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The Detection of New Adverse Drug Reactions

  • Textbook
  • © 1988

Overview

Authors:
  1. M. D. B. Stephens
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Table of contents (10 chapters)

  1. Front Matter

    Pages i-xi
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  2. Introduction

    • M. D. B. Stephens
    Pages 1-27

  3. The Methodology of the Collection of Adverse Event Data in Clinical Trials

    • M. D. B. Stephens
    Pages 28-50

  4. Laboratory Investigations

    • M. D. B. Stephens
    Pages 51-72

  5. The Diagnosis of Adverse Medical Events Associated with Drug Treatment

    • M. D. B. Stephens
    Pages 73-114

  6. The Pre-marketing Establishment of the Side-effect Profile of a New Drug

    • M. D. B. Stephens
    Pages 115-142

  7. Post-marketing Surveillance (PMS)

    • M. D. B. Stephens
    Pages 143-200

  8. Drug Rechallenge

    • M. D. B. Stephens
    Pages 201-209

  9. The Ethical Problems of a Pharmaceutical Physician

    • M. D. B. Stephens
    Pages 210-215

  10. The Collection, Storage, Retrieval and Management of Adverse Drug Reaction Data and Adverse Event Data

    • M. D. B. Stephens
    Pages 216-243

  11. The Regulations Concerning Adverse Reactions

    • M. D. B. Stephens
    Pages 244-290

  12. Back Matter

    Pages 291-366
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Keywords

Bibliographic Information

  • Book Title: The Detection of New Adverse Drug Reactions

  • Authors: M. D. B. Stephens

  • DOI: https://doi.org/10.1007/978-1-349-09887-3

  • Publisher: Red Globe Press London

  • eBook Packages: Biomedical and Life Sciences, Biomedical and Life Sciences (R0)

  • Copyright Information: M.D.B. Stephens 1988

  • Edition Number: 2

  • Number of Pages: XI, 366

  • Additional Information: Previously published under the imprint Palgrave

  • Topics: Pharmacology/Toxicology

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