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Author :
Publisher :
ISBN 13 :
Total Pages : 84 pages
Book Rating : 4.:/5 (319 download)
Download or read book Postmarketing Surveillance of Prescription Drugs written by and published by . This book was released on 1982 with total page 84 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author :
Publisher :
ISBN 13 :
Total Pages : 70 pages
Book Rating : 4.:/5 (826 download)
Download or read book Postmarketing Surveillance of Prescription Drugs written by and published by . This book was released on 1982 with total page 70 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : William M. Wardell
Publisher : Springer Science & Business Media
ISBN 13 : 1468440551
Total Pages : 339 pages
Book Rating : 4.4/5 (684 download)
Download or read book Drug Development, Regulatory Assessment, and Postmarketing Surveillance written by William M. Wardell and published by Springer Science & Business Media. This book was released on 2012-12-06 with total page 339 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume is the outcome of the International School of Phar macology course sponsored as a NATO Advanced Study Institute and held in Erice (Sicily) at the Ettore Majorana Centre for Scientific Culture from October 3 through 12, 1980. The course, which consisted of lectures and teaching seminars, examined issues of international importance in all phases of drug development, assessment, and regu lation. In order to recreate both the atmosphere and substance of the meeting, a variety of materials are included here: the papers pre sented by the lecturers, a selection of key items from the supple mentary materials provided by the lecturers to the participants, notes on issues raised during the discussions, and accounts of certain special sessions arranged in response to interests expressed by those attending. The course covered two broad areas represented here by parts of the book. Part I, "Drug Assessment and Regulation," is based on the nine sessions of the course that ranged in focus from recent developments in the science of clinical pharmacology and drug development to discussions of whether and how the regulation of drug development can (or should) be harmonized internationally. In Part 11, "Postmarketing Surveillance," many aspects of this important subject are presented. Arguments outlining the potential benefits of national and international postmarketing surveillance systems are qualified by consideration of the problems inherent in devising and using these systems.
Author : UNITED STATES. CONGRESS. OFFICE OF TECHNOLOGY ASSESSMENT.
Publisher :
ISBN 13 :
Total Pages : 50 pages
Book Rating : 4.:/5 (131 download)
Download or read book POSTMARKETING SURVEILLANCE OF PRESCRIPTION DRUGS. written by UNITED STATES. CONGRESS. OFFICE OF TECHNOLOGY ASSESSMENT. and published by . This book was released on 1982 with total page 50 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Joint Commission on Prescription Drug Use
Publisher :
ISBN 13 :
Total Pages : 494 pages
Book Rating : 4.3/5 (91 download)
Download or read book Report of Joint Commission on Prescription Drug Use written by Joint Commission on Prescription Drug Use and published by . This book was released on 1980 with total page 494 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Institute of Medicine
Publisher : National Academies Press
ISBN 13 : 0309042860
Total Pages : 241 pages
Book Rating : 4.3/5 (9 download)
Download or read book Modern Methods of Clinical Investigation written by Institute of Medicine and published by National Academies Press. This book was released on 1990-02-01 with total page 241 pages. Available in PDF, EPUB and Kindle. Book excerpt: The very rapid pace of advances in biomedical research promises us a wide range of new drugs, medical devices, and clinical procedures. The extent to which these discoveries will benefit the public, however, depends in large part on the methods we choose for developing and testing them. Modern Methods of Clinical Investigation focuses on strategies for clinical evaluation and their role in uncovering the actual benefits and risks of medical innovation. Essays explore differences in our current systems for evaluating drugs, medical devices, and clinical procedures; health insurance databases as a tool for assessing treatment outcomes; the role of the medical profession, the Food and Drug Administration, and industry in stimulating the use of evaluative methods; and more. This book will be of special interest to policymakers, regulators, executives in the medical industry, clinical researchers, and physicians.
Author : Brian L. Strom
Publisher : Springer Science & Business Media
ISBN 13 : 1489925872
Total Pages : 171 pages
Book Rating : 4.4/5 (899 download)
Download or read book Drug Epidemiology and Post-Marketing Surveillance written by Brian L. Strom and published by Springer Science & Business Media. This book was released on 2013-06-29 with total page 171 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume is a summary of material presented in the course given in the International School of Phannacology on "Drug Epidemiology and Post-Marketing Surveillance" between September 27 and October 8, 1990, at the "Ettore Majorana Center for Scientific Culture" in Erice, Sicily. The course, which was a NATO Advanced Study Institute, included lectures and workshops presented by experts in the new field of phannacoepidemiology. The material covered includes various approaches to spontaneous reporting of adverse drug reactions, including aggregate approaches, such as those used in France, and detailed analyses of individual reports, such as that done in The Netherlands and in Sweden. Also, included are studies using traditional epidemiology methods. In addition, modern pharmacoepidemiology makes considerable use of automated databases. As such, information is presented on their use as well. Phannacoepidemiology started in hospitals and some of the newest work in the field is returning to the hospital as a site for studies. Material on these topics was presented as well. Finally, selected new methodologic developments were outlined in specific examples presented that were of regulatory and commercial importance. This new field of phannacoepidemiology is exploding in interest internationally. Evidence of this is the increasing development of pharmacoepidemiology programs in industry, medical schools, pharmacy schools, and schools of public health. Also, there is a new International Society ofPhannacoepidemiology. Practitioners in this field tend to specialize in either analyses of spontaneous reporting or the use of formal epidemiologic techniques.
Author : Brenda Waning
Publisher :
ISBN 13 : 9780071355070
Total Pages : 209 pages
Book Rating : 4.3/5 (55 download)
Download or read book Pharmacoepidemiology written by Brenda Waning and published by . This book was released on 2001 with total page 209 pages. Available in PDF, EPUB and Kindle. Book excerpt: The not-to-be-missed, benchmark volume on the growing area of stud in the PharmD pharmacy curriculum. Provides a foundation for assessing the nature and extent of drug-taking behaviors. Text is adapted from the author's self-paced learning modules, developed for the Massachusetts College of Pharmacy.
Author : Joint Commission on Prescription Drug Use
Publisher :
ISBN 13 :
Total Pages : 118 pages
Book Rating : 4.:/5 (319 download)
Download or read book Report of Joint Commission of Prescription Drug Use written by Joint Commission on Prescription Drug Use and published by . This book was released on 1980 with total page 118 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Sumner N. Clarren
Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (1 download)
Download or read book The Experiment in Post-marketing Surveillance of Prescription Drugs written by Sumner N. Clarren and published by . This book was released on 1982 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Agency for Healthcare Research and Quality/AHRQ
Publisher : Government Printing Office
ISBN 13 : 1587634333
Total Pages : 385 pages
Book Rating : 4.5/5 (876 download)
Download or read book Registries for Evaluating Patient Outcomes written by Agency for Healthcare Research and Quality/AHRQ and published by Government Printing Office. This book was released on 2014-04-01 with total page 385 pages. Available in PDF, EPUB and Kindle. Book excerpt: This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Author : National Academies of Sciences, Engineering, and Medicine
Publisher : National Academies Press
ISBN 13 : 0309459575
Total Pages : 483 pages
Book Rating : 4.3/5 (94 download)
Download or read book Pain Management and the Opioid Epidemic written by National Academies of Sciences, Engineering, and Medicine and published by National Academies Press. This book was released on 2017-09-28 with total page 483 pages. Available in PDF, EPUB and Kindle. Book excerpt: Drug overdose, driven largely by overdose related to the use of opioids, is now the leading cause of unintentional injury death in the United States. The ongoing opioid crisis lies at the intersection of two public health challenges: reducing the burden of suffering from pain and containing the rising toll of the harms that can arise from the use of opioid medications. Chronic pain and opioid use disorder both represent complex human conditions affecting millions of Americans and causing untold disability and loss of function. In the context of the growing opioid problem, the U.S. Food and Drug Administration (FDA) launched an Opioids Action Plan in early 2016. As part of this plan, the FDA asked the National Academies of Sciences, Engineering, and Medicine to convene a committee to update the state of the science on pain research, care, and education and to identify actions the FDA and others can take to respond to the opioid epidemic, with a particular focus on informing FDA's development of a formal method for incorporating individual and societal considerations into its risk-benefit framework for opioid approval and monitoring.
Author : Joint Commission on Prescription Drug Use
Publisher :
ISBN 13 :
Total Pages : 494 pages
Book Rating : 4.3/5 (243 download)
Download or read book The Final Report: Appendix 2, Minutes of the meetings of the Joint Commission on Prescription Drug Use written by Joint Commission on Prescription Drug Use and published by . This book was released on 1980 with total page 494 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : US Cong Off Tech Assess ...
Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (88 download)
Download or read book Postmarketing surveillance prescription drugs written by US Cong Off Tech Assess ... and published by . This book was released on with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Ronald Marinus Cornelis Herings
Publisher :
ISBN 13 : 9789039301968
Total Pages : 205 pages
Book Rating : 4.3/5 (19 download)
Download or read book Pharmo written by Ronald Marinus Cornelis Herings and published by . This book was released on 199? with total page 205 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Joint Commission on Prescription Drug Use
Publisher :
ISBN 13 :
Total Pages : 188 pages
Book Rating : 4.F/5 ( download)
Download or read book The Final report of the Joint Commission on Prescription Drug Use, Inc written by Joint Commission on Prescription Drug Use and published by . This book was released on 1980 with total page 188 pages. Available in PDF, EPUB and Kindle. Book excerpt:
![Download Assessing the Effectiveness of the Prescription Drug Post-market Surveillance System in Canada [microform]: the Need for a More Active Regulatory Role PDF Online Free](https://books.google.com/books/content/images/frontcover/bvG-ngEACAAJ?fife=w200-h370)
Author : Kontic, A. Sasha
Publisher : Library and Archives Canada = Bibliothèque et Archives Canada
ISBN 13 : 9780494073438
Total Pages : 146 pages
Book Rating : 4.0/5 (734 download)
Download or read book Assessing the Effectiveness of the Prescription Drug Post-market Surveillance System in Canada [microform]: the Need for a More Active Regulatory Role written by Kontic, A. Sasha and published by Library and Archives Canada = Bibliothèque et Archives Canada. This book was released on 2005 with total page 146 pages. Available in PDF, EPUB and Kindle. Book excerpt: Prescription drugs are becoming an increasingly important component of health care in Canada. Therefore, it is important for regulators such as Health Canada to effectively protect the public from the risks of taking prescription medicines. This thesis will begin by summarizing the inherent safety limitations of the drug development process and the history behind the formation of an internationally acceptable post-market monitoring system. It will then analyze the current spontaneous reporting program operated by Health Canada, highlighting procedural and substantive problems that limit the overall effectiveness of the passive post-market surveillance system. The author concludes by exploring new measures that Health Canada can adopt to make the post-marketing surveillance system more active and structured. In particular, the author emphasizes the need to establish an Independent National Drug Agency to reduce conflict of interest in the decision-making process.
