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The Detection of New Adverse Drug Reactions

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Cover of 'The Detection of New Adverse Drug Reactions'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction
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    Chapter 2 The Methodology of the Collection of Adverse Event Data in Clinical Trials
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    Chapter 3 Laboratory Investigations
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    Chapter 4 The Diagnosis of Adverse Medical Events Associated with Drug Treatment
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    Chapter 5 The Pre-marketing Establishment of the Side-effect Profile of a New Drug
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    Chapter 6 Post-marketing Surveillance (PMS)
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    Chapter 7 Drug Rechallenge
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    Chapter 8 The Ethical Problems of a Pharmaceutical Physician
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    Chapter 9 The Collection, Storage, Retrieval and Management of Adverse Drug Reaction Data and Adverse Event Data
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    Chapter 10 The Regulations Concerning Adverse Reactions
Attention for Chapter 2: The Methodology of the Collection of Adverse Event Data in Clinical Trials
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Chapter title
The Methodology of the Collection of Adverse Event Data in Clinical Trials
Chapter number 2
Book title
The Detection of New Adverse Drug Reactions
Published by
Palgrave, London, January 1988
DOI 10.1007/978-1-349-09887-3_2
Book ISBNs
978-1-349-09889-7, 978-1-349-09887-3
Authors

M. D. B. Stephens

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