Product image of Komboglyze (Metformin Hydrochloride, Saxagliptin) supplied by GNH India

Komboglyze

Active Ingredient:
Metformin Hydrochloride, Saxagliptin
Origin:
EU

Komboglyze (Metformin Hydrochloride, Saxagliptin)

Metformin Hydrochloride and Saxagliptin, the active ingredient in Komboglyze, is a Biguanide; DPP‑4 inhibitor presented as a tablet for oral use. It treats type 2 diabetes mellitus in adults.

GNH India supplies Komboglyze as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Astrazeneca Ab

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Indications & Clinical Uses

Komboglyze is indicated for the management of type 2 diabetes mellitus, a chronic metabolic disorder that requires glycaemic control.

  • Type 2 diabetes mellitus: lowers blood glucose levels and improves HbA1c when used with diet and exercise.
  • Inadequate control on metformin alone: adds saxagliptin to achieve target glycaemic goals.
  • Adjunct to lifestyle modification: supports diet and exercise in managing type 2 diabetes.

How It Works

  • Metformin reduces hepatic gluconeogenesis and enhances peripheral insulin sensitivity, while saxagliptin inhibits the enzyme dipeptidyl peptidase‑4 (DPP‑4), leading to increased endogenous incretin levels that augment glucose‑dependent insulin secretion and suppress glucagon release, together providing complementary glucose‑lowering effects.

Side Effects

Komboglyze may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: frequent loose stools.
  • Headache: transient cranial discomfort.
  • Upper respiratory tract infection: mild cold‑like symptoms.
  • Abdominal pain: intermittent discomfort.
  • Vomiting: occasional episodes.

Serious or Rare Side Effects

  • Lactic acidosis: rare but potentially fatal metabolic disturbance.
  • Pancreatitis: severe abdominal pain with elevated enzymes.
  • Severe hypersensitivity: rash, angioedema, or anaphylaxis.
  • Hepatic failure: signs of liver dysfunction.
  • Hypoglycaemia (when combined with insulin or sulfonylureas): dizziness, sweating, confusion.
  • Renal impairment: worsening kidney function.

Precautions & Warnings

Before initiating Komboglyze, clinicians should evaluate patient-specific risk factors and monitor relevant clinical parameters.

  • Renal function assessment: avoid in severe renal impairment.
  • Hepatic function monitoring: use caution in patients with liver disease.
  • Lactic acidosis risk: discontinue if signs of metabolic acidosis appear.
  • Hypoglycaemia potential: monitor when combined with insulin or sulfonylureas.
  • Pregnancy and lactation: assess risk‑benefit, as safety data are limited.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture.

Avoid Interactions

Komboglyze can interact with several medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate lactic acidosis in patients with renal dysfunction.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase saxagliptin exposure.
  • Insulin secretagogues (e.g., sulfonylureas): heighten risk of hypoglycaemia.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect renal clearance of metformin.
  • ACE inhibitors or ARBs: monitor renal function and potassium.
  • Warfarin: occasional alteration of INR, require periodic monitoring.
  • Beta‑blockers: may mask hypoglycaemia symptoms.
  • Alcohol: can potentiate metformin‑related lactic acidosis.

Frequently Asked Questions

Komboglyze is prescribed to improve blood glucose control in adults with type 2 diabetes mellitus, typically as part of a comprehensive treatment plan that includes diet, exercise, and other antidiabetic agents when needed.

Metformin lowers blood glucose by decreasing hepatic glucose production, enhancing insulin‑mediated peripheral glucose uptake, and improving the body’s sensitivity to insulin, thereby helping to reduce fasting and post‑prandial glucose levels.

The specific dose of Komboglyze is determined by the prescribing clinician based on the patient’s individual glycaemic targets, renal function, and concomitant therapies. Patients should follow the prescriber’s instructions exactly.

Safety data for Komboglyze in pregnancy and lactation are limited. Clinicians should weigh potential benefits against risks and consider alternative treatments if safer options are available for pregnant or nursing individuals.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Komboglyze combines a biguanide (metformin) with a DPP‑4 inhibitor (saxagliptin), offering dual mechanisms that improve insulin sensitivity and increase incretin activity. Compared with monotherapy, it can achieve greater HbA1c reduction without the weight gain associated with some other classes such as sulfonylureas.

Komboglyze tablets should be stored at ambient temperature, below 25 °C, in their original blister pack or container, protected from moisture and direct sunlight to maintain stability throughout its shelf life.

Komboglyze is taken orally, usually with meals to reduce gastrointestinal discomfort. The tablet should be swallowed whole with a glass of water and not crushed or chewed unless otherwise directed by a healthcare professional.

Serious risks include lactic acidosis, especially in patients with renal impairment, and pancreatitis. Prompt medical attention is required if patients experience unexplained abdominal pain, rapid breathing, or signs of severe metabolic disturbance.

Komboglyze is contraindicated in individuals with severe renal impairment, known hypersensitivity to metformin or saxagliptin, or a history of lactic acidosis. It should also be avoided in patients with acute or chronic metabolic acidosis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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