The Detection of New Adverse Drug Reactions

Chapter 1 Introduction

Chapter 2 The Methodology of the Collection of Adverse Event Data in Clinical Trials

Chapter 3 Laboratory Investigations

Chapter 4 The Diagnosis of Adverse Medical Events Associated with Drug Treatment

Chapter 5 The Pre-marketing Establishment of the Side-effect Profile of a New Drug

Chapter 6 Post-marketing Surveillance (PMS)

Chapter 8 The Ethical Problems of a Pharmaceutical Physician

Chapter 9 The Collection, Storage, Retrieval and Management of Adverse Drug Reaction Data and Adverse Event Data

Chapter 10 The Regulations Concerning Adverse Reactions