DIAMICRON MR TABLET 60MG

LES LABORATOIRES SERVIER INDUSTRIE - FRANCESERVIER (IRELAND) INDUSTRIES LTD - IRELANDKOTRA PHARMA (M) SDN BHD (MALAYSIA)🇸🇬 Health Sciences Authority

Approval Date: Sep 22, 2010
Approval ID: 3dfb3949c00d7b6b
Company: LES LABORATOIRES SERVIER INDUSTRIE - FRANCESERVIER (IRELAND) INDUSTRIES LTD - IRELANDKOTRA PHARMA (M) SDN BHD (MALAYSIA)
Type: Therapeutic

Approval Details

Approval Id: 3dfb3949c00d7b6b
Drug Name: DIAMICRON MR TABLET 60MG
Product Name: DIAMICRON MR TABLET 60MG
Approval Number: SIN13868P
Approval Date: 2010-09-22
Registrant: SERVIER (S) PTE LTD
Licence Holder: SERVIER (S) PTE LTD
Drug Type: Therapeutic
Forensic Classification: PRESCRIPTION ONLY MEDICINES
Dosage Form: TABLET, FILM COATED, EXTENDED RELEASE
Dosage: DOSAGE AND ADMINISTRATION Oral use. For adult use only. DIAMICRON MR 30mg tablets do not have a break bar and must not be broken in half. Tablets must be administered whole. DIAMICRON MR 60mg tablets have a break bar and may be administered as whole or as half tablets (see Pharmacokinetics – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information). So that the modified release properties of the product can be maintained, DIAMICRON MR 30mg and DIAMICRON MR 60mg tablets should not be chewed or crushed. These products should be taken with food because there is an increased risk of hypoglycemia if a meal is taken late, if an inadequate amount of food is consumed or if the food is low in carbohydrate. It is recommended that the medication be taken at breakfast time. If a dose is forgotten, the dose taken on the next day should not be increased. <ul> <li>A single daily dose provides an effective blood glucose control. The initial recommended dose for these products is 30mg daily, even in elderly patients (≥ 65 years). For DIAMICRON MR 30mg the single daily dose may be between one (30mg) and four (120mg) tablets.</li> <li>For DIAMICRON MR 60mg the single daily dose may be between half a tablet (30mg) and two tablets (120mg).</li> </ul> For both DIAMICRON MR 30mg and DIAMICRON MR 60mg, the daily dose should not exceed 120mg. Previously untreated patients should commence with a dose of 30mg and will benefit from dose titration until the appropriate dose is reached. As with all hypoglycaemic agents, doses should be titrated according to the individual patient's response. Titration should be carried out in steps of 30mg, according to the fasting blood glucose response. Each step should last for at least one month between each increment, except in patients whose blood glucose do not decrease after two weeks of treatment. In this case, it is possible to propose a dosage increase at the end of the 2nd week treatment. Across the dose range, one half of a DIAMICRON MR 60mg tablet, can replace one tablet of DIAMICRON MR 30mg, or one tablet of gliclazide 80mg immediate release (refer to the following table for other dose equivalences). <img src="/TGIF/DiamicronMR-Table1.png" alt="Diamicron MR Dosage Table 1" /> DIAMICRON MR 30mg or DIAMICRON MR 60mg, may be used to replace other antidiabetic treatments without any transitional period. If a patient is switched from a hypoglycaemic sulfonylurea with a prolonged half-life he/she should be carefully monitored (for one to two weeks) in order to avoid hypoglycaemia due to possible residual effects of the previous therapy. DIAMICRON MR 30mg or DIAMICRON MR 60mg, may be given in combination with biguanides, alpha glucosidase inhibitors or insulin. In patients not adequately controlled with DIAMICRON MR concomitant insulin therapy can be initiated under close medical supervision. Elderly subjects: The efficacy and tolerance of the modified release formulation of gliclazide (30mg – 120mg) has been confirmed in clinical trials in subjects over 65 years who were given the same dosage regimen as the general population. The dosage is therefore identical to that recommended for adults under the age of 65 years. Renal insufficiency: The efficacy and tolerance of the modified release formulation of gliclazide (30mg – 120mg) has been confirmed in clinical trials of subjects with mild to moderate renal failure (creatinine clearance of between 15 and 80mL/min) who were given the same dosage regimen as the general population. No dosage adjustment is therefore required in subjects with impaired renal function. In patients at risk of hypoglycaemia: <ul> <li>states of undernourishment or malnutrition,</li> <li>severe or poorly compensated endocrine pathologies (hypopituitarism, hypothyroidism, adrenal insufficiency),</li> <li>withdrawal from prolonged and /or high dose corticosteroid therapy,</li> <li>severe vascular disease (severe coronary heart disease, severe carotid impairment, diffuse vascular disease)</li> </ul> It is recommended that treatment be systematically initiated with a minimal dose of 30mg / day. There are no data or clinical studies in children.
Route Of Administration: ORAL
Indication Info: INDICATIONS DIAMICRON MR 30mg and DIAMICRON MR 60mg are indicated for the treatment of type II diabetes in association with dietary measures and with physical exercise when these measures alone are inadequate to control blood glucose. During controlled clinical trials in patients with type II diabetes, a modified release formulation of gliclazide (30mg – 120mg), taken as a single daily dose, was shown to be effective long term in controlling blood glucose levels, based on monitoring of HbA1c.
Contraindications: CONTRAINDICATIONS DIAMICRON MR 30mg and DIAMICRON MR 60mg are contra-indicated in the following cases: <ul> <li>hypersensitivity to gliclazide, other sulfonylureas, sulphonamides, or to any of the excipients;</li> <li>type 1 diabetes;</li> <li>diabetic pre-coma and coma; diabetic keto-acidosis;</li> <li>severe renal or hepatic insufficiency: in these cases, the use of insulin is recommended;</li> <li>treatment with miconazole (refer to Interactions – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information);</li> <li>pregnancy and lactation (refer to Use in pregnancy and Use in lactation – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).</li> </ul>
Atc Code: A10BB09
Atc Item Name: gliclazide
Pharma Manufacturer Name: SERVIER (S) PTE LTD

Active Ingredients

gliclazide

60mg

GLICLAZIDE

60 MG

Approved

Quick Info

Agency

HSA

Country

🇸🇬

Approval Date

Sep 22, 2010

Approval ID

3dfb3949c00d7b6b

Type

Therapeutic

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