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People with variants in the SLC22A5 gene (often referred to as carnitine transporter deficiency) which results in carnitine deficiency can have skeletal myopathy and/or cardiomyopathy [7]

Understanding how these interactions work helps patients and prescribers plan dosing schedules, watch for warning signs, and reduce the chance of complications like hypoglycemia or delayed drug absorption

If proceeding, use minimum effective investigational dose

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PMID: 67 TaylorSHuangYMallettGStathopoulouCFelizardoTCSunMAet al