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:
adr.reports@tga.gov.au | |
Fax | +61 2 6232 8392 |
Therapeutic Goods Administration PO Box 100 Woden ACT 2606 Australia |
For general privacy information, see Privacy.
Supporting documents
National Adverse Events Following Immunisation (AEFI) reporting form
[Word, 261.6 KB]
National Adverse Events Following Immunisation (AEFI) reporting form
[PDF, 187.09 KB]