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in drug response of the co-administered drugs. Using illustrative case studies and examples, Drug-Drug Interactions for Therapeutic Biologics;
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and bioequivalence for specialty drug products. It describes various scientific approaches and regulatory requirements for manufacturers who;
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and bioequivalence for specialty drug products. It describes various scientific approaches and regulatory requirements for manufacturers who;
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With an emphasis on the fundamental and practical aspects of ADME for therapeutic proteins, this book helps readers strategize, plan and;
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There are few publications about drug interactions in chemotherapy and even less about pediatric oncology treatment. For this reason, the;
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reference is an essential drug-safety tool for patient care, particularly for those on many prescriptions. This new edition has been revised and;
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in integrating these technologies with drug discovery operations will fuel the engine for future innovations. This book cuts across the multiple areas;
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Internationally relied upon by medical practitioners for its unparalleled focus on adverse effects and cutaneous reactions, Litt's Drug;
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Internationally relied upon by medical practitioners for its unparalleled focus on adverse effects and cutaneous reactions, Litt's Drug;
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are available for specific diseases, how selected drugs produce therapeutic benefits, side effects that may occur when taking these drugs, and;
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risk factors before a drug is put to market. The book covers both clinical and nonclinical aspects for understanding drug-drug interactions as;
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The tools for detecting false positives, false negatives, and interference in interactions when testing and monitoring therapeutic drug use;
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updated to provide an overview of the last decade's numerous advances in analytical technologies for detection and quantification of drugs;
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interferences in using immunoassays for therapeutic drug monitoring. This book is essential reading for any clinician, fellow, or trainee who;
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explain their therapeutic use for different skin conditions. The final sections cover related topics such as cost effectiveness and quality;
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book on drug interactions. Based upon thousands of published papers and reports it: * Covers interactions between therapeutic drugs;
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, anti-microbial drug discovery, anti-biofilm therapeutics, and treatment regimes. Given its scope, the book represents a valuable asset for;
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chapter on probe cocktail studies has been included to highlight an important research tool for drug development. These chapters address material;
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Authored by renowned leaders in the field, this comprehensive volume covers all aspects of drug-drug interactions, including preclinical;
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, contraindications, dosage, side effects, pharmacokinetics, and adverse reactions for all approved cardiovascular drugs, including the newest therapeutic;
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sections for easy access: Drug interactions between AEDs; Drug interactions between AEDs and non-AEDs: Interactions affecting AEDs; and Drug;
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(chemical tests) for therapeutic drug monitoring and additional analytical techniques;
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For drugs with a narrow therapeutic index, therapeutic drug monitoring methods are essential for patient management. Although immunoassays;
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therapeutic serum levels, but places equal emphasis on high-alert agents with narrow therapeutic indexes. Each drug chapter is written by clinical;
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In the late 1980s, the median time for FDA to approve a new drug application (NDA) was 29 months. Industry, consumer groups, and FDA agreed;
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For drugs with a narrow therapeutic index, therapeutic drug monitoring methods are essential for patient management. Although immunoassays;
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