metformin
introduction
a biguanide oral hypoglycaemic agent which is very useful in the treatment of patients with insulin resistance
it was developed from the herb Galega officianalis and 1st synthesized in 1922 but overshadowed by the 1st use of insulin in the same year
it was eventually studied in trials for diabetics in 1957 as Glucophage in the same year that a related biguanide, phenformin was studied then energetically marketed globally while metformin was mainly marketed in Europe, particularly, France where it was manufactured.
phenformin was removed from market in 1977 after it was confirmed that it was associated with life threatening lactic acidosis which was initially suggested in 1959. Phenformin was particularly problematic in this regard as it was metabolised by the liver and it accumulates in people with a genetic deficiency of the enzyme cytochrome P450 2D6.
in contrast, metformin is mainly excreted by the kidneys and lactic acidosis is mainly confined to overdoses and those with advanced renal failure.
nevertheless, as a result of these concerns, metformin fell out of favour until its benefits were rediscovered in 1995 leading to it becoming the 1st choice for obese patients with type 2
diabetes mellitus, then in 2012, experts in USA and Europe declared that it should be 1st choice for all patients with type 2 diabetes.
metformin is now also used to Rx
polycystic ovary syndrome (PCOS) (which is associated with insulin resistance), gestational diabetes, and is showing promise in the prevention of cancers such as pancreatic cancer (it appears to lower risk by ~62%) and it may appear to decrease overall cancer risk by 25-37%.
a major issue for ED doctors in patients who take metformin is the significantly increased risk of
radiologic contrast media precautions and adverse reactions in iv contrast media use in radiology such as CT scans which needs active management to prevent nephrotoxicity and subsequent lactic acidosis.
sold under various trade names, including Glucophage XR, Carbophage SR, Riomet, Fortamet, Glumetza, Obimet, Gluformin, Dianben, Diabex, and Diaformin
the slow release versions are mainly to reduce GIT side effects and to improve compliance
tablets are usually 500mg or 1000mg although there is a 850mg immediate release form and a 750mg slow and extended release forms
dose
C/I
adverse effects
diarrhea, cramps, nausea, vomiting and increased flatulence are common
life threatening lactic acidosis is fortunately rare
vitamin B12 malabsorption
mechanism of actions
it improves hyperglyceamia primarily by suppressing glucose production by the liver via activation of AMP-activated protein kinase (AMPK), an enzyme that plays an important role in insulin signaling
it increases insulin sensitivity, enhances peripheral glucose uptake, increases fatty acid oxidation and decreases absorption of glucose from the gastrointestinal tract
it may antagonise the action of
glucagon, thus reducing fasting glucose levels
P/K
slowly absorbed
peak plasma concentrations reached 1-3hrs after oral dose
steady state achieved within 1-2 days of Rx
less than 0.01% is un-ionised in blood, hence it is not lipophilic and does not enter cells readily, although it has a large appparent Vd of 300-1000L after a single dose, presumably as it is mainly distributed to RBC's
it is not metabolised
elimination is renal excretion with average plasma half-life of 6.2hrs, while RBC half life is much longer at ~18 hours
overdose
most common symptoms following overdose appear to include vomiting, diarrhoea, abdominal pain, tachycardia, drowsiness, and, rarely, hypoglycaemia or hyperglycaemia.
the major potentially life-threatening complication of metformin overdose is lactic acidosis, particularly if doses over 5,000mg in adults
in healthy children, unintentional doses of less than 1,700 mg are unlikely to cause any significant toxic effects
metformin.txt · Last modified: 2013/04/11 23:51 (external edit)