Product image of Mifoglame (Sitagliptin) supplied by GNH India

Mifoglame

Active Ingredient:
Sitagliptin
Origin:
EU

Mifoglame (Sitagliptin)

Sitagliptin, the active ingredient in Mifoglame, is a Dipeptidyl peptidase‑4 (DPP‑4) inhibitor presented as an oral formulation for oral use. It is used to improve glycaemic control in adults with type 2 diabetes mellitus.

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

Manufacturer / TM Owner

Bausch Health Ireland Limited

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Indications & Clinical Uses

Mifoglame (sitagliptin) belongs to the DPP‑4 inhibitor class and is employed in the management of type 2 diabetes mellitus.

  • Type 2 diabetes mellitus: improves glycaemic control by enhancing insulin secretion and reducing glucagon release.
  • Monotherapy in type 2 diabetes: can be used alone when diet and exercise are insufficient.
  • Combination therapy: added to metformin or other oral agents to achieve target blood glucose levels.

How It Works

  • Sitagliptin selectively inhibits the enzyme dipeptidyl peptidase‑4 (DPP‑4), which degrades the incretin hormones GLP‑1 and GIP. By preventing this degradation, sitagliptin raises circulating levels of GLP‑1 and GIP, leading to glucose‑dependent stimulation of insulin secretion, suppression of glucagon release, and overall improvement of post‑prandial and fasting blood glucose concentrations.

Side Effects

Sitagliptin is generally well tolerated, but several adverse reactions have been reported.

Common Side Effects

  • Nasopharyngitis: mild upper respiratory tract infection symptoms.
  • Headache: transient mild to moderate pain.
  • Upper respiratory infection: cough, sore throat, or congestion.
  • Gastrointestinal upset: nausea, abdominal discomfort, or diarrhoea.
  • Dizziness: occasional light‑headed sensation.

Serious or Rare Side Effects

  • Pancreatitis: severe abdominal pain requiring immediate medical attention.
  • Severe allergic reactions: rash, angioedema, or anaphylaxis.
  • Joint pain: unexplained arthralgia that may be persistent.
  • Hepatic enzyme elevation: increased ALT/AST levels.
  • Severe hypoglycaemia: especially when combined with insulin or sulfonylureas.

Precautions & Warnings

Before initiating sitagliptin therapy, clinicians should consider several safety aspects.

  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Hepatic impairment: use with caution in moderate to severe liver disease.
  • Concomitant insulin or sulfonylureas: monitor for hypoglycaemia.
  • History of pancreatitis: avoid use and observe for symptoms.
  • Pregnancy and lactation: safety not established; weigh benefits against risks.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture.

Avoid Interactions

Sitagliptin may interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Insulin or sulfonylureas: increased risk of severe hypoglycaemia.
  • Strong DPP‑4 inhibitors (e.g., saxagliptin): additive effect, not recommended.

Moderate Interactions (Monitor Closely)

  • Rifampin: may reduce sitagliptin plasma concentrations.
  • Diuretics: may affect glucose control, requiring monitoring.
  • ACE inhibitors: potential for altered renal function, necessitating observation.

Frequently Asked Questions

Mifoglame contains sitagliptin, a DPP‑4 inhibitor indicated for the treatment of type 2 diabetes mellitus in adults. It helps lower blood glucose levels when used together with diet and exercise, either as monotherapy or in combination with other antidiabetic agents.

Sitagliptin blocks the enzyme dipeptidyl peptidase‑4, which normally breaks down the incretin hormones GLP‑1 and GIP. By preserving these hormones, sitagliptin enhances glucose‑dependent insulin release, reduces glucagon secretion, and improves overall glycaemic control.

The appropriate dose of Mifoglame is determined by the prescribing healthcare professional based on the patient’s clinical condition, renal function, and concomitant therapies. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

The safety of sitagliptin in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

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.

Mifoglame (sitagliptin) differs from sulfonylureas and insulin by acting through the incretin pathway, offering glucose‑dependent insulin release with a lower risk of hypoglycaemia when used alone. Compared with other DPP‑4 inhibitors, its efficacy and safety profile are comparable, but individual patient factors guide the choice.

Mifoglame should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiry date.

Mifoglame is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their healthcare professional.

Serious risks include pancreatitis, severe allergic reactions such as anaphylaxis, and joint pain that may be persistent. Patients should seek immediate medical attention if they experience severe abdominal pain, rash, swelling, or unexplained joint discomfort.

Mifoglame is contraindicated in patients with a known hypersensitivity to sitagliptin or any component of the formulation. Caution is advised for individuals with severe renal or hepatic impairment, a history of pancreatitis, or those taking concomitant insulin or sulfonylureas without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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