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This period is characterized by careful dosage titration, designed to acclimate your body to the medication and minimize potential side effects

This approach enhances patient safety and adherence to prescribed therapies, reducing the likelihood of complications

Methods: In this randomized, double-blind, placebo-controlled, parallel-group study, patients who had end-stage HIV/AIDS with carnitine deficiency and fatigue received 3 g of oral L-carnitine or placebo for 2 weeks, followed by a 2-week, open-label phase with the same amount of L-carnitine for all patients

Patients should choose a timing approach that best supports their adherence and tolerability preferences