Download or read book Martindale written by Sean C. Sweetman and published by . This book was released on 2006-01-01 with total page 3335 pages. Available in PDF, EPUB and Kindle. Book excerpt: This is thirty-fifth edition of Martindale, which provides reliable, and evaluated information on drugs and medicines used throughout the world. It contains encyclopaedic facts about drugs and medicines, with: 5,500 drug monographs; 128,000 preparations; 40,700 reference citations; 10,900 manufacturers. There are synopses of disease treatments which enables identification of medicines, the local equivalent and the manufacturer. It also Includes herbals, diagnostic agents, radiopharmaceuticals, pharmaceutical excipients, toxins, and poisons as well as drugs and medicines. Based on published information and extensively referenced
Download or read book Nursing 2000 Drug Handbook written by Springhouse Publishing and published by . This book was released on 1999 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: For two decades, Nursing Drug Handbook has been the nurse's favorite drug reference. Completely free of commercial bias, it's the oldest, most trusted book of its kind. Each page is packed with accurate, complete, up-to-date drug information. Plus, we've added new features carefully tailored to meet your changing on-the-job needs and preferences. Book jacket.
Download or read book Mosby s Nursing Drug Reference written by and published by . This book was released on 2008 with total page 1310 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Dietary Reference Intakes for Vitamin A Vitamin K Arsenic Boron Chromium Copper Iodine Iron Manganese Molybdenum Nickel Silicon Vanadium and Zinc written by Institute of Medicine and published by National Academies Press. This book was released on 2002-07-19 with total page 804 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume is the newest release in the authoritative series issued by the National Academy of Sciences on dietary reference intakes (DRIs). This series provides recommended intakes, such as Recommended Dietary Allowances (RDAs), for use in planning nutritionally adequate diets for individuals based on age and gender. In addition, a new reference intake, the Tolerable Upper Intake Level (UL), has also been established to assist an individual in knowing how much is "too much" of a nutrient. Based on the Institute of Medicine's review of the scientific literature regarding dietary micronutrients, recommendations have been formulated regarding vitamins A and K, iron, iodine, chromium, copper, manganese, molybdenum, zinc, and other potentially beneficial trace elements such as boron to determine the roles, if any, they play in health. The book also: Reviews selected components of food that may influence the bioavailability of these compounds. Develops estimates of dietary intake of these compounds that are compatible with good nutrition throughout the life span and that may decrease risk of chronic disease where data indicate they play a role. Determines Tolerable Upper Intake levels for each nutrient reviewed where adequate scientific data are available in specific population subgroups. Identifies research needed to improve knowledge of the role of these micronutrients in human health. This book will be important to professionals in nutrition research and education.
Download or read book To Err Is Human written by Institute of Medicine and published by National Academies Press. This book was released on 2000-03-01 with total page 312 pages. Available in PDF, EPUB and Kindle. Book excerpt: Experts estimate that as many as 98,000 people die in any given year from medical errors that occur in hospitals. That's more than die from motor vehicle accidents, breast cancer, or AIDSâ€"three causes that receive far more public attention. Indeed, more people die annually from medication errors than from workplace injuries. Add the financial cost to the human tragedy, and medical error easily rises to the top ranks of urgent, widespread public problems. To Err Is Human breaks the silence that has surrounded medical errors and their consequenceâ€"but not by pointing fingers at caring health care professionals who make honest mistakes. After all, to err is human. Instead, this book sets forth a national agendaâ€"with state and local implicationsâ€"for reducing medical errors and improving patient safety through the design of a safer health system. This volume reveals the often startling statistics of medical error and the disparity between the incidence of error and public perception of it, given many patients' expectations that the medical profession always performs perfectly. A careful examination is made of how the surrounding forces of legislation, regulation, and market activity influence the quality of care provided by health care organizations and then looks at their handling of medical mistakes. Using a detailed case study, the book reviews the current understanding of why these mistakes happen. A key theme is that legitimate liability concerns discourage reporting of errorsâ€"which begs the question, "How can we learn from our mistakes?" Balancing regulatory versus market-based initiatives and public versus private efforts, the Institute of Medicine presents wide-ranging recommendations for improving patient safety, in the areas of leadership, improved data collection and analysis, and development of effective systems at the level of direct patient care. To Err Is Human asserts that the problem is not bad people in health careâ€"it is that good people are working in bad systems that need to be made safer. Comprehensive and straightforward, this book offers a clear prescription for raising the level of patient safety in American health care. It also explains how patients themselves can influence the quality of care that they receive once they check into the hospital. This book will be vitally important to federal, state, and local health policy makers and regulators, health professional licensing officials, hospital administrators, medical educators and students, health caregivers, health journalists, patient advocatesâ€"as well as patients themselves. First in a series of publications from the Quality of Health Care in America, a project initiated by the Institute of Medicine
Download or read book Martindale written by Alison Brayfield and published by . This book was released on 2020-05-22 with total page 4800 pages. Available in PDF, EPUB and Kindle. Book excerpt: Martindale: The Complete Drug Reference provides unbiased and evaluated information on drugs and medicines in use around the world. It is prepared by an experienced team of pharmacists and life scientists who use their professional expertise to select the most clinically relevant and appropriate information from reliable published sources.
Download or read book Mosby s Dental Drug Reference written by Tommy W. Gage and published by . This book was released on 2003 with total page 920 pages. Available in PDF, EPUB and Kindle. Book excerpt: "The CD-ROM provides 115 patient education handouts for drugs prescribed to dental patients that can be customized for your office. Available in English or Spanish. Also on the CD-ROM are 30 full-color images of oral pathologic conditions that may result from drugs patients are taking. New appendices include sample prescriptions and drugs affecting cytochrome P450 enzymes. Detailed coverage of many FDA-approved drugs for 2002, and it was reviewed by expert researchers, scientists, and dental healthcare professionals to ensure that all information is up to date and accurate."--Jacket
Download or read book Mosby s 2021 Nursing Drug Reference E Book written by Linda Skidmore-Roth and published by Elsevier Health Sciences. This book was released on 2020-02-29 with total page 1463 pages. Available in PDF, EPUB and Kindle. Book excerpt: Trusted for over 25 years, this portable, full-color drug reference is easy to navigate and provides safety features that help you practice knowledgeable, safe medication dispensing. Content on more than 5,000 generic and brand-name drugs covers almost every drug you are likely to encounter in clinicals. Side effects information, logically organized by body system and identified as common or life threatening, shows you the important and intricate signs to watch for during assessments. This guide also includes complete pharmacokinetic tables that explain the mechanism and absorption of the drug as well as the action, duration, and excretion of the drug. Whether you’re in the classroom or in clinicals, Mosby's 2021 Nursing Drug Reference, 34th Edition is the all-in-one drug reference you need. Content on more than 5,000 generic and brand-name drugs covers almost every drug you will encounter in clinicals. A Safety Alert feature icon highlights the most critical interactions and side effects that you must be aware of during clinicals. A Black Box Warning feature alerts you to FDA warnings of potentially life-threatening reactions. Bold heading and details on IV drug administration so students can easily find appropriate dosage and IV instructions to help them administer these drugs safely. Side effects information is logically organized by body system and identified as common or life threatening, alerting students to the signs to watch for during assessments. Nursing Process Framework organizes all nursing care steps so students learn how to easily and completely incorporate the nursing process into their clinical experiences. Cross-reference headers in the book listings and in the appendicies make it easier to find the drug content quickly and less likely that students will think a drug is missing if it’s not first found in the book. Complete pharmacokinetic tables explain the mechanism and absorption of the drug, as well as the action, duration, and excretion of the drug. NEW! Approximately 25 monographs on newly released, FDA-approved drugs give you the intricate details you need both in the classroom and clinicals. Each monograph includes new interactions, precautions, alerts, patient teaching instructions, and other need-to-know information — so you’ll feel confident in the accuracy of the information and in preventing medication dispensing errors. NEW! Up-to-date content on drug therapies provides you with instant access to the latest information.
Download or read book Making Medicines Affordable written by National Academies of Sciences, Engineering, and Medicine and published by National Academies Press. This book was released on 2018-03-01 with total page 235 pages. Available in PDF, EPUB and Kindle. Book excerpt: Thanks to remarkable advances in modern health care attributable to science, engineering, and medicine, it is now possible to cure or manage illnesses that were long deemed untreatable. At the same time, however, the United States is facing the vexing challenge of a seemingly uncontrolled rise in the cost of health care. Total medical expenditures are rapidly approaching 20 percent of the gross domestic product and are crowding out other priorities of national importance. The use of increasingly expensive prescription drugs is a significant part of this problem, making the cost of biopharmaceuticals a serious national concern with broad political implications. Especially with the highly visible and very large price increases for prescription drugs that have occurred in recent years, finding a way to make prescription medicinesâ€"and health care at largeâ€"more affordable for everyone has become a socioeconomic imperative. Affordability is a complex function of factors, including not just the prices of the drugs themselves, but also the details of an individual's insurance coverage and the number of medical conditions that an individual or family confronts. Therefore, any solution to the affordability issue will require considering all of these factors together. The current high and increasing costs of prescription drugsâ€"coupled with the broader trends in overall health care costsâ€"is unsustainable to society as a whole. Making Medicines Affordable examines patient access to affordable and effective therapies, with emphasis on drug pricing, inflation in the cost of drugs, and insurance design. This report explores structural and policy factors influencing drug pricing, drug access programs, the emerging role of comparative effectiveness assessments in payment policies, changing finances of medical practice with regard to drug costs and reimbursement, and measures to prevent drug shortages and foster continued innovation in drug development. It makes recommendations for policy actions that could address drug price trends, improve patient access to affordable and effective treatments, and encourage innovations that address significant needs in health care.
Download or read book Lippincott s Critical Care Drug Guide written by Marla J. De Jong and published by Lippincott Williams & Wilkins. This book was released on 2000 with total page 716 pages. Available in PDF, EPUB and Kindle. Book excerpt: Large type and uncluttered design provide quick access to pertinent information immediately. Organized into three parts, this guide provides quick access to essential and easy-to-use information required by CCRNs, CENs and CCNPs. Part 1 is a basic overview of information relating to common conditions such as cardiovascular and respiratory disorders, and provides guidelines for pharmacologic management. Part 2 lists drug monographs in alpha-organized format and focuses on critical care "Need to Know" facts. Part 3 provides you with a unique compendium of information and critical care resources presented in appendices format.
Download or read book Drug Synergism and Dose Effect Data Analysis written by Ronald J. Tallarida and published by CRC Press. This book was released on 2000-07-21 with total page 268 pages. Available in PDF, EPUB and Kindle. Book excerpt: Not since this author's bestselling Manual of Pharmacologic Calculation has there been an available reference for drug data analysis. Incorporating the most relevant parts of that work, Drug Synergism and Dose-Effect Data Analysis focuses on drug combinations and all the quantitative analyses needed to analyze drug combination dose-effect data and to design experiments with two or more compounds. The book contains the statistical methods, the theory, and the computation algorithms needed to analyze single and combination drug data. Numerous examples accompany a presentation that illustrates the calculations and experimental design considerations for modern drug analysis.
Download or read book Profiles of Drug Substances Excipients and Related Methodology written by Harry G. Brittain and published by Academic Press. This book was released on 2011-09-06 with total page 360 pages. Available in PDF, EPUB and Kindle. Book excerpt: Volumes in this widely revered series present comprehensive reviews of drug substances and additional materials, with critical review chapters that summarize information related to the characterization of drug substances and excipients. This organizational structure meets the needs of the pharmaceutical community and allows for the development of a timely vehicle for publishing review materials on this topic. The scope of the Profiles series encompasses review articles and database compilations that fall within one of the following six broad categories: Physical profiles of drug substances and excipients; Analytical profiles of drug substances and excipients; Drug metabolism and pharmacokinetic profiles of drug substances and excipients; Methodology related to the characterization of drug substances and excipients; Methods of chemical synthesis; and Reviews of the uses and applications for individual drug substances, classes of drug substances, or excipients. - Presents comprehensive reviews covering all aspects of drug development and formulation of drugs - Profiles creatine monohydrate and fexofenadine hydrochloride, as well as five others - Meets the information needs of the drug development community
Download or read book Drug Safety written by United States. General Accounting Office and published by . This book was released on 2001 with total page 12 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book A to Z Drug Facts written by David S. Tatro 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: Alphabetically organized, this drug reference integrates successful drug therapy and patient care. Monographs are divided into pharmacological and patient care considerations, and include indications, dosages, and side effects. Includes up-to-date information on more than 4,500 new and orphan drugs. Side effects are organized by body system. 839 illustrations.
Download or read book Bottle of Lies written by Katherine Eban and published by HarperCollins. This book was released on 2020-06-23 with total page 523 pages. Available in PDF, EPUB and Kindle. Book excerpt: A NEW YORK TIMES BESTSELLER * New York Times Notable Book * Best Book of the Year: New York Public Library, Kirkus Reviews, Science Friday With a new postscript by the author From an award-winning journalist, an explosive narrative investigation of the generic drug boom that reveals fraud and life-threatening dangers on a global scale—The Jungle for pharmaceuticals Many have hailed the widespread use of generic drugs as one of the most important public-health developments of the twenty-first century. Today, almost 90 percent of our pharmaceutical market is comprised of generics, the majority of which are manufactured overseas. We have been reassured by our doctors, our pharmacists and our regulators that generic drugs are identical to their brand-name counterparts, just less expensive. But is this really true? Katherine Eban’s Bottle of Lies exposes the deceit behind generic-drug manufacturing—and the attendant risks for global health. Drawing on exclusive accounts from whistleblowers and regulators, as well as thousands of pages of confidential FDA documents, Eban reveals an industry where fraud is rampant, companies routinely falsify data, and executives circumvent almost every principle of safe manufacturing to minimize cost and maximize profit, confident in their ability to fool inspectors. Meanwhile, patients unwittingly consume medicine with unpredictable and dangerous effects. The story of generic drugs is truly global. It connects middle America to China, India, sub-Saharan Africa and Brazil, and represents the ultimate litmus test of globalization: what are the risks of moving drug manufacturing offshore, and are they worth the savings? A decade-long investigation with international sweep, high-stakes brinkmanship and big money at its core, Bottle of Lies reveals how the world’s greatest public-health innovation has become one of its most astonishing swindles.
Download or read book Physician s Drug Handbook written by Michael F. Beers and published by Lippincott Raven. This book was released on 2005 with total page 1396 pages. Available in PDF, EPUB and Kindle. Book excerpt: Physician's Drug Handbook features alphabetically organized monographs on over 900 generic and 2,000 trade name drugs. Each entry includes generic name, U.S. and Canadian trade names, pharmacologic and therapeutic classes, pregnancy risk category, controlled substance schedule, drug forms and strengths, indications, dosages, pharmacodynamics, pharmacokinetics, contraindications and cautions, interactions, adverse reactions, prescriber and patient information, and subsections for pregnant, breast-feeding, pediatric, and geriatric patients. The Eleventh Edition has added more than 50 new drugs, dozens of new indications, herb-drug interactions, Alerts to highlight important information, off-label indications, dosage adjustments, and drug effects on laboratory tests. Readers receive drug updates by e-mail on eDrugInfo.com.
Download or read book Altering American Consciousness written by Caroline Jean Acker and published by Univ of Massachusetts Press. This book was released on 2004 with total page 428 pages. Available in PDF, EPUB and Kindle. Book excerpt: Virtually every American alive has at some point consumed at least one, and very likely more, consciousness altering drug. Yet, if the use of drugs is a constant in American history, the way they have been perceived has varied extensively. Just as the corrupting cigarettes of the early twentieth century ("coffin nails" to contemporaries) became the glamorous accessory of Hollywood stars and American GIs in the 1940s, only to fall into public disfavor later as an unhealthy and irresponsible habit, the social significance of every drug changes over time. The essays in this volume explore these changes, showing how the identity of any psychoactive substance -- from alcohol and nicotine to cocaine and heroin -- owes as much to its users, their patterns of use, and the cultural context in which the drug is taken, as it owes to the drug's documented physiological effects. Rather than seeing licit drugs and illicit drugs, recreational drugs and medicinal drugs, "hard" drugs and "soft" drugs as mutually exclusive categories, the book challenges readers to consider the ways in which drugs have shifted historically from one category to another. -- From publisher's description.
