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Data availability All data used in this paper, including the raw and processed adverse event report dataset, adverse event ontology, drug ontology and the results of our analyses, are shared with the research community via the project website at The raw adverse event reports are obtained from the FDA Adverse Event Reporting System (FAERS): The raw adverse event ontology data from MedDRA are available at which requires subscription

Usage typically ranges from 2 to 4 weeks, depending on the goal and medical advice