Advanced Pharmacology

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Author :
Publisher : Pharmamed Press
ISBN 13 : 9789389354164
Total Pages : 672 pages
Book Rating : 4.3/5 (541 download)

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Book Synopsis Advanced Pharmacology by : Bikash Medhi

Download or read book Advanced Pharmacology written by Bikash Medhi and published by Pharmamed Press. This book was released on 2019-12-02 with total page 672 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Advanced Pharmacology" aimed to deliver such topics of drugs which are very important to be know by any healthcare professional, but found rarely in any books or library. Complete idea of publishing it, is to provide readers a good platform to study the rare topics in pharmacology.This book is recommended for MBBS, MD (Pharmacology), DM (Clinical Pharmacology), Pharm D., M. Pharm and B. Pharm students or any other healthcare professionals. The book is a strong learning aid for post graduate teaching and also helps clinicians or other heathcare professionals understand the pharmacological basis of pharmacotherapeutics through thematic flow diagrams and logical explanations for specialized topics in pharmacology to ease the reading. Book is divided into three sections; Initial two sections of the book deal with basic aspects of clinical pharmacology, regulation and therapeutics; also address the most recent advances in the field. Third section is thoroughly updated to provide readers with an ideal reference that covers wide range of neglected but important topics. It also provides a rich collection of material on critical areas such as medication errors, rational use of drugs, self medication, drug compliance etc. Several other essential regulations framed in India for drugs have been incorporated in the chapters drug policy, drug pricing, orphan drugs etc. Further, critical issues in pharmacology like usage of drugs in pregnancy, renal and hepatic complications, drug-drug interactions etc. are also addressed in a point specific manner to simplify the language to readers. Emerging topics in medical fields like regenerative medicine, nanomedicine, electronic prescribing (e-Rx), drug surveillance systems like Pharmacovigilance, Haemovigilance, Materiovigilance etc. are well explained. Hope, "Advanced Pharmacology", will fulfill the demand and need of healthcare professionals by covering the important and rare topics on drugs.

Advanced Pharmacology for Prescribers

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Publisher : Springer Publishing Company
ISBN 13 : 0826195474
Total Pages : 659 pages
Book Rating : 4.8/5 (261 download)

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Book Synopsis Advanced Pharmacology for Prescribers by : Brent Q. Luu, PharmD, BCPS, BCACP

Download or read book Advanced Pharmacology for Prescribers written by Brent Q. Luu, PharmD, BCPS, BCACP and published by Springer Publishing Company. This book was released on 2021-01-13 with total page 659 pages. Available in PDF, EPUB and Kindle. Book excerpt: Delivers the critical information primary care providers need to be thoroughly informed prescribers This unique resource—an evidence-based pharmacology text and reference for advanced practice students and clinicians—guides users in analyzing the pharmacological foundations of drug therapy and fosters the development of sound clinical judgment in determining the appropriate medication for every patient across the lifespan. Targeting the specific needs of APRN and PA students and clinicians, the text is a “bridge” between standard, lengthy pharmacology texts and quick pocket references that lack information regarding key pharmacotherapy principles. Featuring an applied therapeutic approach to major disorders and their pharmacologic treatment, the book examines how medications act on the body and visa versa, while teaching the rationale for using specific therapeutic agents or drug classes. Each chapter includes case studies that apply the concepts discussed, relevant diagnostic studies, applicable guidelines, genomics, and important lifespan considerations. Of special interest is a chapter on pharmacogenetics explaining the basic principles underlying our current understanding of genetic variations in response to pharmacotherapy and adverse drug reactions. Easily digestible chapters include objectives and review questions. Ancillary resources include an instructor manual with learning objectives, chapter summaries, and case studies; chapter PowerPoint slides; test bank; and image bank. Key Features: Delivers an applied, evidence-based foundation on the basic science underlying prescribing Targets the specific needs of APRN and PA students and professionals and related healthcare providers Provides clinical decision-making tools and principles to support sound prescribing judgment Focuses on synthesizing drugs to manage commonly occurring disorders Includes strategies for addressing the needs of specific populations throughout the lifespan Includes abundant case studies illuminating key concepts Includes a robust instructor manual with learning objectives, chapter summaries, and case studies; PowerPoint slides; test bank; and image bank. Purchase includes access to the eBook for use on most mobile devices or computers.

Principles of Clinical Pharmacology

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Author :
Publisher : Elsevier
ISBN 13 : 0080466427
Total Pages : 567 pages
Book Rating : 4.0/5 (84 download)

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Book Synopsis Principles of Clinical Pharmacology by : Arthur J. Atkinson Jr.

Download or read book Principles of Clinical Pharmacology written by Arthur J. Atkinson Jr. and published by Elsevier. This book was released on 2011-04-28 with total page 567 pages. Available in PDF, EPUB and Kindle. Book excerpt: This revised second edition covers the pharmacologic principles underlying the individualization of patient therapy and contemporary drug development, focusing on the fundamentals that underlie the clinical use and contemporary development of pharmaceuticals. Authors drawn from academia, the pharmaceutical industry and government agencies cover the spectrum of material, including pharmacokinetic practice questions, covered by the basic science section of the certifying examination offered by the American Board of Clinical Pharmacology. This unique reference is recommended by the Board as a study text and includes modules on drug discovery and development to assist students as well as practicing pharmacologists. - Unique breadth of coverage ranging from drug discovery and development to individualization and quality assessment of drug therapy - Unusual cohesive of presentation that stems from author participation in an ongoing popular NIH course - Instructive linkage of pharmacokinetic theory and applications with provision of sample problems for self-study - Wide-ranging perspective of authors drawn from the ranks of Federal agencies, academia and the pharmaceutical industry - Expanded coverage of pharmacogenetics - Expanded coverage of drug transporters and their role in interactions - Inclusion of new material on enzyme induction mechanisms in chapters on drug metabolism and drug interactions - A new chapter on drug discovery that focuses on oncologic agents - Inclusion of therapeutic antibodies in chapter on biotechnology products

Small Animal Clinical Pharmacology

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Publisher : Elsevier Health Sciences
ISBN 13 : 0702028584
Total Pages : 600 pages
Book Rating : 4.7/5 (2 download)

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Book Synopsis Small Animal Clinical Pharmacology by : Jill E. Maddison

Download or read book Small Animal Clinical Pharmacology written by Jill E. Maddison and published by Elsevier Health Sciences. This book was released on 2008 with total page 600 pages. Available in PDF, EPUB and Kindle. Book excerpt: Small Animal Clinical Pharmacology is a practical, clinically-oriented pharmacology text designed to provide the veterinary student and practitioner with all the relevant information needed when designing drug treatment regimens for pets in small animal veterinary practice. Comprehensively updated and revised, the second edition of this core text covers essential new information on drugs used in the management of a range of presenting conditions including heart disease and cardiac arrhythmias. For the second edition new authors, superb new illustrations and a second colour have all been introduced. With its unique approach combining a thorough understanding of the pharmacological action of drugs with a basic understanding of the relevant physiology and pathophysiology of systems and tissues affected, Small Animal Clinical Pharmacology continues to be an indispensable book for all veterinary students and practitioners. Organised by drug class in a uniform and detailed structure which means it is easy to locate key information on dose rates, routes of administration, drug interactions and special considerations at a glance Key chapters based around treatment of disorders of particular body systems, eg cardiovascular and thyroid disorders Essential introductory chapters covering pharmacokinetics, general pharmacological principles and adverse reactions for a thorough basic grounding in the subject All authors are experienced clinicians and recognised experts in their field who bring a down to earth and practical approach to the text

Safety Pharmacology in Pharmaceutical Development

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Author :
Publisher : CRC Press
ISBN 13 : 1439845689
Total Pages : 213 pages
Book Rating : 4.4/5 (398 download)

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Book Synopsis Safety Pharmacology in Pharmaceutical Development by : Shayne C. Gad

Download or read book Safety Pharmacology in Pharmaceutical Development written by Shayne C. Gad and published by CRC Press. This book was released on 2012-04-26 with total page 213 pages. Available in PDF, EPUB and Kindle. Book excerpt: Safety pharmacology is the evaluation and study of the pharmacological effects of a potential drug that are unrelated to the desired therapeutic effect. These effects often present a hazard-particularly in individuals with compromised or limited organ system functions.Safety Pharmacology in Pharmaceutical Development: Approval and Post Marketing Su

Atkinson's Principles of Clinical Pharmacology

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Author :
Publisher : Academic Press
ISBN 13 : 0128198842
Total Pages : 764 pages
Book Rating : 4.1/5 (281 download)

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Book Synopsis Atkinson's Principles of Clinical Pharmacology by : Shiew-Mei Huang

Download or read book Atkinson's Principles of Clinical Pharmacology written by Shiew-Mei Huang and published by Academic Press. This book was released on 2021-10-16 with total page 764 pages. Available in PDF, EPUB and Kindle. Book excerpt: **Selected for Doody's Core Titles® 2024 in Pharmacology**Atkinson's Principles of Clinical Pharmacology, Fourth Edition is the essential reference on the pharmacologic principles underlying the individualization of patient therapy and contemporary drug development. This well-regarded survey continues to focus on the basics of clinical pharmacology for the development, evaluation and clinical use of pharmaceutical products while also addressing the most recent advances in the field. Written by leading experts in academia, industry, clinical and regulatory settings, the fourth edition has been thoroughly updated to provide readers with an ideal reference on the wide range of important topics impacting clinical pharmacology. - Presents the essential knowledge for effective practice of clinical pharmacology - Includes a new chapter and extended discussion on the role of personalized and precision medicine in clinical pharmacology - Offers an extensive regulatory section that addresses US and international issues and guidelines - Provides extended coverage of earlier chapters on transporters, pharmacogenetics and biomarkers, along with further discussion on "Phase 0" studies (microdosing) and PBPK

Drug Discovery and Development - E-Book

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Publisher : Elsevier Health Sciences
ISBN 13 : 0702053163
Total Pages : 361 pages
Book Rating : 4.7/5 (2 download)

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Book Synopsis Drug Discovery and Development - E-Book by : Raymond G Hill

Download or read book Drug Discovery and Development - E-Book written by Raymond G Hill and published by Elsevier Health Sciences. This book was released on 2012-07-20 with total page 361 pages. Available in PDF, EPUB and Kindle. Book excerpt: The modern pharmacopeia has enormous power to alleviate disease, and owes its existence almost entirely to the work of the pharmaceutical industry. This book provides an introduction to the way the industry goes about the discovery and development of new drugs. The first part gives a brief historical account from its origins in the mediaeval apothecaries' trade, and discusses the changing understanding of what we mean by disease, and what therapy aims to achieve, as well as summarising case histories of the discovery and development of some important drugs. The second part focuses on the science and technology involved in the discovery process: the stages by which a promising new chemical entity is identified, from the starting point of a medical need and an idea for addressing it. A chapter on biopharmaceuticals, whose discovery and development tend to follow routes somewhat different from synthetic compounds, is included here, as well as accounts of patent issues that arise in the discovery phase, and a chapter on research management in this environment. The third section of the book deals with drug development: the work that has to be undertaken to turn the drug candidate that emerges from the discovery process into a product on the market. - The definitive introduction to how a pharmaceutical company goes about its business of discovering and developing drugs. The second edition has a new editor: Professor Raymond Hill ● non-executive director of Addex Pharmaceuticals, Covagen and of Orexo AB ● Visiting Industrial Professor of Pharmacology in the University of Bristol ● Visiting Professor in the School of Medical and Health Sciences at the University of Surrey ● Visiting Professor in Physiology and Pharmacology at the University of Strathclyde ● President and Chair of the Council of the British Pharmacological Society ● member of the Nuffield Council on Bioethics and the Advisory Council on Misuse of Drugs. New to this edition: - Completely rewritten chapter on The Role of Medicinal Chemistry in the Drug Discovery Process. - New topic - DMPK Optimization Strategy in drug discovery. - New chapter on Scaffolds: Small globular proteins as antibody substitutes. - Totally updated chapters on Intellectual Property and Marketing - 50 new illustrations in full colour Features - Accessible, general guide to pharmaceutical research and development. - Examines the interfaces between cost and social benefit, quality control and mass production, regulatory bodies, patent management, and all interdisciplinary intersections essential to effective drug development. - Written by a strong team of scientists with long experience in the pharmaceutical industry. - Solid overview of all the steps from lab bench to market in an easy-to-understand way which will be accessible to non-specialists. From customer reviews of the previous edition: '... it will have everything you need to know on this module. Deeply referenced and, thus, deeply reliable. - Highly Commended in the medicine category of the BMA 2006 medical book competition - Winner of the Royal Society of Medicine Library Prize for Medical Book of the Year

A Comprehensive Guide to Toxicology in Nonclinical Drug Development

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Author :
Publisher : Academic Press
ISBN 13 : 0128036214
Total Pages : 988 pages
Book Rating : 4.1/5 (28 download)

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Book Synopsis A Comprehensive Guide to Toxicology in Nonclinical Drug Development by : Ali S. Faqi

Download or read book A Comprehensive Guide to Toxicology in Nonclinical Drug Development written by Ali S. Faqi and published by Academic Press. This book was released on 2016-11-03 with total page 988 pages. Available in PDF, EPUB and Kindle. Book excerpt: A Comprehensive Guide to Toxicology in Nonclinical Drug Development, Second Edition, is a valuable reference designed to provide a complete understanding of all aspects of nonclinical toxicology in the development of small molecules and biologics. This updated edition has been reorganized and expanded to include important topics such as stem cells in nonclinical toxicology, inhalation and dermal toxicology, pitfalls in drug development, biomarkers in toxicology, and more. Thoroughly updated to reflect the latest scientific advances and with increased coverage of international regulatory guidelines, this second edition is an essential and practical resource for all toxicologists involved in nonclinical testing in industry, academic, and regulatory settings. - Provides unique content that is not always covered together in one comprehensive resource, including chapters on stem cells, abuse liability, biomarkers, inhalation toxicology, biostatistics, and more - Updated with the latest international guidelines for nonclinical toxicology in both small and large molecules - Incorporates practical examples in order to illustrate day-to-day activities and the expectations associated with working in nonclinical toxicology

Pharmacology in Drug Discovery and Development

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Publisher : Academic Press
ISBN 13 : 0128037539
Total Pages : 340 pages
Book Rating : 4.1/5 (28 download)

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Book Synopsis Pharmacology in Drug Discovery and Development by : Terry P. Kenakin

Download or read book Pharmacology in Drug Discovery and Development written by Terry P. Kenakin and published by Academic Press. This book was released on 2016-10-21 with total page 340 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmacology in Drug Discovery and Development: Understanding Drug Response, Second Edition, is an introductory resource illustrating how pharmacology can be used to furnish the tools necessary to analyze different drug behavior and trace this behavior to its root cause or molecular mechanism of action. The concepts discussed in this book allow for the application of more predictive pharmacological procedures aimed at increasing therapeutic efficacy that will lead to more successful drug development. Chapters logically build upon one another to show how to characterize the pharmacology of any given molecule and allow for more informed predictions of drug effects in all biological systems. New chapters are dedicated to the interdisciplinary drug discovery environment in both industry and academia, and special techniques involved in new drug screening and lead optimization. This edition has been fully revised to address the latest advances and research related to real time kinetic assays, pluridimensional efficacy, signaling bias, irreversible and chemical antagonism, allosterically-induced bias, pharmacokinetics and safety, target and pathway validation, and much more. With numerous valuable chapter summaries, detailed references, practical examples and case studies throughout, Dr. Kenakin successfully navigates a highly complex subject, making it accessible for students, professors, and new researchers working in pharmacology and drug discovery. - Includes example-based cases that illustrate how the pharmacological concepts discussed in this book lead to practical outcomes for further research - Provides vignettes on those researchers and scientists who have contributed significantly to the fields of pharmacology and drug discovery throughout history - Offers sample questions throughout the book and an appendix containing answers for self-testing and retention

Basic Principles of Drug Discovery and Development

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Publisher : Academic Press
ISBN 13 : 0128172150
Total Pages : 738 pages
Book Rating : 4.1/5 (281 download)

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Book Synopsis Basic Principles of Drug Discovery and Development by : Benjamin E. Blass

Download or read book Basic Principles of Drug Discovery and Development written by Benjamin E. Blass and published by Academic Press. This book was released on 2021-03-30 with total page 738 pages. Available in PDF, EPUB and Kindle. Book excerpt: Basic Principles of Drug Discovery and Development presents the multifaceted process of identifying a new drug in the modern era, which requires a multidisciplinary team approach with input from medicinal chemists, biologists, pharmacologists, drug metabolism experts, toxicologists, clinicians, and a host of experts from numerous additional fields. Enabling technologies such as high throughput screening, structure-based drug design, molecular modeling, pharmaceutical profiling, and translational medicine are critical to the successful development of marketable therapeutics. Given the wide range of disciplines and techniques that are required for cutting edge drug discovery and development, a scientist must master their own fields as well as have a fundamental understanding of their collaborator's fields. This book bridges the knowledge gaps that invariably lead to communication issues in a new scientist's early career, providing a fundamental understanding of the various techniques and disciplines required for the multifaceted endeavor of drug research and development. It provides students, new industrial scientists, and academics with a basic understanding of the drug discovery and development process. The fully updated text provides an excellent overview of the process and includes chapters on important drug targets by class, in vitro screening methods, medicinal chemistry strategies in drug design, principles of in vivo pharmacokinetics and pharmacodynamics, animal models of disease states, clinical trial basics, and selected business aspects of the drug discovery process. - Provides a clear explanation of how the pharmaceutical industry works, as well as the complete drug discovery and development process, from obtaining a lead, to testing the bioactivity, to producing the drug, and protecting the intellectual property - Includes a new chapter on the discovery and development of biologics (antibodies proteins, antibody/receptor complexes, antibody drug conjugates), a growing and important area of the pharmaceutical industry landscape - Features a new section on formulations, including a discussion of IV formulations suitable for human clinical trials, as well as the application of nanotechnology and the use of transdermal patch technology for drug delivery - Updated chapter with new case studies includes additional modern examples of drug discovery through high through-put screening, fragment-based drug design, and computational chemistry

Clinical Pharmacology: Current Topics and Case Studies

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Publisher : Springer Science & Business Media
ISBN 13 : 3709101441
Total Pages : 438 pages
Book Rating : 4.7/5 (91 download)

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Book Synopsis Clinical Pharmacology: Current Topics and Case Studies by : Markus Müller

Download or read book Clinical Pharmacology: Current Topics and Case Studies written by Markus Müller and published by Springer Science & Business Media. This book was released on 2011-02-04 with total page 438 pages. Available in PDF, EPUB and Kindle. Book excerpt: Today we witness an eventful time in which the powerful new forces of genomics, information technology and economics are rapidly changing the science and art of medicine. This will require more specialization than ever before. However, there is also an increasing demand for an integrated approach, which is provided by the discipline of Clinical Pharmacology (CP). CP pursues a scientific goal by studying drug action in patients and volunteers, a clinical goal by administering appropriate drug therapy and a regulatory goal by assessing the risk/benefit ratio of drug candidates in drug development and reimbursement. This introduction to current topics of CP covers traditional topics of clinical drug research and trial methodology but also provides insight in current topics like genomics, imaging technology and issues in drug reimbursement. A number of concrete case studies in clinical drug research and development help to give a better understanding of the general principles of CP.

Drug Discovery and Evaluation

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Publisher : Springer Science & Business Media
ISBN 13 : 366203333X
Total Pages : 790 pages
Book Rating : 4.6/5 (62 download)

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Book Synopsis Drug Discovery and Evaluation by : Hans G. Vogel

Download or read book Drug Discovery and Evaluation written by Hans G. Vogel and published by Springer Science & Business Media. This book was released on 2013-04-17 with total page 790 pages. Available in PDF, EPUB and Kindle. Book excerpt: This reference book contains a comprehensive selection of the most frequently used assays for reliably detecting pharmacological effects of potential drugs, including tests for cardiovascular, analgesic, psychotropic, metabolic, endocrine, respiratory, renal, and immunomodulatory activities. Each of the over 700 assays comprises a detailed protocol with the purpose and rationale of the method, a description of the experimental procedure, a critical assessment of the results and their pharmacological and clinical relevance, and pertinent references. Identification of specific tests is facilitated by the enclosed CD-ROM which allows for a quick and full text research. An appendix with guidelines and legal regulations for animal experiments in various countries will help to plan these experiments properly in accordance with the welfare of laboratory animals.

Pharmacology: An Essential Textbook

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Publisher : Thieme
ISBN 13 : 1626237417
Total Pages : 1354 pages
Book Rating : 4.6/5 (262 download)

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Book Synopsis Pharmacology: An Essential Textbook by : Mark A. Simmons

Download or read book Pharmacology: An Essential Textbook written by Mark A. Simmons and published by Thieme. This book was released on 2020-11-11 with total page 1354 pages. Available in PDF, EPUB and Kindle. Book excerpt: The perfect pharmacology study tool for the classroom and examinations! Pharmacology: An Essential Textbook, Second Edition by Mark Simmons covers pharmacology facts and concepts necessary for success in the classroom and on board examinations. The clear and concise text presents important, clinically relevant pharmacology knowledge and concepts students must master. The updated edition includes the addition of new drugs, a chapter on water and fatsoluble vitamins, a greater number of clinical questions, and a fresh design. Key Features Hundreds of full-color illustrations, beautiful infographics, and summary tables provide visual depictions of important concepts The succinct, bullet-point format focuses on must-master information Flow charts used to delineate drug effects make complex interactions between different cells and organs easier to comprehend Sidebars build on and integrate learning across the basic sciences and apply it to the clinical setting Nearly 200 board-style and factual self-testing questions with explanatory answers are ideal for exam practice An additional 200 questions and answers are available online at MedOne via the scratch-off code in the book This is an invaluable resource for medical and nursing school pharmacology courses, pharmacy school students, other health professionals studying pharmacology, and advanced undergraduate courses in pharmacology or pharmaceutical sciences. This book provides robust test prep for the USMLE® Step 1, COMLEX Level 1, NAPLEX, NCLEX and other licensing exams.

Advanced Issue Resolution in Safety Pharmacology

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Publisher : Academic Press
ISBN 13 : 9780128122068
Total Pages : 0 pages
Book Rating : 4.1/5 (22 download)

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Book Synopsis Advanced Issue Resolution in Safety Pharmacology by : Mary Jeanne Kallman

Download or read book Advanced Issue Resolution in Safety Pharmacology written by Mary Jeanne Kallman and published by Academic Press. This book was released on 2018-09-07 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Advanced Issue Resolution in Safety Pharmacology not only discusses unique issues that may emerge during the development of new medicines, but also provides detailed insights on how to resolve them. The book employs a valuable strategy that integrates preclinical findings with the clinical resolution of those findings. In addition, it introduces key interdisciplinary topics in an accessible and systematic format. Edited and written by leaders in the field of safety pharmacology, this book considerably advances the discussion on issue resolution topics, thus raising them to the next level of importance by providing scientists with an indispensable resource on solving safety issues.

Concepts and Principles of Pharmacology

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Author :
Publisher : Springer Nature
ISBN 13 : 3030353621
Total Pages : 457 pages
Book Rating : 4.0/5 (33 download)

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Book Synopsis Concepts and Principles of Pharmacology by : James E. Barrett

Download or read book Concepts and Principles of Pharmacology written by James E. Barrett and published by Springer Nature. This book was released on 2019-12-24 with total page 457 pages. Available in PDF, EPUB and Kindle. Book excerpt: Celebrating 100 years of HEP, this volume will discuss key pharmacological discoveries and concepts of the past 100 years. These discoveries have dramatically changed the medical treatment paradigms of many diseases and these concepts have and will continue to shape discovery of new medicinies. Newly evolving technologies will similarly be discussed as they will shape the future of the pharmacology and, accordingly, medical therapy.

Practical Manual of Experimental and Clinical Pharmacology

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Author :
Publisher : Jaypee Brothers,Medical Publishers Pvt. Limited
ISBN 13 : 9789386150721
Total Pages : 430 pages
Book Rating : 4.1/5 (57 download)

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Book Synopsis Practical Manual of Experimental and Clinical Pharmacology by : Bikash Mehdi

Download or read book Practical Manual of Experimental and Clinical Pharmacology written by Bikash Mehdi and published by Jaypee Brothers,Medical Publishers Pvt. Limited. This book was released on 2016-10-26 with total page 430 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Bioequivalence and Statistics in Clinical Pharmacology

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Author :
Publisher : CRC Press
ISBN 13 : 1466585218
Total Pages : 434 pages
Book Rating : 4.4/5 (665 download)

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Book Synopsis Bioequivalence and Statistics in Clinical Pharmacology by : Scott D. Patterson

Download or read book Bioequivalence and Statistics in Clinical Pharmacology written by Scott D. Patterson and published by CRC Press. This book was released on 2017-03-27 with total page 434 pages. Available in PDF, EPUB and Kindle. Book excerpt: Maintaining a practical perspective, Bioequivalence and Statistics in Clinical Pharmacology, Second Edition explores statistics used in day-to-day clinical pharmacology work. The book is a starting point for those involved in such research and covers the methods needed to design, analyze, and interpret bioequivalence trials; explores when, how, and why these studies are performed as part of drug development; and demonstrates the methods using real world examples. Drawing on knowledge gained directly from working in the pharmaceutical industry, the authors set the stage by describing the general role of statistics. Once the foundation of clinical pharmacology drug development, regulatory applications, and the design and analysis of bioequivalence trials are established, including recent regulatory changes in design and analysis and in particular sample-size adaptation, they move on to related topics in clinical pharmacology involving the use of cross-over designs. These include, but are not limited to, safety studies in Phase I, dose-response trials, drug interaction trials, food-effect and combination trials, QTc and other pharmacodynamic equivalence trials, proof-of-concept trials, dose-proportionality trials, and vaccines trials. This second edition addresses several recent developments in the field, including new chapters on adaptive bioequivalence studies, scaled average bioequivalence testing, and vaccine trials. Purposefully designed to be instantly applicable, Bioequivalence and Statistics in Clinical Pharmacology, Second Edition provides examples of SAS and R code so that the analyses described can be immediately implemented. The authors have made extensive use of the proc mixed procedures available in SAS.