Will the future of pharmacovigilance be more automated?

Author:

Salvo Francesco12ORCID,Micallef Joelle3,Lahouegue Amir4,Chouchana Laurent5ORCID,Létinier Louis126,Faillie Jean-Luc7,Pariente Antoine12ORCID

Affiliation:

1. University of Bordeaux, Inserm, BPH, Team AHeaD, Bordeaux, France

2. CHU de Bordeaux, Service de Pharmacologie Medicale, Bordeaux, France

3. Pharmacovigilance Centre, Department of Clinical Pharmacology and Pharmacovigilance, University of Aix Marseille, INSERM UMR 1106 Institut de Neurosciences des Systèmes, Marseille, France

4. Department of Pharmacovigilance and Medical Information, Astrazeneca, Courbevoie, France

5. Regional Center of Pharmacovigilance, Pharmacology Department, Cochin Port Royal University Hospital, Paris, France

6. Synapse Medicine, Bordeaux, France

7. Inserm, Departement de Pharmacologie Medicale Et Toxicologie, Centre Regional de PV, Institut Desbrest D’epidemiologie Et de Sante Publique, CHU de Montpellier, Universite Montpellier, Montpellier, France

Publisher

Informa UK Limited

Subject

Pharmacology (medical),General Medicine

Reference50 articles.

1. EMA. Good pharmacovigilance practices; 2018. [cited Mar 17, 2023]. Available from: https://www.ema.europa.eu/en/human-regulatory/post-authorisation/pharmacovigilance/good-pharmacovigilance-practices

2. US FDA. Good pharmacovigilance practices and pharmacoepidemiologic assessment. [cited Mar 17, 2023]. Available from: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/good-pharmacovigilance-practices-and-pharmacoepidemiologic-assessment

3. Desogestrel and panic attacks - a new suspected adverse drug reaction reported by patients and health care professionals on spontaneous reports

4. What place for intelligent automation and artificial intelligence to preserve and strengthen vigilance expertise in the face of increasing declarations?

5. Under-reporting of adverse drug reactions in general practice

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