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NAXGLIM-M1

For Newly Diagnosed Obese Diabetes Patient — Glimepiride 1mg Tablets IP & Metformin Hydrochloride 500mg (SR)

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NAXGLIM-M1 Product Carton 10×10 Tablets

Overview

NAXGLIM-M1 is specifically formulated for newly diagnosed obese diabetic patients who require effective dual-mechanism glycaemic control from the outset. Each tablet combines Glimepiride 1mg (a third-generation sulfonylurea) with Metformin Hydrochloride 500mg in a sustained-release matrix.

The combination addresses two core defects in Type 2 Diabetes simultaneously — insufficient insulin secretion and peripheral insulin resistance — making it particularly well-suited for obese patients who commonly present with both pathologies at diagnosis.

Indications

  • Newly diagnosed obese patients with Type 2 Diabetes Mellitus
  • Patients requiring dual oral antidiabetic therapy from initiation
  • Co-morbid diabetic patients with hypertension, hyperlipidaemia, or cardiac disease
  • Type 2 DM patients where monotherapy has not achieved glycaemic targets

Key Benefits

01
Improves Insulin Secretory Deficit

Glimepiride stimulates pancreatic β-cells to correct the relative insulin secretory deficit found in most newly diagnosed diabetic patients, helping restore physiological insulin response.

02
Convenient for Co-morbid Patients

The combination is particularly suitable for patients with concurrent hypertension, hyperlipidaemia, and cardiac disease — offering effective glycaemic control without adding cardiovascular risk.

03
Less Prone to Hypoglycaemia

Glimepiride 1mg — the lowest effective sulfonylurea dose — combined with SR-Metformin produces a significantly lower risk of hypoglycaemic episodes compared to higher-dose or older sulfonylurea regimens.

Dosage & Administration

  • Standard dose: 1 tablet once or twice daily with meals
  • Titration: Initiate with once-daily dosing; increase frequency after 4–8 weeks if HbA1c target not achieved
  • Must be taken with food to minimise hypoglycaemia risk (glimepiride) and GI effects (metformin)
  • Swallow whole — SR matrix must not be crushed or split
  • Monitor renal function (eGFR) at least annually; withhold if eGFR < 30

Contraindications

  • Type 1 diabetes mellitus or diabetic ketoacidosis
  • eGFR < 30 mL/min/1.73m² (severe renal impairment)
  • Hypersensitivity to glimepiride, sulfonamides, metformin, or any excipient
  • Acute or chronic hepatic impairment (lactic acidosis risk)
  • Acute conditions with risk of renal deterioration (severe infection, dehydration, surgery)
  • Pregnancy and lactation
  • Iodinated contrast administration — temporarily discontinue 48 hours prior