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Books in Drug adverse reactions and interactions

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    • Computational Methods in Medicinal Chemistry, Pharmacology, and Toxicology

      • 1st Edition
      • June 18, 2025
      • Muhammad Ishfaq
      • English
      • Paperback
        9 7 8 0 4 4 3 3 3 0 2 4 7
      • eBook
        9 7 8 0 4 4 3 3 3 0 2 5 4
      Computational Methods in Medicinal Chemistry, Pharmacology, and Toxicology is a comprehensive resource that offers an advanced overview of computational techniques employed in drug discovery, design, and toxicity prediction. The book discusses various topics, including molecular modeling, virtual screening, machine learning, and network pharmacology. It serves as an essential guide for researchers, practitioners, and students in pharmacology, toxicology, medicinal chemistry, bioinformatics, and systems biology fields, showcasing practical applications and future perspectives on new technologies. In addition to covering computational approaches, the book provides real-world examples of drug discovery, candidate optimization, and safety assessment.Other sections explore computer applications in pharmacology and toxicology and discusses the importance of these methods in advancing medicinal research.

    • Essentials of Translational Pediatric Drug Development

      • 1st Edition
      • July 22, 2024
      • Elke Gasthuys + 3 more
      • English
      • Paperback
        9 7 8 0 3 2 3 8 8 4 5 9 4
      • eBook
        9 7 8 0 3 2 3 9 0 4 2 9 2
      Essentials of Translational Pediatric Drug Development: From Past Needs to Future Opportunities provides integrated and up-to-date insights relevant for both translational researchers and clinicians active in the field of pediatric drug development. The book covers all key aspects from different stakeholder perspectives, providing a literature overview and careful reflection on state-of-the-art approaches. It will be an ideal guide for researchers in the field who are designing and performing high quality, innovative pediatric-adapted drug development by helping them define needs/challenges and possible solutions that advance and harmonize pediatric drug development.Despite the broad consensus that children merit the same quality of drug treatment as any other age group, children remain frequently neglected during drug research and development. Even with the adoption of multiple legislations addressing this problem, the lack of efficacy and safety data of marketed as well as newly developed drugs still remain in the pediatric population.

    • Deprescribing and Polypharmacy in an Aging Population

      • 1st Edition
      • August 22, 2023
      • Ali Elbeddini
      • English
      • Paperback
        9 7 8 0 3 2 3 9 9 1 3 8 4
      • eBook
        9 7 8 0 3 2 3 9 9 3 8 1 4
      Deprescribing and Polypharmacy in an Aging Population supports healthcare professionals across global healthcare institutions in reducing polypharmacy-related drug replated problems (DRPs) by working with patients, families, interprofessional healthcare professionals, and educational institutions to develop, implement, test, improve upon, and educate on strategies for deprescribing and optimizing patient safety. Polypharmacy, the use of multiple medications at the same time by one person, is very common in various patient populations, including those who lack primary physicians, patients with mental health conditions, patients with multiple chronic conditions, and in the aging population.

    • Handbook of Basic and Clinical Ocular Pharmacology and Therapeutics

      • 1st Edition
      • July 25, 2022
      • Sunny Ohia + 1 more
      • English
      • Paperback
        9 7 8 0 1 2 8 1 9 2 9 1 7
      • eBook
        9 7 8 0 1 2 8 1 9 2 9 2 4
      Handbook of Basic and Clinical Ocular Pharmacology and Therapeutics provides a review of the basic anatomy, physiology, biochemistry and pathology of the eye with a focus drug therapy, drug delivery and use of therapeutic medical miniature devices. An understanding of the pharmacological actions of drugs acting on the eye requires the student and health care practitioner to learn additional principles in basic and clinical sciences that are unique to this organ. As a sensory organ, the eye is relatively inaccessible to the systemic circulation due to the blood-vitreous, blood-aqueous and blood-retinal barriers. Consequently, the administration of drugs for therapeutic effects in the eye necessitates an understanding of physico-chemical properties of the molecules and pharmacokinetic principles involved in the access to its site of action via topical, intracameral and intravitreal administration. This book includes information on the general principles of pharmacokinetics and pharmacodynamics of drugs as it pertains to the eye and in combating ocular disorders and diseases. Using a disease-themed approach, the book discusses basic and clinical pharmacological principles involved in the therapy of these diseases including the ocular side effect of systemically-adminis... drugs, drugs used in ophthalmic surgery and miscellaneous agents, the therapeutic utility of biologics, drug conjugates, combination products, gene and cellular therapy are also covered. Handbook of Basic and Clinical Ocular Pharmacology and Therapeutics is useful as a primary and secondary source of reference for up-to-date information about the pharmacological mechanisms of action, pharmacokinetics, side effects, drug-drug interactions and therapeutic indications of drugs for pharmacologists, pharmaceutical scientists, students in the health care disciplines (nursing, pharmacy, optometry, medical), and practitioners in optometry and ophthalmology.

    • Atkinson's Principles of Clinical Pharmacology

      • 4th Edition
      • October 16, 2021
      • Shiew-Mei Huang + 3 more
      • English
      • Hardback
        9 7 8 0 1 2 8 1 9 8 6 9 8
      • eBook
        9 7 8 0 1 2 8 1 9 8 8 4 1
      **Selected for Doody’s Core Titles® 2024 in Pharmacology**Atkins... Principles of Clinical Pharmacology, Fourth Edition is the essential reference on the pharmacologic principles underlying the individualization of patient therapy and contemporary drug development. This well-regarded survey continues to focus on the basics of clinical pharmacology for the development, evaluation and clinical use of pharmaceutical products while also addressing the most recent advances in the field. Written by leading experts in academia, industry, clinical and regulatory settings, the fourth edition has been thoroughly updated to provide readers with an ideal reference on the wide range of important topics impacting clinical pharmacology.

    • Nutraceuticals

      • 2nd Edition
      • January 27, 2021
      • Ramesh C. Gupta + 2 more
      • English
      • Hardback
        9 7 8 0 1 2 8 2 1 0 3 8 3
      • eBook
        9 7 8 0 1 2 8 2 1 2 4 6 2
      Nutraceuticals: Efficacy, Safety and Toxicity, Second Edition, brings together everything that is currently known about nutraceuticals and their potential toxic effects. The book introduces readers to nutraceuticals, herbal medicines, Ayurvedic medicines, prebiotics, probiotics, adaptogens, and their uses and specific applications. This essential reference discusses the mechanism of action for the judicious use of these nutraceuticals and the best tools for their evaluation before detailing the safety and toxicity of nutraceuticals and interactions with other therapeutic drugs. Finally, and crucially, regulatory aspects from around the world are covered. Completely revised and updated, this updated edition provides toxicologists, pharmacologists, pharmaceutical scientists, and those interested in medicinal plants and natural products with a comprehensive overview of the most effective tools upon which to evaluate the safety and toxicity of nutraceuticals, prebiotics, probiotics and alternative medicines.

    • Drug Delivery Devices and Therapeutic Systems

      • 1st Edition
      • November 7, 2020
      • Eric Chappel
      • English
      • Paperback
        9 7 8 0 1 2 8 1 9 8 3 8 4
      • eBook
        9 7 8 0 1 2 8 1 9 8 3 9 1
      Drug Delivery Devices and Therapeutic Systems examines the current technology and innovations moving drug delivery systems (DDS) forward. The book provides an overview on the therapeutic use of drug delivery devices, including design, applications, and a description of the design of each device. While other books focus on the therapy, the primary emphasis in this book is on current technologies for DDS applications, including microfluidics, nanotechnology, biodegradable hydrogel and microneedles, with a special emphasis on wearable DDS. As part of the Developments in Biomedical Engineering and Bioelectronics series, this book is written by experts in the field and informed with information directly from manufacturers. Pharmaceutical scientists, medical researchers, biomedical engineers and clinical professionals will find this an essential reference.

    • Drug Safety in Developing Countries

      • 1st Edition
      • June 3, 2020
      • Yaser Mohammed Al-Worafi
      • English
      • Paperback
        9 7 8 0 1 2 8 1 9 8 3 7 7
      • eBook
        9 7 8 0 1 2 8 2 0 4 1 2 2
      Drug Safety in Developing Countries: Achievements and Challenges provides comprehensive information on drug safety issues in developing countries. Drug safety practice in developing countries varies substantially from country to country. This can lead to a rise in adverse reactions and a lack of reporting can exasperate the situation and lead to negative medical outcomes. This book documents the history and development of drug safety systems, pharmacovigilance centers and activities in developing countries, describing their current situation and achievements of drug safety practice. Further, using extensive case studies, the book addresses the challenges of drug safety in developing countries.

    • Medicinal Plants in Asia and Pacific for Parasitic Infections

      • 1st Edition
      • October 20, 2020
      • Christophe Wiart
      • English
      • Paperback
        9 7 8 0 1 2 8 1 6 8 1 1 0
      • eBook
        9 7 8 0 1 2 8 1 6 8 1 2 7
      Medicinal Plants in Asia and Pacific for Parasitic Infections: Botany, Ethnopharmacology, Molecular Basis, and Future Prospect offers an in-depth view into antiprotozoal pharmacology of natural products from medicinal plants in Asia with an emphasis on their molecular basis, cellular pathways, and cellular targets. This book provides scientific names, botanical classifications, botanical description, medicinal uses, chemical constituents and antiprotozoal activity of more than 100 Asian medicinal plants, with high quality original botanical plates, chemical structures, and pharmacological diagrams and lists hundreds of carefully selected references. It also examines the pharmacological and medicinal applications of Asian medicinal plants especially in drug development for protozoan prevention and treatment. Medicinal Plants in Asia and Pacific for Parasitic Infections is a research tool and resource for the discovery of leads for the treatment of protozoal diseases based on interrelated botanical, biochemical, ethnopharmacological... phylogenetic, pharmacological, and chemical information.

    • Post-Authorization Safety Studies of Medicinal Products

      • 1st Edition
      • June 19, 2018
      • Ayad K. Ali + 1 more
      • English
      • Hardback
        9 7 8 0 1 2 8 0 9 2 1 7 0
      • eBook
        9 7 8 0 1 2 8 0 9 2 0 8 8
      Post-Authorization Safety Studies of Medicinal Products: The PASS Book bridges the gap in the literature by providing a complete look at post-authorization safety studies and important pharmacoepidemiology and pharmacovigilance aspects. It covers various types and limitations of active surveillance programs, including the use of large databases and disparate data sources for rapid signal detection, as well as novel and advanced design and analysis approaches for causal interference from observational data. This book serves as an important reference for pharmacovigilance scientists and pharmacoepidemiologi... who are searching for the appropriate study design to answer safety research questions. Readers will be able to effectively and efficiently design and interpret findings from post-authorization safety studies with the goal of improving the benefit-risk balance of a drug in order to optimize patient safety.