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July 20: Four years after it was rejected by the FDA due to safety concerns, Daiichi Sankyos Vanflyta (quizartinib) won approval to treat patients with acute myeloid leukemia that has a FLT3-ITD gene mutation

Specifically, MEM alleviated inflammatory processes mediated by chronical lipopolysaccharide administration into the basal forebrain of mice [8183]

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Avoid mixing it directly with strong actives like vitamin C or retinoids in the same routine, as this may reduce effectiveness or cause irritation

So, who is most at risk for developing this deficiency

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