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National Adverse Events Following Immunisation (AEFI) reporting form
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
For general privacy information, see Privacy.