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In rare cases, allergic reactions may occur

The essential link between the mitochondrial carnitine transport and FAO is demonstrated by the life-threatening inherited carnitine/acylcarnitine translocase deficiency (OMIM 613698) that, in contrast to the PCD caused by OCTN2 defects, cannot be compensated by the administration of carnitine (Indiveri et al., 2011)

Journal of Pediatric Gastroenterology and Nutrition, 60(6), 802810

A slowdown during GLP-1 therapy does not necessarily mean treatment has failed

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This suggests the resistance occurs further along in the biological pathway