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Competitive athletes should avoid consumption

Lidocaine is extensively metabolized in the liver, so drugs that decrease hepatic blood flow (e.g., propranolol) or inhibit CYP1A2/CYP3A4 (e.g., fluvoxamine, ketoconazole, clarithromycin) may elevate systemic concentrations and increase the risk of central nervous system or cardiovascular toxicity

Both peptides share the same amino acid sequence from human growth hormone (positions 176-191)

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However, the absence of human clinical trials means the safety profile in humans is entirely unknown

Notable interactions include: Many med spa intake processes are streamlined for speed and convenience, which can mean medication review is either rushed or skipped entirely