Product image of Jytaglen Plus (Metformin Hydrochloride, Sitagliptin) supplied by GNH India

Jytaglen Plus

Active Ingredient:
Metformin Hydrochloride, Sitagliptin
Origin:
EU

Jytaglen Plus (Metformin Hydrochloride, Sitagliptin)

Metformin Hydrochloride, the active ingredient in Jytaglen Plus, is a biguanide presented as an oral tablet for oral use. It is used to improve glycemic control in adults with type 2 diabetes mellitus, often in combination with other antidiabetic agents.

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

Manufacturer / TM Owner

Mediapharm Ltd

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Indications & Clinical Uses

Jytaglen Plus is an oral antidiabetic combination that targets hyperglycaemia in type 2 diabetes mellitus.

  • Type 2 diabetes mellitus (monotherapy): lowers fasting and post‑prandial glucose levels when used alone.
  • Type 2 diabetes mellitus (add‑on to metformin): provides additional glucose reduction for patients inadequately controlled on metformin alone.
  • Type 2 diabetes mellitus (add‑on to sulfonylurea or insulin): enhances overall glycaemic control when combined with other glucose‑lowering agents.

How It Works

  • Metformin reduces hepatic gluconeogenesis and increases peripheral insulin sensitivity, while sitagliptin blocks the dipeptidyl peptidase‑4 enzyme, raising endogenous incretin (GLP‑1 and GIP) levels. The combined actions enhance glucose‑dependent insulin secretion, suppress glucagon release, and improve overall glycaemic regulation without causing hypoglycaemia when used appropriately.

Side Effects

Jytaglen Plus may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhoea: loose stools, usually early in therapy.
  • Headache: occasional tension‑type headache.
  • Upper respiratory tract infection: nasopharyngitis symptoms.
  • Dizziness: transient light‑headedness.
  • Abdominal discomfort: mild cramping or bloating.

Serious or Rare Side Effects

  • Lactic acidosis: rare but life‑threatening metabolic disturbance.
  • Severe hypoglycaemia: especially when combined with insulin or sulfonylureas.
  • Pancreatitis: acute inflammation of the pancreas.
  • Allergic reactions: rash, angio‑edema, or anaphylaxis.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient‑specific risk factors and monitor relevant clinical parameters.

  • Renal function: evaluate eGFR to avoid accumulation and lactic acidosis risk.
  • Hepatic function: assess liver enzymes, as impairment may increase adverse events.
  • Cardiovascular status: monitor for heart failure exacerbation.
  • Concomitant hypoglycaemic agents: adjust doses to prevent severe hypoglycaemia.
  • Pregnancy and lactation: weigh benefits against potential risks; use only if clearly needed.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Jytaglen Plus can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Severe renal impairment: markedly increases metformin exposure and lactic acidosis risk.
  • Iodinated contrast agents: may precipitate acute kidney injury, necessitating temporary discontinuation.
  • Alcohol abuse: potentiates metformin‑related lactic acidosis.

Moderate Interactions (Monitor Closely)

  • Sulfonylureas or insulin: heightened hypoglycaemia; dose adjustments may be required.
  • Diuretics (especially thiazides): may reduce renal clearance of metformin.
  • ACE inhibitors or ARBs: monitor renal function and electrolytes.
  • CYP3A4 inhibitors (e.g., ketoconazole): may increase sitagliptin levels.

Frequently Asked Questions

Jytaglen Plus is an oral fixed‑dose combination of metformin hydrochloride and sitagliptin indicated for improving glycaemic control in adults with type 2 diabetes mellitus, either as monotherapy or as part of a broader antidiabetic regimen.

Metformin lowers blood glucose primarily by inhibiting hepatic gluconeogenesis and enhancing peripheral insulin sensitivity, which reduces the amount of glucose released into the bloodstream and improves cellular uptake of glucose.

The prescribed dose of Jytaglen Plus is determined by the treating physician based on the patient’s individual clinical profile, renal function, and response to therapy. Patients should follow the exact dosing instructions provided by their healthcare professional.

Use of Jytaglen Plus during pregnancy or lactation should only occur when the potential benefits outweigh the possible risks. Clinicians must evaluate each case individually, and women who are pregnant, planning pregnancy, or breastfeeding should discuss treatment options with their doctor.

To request Jytaglen Plus, 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.

Compared with metformin alone, the addition of sitagliptin provides complementary glucose‑lowering mechanisms, often achieving better glycaemic control without a substantial increase in hypoglycaemia risk. It offers an alternative to other combination therapies such as metformin‑sulfonylurea or insulin‑based regimens.

Jytaglen Plus should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the tablets from moisture, excessive heat and direct sunlight to maintain product stability.

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

The most serious adverse events include lactic acidosis, severe hypoglycaemia (especially when combined with insulin or sulfonylureas), acute pancreatitis, and rare severe skin reactions such as Stevens‑Johnson syndrome. Prompt medical attention is required if any of these occur.

Jytaglen Plus is contraindicated in patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), known hypersensitivity to metformin or sitagliptin, and those with a history of lactic acidosis. Caution is also advised for individuals with hepatic disease, heart failure, or a history of pancreatitis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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