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The Case of the Man Overboard

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A Michaela McPherson Mystery

By

Judith Lucci

Copyright © 2018 by Judith Lucci

All rights reserved. No part of this book may be reproduced in any form or by any electronic or mechanical means, including information storage and retrieval systems, without permission in writing from the author, except by a reviewer who may quote brief passages in a review.

The characters and events in this book are fictitious. Any similarity to real persons, living or dead, is coincidental and not intended by the author.

Acknowledgements

Many thanks for the encouragement of my fans, friends, and family as I completed The Case of the Man Overboard. Without your support and the support of those read my books, I wouldn’t write. I’d like to give a special note of thanks to Eric Blumensen for his help in the preparation of this book and to my incredible editors and street team for their thoughtful review of my work. Thanks to all of  you for your help!

DEDICATION

This book is dedicated to the authors of the following article that was published as a Special Communication of Journal of the American Medical Association.  The abstract is included here.

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THE HIGH COST OF PRESCRIPTION Drugs in the United States Origins and Prospects for Reform

Aaron S. Kesselheim, MD, JD, MPH1Jerry Avorn, MD1Ameet Sarpatwari, JD, PhD1

The increasing cost of prescription drugs in the United States has become a source of concern for patients, prescribers, payers, and policy makers.

Objectives  To review the origins and effects of high drug prices in the US market and to consider policy options that could contain the cost of prescription drugs.

Evidence  We reviewed the peer-reviewed medical and health policy literature from January 2005 to July 2016 for articles addressing the sources of drug prices in the United States, the justifications and consequences of high prices, and possible solutions.

Findings  Per capita prescription drug spending in the United States exceeds that in all other countries, largely driven by brand-name drug prices that have been increasing in recent years at rates far beyond the consumer price index. In 2013, per capita spending on prescription drugs was $858 compared with an average of $400 for nineteen other industrialized nations. In the United States, prescription medications now comprise an estimated seventeen percent of overall personal health care services. The most important factor that allows manufacturers to set high drug prices is market exclusivity, protected by monopoly rights awarded upon Food and Drug Administration approval and by patents. The availability of generic drugs after this exclusivity period is the main means of reducing prices in the United States, but access to them may be delayed by numerous business and legal strategies. The primary counterweight against excessive pricing during market exclusivity is the negotiating power of the payer, which is currently constrained by several factors, including the requirement that most government drug payment plans cover nearly all products. Another key contributor to drug spending is physician prescribing choices when comparable alternatives are available at different costs. Although prices are often justified by the high cost of drug development, there is no evidence of an association between research and development costs and prices; rather, prescription drugs are priced in the United States primarily on the basis of what the market will bear.

Conclusions and Relevance  High drug prices are the result of the approach the United States has taken to granting government-protected monopolies to drug manufacturers, combined with coverage requirements imposed on government-funded drug benefits. The most realistic short-term strategies to address high prices include enforcing more stringent requirements for the award and extension of exclusivity rights; enhancing competition by ensuring timely generic drug availability; providing greater opportunities for meaningful price negotiation by governmental payers; generating more evidence about comparative cost-effectiveness of therapeutic alternatives; and more effectively educating patients, prescribers, payers, and policy makers about these choices.

Source: https://jamanetwork.com/journals/jama/article-abstract/2545691