Adverse events (‘side effects’) reporting survey

5 April 2018

Investigation of adverse event ('side effect') reports is an important way that the Therapeutic Goods Administration (TGA) monitors the safety of medicines and vaccines used in Australia.

We are undertaking a survey to seek information about your experiences and attitudes towards key issues related to medicines and their use. Your responses will help the TGA improve the way we collect and use adverse event reports.

Both health professionals and consumers can provide vital first-hand information about their experiences with medicines and vaccines and how these have affected them.

All responses are anonymous and this survey does not collect any personally identifying information.

We'd ask that consumers and health professionals select the appropriate survey link below.

Consumer
(time estimate 5-10 minutes)
Health professional
(time estimate about 10 minutes)

The TGA thanks you for your time.