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TOPIC 3: DIAGNOSIS AND MANAGEMENT OF ADVERSE DRUG REACTIONS
Session Chair(s)
Gaby L. Danan, MD, PHD
Pharmacovigilance Expert, GLD, France
Phil Tregunno
Deputy Director - Patient Safety Monitoring, Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom
Pharmacovigilance is first based on the medical assessment of the adverse events passively or actively collected in organised schemes. It is then essential to be able to identify consistently the nature of events and their seriousness as well as to assess causality with the suspect drug(s). This session will provide some clues for the recognition of two serious events involving target organs of drug toxicity.
Speaker(s)
Gaby L. Danan, MD, PHD
Pharmacovigilance Expert, GLD, France
Medical Evaluation of Adverse Drug Reactions
Gaby L. Danan, MD, PHD
Pharmacovigilance Expert, GLD, France
Drug-Induced Liver Injury
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