On November 6, 1995, the Institute of Medicine's Vaccine Safety Forum convened a workshop on detecting and responding to adverse events following vaccination. Workshop speakers and participants discussed the difficulties in detecting adverse events, current adverse events detection and response methods and procedures, suggestions for improving the means of detecting and responding to adverse events following vaccination, and future areas of research. This document represents a summary of that workshop.
- Vaccine Safety Forum
- Copyright
- Preface
- Contents
- Detecting and Responding to Adverse Events Following Vaccination: Workshop Summary
- EXECUTIVE SUMMARY
- INTRODUCTION
- DIFFICULTIES IN DETECTING ADVERSE EVENTS FOLLOWING VACCINATION
- CURRENT ADVERSE EVENT DETECTION AND RESPONSE PROCEDURES
- Vaccine Adverse Event Reporting System
- Large Linked Databases
- Surveillance by Vaccine Manufacturers
- Food and Drug Administration
- IMPROVING DETECTION OF AND RESPONSE TO ADVERSE EVENTS
- Increasing Reporting to VAERS
- Improving the Quality of Information in VAERS
- Improving Vaccine Lot Information
- Improving the Usefulness of LLDB Data
- Clinical Trials
- Comparison Studies
- ADDITIONAL AREAS FOR RESEARCH
- REFERENCES
- WORKSHOP AGENDA
- INSTITUTE OF MEDICINE VACCINE SAFETY FORUM
- PARTICIPANTS
- Research to Identify Risks for Adverse Events Following Vaccination: Biological Mechanisms and Possible Means of Prevention
- EXECUTIVE SUMMARY
- INTRODUCTION
- IMMUNE RESPONSE TO VACCINE ANTIGENS
- GENETIC FACTORS AFFECTING DEVELOPMENT OF AUTOIMMUNITY
- RESEARCH ON IDENTIFYING POPULATIONS AT RISK FOR ADVERSE EVENTS
- Arthritis and Rubella Vaccine
- Anaphylaxis and Measles, Mumps, and Rubella Vaccine
- Convulsions and DPT
- High-Titer Measles Vaccine
- Multiple Sclerosis or Guillain-Barre Syndrome and Vaccines
- Multiple-Antigen Vaccination and Adverse Immune Responses
- RESEARCH OPPORTUNITIES
- REFERENCES
- WORKSHOP AGENDA
- INSTITUTE OF MEDICINE VACCINE SAFETY FORUM
- PARTICIPANTS
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