Download or read book ISE Pharmacology written by Henry Hitner and published by . This book was released on 2021 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The SAGE Encyclopedia of Pharmacology and Society written by Sarah E. Boslaugh and published by SAGE Publications. This book was released on 2015-09-15 with total page 1883 pages. Available in PDF, EPUB and Kindle. Book excerpt: The SAGE Encyclopedia of Pharmacology and Society explores the social and policy sides of the pharmaceutical industry and its pervasive influence in society. While many technical STM works explore the chemistry and biology of pharmacology and an equally large number of clinically oriented works focus on use of illegal drugs, substance abuse, and treatment, there is virtually nothing on the immensely huge business (“Big Pharma”) of creating, selling, consuming, and regulating legal drugs. With this new Encyclopedia, the topic of socioeconomic, business and consumer, and legal and ethical issues of the pharmaceutical industry in contemporary society around the world are addressed. Key Features: 800 signed articles, authored by prominent scholars, are arranged A-to-Z and published in a choice of electronic or print formats Although arranged A-to-Z, a Reader's Guide in the front matter groups articles by thematic areas Front matter also includes a Chronology highlighting significant developments in this field All articles conclude with Further Readings and Cross References to related articles Back matter includes an annotated Resource Guide to further research, a Glossary, Appendices (e.g., statistics on the amount and types of drugs prescribed, etc.), and a detailed Index The Index, Reader’s Guide, and Cross References combine for search-and-browse capabilities in the electronic edition The SAGE Encyclopedia of Pharmacology and Society is an authoritative and rigorous source addressing the pharmacology industry and how it influences society, making it a must-have reference for all academic libraries as a source for both students and researchers to utilize.
Download or read book Quantitative Pharmacology and Individualized Therapy Strategies in Development of Therapeutic Proteins for Immune Mediated Inflammatory Diseases written by Honghui Zhou and published by John Wiley & Sons. This book was released on 2019-03-19 with total page 512 pages. Available in PDF, EPUB and Kindle. Book excerpt: Thorough Overview Identifies and Addresses Critical Gaps in the Treatment of Several Chronic Diseases With increasing numbers of patients suffering from Immune-Mediated Inflammatory Diseases (IMIDs), and with the increasing reliance on biopharmaceuticals to treat them, it is imperative that researchers and medical practitioners have a thorough understanding of the absorption, distribution, metabolism and excretion (ADME) of therapeutic proteins as well as translational pharmacokinetic/pharmacodynamic (PK/PD) modeling for them. This comprehensive volume answers that need to be addressed. Featuring eighteen chapters from world-renowned experts and opinion leaders in pharmacology, translational medicine and immunology, editors Honghui Zhou and Diane Mould have curated a much-needed collection of research on the advanced applications of pharmacometrics and systems pharmacology to the development of biotherapeutics and individualized treatment strategies for the treatment of IMIDs. Authors discuss the pathophysiology of autoimmune diseases in addition to both theoretical and practical aspects of quantitative pharmacology for therapeutic proteins, current translational medicine research methodologies and novel thinking in treatment paradigm strategies for IMIDs. Other notable features include: • Contributions from well-known authors representing leading academic research centers, specialized contract research organizations and pharmaceutical industries whose pipelines include therapeutic proteins • Chapters on a wide range of topics (e.g., pathophysiology of autoimmune diseases, biomarkers in ulcerative colitis, model-based meta-analysis use in the development of therapeutic proteins) • Case studies of applying quantitative pharmacology approaches to guiding therapeutic protein drug development in IMIDs such as psoriasis, inflammatory bowel disease, multiple sclerosis and lupus Zhou and Mould’s timely contribution to the critical study of biopharmaceuticals is a valuable resource for any academic and industry researcher working in pharmacokinetics, pharmacology, biochemistry, or biotechnology as well as the many clinicians seeking the safest and most effective treatments for patients dealing with chronic immune disorders.
Download or read book Essential CNS Drug Development written by Amir Kalali and published by Cambridge University Press. This book was released on 2012-06-07 with total page 219 pages. Available in PDF, EPUB and Kindle. Book excerpt: Presents the complicated process of CNS drug development in a way that is engaging and informative for professionals and students.
Download or read book Handbook s written by University of the State of New York and published by . This book was released on 1920 with total page 5146 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Clinical Pharmacology Made Ridiculously Simple Rev Ed Ise written by James M. Olson (Medical scientist) and published by . This book was released on 2000-03-01 with total page 163 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Therapeutic Potential of the Cannabinoid CB2 Receptor written by Reem Smoum and published by Frontiers Media SA. This book was released on 2022-11-14 with total page 178 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The Journal of Pharmacology and Experimental Therapeutics written by and published by . This book was released on 1977 with total page 890 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Accurate Results in the Clinical Laboratory written by Amitava Dasgupta and published by Elsevier. This book was released on 2019-07-20 with total page 510 pages. Available in PDF, EPUB and Kindle. Book excerpt: Accurate Results in the Clinical Laboratory: A Guide to Error Detection and Correction, Second Edition, provides a comprehensive review of the factors leading to errors in all areas of clinical laboratory testing. This trusted guide addresses interference issues in all laboratory tests, including patient epigenetics, processes of specimen collection, enzymes and biomarkers. Clinicians and laboratory scientists will both benefit from this reference that applies discussions to both accurate specimen analysis and optimal patient care. Hence, this is the perfect reference for clinical laboratorians, from trainees, to experienced pathologists and directors. Provides comprehensive coverage across endocrine, oncology, hematology, immunohistochemistry, immunology, serology, microbiology, and molecular testing Includes new case studies that highlight clinical relevance and errors to avoid Highlights the best titles published within a variety of medical specialties Reviewed by medical librarians and content specialists, with key selections compiled in their annual list
Download or read book Drug Safety written by United States. Congress. House. Committee on Government Operations and published by . This book was released on 1964 with total page 1600 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book A Legislative History of the Federal Food Drug and Cosmetic Act and Its Amendments written by and published by . This book was released on 1979 with total page 916 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmacology for Nurse Anesthesiology written by Richard Ouellette and published by Jones & Bartlett Publishers. This book was released on 2011 with total page 561 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmacology for Nurse Anesthesiology provides appropriate chemical, biological, and physical information of the actions, interactions, and reactions of medication, particularly as they apply and impact the practice of nurse anesthesia. Written by CRNAs for CRNAs, the information about various drugs is based on theoretical aspects based in chemistry, biochemistry, biology, and physics/biophysics and practical aspects straight from actual CRNAs who administer and deal with the medications on a case-by-case, daily basis. The perfect resource for both practicing professionals and students in CRNA programs!
Download or read book Drug Information written by Bonnie Snow and published by Scarecrow Press. This book was released on 1999 with total page 772 pages. Available in PDF, EPUB and Kindle. Book excerpt: Designed for use as a self-study text, as a course text in more formal instruction programs, or as a refresher for the busy professional, the book includes valuable background data on legal and regulatory issues, as well as pharmaceutical technology.
Download or read book Drug Induced Liver Disease written by Neil Kaplowitz and published by CRC Press. This book was released on 2002-10-16 with total page 790 pages. Available in PDF, EPUB and Kindle. Book excerpt: Featuring more than 4100 references, Drug-Induced Liver Disease will be an invaluable reference for gastroenterologists, hepatologists, family physicians, internists, pathologists, pharmacists, pharmacologists, and clinical toxicologists, and graduate and medical school students in these disciplines.
Download or read book Medicinal Plants of the Asia Pacific written by Christophe Wiart and published by World Scientific. This book was released on 2006-01-11 with total page 756 pages. Available in PDF, EPUB and Kindle. Book excerpt: ' This invaluable book provides a readable, introductory text to the fascinating subject of drug discovery from the medicinal plants of Asia-Pacific. A carefully designed layout presents more than 400 medicinal plants, and includes description of compound structure, molecular properties, pharmacology and clinical uses. With its broad scope and extensive compound listings, this is a premier reference source for natural products research using a pharmacological approach. Starting from a collection of plants in the rainforests of Asia-Pacific, Wiart shows how the present state of knowledge fosters a whole new way of looking at the discovery of drugs from medicinal plants. Wiart uses his approach to deal with a remarkable array of fundamental problems: from the phylogeny of plants, to the molecular basis of activity, limitations of phytochemistry, and the possibility of a truly fundamental theory of ethnopharmacology. Written with exceptional clarity, and illustrated by more than 300 original pictures and 400 chemical structures, this seminal book allows scientists and non-scientists alike to participate in what promises to be a major intellectual revolution. Contents:Class MAGNOLIOPSIDA Cronquist, Takhtajan & Zimmermann, 1966, the Dicotyledons:Subclass MAGNOLIIDAE Takhtajan 1966Subclass HAMAMELIDAE Takhtajan 1966Subclass CARYOPHYLLIDAE Takhtajan 1966Subclass DILLENIIDAE Takhtajan 1966Subclass ROSIDAE Takhtajan 1966Subclass ASTERIDAE Takhtajan 1966Class LILIOPSIDA Cronquist, Takhtajan & Zimmermann 1966, the Monocotyledons:Subclass ARECIDAE Takhtajan 1966Subclass COMMELINIDAE Takhtajan 1966Subclass ZINGIBERIDAE Cronquist 1978Subclass LILIIDAE Takhtajan 1966 Readership: Students, academics and researchers in pharmacology, toxicology, biotechnology, natural product research, medicinal chemistry, oncology, microbiology, alternative medicine and food sciences; pharmaceutical companies. Keywords:Drug Discovery;Medicinal Plants;Asia-Pacific;EthnopharmacologyKey Features:This book offers, for the very first time, a systematic and a comprehensive coverage of medicinal plants of the Asia-Pacific, one of the richest regions in biodiversityIt is a premier source of reference on traditional medicinal herbs and development of drugs from natural resourcesIt provides a detailed and fascinating ethnopharmacological account of over 400 plant species, illustrated with more than 300 original picture, 400 chemical structures, and contains thousands of referencesReviews: “Christophe Wiart has produced a magnificent book covering all pertinent aspects of the potential medicinal plants of the Asia-Pacific Region. Plants (dicots and moncots) are organized by class, subclass, order, family, genus and species. More than 315 species of plants are included in this tome. Botanical descriptions are first given for each family with a general statement of the potential pharmaceutical interest for the family, followed by discussions of the physical characteristics of each species, uses in the region and pharmaceutical interests in the species; the pharmacology, including potential toxicity, of extracts of each plant and an indication of the major pharmacologically active principles, with their structures are mentioned. Photographs and/or line drawings are included for each species … I have never seen such a book that has been this carefully prepared, so botanists, chemists, pharmacognosists, and pharmacologists having any interest in the medicinal or potentially medicinal higher plants of the Asia-Pacific Region, will be satisfied in the book content. The book will be found useful by academic, industrial and government scientists having any interest in the potential of plants as a source of new drugs.” Professor Norman Farnsworth University of Illinois at Chicago, USA “It will be an invaluable resource for doctors, pharmacists, plant scientists, pharmaceutical companies and conservationists in the region, and to all who are interested in medicinal plants.” Professor Nina L Etkin University of Hawaii, USA “‘Medicinal plants of Asia-Pacific: Drugs for the Future?’ offers researchers a strong foundation from which to advance the field of ethnopharmacology.” Professor Elizabeth M Williamson University of Reading, UK '
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 568 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
Download or read book A Comprehensive Guide to Toxicology in Nonclinical Drug Development written by Ali S. Faqi and published by Elsevier. This book was released on 2024-02-11 with total page 1074 pages. Available in PDF, EPUB and Kindle. Book excerpt: A Comprehensive Guide to Toxicology in Nonclinical Drug Development, Third Edition is a valuable reference providing a complete understanding of all aspects of nonclinical toxicology in pharmaceutical research. This updated edition has been expanded and re-developed covering a wide-range of toxicological issues in small molecules and biologics. Topics include ADME in drug discovery, pharmacokinetics, toxicokinetics, formulations, and genetic toxicology testing. The book has been thoroughly updated throughout to reflect the latest scientific advances and includes new information on antiviral drugs, anti-diabetic drugs, immunotherapy, and a discussion on post-pandemic drug development challenges and opportunities. This is an essential and practical resource for all toxicologists involved in nonclinical testing in industry, academic, and regulatory settings. Provides updated, unique content not covered in one comprehensive resource, including chapters on stem cells, antiviral drugs, anti-diabetic drugs, and immunotherapy Includes 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 expectations associated with working in nonclinical toxicology
