Reporting adverse drug events to the Therapeutic Goods Administration
- PMID: 33664539
- PMCID: PMC7900275
- DOI: 10.18773/austprescr.2020.077
Reporting adverse drug events to the Therapeutic Goods Administration
Keywords: Therapeutic Goods Administration; adverse drug reaction reporting systems; drug-related side effects and adverse reactions.
Conflict of interest statement
Conflict of interest: none declared
References
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- Therapeutic Goods Administration. Half yearly performance snapshot: July to December 2019. Canberra: Commonwealth of Australia; 2020. https://www.tga.gov.au/publication/half-yearly-performance-snapshot-july... [cited 2021 Jan 4]
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- Mackay K. Showing the blue card: reporting adverse reactions. Aust Prescr 2005;28:140-2. 10.18773/austprescr.2005.107 - DOI
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- Wiktorowicz ME, Lexchin J, Paterson M, Mintzes B, Metge C, Light D, et al. Research networks involved in post-market pharmacosurveillance in the United States, United Kingdom, France, New Zealand, Australia, Norway and European Union: lessons for Canada. Edmonton (AB): Canadian Patient Safety Institute; 2008. https://www.patientsafetyinstitute.ca/en/toolsResources/ Research/commis... researchResults.aspx [cited 2021 Jan 4]
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