Buch, Englisch, 680 Seiten, Format (B × H): 178 mm x 254 mm
Buch, Englisch, 680 Seiten, Format (B × H): 178 mm x 254 mm
ISBN: 978-3-031-51088-5
Verlag: Springer
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.
Zielgruppe
Graduate
Autoren/Hrsg.
Fachgebiete
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Pharmazie
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizinische Fachgebiete Pharmakologie, Toxikologie
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizin, Gesundheitswesen Public Health, Gesundheitsmanagement, Gesundheitsökonomie, Gesundheitspolitik
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Zahnmedizin
- Wirtschaftswissenschaften Betriebswirtschaft Bereichsspezifisches Management Betriebliches Gesundheitsmanagement
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Pflege Krankenpflege
Weitere Infos & Material
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.