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International Epidemiology Databases to Evaluate AIDS

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Clinical Outcomes

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The Clinical Outcomes and Pharmacovigilance WG is focused on research around adverse events among persons treated and untreated with HIV/AIDS in IeDEA. This Working Group consists of a representative from each IeDEA region, as well as program staff from DAIDS.

Purpose:

  • To optimize the aggregation of data on adverse events at IeDEA sites to allow for meaningful research on adverse events in diverse populations and across IeDEA regions.
  • To work within IeDEA, and with global partners, to develop a pharmacovigilence system at IeDEA sites to describe the incidence and prevalence of adverse events among persons receiving care.
  • To identify risk factors for adverse events.
  • To conduct research on the clinical management of adverse events in diverse patient populations

 

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