Individual Patient Data Meta-Analysis to address Adverse Drug Events across the continuum of care
Description
Overall objectives:
- To conduct an individual patient data meta-analysis (IPD-MA) of studies with clinically adjudicated adverse drug events (ADEs)
- To create a pooled dataset of patient characteristics and ADEs from studies that submitted their data
- To conduct research using this pooled dataset aiming to reducing the occurrence off ADEs
Who is the principal investigator?
Dr. Fatma Karapinar-Çarkit and Dr. Daniala Weir (University Utrecht)
Team
Dr. Thomas Kempen
Dr. Sophie Bots
Dr. Ania Syrowatka
Dr. Joanna Klopotowska
Dr. Zuzana Ocovska
Dr. Robyn Tamblyn
Dr. Emily McDonald
Dr. Brooke Levis
Dr. Lisa McCarthy
Dr. Corrine Hohl
Dr. Catriona Cahir
Dr. Lina Heier
Who is collaborating?
Utrecht UMC
Amsterdam UMC
Charles University (Prague)
McGill University (Montreal)
University of Toronto (Toronto)
University of British Columbia (Vancouver)
Royal College of Surgeons in Ireland University (Dublin)
Are we looking for students or researchers to collaborate on this project?
We offer both short-and long-term internships for students interested in areas such as adverse drug reactions, adverse drug events, medication safety in general.
Also, visit our Vacancies page.
Contact for internship or collaboration and general questions
Dr. Karapinar-Carkit (f.karapinar@mumc.nl) and Dr. Daniala Weir (d.l.weir@uu.nl)