Mutations in the gene encoding OCTN2, SLC22A5 , can impair fatty acid metabolism and lead to systemic primary carnitine deficiency (SPCD, OMIM 212140) 8 , an autosomal recessive disorder whose clinical manifestations include cardiomyopathy, hypoglycemia, chronic muscle weakness and liver dysfunction 9
When to contact a healthcare provider Contact your prescriber if headaches are severe enough to interfere with daily activities
Clinical Insight on Semaglutide for Chronic Weight Management in Adults: Patient Selection and Special Considerations
Helps Lower Fatigue: Restoring vitamin B12 to healthy levels can treat anemia, help with conversion of macronutrients and production of creatine (beneficial for building muscle mass), and reduce muscle weakness
M.AxelmanK.ForsellC.et al (2001)
Schlwicke Engstrm K, Strmberg U, Lundh T, Johansson I, Vessby B, Hallmans G, Skerfving S, Broberg K