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Documenting Adverse Events
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Adverse Events: Documenting, Recording, and Reporting
Identifying adverse drug event information in clinical notes with distributional semantic representations of context - ScienceDirect
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Monitoring adverse social and medical events in public health trials: assessing predictors and interpretation against a proposed model of adverse event reporting | Trials | Full Text
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Introduction to Collecting and Reporting Adverse Events in Clinical Research
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Adverse Event Detection, Processing, and Reporting - Registries for Evaluating Patient Outcomes - NCBI Bookshelf
Reporting Adverse Drug Events
Adverse Events Distribution
