Naina Mohamed Pakkir Maideen
1*, Abdurazak Jumale
1, Rajkapoor Balasubramaniam
21 Dubai Health Authority, Dubai, United Arab Emirates.
2 Department of Pharmacology, Faculty of Medicine, Sebha University, Sebha, Libya.
Abstract
Metformin is a most widely used medication all
around the world to treat Type 2 diabetes mellitus. It is also found to be
effective against various conditions including, Prediabetes, Gestational
diabetes mellitus (GDM), Polycystic Ovarian Syndrome (PCOS), Obesity, Cancer,
etc. It is a cationic drug and it depends Organic Cation Transporters (OCTs)
and Multidrug and Toxin Extruders (MATEs) mostly for its pharmacokinetics
movement. The probability of drug interaction increases with the number of
concomitant medications. This article focuses the drug interactions of
metformin and most of them are linked to the inhibition of OCTs and MATEs
leading to increased plasma metformin concentrations and subsequent elevation
of risk of Metformin Associated Lactic Acidosis (MALA). By identifying the
drugs inhibiting OCTs and MATEs, the healthcare professionals can predict the
drug interactions of metformin.