1. Pouliot A, Vaillancourt R, Stacey D, Suter P. Defining and identifying concepts of medication literacy: an international perspective. Res Soc Adm Pharm. 2018;14(9):797–804. https://doi.org/10.1016/j.sapharm.2017.11.005.
2. Puil L, Lexchin J, Bero L, Mangin D, Hallgreen CE, Wong GWK, Mintzes B. The impact of post-market regulatory safety advisories on patients, prescribers, and the healthcare system. Cochrane Database Syst Rev. 2019;(12) https://doi.org/10.1002/14651858.CD013510.
3. U.S. Food and Drug Administration. FDA Adverse Event Reporting System (FAERS) Public Dashboard; 2021. https://www.fda.gov/drugs/questions-and-answers-fdas-adverse-event-reporting-system-faers/fda-adverse-event-reporting-system-faers-public-dashboard. Accessed 03 April 2023.
4. European Medicines Agency. Online access to suspected side-effect reports; n.d.. https://www.adrreports.eu/en/. Accessed 03 April 2023.
5. Australian Government Department of Health and Aged Care Therapeutic Goods Administration. Database of Adverse Event Notifications (DAEN); 2023. https://www.tga.gov.au/safety/safety/safety-monitoring-daen-database-adverse-event-notifications/database-adverse-event-notifications-daen. Accessed 16 Feb 2023.