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Dawed, A.Y., Zhou, K., van Leeuwen, N., Mahajan, A., Robertson, N., Koivula, R., et al. (2019) Variation in the Plasma Membrane Monoamine Transporter (PMAT) (Encoded by SLC29A4) and Organic Cation Transporter 1 (OCT1) (Encoded by SLC22A1) and Gastrointestinal Intolerance to Metformin in Type 2 Diabetes: An IMI Direct Study. Diabetes Care, 42, 1027-1033.
https://doi.org/10.2337/dc18-2182

has been cited by the following article:

• TITLE: Metformin—Pharmacokinetic and Pharmacodynamics Journey Through the Body

  AUTHORS: Alycia Lewis, Kelley Williams, Terry Oroszi

  KEYWORDS: Diabetes, Metformin, Pharmacokinetic, Pharmacodynamic, Personalized Medicine

  JOURNAL NAME: Pharmacology & Pharmacy, Vol.15 No.12, December 13, 2024

  ABSTRACT: Metformin is a commonly prescribed drug used to treat type 2 diabetes. The drug works by decreasing the amount of glucose the liver produces, increasing the sensitivity of muscle cells to insulin, and delaying the absorption of glucose in the intestines. Approximately 50% - 55% of metformin is absorbed in the small intestines. Most of the drug is excreted in the urine, so a patient with renal impairment may need a lower dose of the drug. Common side effects include nausea, vomiting, and diarrhea. Metformin may increase the risk of vitamin B12 deficiency. A rare but serious complication of metformin treatment is lactic acidosis, which is characterized by a blood pH of less than 7.35 and a plasma lactate concentration of greater than 5.0 mmol/L. The risk of lactic acidosis increases with the dose of metformin. The current recommended maximum dose of metformin is 2.0 g per day.