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Regulatoryretatrutidesemaglutidetgagray market

TGA reports torn oesophagus after unapproved retatrutide contained semaglutide

Laboratory testing found the black-market product held semaglutide at roughly eight times the concentration of approved semaglutide medicines.

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By Daniel Okafor · Regulatory Correspondent
Sep 14 04:33 ETSource: SSBCrack

The wire

  1. 01Australia's Therapeutic Goods Administration said a patient was hospitalised with a torn oesophagus after uncontrollable vomiting; testing of the product sold as retatrutide found semaglutide at about eight times the concentration of approved products.
  2. 02Gastroenterologist Darcy Holt said an untreated oesophageal rupture can be life-threatening and that he now asks about peptide use routinely, having seen a marked rise in patients reporting unapproved retatrutide.
  3. 03The TGA reiterated retatrutide is still in human clinical trials and unapproved, and warned of unknown contents and non-sterility; liver toxicity and severe secretory diarrhoea have also been reported.

From the source

Patient suffers torn oesophagus after using unapproved weight-loss peptide retatrutide

A patient has faced severe health consequences after using an unapproved peptide marketed as the weight-loss drug retatrutide, leading to hospitalisation for a torn oesophagus. The Therapeutic Goods Administration (TGA) disclosed this alarming case to the media as part of its ongoing warnings about the dangers of unapproved peptides.

Read at news.ssbcrack.com