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The potential consequences of improper retatrutide preparation include: Overdose or underdose Errors in volume or concentration can result in receiving far more or far less active compound than intended, with unpredictable clinical consequences Injection-site reactions Including pain, redness, swelling, or abscess formation, particularly if aseptic technique is not maintained Systemic infection Contaminated solutions can introduce bacteria or other pathogens directly into subcutaneous tissue or the bloodstream Allergic or anaphylactic reactions Peptide aggregates or contaminants in unregulated products may trigger immune responses Gastrointestinal adverse effects GLP-1 receptor agonists as a class are associated with nausea, vomiting, diarrhoea, and constipation

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