Peter N. Bennett MD FRCP DPMSA, Morris J. Brown MA MSc FRCP's Clinical Pharmacology, 10th edition PDF

By Peter N. Bennett MD FRCP DPMSA, Morris J. Brown MA MSc FRCP FAHA FMedSci

ISBN-10: 0443102449

ISBN-13: 9780443102448

This publication is for college students, medical professionals and certainly for all all for evidence-based drug remedy. a data of pharmacological and healing rules is key if drugs/medicines are for use correctly and successfully for more and more trained and demanding sufferers. medical professionals who know how medicinal drugs get into the physique, how they produce their results, what occurs to them within the physique, and the way proof in their healing impact is classified, will pick out medicinal drugs extra skilfully, and use them extra effectively than those that don't. the foundations concerned are neither so a number of nor so obscure as to discourage any prescriber, together with these whose basic pursuits lie somewhere else than in pharmacology. All who use medicinal drugs can't get away both the ethical or the felony 'duty of care' to prescribe in an educated and liable way.Introductory first 3 sections conceal basic precept of medical pharmacology; 5 next sections hide drug therapy of ailment organised by way of physique systemRetains approachable type set by means of the unique writer, Professor LaurenceEmphasis all through is on evidence-based and secure drug prescribingNew color designIncreased use of graphicsSlightly shorter through removing of old-fashioned fabric

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Extra info for Clinical Pharmacology, 10th edition

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Human pharmacology (20 to 50 subjects) o healthy volunteers or volunteer patients, according to the class of drug and its safety o pharmacokinetics (absorption, distribution, metabolism, excretion) o pharmacodynamics (biological effects) where practicable, tolerability, safety, efficacy. Phase 2. Therapeutic exploration (50 to 300 subjects) o patients o pharmacokinetics and pharmacodynamic dose-ranging, in carefully controlled studies for efficacy and safety,11 which may involve comparison with placebo.

Such techniques can deliver hormones and autacoids in commercial amounts (such as insulin and growth hormone, erythropoietins, cell growth factors and plasminogen activators, interferons, vaccines and immune antibodies). Transgenic animals (that breed true for the gene) are also being developed as models for human disease as well as for production of medicines. The polymerase chain reaction (PCR) is a method of gene amplification that does not require living cells; it takes place in vitro and can produce (in a cost-effective way) commercial quantities of pure potential medicines.

A further risk is that this 'production line' approach could lead to a loss of integration of the established specialities (chemistry, biochemistry, pharmacology) and to an overall lack of understanding of how physiological and pathophysiological processes contribute to the interaction of drug and disease. New drugs could be targeted at selected groups of patients based on their genetic make-up. This concept of 'the right medicine for the right patient' is the basis of pharmacogenetics (see p. 105), the genetically determined variability in drug response.

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Clinical Pharmacology, 10th edition by Peter N. Bennett MD FRCP DPMSA, Morris J. Brown MA MSc FRCP FAHA FMedSci

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