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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
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Our team has spent the last three years working with researchers investigating peptide applications beyond the typical performance and recovery focus
Diabetes Care 28 , 177185 (2005)
It helps promote and speed up the repair and regeneration of the lower and upper GI tract
TB500 is supplied as lyophilised powder for in vitro and laboratory research use only
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