Ethical and Scientific Issues in Studying the Safety of Approved Drugs Book [PDF] Download

Download the fantastic book titled Ethical and Scientific Issues in Studying the Safety of Approved Drugs written by Institute of Medicine, available in its entirety in both PDF and EPUB formats for online reading. This page includes a concise summary, a preview of the book cover, and detailed information about "Ethical and Scientific Issues in Studying the Safety of Approved Drugs", which was released on 30 July 2012. We suggest perusing the summary before initiating your download. This book is a top selection for enthusiasts of the Medical genre.

Summary of Ethical and Scientific Issues in Studying the Safety of Approved Drugs by Institute of Medicine PDF

An estimated 48 percent of the population takes at least one prescription drug in a given month. Drugs provide great benefits to society by saving or improving lives. Many drugs are also associated with side effects or adverse events, some serious and some discovered only after the drug is on the market. The discovery of new adverse events in the postmarketing setting is part of the normal natural history of approved drugs, and timely identification and warning about drug risks are central to the mission of the Food and Drug Administration (FDA). Not all risks associated with a drug are known at the time of approval, because safety data are collected from studies that involve a relatively small number of human subjects during a relatively short period. Written in response to a request by the FDA, Ethical and Scientific Issues in Studying the Safety of Approved Drugs discusses ethical and informed consent issues in conducting studies in the postmarketing setting. It evaluates the strengths and weaknesses of various approaches to generate evidence about safety questions, and makes recommendations for appropriate followup studies and randomized clinical trials. The book provides guidance to the FDA on how it should factor in different kinds of evidence in its regulatory decisions. Ethical and Scientific Issues in Studying the Safety of Approved Drugs will be of interest to the pharmaceutical industry, patient advocates, researchers, and consumer groups.


Detail About Ethical and Scientific Issues in Studying the Safety of Approved Drugs PDF

  • Author : Institute of Medicine
  • Publisher : National Academies Press
  • Genre : Medical
  • Total Pages : 292 pages
  • ISBN : 0309218160
  • PDF File Size : 50,7 Mb
  • Language : English
  • Rating : 4/5 from 21 reviews

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Ethical Issues in Studying the Safety of Approved Drugs

Ethical Issues in Studying the Safety of Approved Drugs
  • Publisher : Unknown Publisher
  • File Size : 53,6 Mb
  • Release Date : 16 June 2024
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The FDA requested that the IOM examine the ethical and informed consent issues that should be considered when conducting clinical trials to evaluate drug safety. This report outlines when and

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  • Release Date : 13 October 2012
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The Best Pharmaceuticals for Children Act (BPCA) and the Pediatric Research Equity Act (PREA) were designed to encourage more pediatric studies of drugs used for children. The FDA asked the

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  • Publisher : National Academies Press
  • File Size : 25,6 Mb
  • Release Date : 07 April 2000
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The Institute of Medicine's (IOM's) Roundtable on Research and Development of Drugs, Biologics, and Medical Devices evolved from the Forum on Drug Development, which was established in 1986. Sponsor representatives and

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  • File Size : 21,7 Mb
  • Release Date : 27 February 2007
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In the wake of publicity and congressional attention to drug safety issues, the Food and Drug Administration (FDA) requested the Institute of Medicine assess the drug safety system. The committee

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  • File Size : 51,8 Mb
  • Release Date : 08 February 2009
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Environmental health decision making can be a complex undertaking, as there is the need to navigate and find balance among three core elements: science, policy, and the needs of the

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  • Publisher : National Academies Press
  • File Size : 47,7 Mb
  • Release Date : 06 February 2003
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When 18-year-old Jesse Gelsinger died in a gene transfer study at the University of Pennsylvania, the national spotlight focused on the procedures used to ensure research participants' safety and their

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  • File Size : 40,5 Mb
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The Transformational Medical Technologies (TMT) has been a unique component of the U.S. Department of Defense (DoD) medical biodefense efforts since 2006. Its mission is to advance countermeasure research and

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  • Publisher : Unknown Publisher
  • File Size : 29,9 Mb
  • Release Date : 05 June 2019
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Scientific research ethics vary by discipline and by country, and this analysis sought to understand those variations. The authors reviewed literature and conducted interviews to provide researchers, government officials, and