Read the reporting adverse events overview to learn more, including what type of details should be included in a report, what will happen to a report once we receive it, and other frequently asked questions.
You can also find a list of adverse events that have already been reported to the TGA in the Database of Adverse Event Notifications (DAEN).
-
PageReport counterfeit products, suspicious or illegal activity, or make a complaint about non-compliant advertising.
-
PageYou can report a side effect, reaction or other problem with a therapeutic good. Your report can help keep others safe.
-
PageReport an adverse event or problem related to a medicine, vaccine or medical device as a health professional.
-
PageAs the sponsor of a medicine or a medical device in Australia, you have a responsibility to report adverse events.
Topics