Concerns regarding the public health risks associated with unapproved peptide products

This is a joint statement from Dr Amanda Cuss, Acting Chief Medical Adviser – Health Products Regulation Group at the Therapeutic Goods Administration (TGA) and Professor Michael Kidd AO, Australia’s Chief Medical Officer (CMO).

Date published:
Media type:
Statement
Audience:
General public

Australia’s health leaders are increasingly concerned about the growing availability, promotion and use of unapproved peptide products in Australia.

Reports received by the Therapeutic Goods Administration (TGA), along with hospitalisation data from states and territories, have identified serious adverse effects associated with the use of unapproved peptides. These include:

  • liver damage
  • severe allergic reactions requiring hospitalisation, and
  • inflammation and other health complications requiring medical attention.

Unapproved peptide products that are not included in the Australian Register of Therapeutic Goods have not been evaluated by the TGA for safety, quality or effectiveness. These can include products containing BPC‑157, GHK‑Cu, TB‑500, retatrutide and CJC‑1295.

Read the full joint statement on the TGA website

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