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View Rights PortalWolters Kluwer Law & Business delivers expert content and solutions in the areas of law, corporate compliance, health compliance, reimbursement, and legal education.
View Rights PortalTrinity Publishing NZ Ltd has been producing children's books since 1997 in Australasia whilst sailing in the South Pacific islands. Since 2018 we have also begun producing work for a European readership..We love visiting the place where our book subjects live and play.
View Rights PortalThe heroic story of the invention of antidepressants is a key part of the psychopharmaceutical turn. On Trial revolves around one of its pioneers, psychiatrist Roland Kuhn, who practiced in Münsterlingen, a state-run psychiatric hospital in Switzerland. Kuhn became famous for the 'discovery' of the first antidepressant, Tofranil, and more recently notorious for his numerous trials on often unsuspecting patients. Largely based on the extensive and previously inaccessible sources of Kuhn's private archive, the book delves into the early days of industry-sponsored clinical research in psychiatry. It examines how the clinic, patients, doctors, nursing staff, corporations, and authorities interacted in the trials. Conducted from the 1940s to 1980s, the Münsterlingen drug trials are historicised and situated in the period's evolving landscape of experimentation.
For 20 years, Drug Profiles has provided pharmacies with the best possible preparation,whether for the initial patient consultation when a drug is first prescribed or for providing advice on self-medication.■ more than 300 completely revised profiles on the most common active substances■ pictograms illustrating proper administration■ colour-coded patient information■ 31 new substance profilesEnabling pharmacists to provide their patients with expert advice on drug therapy.New: Important information and suggested wording for the “special information”column in the standardized medication plan required by German law since 2016.
For half a century, “Mutschler” has been the standard reference work on pharmacology and toxicology – always forward-looking and at the cutting edge. The 11th edition continues this approach: ■ Up-to-the-minute: new drugs, including biologicals, relevant guidelines in the context of evidence-based medicine ■ Clearly structured: completely new layout with the focus on indication-related pharmacotherapy; uniformly constructed concise chapters ■ Well-illustrated: with many figures and tables, completely revised ■ Easy to remember: readily understandable explanations – even of complex issues ■ Critical: objective, independent assessment of the clinical value of drugs and drug groups ■ Comprehensive: with short introductions into the principles of anatomy, physiology and pathophysiology in the individual chapters ■ Reliable: full coverage of the subjects usually tested in the medical and pharmaceutical state examinations The proven source for complete knowledge about the actions of drugs: for students and practitioners.
Many of us have to take drugs on a regular basis. But birth control pills, antibiotics, blood pressure medication, statins, diabetes medication, diuretics, anti-cancer drugs, gastrointestinal remedies or preparations against osteoporosis can all rob the body of essential vitamins and minerals. Often, drug-related micronutrient deficiency is the unrecognized cause of drug side effects. Symptoms such as exhaustion, depression, lack of concentration, irritability, sleep disorders or even dementia can result. Such problems can be prevented. Informed patients can take preventive measures, avoid unwanted side effects and make their drug therapy more effective. This guide explains what to watch out for and how to improve quality of life.
Several different pills prescribed by many different physicians: pharmacists encounter patients in this situation every day! What at first seems quite normal can, on closer inspection, be fraught with considerable risks of drug-related problems. Using this analysis as a core component of medication management, pharmacies have the key risk minimisation tool at their disposal. The authors guide their readers step by step through the discussions with the patient, the stages of the analysis, and the clear documentation. Case examples reflect on the content and illustrate implementation. The launch of pharmaceutical services enables an improvement in the safety and efficacy of customers‘ drug therapy in the pharmacy by means of the service „Extended medication counselling for polymedication“. Everything pharmacists need to know for the necessary medication analysis can be found in this book. This completely revised 2nd edition includes: - Important information on pharmaceutical services - Illustrative case examples on many indications - QR codes that lead to additional digital material Whether it is a detailed adjustment or a major change to medication: every patient benefits from the intervention.
Embryo research, cloning, assisted conception, neonatal care, saviour siblings, organ transplants, drug trials - modern developments have transformed the field of medicine almost beyond recognition in recent decades and the law struggles to keep up. In this highly acclaimed and very accessible book, now in its sixth edition, Margaret Brazier and Emma Cave provide an incisive survey of the legal situation in areas as diverse as fertility treatment, patient consent, assisted dying, malpractice and medical privacy. The book has been fully revised and updated to cover the latest cases, from assisted dying to informed consent; legislative reform of the NHS, professional regulation and redress; European regulations on data protection and clinical trials; and legislation and policy reforms on organ donation, assisted conception and mental capacity. Essential reading for healthcare professionals, lecturers, medical and law students, this book is of relevance to all whose perusal of the daily news causes wonder, hope and consternation at the advances and limitations of medicine, patients and the law.
Embryo research, cloning, assisted conception, neonatal care, saviour siblings, organ transplants, drug trials - modern developments have transformed the field of medicine almost beyond recognition in recent decades and the law struggles to keep up. In this highly acclaimed and very accessible book, now in its sixth edition, Margaret Brazier and Emma Cave provide an incisive survey of the legal situation in areas as diverse as fertility treatment, patient consent, assisted dying, malpractice and medical privacy. The book has been fully revised and updated to cover the latest cases, from assisted dying to informed consent; legislative reform of the NHS, professional regulation and redress; European regulations on data protection and clinical trials; and legislation and policy reforms on organ donation, assisted conception and mental capacity. Essential reading for healthcare professionals, lecturers, medical and law students, this book is of relevance to all whose perusal of the daily news causes wonder, hope and consternation at the advances and limitations of medicine, patients and the law.
Embryo research, cloning, assisted conception, neonatal care, saviour siblings, organ transplants, drug trials - modern developments have transformed the field of medicine almost beyond recognition in recent decades and the law struggles to keep up. In this highly acclaimed and very accessible book, now in its sixth edition, Margaret Brazier and Emma Cave provide an incisive survey of the legal situation in areas as diverse as fertility treatment, patient consent, assisted dying, malpractice and medical privacy. The book has been fully revised and updated to cover the latest cases, from assisted dying to informed consent; legislative reform of the NHS, professional regulation and redress; European regulations on data protection and clinical trials; and legislation and policy reforms on organ donation, assisted conception and mental capacity. Essential reading for healthcare professionals, lecturers, medical and law students, this book is of relevance to all whose perusal of the daily news causes wonder, hope and consternation at the advances and limitations of medicine, patients and the law.
With the huge number of medicinal products, it is easy to get lost in the pharmaceutical jungle. Clearly divided into over-the-counter medicines, prescription-only drugs and narcotics, the flashcards make it easier for beginners to learn the material. In this way, information about - Indications and mechanisms of action - Doses and available dosage forms - Instructions for use and special features can be repeated and consolidated. The new check section summarises the important side effects, interactions and contraindications. So now nothing stands in the way of successfully advising patients!
In the last stage of life, it is all about giving care in a professional manner and providing efficient relief of suffering. In addition to all the important key points about in-label use, this book consisting of drug monographs, includes: - Information about off-label indications with dosages, - Lists of the different dosage forms available, - Instructions about use in renal failure. A clear structure and icons enable rapid orientation in everyday practice. Focussed knowledge at your fingertips? That’s aporello!
Intoxicating? Intoxicating drugs are as old as mankind itself. Whether herbal or produced synthetically in a laboratory, their variety is almost limitless. And every year, more substances are added to the list. Niels Eckstein, who is a Professor of Drug Regulatory Affairs and Pharmacology and a long-standing expert in the narcotics scene, explores the abysses of the darknet and dealer hell, provides insider information, conducts interviews with dealers and producers, and offers profound insights into the bizarre, parallel world of intoxicating substances. At the same time, the author takes a thorough look at the chemistry of the different substance classes and the neurobiological basis of addiction. He also covers production and assesses the danger and addiction potential of designer drugs, BTM, NPS, medicinal drugs and doping substances. This book outlines the political and sociopolitical dimensions of the use of psychoactive substances, classifies them legally, describes risks, approaches, and help strategies, highlights routes out of drug problems and alternatives to drug prohibition, and comments on the opioid crisis in the United States and the „war on drugs.“ “I don‘t care how it‘s regulated: if he wants it and can pay for it, he gets it. If I get caught, I‘ll go to jail for a few years, whether it‘s for a kilo of coke, meph or testo, it doesn‘t matter.“ – In an interview with a dealer
The purpose of this book is to support general practitioners in finding the optimum, guideline-compliant therapy for their patients. The focus is on the clinical pictures of depression, psychosis as well as anxiety and sleep disorders and the handling of psychiatric emergencies. The reader will learn everything about the epidemiology, aetiology, diagnosis and medical treatment of these diseases, about switching therapy and about treatment in pregnancy and lactation. All the available psychotropic drugs and their pharmacological properties are described in detail – including key specific features of active substances and drug safety aspects. The table of substances in the appendix provides a clear summary of the information and simplifies the choice of the appropriate drug. The extras: - 13 factsheets with concise, summarised information to cope with tricky situations in the practice - The authors take the current treatment guidelines from Germany, Austria and Switzerland into account and name examples of proprietary medicinal products in the three countries.
Quick and comprehensive information on psychotropic drugs for adults. The “Clinical Handbook of Psychotropic Drugs” has become a standard reference and working tool for psychiatrists, psychologists, physicians, pharmacists, nurses, and other mental health professionals Independent, unbiased, uptodate Packed with unique, easy-to-read comparison charts and tables (dosages, side effects, pharmacokinetics, interactions …) for a quick overview of treatment options Succinct, bulleted information on all classes of medication: on- and off-label indications, (US FDA, Health Canada), recommended dosages, US and Canadian trade names, side effects, interactions, pharmacodynamics, precautions in the young, the elderly, and pregnancy, nursing implications, and much more – all you need to know for each class of drug Potential interactions and side effects summarized in comparison charts With instantly recognizable icons and in full color throughout, allowing you to fnd at a glance all the information you seek Clearly written patient information sheets available for download as printable PDF files
The new Teuscher covers the range of relevant areas of biogenic drug substances and medicinal products. In its time-honoured way, it conveys knowledge about the ■ Nature, origin and processing of crude drugs ■ Structure, biosynthesis and metabolism of the constituents ■ Preparation, pharmacology and use of the active substances ■ Dosage and side effects of the medicinal products derived from them The book deals with both classically produced and genetically engineered antibiotics, hormones, enzymes as well as blood and immunological products. Completely new chapters discuss cytokines, gene therapy, use of stem cells and traditional Chinese medicine. For generations, the textbook and companion for both students and fully qualified professionals!
The selection of a drug as well as the determination of the appropriate dosage form and the correct dosage, are two of the difficult tasks faced by a physician. This is particularly the case in paediatrics, where drugs are very often used outside of their licensed indications and hence no dosage recommendations are available. This standard work provides the reliable information that is needed: - Dosages of more than 300 medicines - Differentiation according to age and weight - Details of paediatric licensing - Off-label dosages according to the literature and experience - Contraindications and frequency of undesirable effects. Numerous active substances have been newly included in this 16th edition. Essential for physicians and also indispensable for pharmacists when checking prescriptions for plausibility.
The handling of drug interactions in the pharmacy has an important significance. A well-functioning interaction management system increases the safety of drug therapy for patients, promotes interdisciplinary exchange between physician and pharmacist, and boosts the skills of the local pharmacy. The author, an experienced practitioner, has developed standard templates for successfully communicating the most commonly occurring, clinically relevant interactions: - Decision aids in the form of flowcharts: When and how should the communication with the physician take place? - Aids to communication as sample forms that can be tailored to the individual pharmacy: What information does the physician need, what solutions does the pharmacy suggest? The forms cover both general interactions and specific interaction pairs and mechanisms: The appropriate solution for every interaction!
The consistent and evidence-based development of Korean medicine in many clinical application areas has significantly improved its international status in recent years. The basis for this development is one of the most important medical books in Korea, the „Donguibogam“, a clinical lexicon of applications compiled about 400 years ago; at that time the traditional work also enjoyed the highest recognition in China. In 2009 it was included in the „Memory of the World“ register of UNESCO. Even now after 400 years, it still serves as a manual for writing prescriptions for many physicians in Korea, and testifies that the understanding of nature and human disease patterns is still current and clinically applicable even in the modern industrialised world. This work provides ■ understanding for Korean medicine, ■ many selected medicinal formulations and their fields of application, ■ the description and evaluation of important traditional single remedies, ■ the corresponding drug monographs with information on analytical testing
The ward pharmacist in the hospital is like the airbag in a car. As part of a fail-safe system, they monitor and optimise the patient’s drug therapy. Ward pharmacists work hand in hand with medical and nursing staff. That situation is also reflected in this workbook. All the cases presented were patients who had been cared for, evaluated and documented by a physician-pharmacist duo or similar team with combined medical and pharmaceutical expertise. The editorial team considered it important to illustrate all critical indications typically encountered in a hospital. In assessing and selecting the examples, they were able to draw upon the many years’ experience of their pioneering work as hospital and ward pharmacists. Practical tips, checklists, comments and advice for working in the ward environment round off the individual chapters. By learning from actual cases, this book offers the unique chance to develop an instinct for the pitfalls of drug safety. That applies to those who have successfully completed further training in the field of “Medication Management in the Hospital” and for all who wish to ensure the optimum treatment for their patients through competent work in clinical pharmacy.
This book is available as an open access ebook under a CC-BY-NC-ND licence. Through its study of diabetes care in twentieth-century Britain, Managing diabetes, managing medicine offers the first historical monograph to explore how the decision-making and labour of medical professionals became subject to bureaucratic regulation and managerial oversight. Where much existing literature has cast health care management as either a political imposition or an assertion of medical control, this work positions managerial medicine as a co-constructed venture. Although driven by different motives, doctors, nurses, professional bodies, government agencies and international organisations were all integral to the creation of managerial systems, working within a context of considerable professional, political, technological, economic and cultural change.
The risks in connection with the unborn child and infant when prescribing and dispensing medicinal products are adequately known. However, a sound knowledge of safety issues and precise recommendations – rather than the blanket forgoing of medicinal treatment – is crucial for providing expert, professional advice. To meet this special responsibility, a reliable source of information is essential. The now ninth edition of this standard reference work provides the necessary professional knowledge not only for all physicians and pharmacists who wish to support their pregnant and breast-feeding patients through competent advice, but also for midwives: - Information about embryonal development and developmental disorders - Well over 1000 drug substances with all important medicinal products, assessed individually - Classification according to FDA and ADEC - Differentiated risk assessment, based on current literature - Personal recommendations of the experienced and well-known team of authors from the realms of gynaecology, paediatric medicine and clinical pharmacology. The new edition contains many new assessments from current studies.