Product image of Jazeta (Sitagliptin Hydrochloride) supplied by GNH India

Jazeta

Active Ingredient:
Sitagliptin Hydrochloride
Origin:
EU

Jazeta (Sitagliptin Hydrochloride)

Sitagliptin Hydrochloride, the active ingredient in Jazeta, is a DPP‑4 inhibitor presented as a tablet for oral use. It is indicated for the management of type 2 diabetes mellitus in adults, helping to improve glycemic control when combined with diet and exercise.

GNH India supplies Jazeta as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on quality assurance and regulatory compliance. Our distribution network ensures timely delivery across multiple regions and adherence to local import requirements.

Manufacturer / TM Owner

Zentiva, K.S.

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Indications & Clinical Uses

  • Jazeta (sitagliptin hydrochloride) is used in the DPP‑4 inhibitor class to manage hyperglycemia in type 2 diabetes.
  • Type 2 diabetes mellitus: improves glycemic control as an adjunct to diet and exercise, alone or with other antidiabetic agents.
  • Inadequate control on metformin: provides additional glucose‑lowering effect when added to metformin therapy.
  • Combination with sulfonylureas: enhances insulin secretion while reducing the risk of hypoglycemia compared with sulfonylurea monotherapy.

How It Works

  • Sitagliptin selectively inhibits the enzyme dipeptidyl peptidase‑4 (DPP‑4), which results in increased circulating levels of the incretin hormones GLP‑1 and GIP. Elevated incretins enhance glucose‑dependent insulin secretion from pancreatic β‑cells and suppress glucagon release from α‑cells, thereby lowering post‑prandial and fasting blood glucose concentrations.

Side Effects

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: transient cranial discomfort.
  • Upper respiratory tract infection: symptoms such as sore throat or congestion.
  • Diarrhea: loose stools that are usually self‑limiting.
  • Hypoglycemia (when combined with insulin or sulfonylureas): low blood sugar episodes.

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.
  • Elevated liver enzymes: abnormal hepatic function tests.
  • Bullous pemphigoid: rare autoimmune skin disorder.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Renal impairment: dose adjustment may be required based on renal function.
  • Hepatic impairment: use with caution in patients with liver disease.
  • History of pancreatitis: avoid or monitor closely for recurrent episodes.
  • Concurrent insulin or sulfonylureas: increased risk of hypoglycemia; monitor glucose levels.
  • Elderly patients: assess renal function regularly as clearance may decline.
  • Store at ambient temperature below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Jazeta may interact with other medicines as follows:

Major Interactions (Avoid)

  • Insulin: combined use can cause severe hypoglycemia.
  • Sulfonylureas: additive risk of low blood glucose.
  • Strong CYP3A4 inhibitors: may increase sitagliptin exposure.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect glycemic control; monitor blood glucose.
  • ACE inhibitors: monitor renal function when used together.
  • Rifampin: may reduce sitagliptin plasma concentrations, potentially diminishing efficacy.

Frequently Asked Questions

Jazeta contains sitagliptin hydrochloride and is prescribed to improve blood glucose control in adults with type 2 diabetes mellitus. It is used as part of a comprehensive treatment plan that includes diet, exercise, and may be combined with other antidiabetic medications.

Sitagliptin works by selectively inhibiting the enzyme dipeptidyl peptidase‑4 (DPP‑4). This inhibition raises levels of the incretin hormones GLP‑1 and GIP, which increase insulin secretion and decrease glucagon release in a glucose‑dependent manner, thereby lowering blood sugar.

The appropriate dose of Jazeta is determined by the prescribing healthcare professional based on the patient’s clinical condition, renal function, and concomitant therapies. Dosage may be adjusted over time to achieve optimal glycemic control.

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

To order Jazeta, 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, sitagliptin does not typically cause gastrointestinal upset and can be added when metformin alone is insufficient. Unlike sulfonylureas, it has a lower intrinsic risk of hypoglycemia because its insulin‑stimulating effect is glucose‑dependent.

Jazeta tablets should be stored at ambient temperature below 25 °C, in the original packaging, protected from moisture and direct light. Keep the product out of reach of children and do not use after the expiry date printed on the label.

Jazeta 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.

The most serious adverse events associated with sitagliptin include acute pancreatitis, severe hypersensitivity reactions such as anaphylaxis or angioedema, and, when combined with insulin or sulfonylureas, potentially dangerous hypoglycemia. Prompt medical attention is required if any of these occur.

Jazeta is contraindicated in patients with type 1 diabetes, diabetic ketoacidosis, or a known hypersensitivity to sitagliptin or any of the tablet’s excipients. Caution is also advised for individuals with severe renal impairment, as dose adjustment may be required.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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