Adverse Event Reporting

Adverse Event Reporting is a regulatory and safety-monitoring process in clinical research and healthcare practice that systematically documents, evaluates, and communicates unexpected or harmful medical occurrences associated with therapeutic interventions to ensure patient safety, regulatory compliance, and quality improvement.

2.4K

Publications

146.8K

Citations

10.6K

Authors

3K

Institutions

Publications per year

2017–2026

808

Authors

10.6K

  1. EB
    Ethan Basch

    University of North Carolina at Chapel Hill, United States

    30 publications · 4.6K citations

    25

    h-index

  2. AJ
    Alan J. Forster

    University of Ottawa, Canada

    19 publications · 2.4K citations

    18

    h-index

  3. BB
    Bryce B. Reeve

    University of North Carolina at Chapel Hill, United States

    20 publications · 3.4K citations

    16

    h-index

  4. RB
    Robert Ball

    Center for Biologics Evaluation and Research, United States

    16 publications · 1K citations

    16

    h-index

  5. ER
    Emanuel Raschi

    University of Bologna, Italy

    18 publications · 925 citations

    16

    h-index

1–5 of 10.6K

Venues

  1. Drug Safety

    98 publications · 5K citations

    42

    h-index

  2. PubMed

    Repository · 117 publications · 7.2K citations

    36

    h-index

  3. BMJ Quality & Safety

    43 publications · 5.1K citations

    34

    h-index

  4. BMJ Quality & Safety

    42 publications · 2.6K citations

    28

    h-index

  5. Pharmacoepidemiology and Drug Safety

    51 publications · 3.7K citations

    27

    h-index

1–5