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Clinical documents : ER records, imaging or tests (HIDA scan, CT for obstruction, gastric-emptying studies), operative and pathology reports

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The TGA has specifically identified retatrutide as an example of an unapproved peptide product and warns that unapproved therapeutic goods have not been evaluated by the agency for safety, quality, or effectiveness

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Each starts at a low dose that can be increased every four weeks as tolerated and needed