mi-erasmusmc / Dracula

A drug - adverse event mapper for clinicaltrials.gov
Apache License 2.0
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Dracula - A Clinical Trials Drug - Adverse Event Mapper

Dracula is a tool to be used in combination with the CTTI AACT database. It does two things: First, it generates an additional table called 'result_group_ingredient' that links the reported adverse events from the 'result_groups' table to an RxNorm ID of the drugs provided to the specific group for which this adverse event occurred. Second it adds a pt_code column to the reported_events table containing the MedDRA preferred term code for the specific adverse event.

Note: The master branch of this project should work, but the project as whole is still under construction. Although a decent effort is made to make this mapping decent, Dracula is not perfect. Contributions, comments and suggestions are very much welcome.

REQUIREMENTS

HOW TO RUN

OPTIONS

There are two extra settings that you can configure in the Settings.toml file.

  1. skip_meddra If you want to skip the MedDRA step set this to true.
  2. meddra_precision The meddra normalization relies on some fuzzy matching. Tell Dracula how fuzzy you would like to accept the results on a scale of 1-5 with 5 being super wild (wilder is also a bit slower).

TODO: