MEIJUMET

Posology Adults with normal renal function (GFR≥ 90 mL/min) Reduction in the risk or delay of the onset of type 2 diabetes • Metformin should only be considered where intensive lifestyle modifications for 3 to 6 months have not resulted in adequate glycaemic control.

• The therapy should be initiated with one tablet Meijumet 500 mg once daily with the evening meal. • After 10 to 15 days dose adjustment on the basis of blood glucose measurements is recommended (OGTT and/or FPG and/or HbA1C values to be within the normal range).

A slow increase of dose may improve gastro- intestinal tolerability. The maximum recommended dose is 4 tablets (2000 mg) once daily with the evening meal. • It is recommended to regularly monitor (every 3-6 months) the glycaemic status (OGTT and/or FPG and/or HbA1c value) as well as the risk factors to evaluate whether treatment needs to be continued, modified or discontinued.

• A decision to re-evaluate therapy is also required if the patient subsequently implements improvements to diet and/or exercise, or if changes to the medical condition will allow increased lifestyle interventions to be possible. Monotherapy in Type 2 diabetes mellitus and combination with other oral antidiabetic agents: • Meijumet 1000 mg should be taken once daily with the evening meal at a maximum recommended dose of 2 tablets per day.

• Meijumet 1000 mg is intended as a maintenance therapy for patients currently treated with either 1000 mg or 2000 mg of metformin hydrochloride. On switch, the daily dose of Meijumet should be equivalent to the current daily dose of metformin hydrochloride.

• In patients treated with metformin hydrochloride at a dose above 2000 mg daily, switching to Meijumet is not recommended. • For patients new to metformin hydrochloride, the usual starting dose of Meijumet is 500 mg once daily given with the evening meal.

After 10 to 15 days the dose should be adjusted on the basis of blood glucose measurements. A slow increment in dose may improve gastrointestinal tolerability. • If glycaemic control is not achieved on once daily dosing of Meijumet at a maximum dose of 2000 mg a day, then a twice daily dosing schedule should be considered with both doses being given with food, at the time of the morning and evening meals.

If glycaemic control is still not achieved, patients may be switched to standard metformin hydrochloride tablets to a maximum dose of 3000 mg daily. . • In the event of transfer from another oral antidiabetic agent, titration should begin with Meijumet 500 mg before switching to Meijumet 1000 mg as indicated above.

In post marketing data and in controlled clinical studies, adverse event reporting in patients treated with Metformin hydrochloride prolonged release tablets was similar in nature and severity to that reported in patients treated with Metformin immediate release.

During treatment initiation, the most common adverse reactions are nausea, vomiting, diarrhoea, abdominal pain and loss of appetite, which resolve spontaneously in most cases. The following adverse reactions may occur with Meijumet Tablets Frequencies are defined as follows: very common: ≥1/10; common ≥1/100, <1/10; uncommon ≥1/1,000, <1/100; rare ≥1/10,000, <1/1,000; very rare <1/10,000.

Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness. 4). 4. Special warnings and precautions for use).

Nervous system disorders:

Common: • Taste disturbance Gastrointestinal disorders: Very common: • Gastrointestinal disorders such as nausea, vomiting, diarrhoea, abdominal pain and loss of appetite. These undesirable effects occur most frequently during initiation of therapy and resolve spontaneously in most cases.

A slow increase of the dose may also improve gastrointestinal tolerability.

Hepatobiliary disorders:

Very rare: • Isolated reports Liver function tests abnormalities or hepatitis resolving upon metformin discontinuation.

Skin and subcutaneous tissue disorders:

Very rare: • Skin reactions such as erythema, pruritus and urticaria. Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product.

Lactic acidosis:

Lactic acidosis, a very rare but serious metabolic complication, most often occurs at acute worsening of renal function or cardiorespiratory illness or sepsis. Metformin accumulation occurs at acute worsening of renal function and increases the risk of lactic acidosis.

In case of dehydration (severe diarrhoea or vomiting, fever or reduced fluid intake), metformin should be temporarily discontinued and contact with a health care professional is recommended. Medicinal products that can acutely impair renal function (such as antihypertensives, diuretics and NSAIDs) should be initiated with caution in metformin-treated patients.

5). Patients and/or care-givers should be informed of the risk of lactic acidosis. Lactic acidosis is characterised by acidotic dyspnoea, abdominal pain, muscle cramps, asthenia and hypothermia followed by coma. In case of suspected symptoms, the patient should stop taking metformin and seek immediate medical attention.

35), increased plasma lactate levels (>5 mmol/L) and an increased anion gap and lactate/pyruvate ratio.

Patients with known or suspected mitochondrial diseases:

In patients with known mitochondrial diseases such as Mitochondrial Encephalopathy with Lactic Acidosis, and Stroke-like episodes (MELAS) syndrome and Maternal inherited diabetes and deafness (MIDD), metformin is not recommended due to the risk of lactic acidosis exacerbation and neurologic complications which may lead to worsening of the disease.

In case of signs and symptoms suggestive of MELAS syndrome or MIDD after the intake of metformin, treatment with metformin should be withdrawn immediately and prompt diagnostic evaluation should be performed. 2. 3. Cardiac function Patients with heart failure are more at risk of hypoxia and renal insufficiency.

1. • Any type of acute metabolic acidosis (such as lactic acidosis, diabetic ketoacidosis). • Diabetic pre-coma. • Severe renal failure (GFR <30 mL/min). • Acute conditions with the potential to alter renal function such as: - Dehydration, - severe infection, - shock, • Disease which may cause tissue hypoxia (especially acute disease, or worsening of chronic disease) such as: - decompensated heart failure, - respiratory failure, - recent myocardial infarction, - shock • Hepatic insufficiency, acute alcohol intoxication, alcoholism.