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Efficacy and safety of meal-time administration of short-acting exenatide for glycaemic control in type 1 diabetes (MAG1C): a randomised, double-blind, placebo-controlled trial
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In pre- and postnatal development studies in pregnant rats, empagliflozin was administered from gestation day 6 through to lactation day 20 (weaning) at up to 100 mg/kg/day (approximately 16-times the 25 mg maximum clinical dose) without maternal toxicity
J Clin Endocrinol Metab 2019;104:2463-72.ArticlePubMed 43
About the Author Pamela Maragliano, DMD Pamela Maragliano, DMD, is the chief editor of Dental Economics
