Principles and Practice of Pharmacovigilance and Drug Safety
Editat de Jimmy Jose, Anthony R. Cox, Vibhu Paudyalen Limba Engleză Hardback – 28 oct 2024
A holistic approach is taken with each chapter written from the perspective of a practitioner, industry personnel, researcher, or regulator, creating a synergy between drug safety, pharmacovigilance, and clinical practice. Chapters offer key material on adverse drug reactions, medication errors, prescribing safety, pharmacovigilance as well as data sources used in drug safety and pharmacovigilance. Each chapter is structured as a self-contained learning resource, with learning objectives, and worked cases. The book is suitable for undergraduate healthcare professions, postgraduate students, researchers, clinical practitioners – including those with prescribing responsibilities. It will also be useful for professionals moving from a clinical practice role to a specialist pharmacovigilance role. For those already in a pharmacovigilance role, the book offers insight into the theory and practice of drug safety and pharmacovigilance in clinical settings.
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Specificații
ISBN-13: 9783031510885
ISBN-10: 3031510887
Ilustrații: X, 680 p. 49 illus., 42 illus. in color.
Dimensiuni: 178 x 254 mm
Greutate: 1.2 kg
Ediția:1st ed. 2024
Editura: Springer International Publishing
Colecția Springer
Locul publicării:Cham, Switzerland
ISBN-10: 3031510887
Ilustrații: X, 680 p. 49 illus., 42 illus. in color.
Dimensiuni: 178 x 254 mm
Greutate: 1.2 kg
Ediția:1st ed. 2024
Editura: Springer International Publishing
Colecția Springer
Locul publicării:Cham, Switzerland
Cuprins
Part I. Principles and Practice of Pharmacovigilance and Drug Safety.- Overview of Drug Safety.- An Overview Of Immunological Reactions To Drugs.- Predisposing Factors for Adverse Drug Reactions.- Drug interactions and their management.- Economics of medication safety.- Principles Of Pharmacovigilance And Drug Regulation.- Clinical Trials Safety Data.- Causality Assessment in Pharmacovigilance.- A Retrospective and Prospective Look at Pharmacoepidemiology.- Communicating drug safety.- Patient involvement in pharmacovigilance.- Collaborative Approaches to Establishing and Implementing Pharmacovigilance Systems.- Part II. Safer Prescribing and Drug use in Practice.- Medication Errors in Healthcare.- Spontaneous Reporting Systems.- Methods to Identify, Prevent, Predict and Manage Adverse Drug Reactions in Pharmacovigilance and Clinical Practice.- Ethics in Pharmacovigilance.- Information Sources for Drug Safety and Communicating Risks in Clinical Practice.- Polypharmacy and Deprescribing.- Medication Prescribing and Safety Monitoring in Paediatrics.- Prescribing and Safety Monitoring in the Older Person.- Safe Prescribing and Drug use in Pregnancy and Breastfeeding.- Safe Prescribing in Patients with Renal and Hepatic Diseases.- Clinical Application of Pharmacogenomics in Improving Drug Safety.
Notă biografică
Dr. Jimmy Jose is an Associate Professor in Pharmacy Practice/Clinical Pharmacy in School of Pharmacy at the University of Nizwa, Sultanate of Oman. His previous major academic appointments include in International Medical University, Malaysia. Dr. Jose was awarded his PhD in the field of pharmacovigilance in 2008. He is an experienced teacher; MPharm, PharmD, M Pharm program (twinning program with University of Strathclyde) and BPharm. He was trained in clinical pharmacy at Michigan hospitals, USA, and has international clinical pharmacy hospital service experience in both Oman and India. His primary field of research is hospital-based pharmacovigilance. He has published a book chapter on pharmacovigilance and around 45 articles in peer reviewed journals. He serves as an Associate Editor for the journal Pharmacoepidemiology and Drug Safety and as an Editorial/Advisory Board Member for various other journals including International Journal of Pharmacy Practice and European Journal of Hospital Pharmacy.
Dr. Vibhu Paudyal is an Associate Professor of Clinical Pharmacy at University of Birmingham, UK. He trained with GlaxoSmithKline Pharmaceuticals soon after his BPharm degree and worked as an industrial pharmacist. He then undertook postgraduate MSc studies in Clinical Pharmacology and PhD in Pharmacy Practice. He is the Fellow of European Society of Clinical Pharmacy (ESCP) and past chair of ESCP Research Committee. He has researched and published extensively in the area of drug safety and pharmacovigilance including theory informed research to understand and mitigate medication errors in healthcare settings and on the perspectives of non-medical prescribers on safety. He has supervised 12 PhDs to completion and published over 120 peer reviewed published papers. He is also the Associate Editor of International Journal of Clinical Pharmacy. He has led externally funded research programmes including those funded by UK NIHR as the Chief Investigator.
Dr. Anthony Cox is a Reader in Clinical Pharmacy and Drug Safety at the University of Birmingham, UK. A hospital pharmacist with 20 years experience, he obtained his PhD in pharmacovigilance while working at the MHRA’s Yellow Card Centre West Midlands – where he holds an honorary position. He has published several book chapters on drug safety, and research on pharmacovigilance, the use of medicines by patients, and other areas related to safe use of medicines. He is the Head of Education at the School of Pharmacy and leads the Medicines Safety Research Group at the University of Birmingham. He has been an external examiner for three postgraduate pharmacovigilance programmes. He is a member of the editorial board of the International Journal of Pharmacy Practice, and serves on the Royal Pharmaceutical Society’s Medication Safety Working Group. He is a fellow of both the Royal Pharmaceutical Society and the British Pharmacological Society.
Textul de pe ultima copertă
The science of drug safety and pharmacovigilance has rapidly evolved in the 21st century. The knowledge and principles it contains are of increasing importance in clinical and practice settings. The aim of this book is to deal with the gap in knowledge about pharmacovigilance and drug safety, including the application of pharmacovigilance knowledge to individual patient cases in clinical practice.
A holistic approach is taken with each chapter written from the perspective of a practitioner, industry personnel, researcher, or regulator, creating a synergy between drug safety, pharmacovigilance, and clinical practice. Chapters offer key material on adverse drug reactions, medication errors, prescribing safety, pharmacovigilance as well as data sources used in drug safety and pharmacovigilance. Each chapter is structured as a self-contained learning resource, with learning objectives, and worked cases. The book is suitable for undergraduate healthcare professions, postgraduate students, researchers, clinical practitioners – including those with prescribing responsibilities. It will also be useful for professionals moving from a clinical practice role to a specialist pharmacovigilance role. For those already in a pharmacovigilance role, the book offers insight into the theory and practice of drug safety and pharmacovigilance in clinical settings.
A holistic approach is taken with each chapter written from the perspective of a practitioner, industry personnel, researcher, or regulator, creating a synergy between drug safety, pharmacovigilance, and clinical practice. Chapters offer key material on adverse drug reactions, medication errors, prescribing safety, pharmacovigilance as well as data sources used in drug safety and pharmacovigilance. Each chapter is structured as a self-contained learning resource, with learning objectives, and worked cases. The book is suitable for undergraduate healthcare professions, postgraduate students, researchers, clinical practitioners – including those with prescribing responsibilities. It will also be useful for professionals moving from a clinical practice role to a specialist pharmacovigilance role. For those already in a pharmacovigilance role, the book offers insight into the theory and practice of drug safety and pharmacovigilance in clinical settings.
Caracteristici
Offers insight into pharmacovigilance and drug safety in a clinical context rather than a more restricted focus Addresses UG/PG professions who will be future prescribers Each chapter is structured as a self-contained learning resource with learning objectives and worked cases