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Book Red Book

    Book Details:
  • Author :
  • Publisher :
  • Release : 2006
  • ISBN :
  • Pages : 1066 pages

Download or read book Red Book written by and published by . This book was released on 2006 with total page 1066 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Pdr Pharmacopoeia Pocket Dosing Guide 5

Download or read book Pdr Pharmacopoeia Pocket Dosing Guide 5 written by PDR Staff and published by Physician's Desk Reference (PDR). This book was released on 2003 with total page 300 pages. Available in PDF, EPUB and Kindle. Book excerpt: Buy 5 get 1 free special offer pre-pack.

Book The Merck Veterinary Manual

Download or read book The Merck Veterinary Manual written by Merck and Co., Inc. Staff and published by . This book was released on 2003-11 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: For more than forty years, animal health professionals have turned to the Merck Veterinary Manualfor integrated, concise and reliable veterinary information. Now this manual covering the diagnosis, treatment, and prevention of diseases of companion, food and zoo animals.is available on an easy-to-use, fully searchable CD-ROM. The CD includes the full text of The Merck Veterinary Manual 8/e and has been enhanced with picture links featuring original anatomical artwork and numerous clinical and diagnostic illustrations, table links and quick search links that provide quick accesss to cross referenced text.

Book The British National Bibliography

Download or read book The British National Bibliography written by Arthur James Wells and published by . This book was released on 2009 with total page 2744 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Pharmacology Clear   Simple

Download or read book Pharmacology Clear Simple written by Cynthia J Watkins and published by F.A. Davis. This book was released on 2018-04-18 with total page 530 pages. Available in PDF, EPUB and Kindle. Book excerpt: Here’s the must-have knowledge and guidance you need to gain a solid understanding of pharmacology and the safe administration of medications in one text. A body systems approach to pharmacology with a basic math review and a focus on drug classifications prepare you for administering specific drugs in the clinical setting.

Book Tarascon Pocket Pharmacopoeia 2014 Deluxe Lab Coat Edition

Download or read book Tarascon Pocket Pharmacopoeia 2014 Deluxe Lab Coat Edition written by and published by Jones & Bartlett Publishers. This book was released on 2013-12-04 with total page 451 pages. Available in PDF, EPUB and Kindle. Book excerpt: Used by prescribers around the world, including: physicians, pharmacists, nurses, physician assistants, dentists and medical transcriptionist, the Tarascon Pharmacopoeia® 2014 Deluxe Lab Coat Edition continues its tradition as the leading portable drug reference packed with vital drug information to help clinicians make better decisions at the point of care. The Tarascon Pharmacopoeia® 2014 Deluxe Lab Coat Edition is an expanded version of the Classic Shirt-Pocket Edition, containing more drugs, black box warnings, evidence-based off-label indications for adults and pediatric patients, and additional tables. This reference also includes typical drug dosing (all FDA approved), available trade and generic formulations, metabolism, safety in pregnancy and lactation, relative drug pricing information, Canadian trade names, and an herbal & alternative therapies section. Multiple tables supplement the drug content, including opioid equivalency, emergency drug infusions, cardiac dysrhythmia protocols, pediatric drug dosing, and much more.

Book Handbook of Bioequivalence Testing

Download or read book Handbook of Bioequivalence Testing written by Sarfaraz K. Niazi and published by CRC Press. This book was released on 2007-08-22 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct efficient and successful bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence, and advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more difficult to conduct and summarize. The Handbook of Bioequivalence Testing offers a complete description of every aspect of bioequivalence testing. Features: Describes the current analytical methods used in bioequivalence testing, as well as their respective strengths and limitations Discusses worldwide regulatory requirements for filing for approval of generic drugs Covers GLP, GCP, and 21 CFR compliance requirements for qualifying studies for regulatory submission and facility certification Includes actual examples of reports approved by regulatory authorities to illustrate various scientific, regulatory, and formatting aspects Provides a list of vendors for the software used to analyze bioequivalence studies and recommendations Explains how to apply for a waiver, how to secure regulatory approval of reports, and how to obtain regulatory certification of facilities conducting bioequivalence studies

Book Handbook of Essential Oils

Download or read book Handbook of Essential Oils written by K. Husnu Can Baser and published by CRC Press. This book was released on 2009-12-28 with total page 994 pages. Available in PDF, EPUB and Kindle. Book excerpt: Egyptian hieroglyphs, Chinese scrolls, and Ayurvedic literature record physicians administering aromatic oils to their patients. Today society looks to science to document health choices and the oils do not disappoint. The growing body of evidence of their efficacy for more than just scenting a room underscores the need for production standards, quality control parameters for raw materials and finished products, and well-defined Good Manufacturing Practices. Edited by two renowned experts, the Handbook of Essential Oils covers all aspects of essential oils from chemistry, pharmacology, and biological activity, to production and trade, to uses and regulation. Bringing together significant research and market profiles, this comprehensive handbook provides a much-needed compilation of information related to the development, use, and marketing of essential oils, including their chemistry and biochemistry. A select group of authoritative experts explores the historical, biological, regulatory, and microbial aspects. This reference also covers sources, production, analysis, storage, and transport of oils as well as aromatherapy, pharmacology, toxicology, and metabolism. It includes discussions of biological activity testing, results of antimicrobial and antioxidant tests, and penetration-enhancing activities useful in drug delivery. New information on essential oils may lead to an increased understanding of their multidimensional uses and better, more ecologically friendly production methods. Reflecting the immense developments in scientific knowledge available on essential oils, this book brings multidisciplinary coverage of essential oils into one all-inclusive resource.

Book Countering the Problem of Falsified and Substandard Drugs

Download or read book Countering the Problem of Falsified and Substandard Drugs written by Institute of Medicine and published by National Academies Press. This book was released on 2013-06-20 with total page 377 pages. Available in PDF, EPUB and Kindle. Book excerpt: The adulteration and fraudulent manufacture of medicines is an old problem, vastly aggravated by modern manufacturing and trade. In the last decade, impotent antimicrobial drugs have compromised the treatment of many deadly diseases in poor countries. More recently, negligent production at a Massachusetts compounding pharmacy sickened hundreds of Americans. While the national drugs regulatory authority (hereafter, the regulatory authority) is responsible for the safety of a country's drug supply, no single country can entirely guarantee this today. The once common use of the term counterfeit to describe any drug that is not what it claims to be is at the heart of the argument. In a narrow, legal sense a counterfeit drug is one that infringes on a registered trademark. The lay meaning is much broader, including any drug made with intentional deceit. Some generic drug companies and civil society groups object to calling bad medicines counterfeit, seeing it as the deliberate conflation of public health and intellectual property concerns. Countering the Problem of Falsified and Substandard Drugs accepts the narrow meaning of counterfeit, and, because the nuances of trademark infringement must be dealt with by courts, case by case, the report does not discuss the problem of counterfeit medicines.

Book Dictionary of Pharmaceutical Medicine

Download or read book Dictionary of Pharmaceutical Medicine written by Gerhard Nahler and published by Springer Science & Business Media. This book was released on 2013-06-29 with total page 186 pages. Available in PDF, EPUB and Kindle. Book excerpt: This dictionary is aimed primarily at the beginners entering the new discipline of Pharmaceutical Medicine, an area comprising aspects of toxicology, pharmacology, pharmaceutics, epidemiology, statistics, drug regulatory and legal affairs, medicine and marketing. But also more experienced colleagues in departments engaged in clinical development as well as researchers and marketing experts in the pharmaceutical industry will find concise and up-to-date information. The book is completed by a list of a about 1000 abbreviations encountered in pharmaceutical medicine and a compilation of important addresses of national and international health authorities.

Book Pharmaceutical Dosage Forms and Drug Delivery Systems

Download or read book Pharmaceutical Dosage Forms and Drug Delivery Systems written by Howard C. Ansel and published by Lippincott Williams & Wilkins. This book was released on 1999 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: This work covers the entire scope of pharmaceutics, from the basics of drug dosage and routes of administration to the finer points of drug discovery, drug product development, legislation and regulations governing quality standards and product approval for marketing.

Book Pharmacy Informatics

    Book Details:
  • Author : Philip O. Anderson
  • Publisher : CRC Press
  • Release : 2009-12-01
  • ISBN : 1420071769
  • Pages : 308 pages

Download or read book Pharmacy Informatics written by Philip O. Anderson and published by CRC Press. This book was released on 2009-12-01 with total page 308 pages. Available in PDF, EPUB and Kindle. Book excerpt: Applies the Principles of Informatics to the Pharmacy ProfessionEmphasizes Evidence-Based Practice and Quality Improvement ApproachesLeading the way in the integration of information technology with healthcare, Pharmacy Informatics reflects some of the rapid changes that have developed in the pharmacy profession. Written by educators and profession

Book Duke s Handbook of Medicinal Plants of the Bible

Download or read book Duke s Handbook of Medicinal Plants of the Bible written by James A. Duke and published by CRC Press. This book was released on 2007-12-26 with total page 554 pages. Available in PDF, EPUB and Kindle. Book excerpt: Readers have come to depend on Jim Duke's comprehensive handbooks for their ease of use and artful presentation of scientific information. Following the successful format of his other CRC handbooks, Duke's Handbook of Medicinal Plants of the Bible contains 150 herbs listed alphabetically and by scientific name. Each entry provides illustrations of the plant, synonyms, notes, common names, activities, indications, dosages, downsides and interactions, natural history, and extracts. It includes Biblical quotes as well as comments on points of interest.

Book Drug Benefits and Risks

    Book Details:
  • Author : Chris J. van Boxtel
  • Publisher : John Wiley & Sons
  • Release : 2001-11-28
  • ISBN : 9780471899273
  • Pages : 738 pages

Download or read book Drug Benefits and Risks written by Chris J. van Boxtel and published by John Wiley & Sons. This book was released on 2001-11-28 with total page 738 pages. Available in PDF, EPUB and Kindle. Book excerpt: This is an inclusive reference exploring the scientific basis and practice of drug therapy. The key concept is to look at the balance between the benefits and risks of drugs but in this context also the social impact which drugs have in modern societies is highlighted. Taking an evidence-based approach to the problem, the practice of clinical pharmacology and pharmacotherapy in the developing as well as the developed world is examined. For this purpose the book * Covers general clinical pharmacology, pharmacology of various drug groups and the treatments specific to various diseases * Gives guidance on how doctors should act so that drugs can be used effectively and safely * Encourages the rational use of drugs in society This book brings together a large amount of excellent content that will be invaluable for anyone working within, or associated with, the field of clinical pharmacology and pharmacotherapy - undergraduates, postgraduates, regulatory authorities and the pharmaceutical industry.

Book The Globalization of Crime

Download or read book The Globalization of Crime written by United Nations Office on Drugs and Crime and published by UN. This book was released on 2010 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: In The globalization of crime: a transnational organized crime threat assessment, UNODC analyses a range of key transnational crime threats, including human trafficking, migrant smuggling, the illicit heroin and cocaine trades, cybercrime, maritime piracy and trafficking in environmental resources, firearms and counterfeit goods. The report also examines a number of cases where transnational organized crime and instability amplify each other to create vicious circles in which countries or even subregions may become locked. Thus, the report offers a striking view of the global dimensions of organized crime today.

Book Community Pharmacy

    Book Details:
  • Author : Paul Rutter
  • Publisher : Elsevier Health Sciences
  • Release : 2016-12-03
  • ISBN : 0702069965
  • Pages : 400 pages

Download or read book Community Pharmacy written by Paul Rutter and published by Elsevier Health Sciences. This book was released on 2016-12-03 with total page 400 pages. Available in PDF, EPUB and Kindle. Book excerpt: Now in its fourth edition, this best-selling book is fully updated to address the ever increasing demands on healthcare professionals to deliver high-quality patient care. A multitude of factors impinge on healthcare delivery today, including an ageing population, more sophisticated medicines, high patient expectation and changing health service infrastructure. Time demands on primary care doctors have caused other models of service delivery to be adopted across the world, leading to ongoing changes in the traditional boundaries of care between doctors, nurses, and pharmacists. Certain medical tasks are now being performed by nurses and pharmacists, for example prescribing. Healthcare policies to encourage patients to manage their own health have led to more medicines becoming available over the counter, allowing community pharmacists to manage and treat a wide range of conditions. Further deregulation of medicines to treat acute illness from different therapeutic areas seems likely. Government policy now encourages chronic disease management as a self-care activity, and could well be the largest area for future growth of reclassification of medicines. Pharmacists, now more than ever before, need to be able to recognise the signs and symptoms, and use an evidence-based approach to treatment. Community Pharmacy is intended for all non-medical prescribers but especially for pharmacists, from undergraduate students to experienced practitioners. Key features - Guidance for arriving at a differential diagnosis - Practical prescribing tips - Trigger points for referral boxes - Other hints and tips boxes - Specific questions to ask boxes - Case studies - Self-assessment questions Consistent approach gives: - Anatomy overview - History taking and physical examination - Prevalence and epidemiology - Aetiology - Arriving at a differential diagnosis - Clinical features - Conditions to eliminate Likely causes Unlikely causes Very unlikely causes - Evidence base for OTC medicine - Practical prescribing and product selection - More on the examination of eyes, ears and mouth - New sections on future-proofing (vaccinations etc.) - New material covering inter-professional education for clinical skills. Now with a free accompanying e-book on StudentConsult which also gives additional material on: - evidence-based medicine - videos on physical examination - additional written case studies - more multiple-choice questions

Book Real World Drug Discovery

Download or read book Real World Drug Discovery written by Robert M. Rydzewski and published by Elsevier. This book was released on 2010-07-07 with total page 535 pages. Available in PDF, EPUB and Kindle. Book excerpt: Drug discovery increasingly requires a common understanding by researchers of the many and diverse factors that go into the making of new medicines. The scientist entering the field will immediately face important issues for which his education may not have prepared him: project teams, patent law, consultants, target product profiles, industry trends, Gantt charts, target validation, pharmacokinetics, proteomics, phenotype assays, biomarkers, and many other unfamiliar topics for which a basic understanding must somehow be obtained. Even the more experienced scientist can find it frustratingly difficult to get an overview of the many factors involved in modern drug discovery and often only after years of exploring does a whole and integrated picture emerge in the mind of the researcher.Real World Drug Discovery: A Chemist's Guide to Biotech and Pharmaceutical Research presents this kind of map of the landscape of drug discovery. In a single, readable volume it outlines processes and explains essential concepts and terms for the recent science graduate wondering what to expect in pharma or biotech, the medicinal chemist seeking a broader and more timely understanding of the industry, or the contractor or collaborator whose understanding of the commercial drug discovery process could increase the value of his contribution to it. - Interviews with well-known experts in many of the fields involved, giving insightful comments from authorities on many of the sub-disciplines important to cutting edge drug discovery. - Helpful suggestions gleaned from years of experience in biotech and pharma, which represents a repository drug discovery "lore" not previously available in any book. - "Periodic Table of Drugs" listing current top-selling drugs arranged by target and laid out so that structural similarities and differences are plain and clear. - Extensive use of diagrams to illustrate concepts like biotech startup models, preteomic profiling for target identification, Gantt charts for project planning, etc.