The PharmaPendium Safety Module API allows developers to retrieve adverse event data that is normalized to MedDRA. This data is manually extracted from FDA and EMA approval documents and literature and is linked to the dose, dose type, route of administration, drug, source document, and year. PharmaPendium is Elsevier's collection of fully-searchable drug approval documents and extracted data for informing drug development decisions.
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So far, we don't have a record of any changes to this API