National Adverse Events Following Immunisation (AEFI) reporting form

4 August 2016

Suspected adverse events that occur after having a vaccination can be reported to the TGA. These reports provide important information for the TGA's safety monitoring program.

A completed AEFI form can be submitted to the TGA via:

Fax +61 2 6232 8392

Therapeutic Goods Administration
PO Box 100
Woden ACT 2606

For general privacy information, see Privacy.

AEFI reporting form

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