Metformin Hydrochloride Modified Release.
- Treatment of type 2 diabetes mellitus in adults, particularly in overweight individuals, when dietary management and physical alone does not result in adequate glycaemic management.
- Metformin may be used as monotherapy or in combination with other oral hypoglycaemic agents, or with insulin.
- Maximum dose of Metformin modified release tablets is 2000mg per day.
- Metformin modified release tablet shells do not dissolve and may appear in the faeces. When individuals are commenced on this medicine, please advise them of this fact.
Renal Insufficiency – Metformin is entirely renally excreted and accumulates in those individuals with renal insufficiency. It is recommended creatinine clearance and/or serum creatinine levels are determined before initiating treatment and regularly thereafter (at least annually for those individuals with normal renal function). Renal function should be checked at least two to four times a year for those individuals whose serum creatinine levels are at the upper limit of normal and for elderly individuals. Current recommendations for metformin are CrCl 60-90 mL/min dose of metformin 2g daily, 30-60 mL/minute 1g daily. Metformin should be ceased if eGFR falls below 30 mL/min/1.73 m2. Diabetes Medsscheck referral to health care professions annual cycle of care.
- Hepatic insufficiency Metformin should not be used in liver failure due to the increased risk of lactic acidosis.
- There is no data for the use of metformin modified release in children.
- Lactic acidosis – Life threatening lactic acidosis can occur due to metformin accumulating in susceptible individuals. Early warning symptoms include anorexia, nausea, vomiting, abdominal pain, and cramps. Risks factors include renal dysfunction, old age, and doses of metformin >2g daily. It can also be associated with prolonged fasting, excessive alcohol, and hepatic dysfunction. Diabetes Medscheck counseling on side effect profile.
- Discontinue metformin 48 hours before surgery, if possible. It is common practice not to restart metformin for 2 days after surgery and once the individual is eating and drinking normally. Diabetes Medscheck side effect profile.
- Gastrointestinal- diarrhoea, nausea, vomiting, abdominal pain, and loss of appetite. Starting with a low dose and increasing slowly can help with these side effects. Taking medicine with meals can also reduce the unwanted effects. Altered taste is also commonly reported with metformin.
- Dermatological -skin reactions including urticaria, erythema, and pruritus.
- Lactic acidosis reduced vitamin B12 absorption.
- Reduced vitamin B12 absorption.
- Isolated reports of liver function test abnormalities or hepatitis. This has resolved after the metformin has ceased.
- Hypersensitivity to metformin or any of the excipients.
- Renal failure or dysfunction, any acute condition that has the potential to lower renal function (dehydration, severe infection, shock, contrast dye).
- Ketoacidosis due to diabetes, diabetic precoma.
- Renal failure or renal dysfunction.
- Any acute condition that has the potential to lower renal function (dehydration, severe infection, shock, contrast dye).
- Major surgery.
- Severe hepatic dysfunction.
- Acute or chronic disease that can cause tissue hypoxia (cardiac failure, MI, pancreatitis, sepsis).
Plasma protein binding of metformin is negligible.
For more detailed information on this product please consult the product information.