Fundamentals of Pediatric Drug Dosing
Editat de Iftekhar Mahmood, Gilbert Burckarten Limba Engleză Hardback – 10 noi 2016
With the advent of pediatric exclusivity, and requirements to conduct clinical studies in children, an emphasis has been placed on finding a safe and efficacious dose of a drug in children. Children are not ‘small adults’, and drug dosing in this population requires special consideration. There are subtle physiological and biochemical differences among neonates, infants, children, adolescents and adults and dosing in pediatrics requires proper understanding of these factors. Furthermore, dosing in children, as in adults, should be based on pharmacokinetic and pharmacodynamic data. This is an evolving area, as pediatric pharmacokinetic studies are becoming mandatory for getting approval of new drugs in this population.
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Specificații
ISBN-13: 9783319437521
ISBN-10: 3319437526
Pagini: 160
Ilustrații: VIII, 146 p. 12 illus. in color.
Dimensiuni: 155 x 235 x 15 mm
Greutate: 0.45 kg
Ediția:1st ed. 2016
Editura: Springer International Publishing
Colecția Adis
Locul publicării:Cham, Switzerland
ISBN-10: 3319437526
Pagini: 160
Ilustrații: VIII, 146 p. 12 illus. in color.
Dimensiuni: 155 x 235 x 15 mm
Greutate: 0.45 kg
Ediția:1st ed. 2016
Editura: Springer International Publishing
Colecția Adis
Locul publicării:Cham, Switzerland
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Cuprins
1. Pediatric Drug Development and the Regulatory Changes that are Creating the Science of Pediatric Dosing.- 2. Pediatric Physiology.- 3. Developmental Pharmacology: Impact on Pharmacokinetics and Pharmacodynamics of Drugs.- 4. Pediatric Clinical Trial Design and Dosing.- 5. Applicaton of Allometric Principles in Pediatric Drug Development.- 6. Population Pharmacokinetics in Pediatric Drug Development.- 7. Scaling Dose-Exposure-Response from Adults to Children.- 8. Applications of Physiologically-Based Pharmacokinetic (PBPK) Models for Pediatric Populations.- 9. Perinatal Pharmacology and Maternal/Fetal Dosing.
Recenzii
“The purpose is to review the evolution of pediatric research as it relates to pediatric drug dosing, an extremely worthy goal. … This book will meet the needs of these readers, particularly those interested in conducting research in children and students and clinicians who want to obtain a more in-depth understanding of dosing medications in pediatric patients. … I am unaware of another book on this subject, particularly for individuals involved in developing and conducting research in this patient population.” (Ina Lee Calligaro, Doody's Book Reviews, February, 2017)
Notă biografică
Iftekhar Mahmood, Ph. D., is a clinical Pharmacologist at the Center for Biologic Evaluation and Research (CBER), FDA. He holds a Bachelor of Pharmacy degree and a Ph.D. degree in Pharmaceutical Sciences with specialization in pharmacokinetics. Dr. Mahmood joined the FDA in December 1993 and for more than 8 years served as a clinical pharmacologist dealing with neuro-pharmacology products in Center for Drug Evaluation and Research (CDER). Since last 10 years, Dr. Mahmood has been a clinical pharmacologist for therapeutic proteins and blood products. Dr. Mahmood is involved in several CBER and CDER working groups. Dr. Mahmood has published more than 100 scientific papers in peer-reviewed scientific journals. He is author of the books “Interspecies Pharmacokinetic Scaling”, “Pediatric Pharmacology and Pharmacokinetics”, and “Pharmacokinetic Allometric Scaling in Pediatric Drug Development”. Dr. Mahmood is the recipient of several CDER Intramural Research Grantsas well as the recipient of several CDER and CBER awards.
Division of Hematology Clinical Review Branch, Office of Blood Review & Research (OBRR), Center for Biologics Evaluation and Research, Food & Drug Administration, 10903 New Hampshire Avenue, Silver Spring, MD 20993-0002, USA.
Dr. Gilbert Burckart is presently Associate Director for Pediatrics, Office of Clinical Pharmacology, U.S. Food and Drug Administration. Dr. Burckart received his B.S. in Pharmacy from the University of Pittsburgh in 1972, his Pharm.D. from the University of Kentucky in 1975, and did his pediatric residency at University of Kentucky in Lexington and Norton Children’s Hospital in Louisville. He served on the faculties of the State University of New York at Buffalo at Buffalo Children’s Hospital, the University of Tennessee at LeBonheur Children’s Hospital, and the University of Pittsburgh and the Pittsburgh Children’s Hospital. In 2003, he moved to the University ofSouthern California in Los Angeles, where he was Chairman of the Department of Pharmacy, and Professor of Pharmacy and Professor of Pediatrics.
Dr. Burckart has previously served as the President of the American College of Clinical Pharmacy, and as President of the American College of Clinical Pharmacology.
Dr. Burckart moved to the US FDA in 2008. His duties include participation in the FDA’s Pediatric Review Committee.
Division of Hematology Clinical Review Branch, Office of Blood Review & Research (OBRR), Center for Biologics Evaluation and Research, Food & Drug Administration, 10903 New Hampshire Avenue, Silver Spring, MD 20993-0002, USA.
Dr. Gilbert Burckart is presently Associate Director for Pediatrics, Office of Clinical Pharmacology, U.S. Food and Drug Administration. Dr. Burckart received his B.S. in Pharmacy from the University of Pittsburgh in 1972, his Pharm.D. from the University of Kentucky in 1975, and did his pediatric residency at University of Kentucky in Lexington and Norton Children’s Hospital in Louisville. He served on the faculties of the State University of New York at Buffalo at Buffalo Children’s Hospital, the University of Tennessee at LeBonheur Children’s Hospital, and the University of Pittsburgh and the Pittsburgh Children’s Hospital. In 2003, he moved to the University ofSouthern California in Los Angeles, where he was Chairman of the Department of Pharmacy, and Professor of Pharmacy and Professor of Pediatrics.
Dr. Burckart has previously served as the President of the American College of Clinical Pharmacy, and as President of the American College of Clinical Pharmacology.
Dr. Burckart moved to the US FDA in 2008. His duties include participation in the FDA’s Pediatric Review Committee.
Textul de pe ultima copertă
Focused on pediatric physiology, pharmacology, pharmacokinetics and pharmacodynamics, this book illustrates the differences between the pediatric population and adults; knowledge of extreme importance not only during pediatric drug development but also in the clinical practice. Physicians, nurses, clinical pharmacologists, researchers and healthcare professionals will find this an invaluable resource.
With the advent of pediatric exclusivity, and requirements to conduct clinical studies in children, an emphasis has been placed on finding a safe and efficacious dose of a drug in children. Children are not ‘small adults’, and drug dosing in this population requires special consideration. There are subtle physiological and biochemical differences among neonates, infants, children, adolescents and adults and dosing in pediatrics requires proper understanding of these factors. Furthermore, dosing in children, as in adults, should be based on pharmacokinetic and pharmacodynamic data. This is an evolving area, as pediatric pharmacokinetic studies are becoming mandatory for getting approval of new drugs in this population.
With the advent of pediatric exclusivity, and requirements to conduct clinical studies in children, an emphasis has been placed on finding a safe and efficacious dose of a drug in children. Children are not ‘small adults’, and drug dosing in this population requires special consideration. There are subtle physiological and biochemical differences among neonates, infants, children, adolescents and adults and dosing in pediatrics requires proper understanding of these factors. Furthermore, dosing in children, as in adults, should be based on pharmacokinetic and pharmacodynamic data. This is an evolving area, as pediatric pharmacokinetic studies are becoming mandatory for getting approval of new drugs in this population.
Caracteristici
Collects information on physiological, pharmacological, and pharmacokinetic differences between the pediatric population and adults, providing a comprehensive overview to the reader Discusses the importance and complexities of clinical trial design in pediatrics Provides the reader with different aspects of modeling and simulation in pediatrics, which can be applied during drug development Describes the principles and application of allometry to the prediction of PK parameters as well as dose selection in pediatric population