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Notably, this low dose outperformed even some existing obesity medications at the time, without the troublesome side effects
Without intrinsic factor, the small intestine cannot efficiently absorb dietary B12 through the normal receptor-mediated pathway
(Source: Padhi S, Sarangi R, Ramdas A, et al
Preclinical toxicology studies in rats and dogs at doses up to 20 times the projected human therapeutic dose showed no organ toxicity, no changes in IGF-1 levels, and no alterations in glucose homeostasis [4]
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