Adverse Events

Consumers, health professionals and industry can access online information about adverse events to medicines that have been reported to the Therapeutic Goods Administration (TGA) since 1971.

The TGA and the New Zealand regulator, Medsafe, have worked together on the development of two publicly accessible databases that provide information on adverse events reported to each organisation. This project is part of the staged implementation of the move to becoming the Australia New Zealand Therapeutic Products Agency. Go to: