consensus ISBN 0151008779 view that “the misconduct be committed intentionally, or knowingly, or Reviewed by Sheldon Krimsky in reckless disregard of accepted practices” (p. 188). Just being sloppy and making mistakes is not currently sufficient for a finding of misconduct. Myth #3: The peer review system is the best thing science has going for it Anyone who has read Horace Freeland Judson’s magnum opus on the his- in its pursuit of certifiable knowledge. There is undoubtedly a two-class sys- tory of molecular biology, The Eighth Day of Creation, which gives homage tem in the world of journals: those that are refereed and those that are not. http://www.nature.com/naturemedicine to the creative power and intellect of the new breed of molecular geneticists, Peer review has been likened to Winston Churchill’s view of democracy. It might be surprised to learn that his latest book is a no-nonsense exposé of is a flawed system that is better than any of its alternatives. -
Bias, Conflict, and Manipulation in Scientific Evidence
Boston College Law Review Volume 61 Issue 6 Article 5 6-26-2020 Industry-Influenced vidence:E Bias, Conflict, and Manipulation in Scientific videnceE Dean A. Elwell Boston College Law School, [email protected] Follow this and additional works at: https://lawdigitalcommons.bc.edu/bclr Part of the Courts Commons, Evidence Commons, and the Supreme Court of the United States Commons Recommended Citation Dean A. Elwell, Industry-Influenced vidence:E Bias, Conflict, and Manipulation in Scientificvidence E , 61 B.C.L. Rev. 2155 (2020), https://lawdigitalcommons.bc.edu/bclr/vol61/iss6/5 This Notes is brought to you for free and open access by the Law Journals at Digital Commons @ Boston College Law School. It has been accepted for inclusion in Boston College Law Review by an authorized editor of Digital Commons @ Boston College Law School. For more information, please contact [email protected]. INDUSTRY-INFLUENCED EVIDENCE: BIAS, CONFLICT, AND MANIPULATION IN SCIENTIFIC EVIDENCE Abstract: In 2008, in Exxon Shipping Co. v. Baker, the U.S. Supreme Court re- fused to consider scientific studies that a litigant had funded. Despite this rejection, many courts have failed even to recognize the dangers of relying on such potential- ly biased research. As a result, standards for the admission of scientific evidence have evolved without accounting for the risks posed by industry-influenced evi- dence. This Note argues for meaningful admissibility reviews via mandatory dis- closure of industry influence. In this context, the evidentiary fraud doctrine should guide applications of Frye v. United States and Daubert v. Merrell Dow Pharma- ceuticals, Inc. -
WHEN CONFLICT-OF-INTEREST IS a FACTOR in SCIENTIFIC MISCONDUCT Sheldon Krimsky*
Med Law (2007) 26:447-463 Medicine and Law ©YOZMOT 2007 Defining Scientific Misconduct WHEN CONFLICT-OF-INTEREST IS A FACTOR IN SCIENTIFIC MISCONDUCT Sheldon Krimsky* ABSTRACT: Under the guidelines adopted by the United States (U.S.) Office of Research Integrity (ORI), scientific misconduct is defined by one or more of three activities: fabrication of data, falsification of results, and plagiarism or the improper appropriation of other people’s ideas or written work. This paper discusses whether three other breaches in scientific ethics, namely ghost writing, fabricating credentials, and failure to disclose conflicts of interest, rise to the level of scientific misconduct. After discussing the funding effect in science, the paper argues that, like ghost writing and fabricated credentials, conflicts of interest can bias the outcome of research. Thus, lack of transparency to reviewers, journals and readers for conflicts of interest should be considered a form of scientific misconduct. Keywords: Conflict of interest; ghostwriting; office of research integrity (USA); vigor study. INTRODUCTION According to the Office of Research Integrity (ORI) of the United States (U.S.) Department of Health and Human Services, scientific misconduct is defined by three terms: fabrication, falsification and plagiarism. Scientists found guilty of fabricating, or making up data or results and reporting them, who falsify or consciously manipulate research results, or who appropriate other people’s ideas, processes or results without giving them credit could, under ORI’s definition, be found guilty of scientific misconduct. These breaches in scientific ethics, however, are not the only ones. Among others are fabricating one’s credentials, taking credit in a publication without personal contribution, and failure to disclose a conflict of interest.