Product image of Incresync (Pioglitazone, Alogliptin) supplied by GNH India

Incresync

Active Ingredient:
Pioglitazone, Alogliptin
Origin:
EU

Incresync (Pioglitazone, Alogliptin)

Pioglitazone and Alogliptin, the active ingredients in Incresync, are a thiazolidinedione and a DPP‑4 inhibitor presented as oral tablets for systemic use. They are indicated for the management of type 2 diabetes mellitus in adult patients when diet, exercise, and monotherapy are insufficient. Together they improve insulin sensitivity and raise endogenous incretin levels, supporting better glycaemic control. The combination targets two complementary pathways to enhance glucose regulation.

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

Manufacturer / TM Owner

Takeda Pharma A/S

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Indications & Clinical Uses

Incresync combines a thiazolidinedione and a DPP‑4 inhibitor to improve glycaemic control in type 2 diabetes.

  • Type 2 diabetes mellitus: lowers fasting and post‑prandial blood glucose when added to diet and exercise.
  • Inadequate control on monotherapy: provides additional glucose‑lowering effect as part of combination therapy.
  • Adults requiring improved insulin sensitivity: enhances peripheral insulin action while augmenting incretin‑mediated insulin secretion.

How It Works

  • Pioglitazone binds to and activates the nuclear peroxisome proliferator‑activated receptor‑γ (PPARγ), modulating gene expression to increase peripheral insulin sensitivity and glucose uptake. Alogliptin selectively inhibits the enzyme dipeptidyl peptidase‑4 (DPP‑4), preventing degradation of the incretin hormones GLP‑1 and GIP, thereby prolonging their action to stimulate glucose‑dependent insulin secretion and suppress glucagon release. The dual action addresses both insulin resistance and impaired insulin secretion.

Side Effects

Incresync may be associated with a range of adverse reactions, which are reported in clinical use.

Common Side Effects

  • Edema: swelling of the lower extremities.
  • Weight gain: modest increase in body weight.
  • Upper respiratory tract infection: symptoms such as cough or sore throat.
  • Headache: mild to moderate intensity.
  • Nausea: occasional stomach discomfort.

Serious or Rare Side Effects

  • Congestive heart failure exacerbation: worsening of pre‑existing heart failure.
  • Hepatic injury: elevated liver enzymes or hepatitis.
  • Severe hypoglycaemia: especially when combined with insulin or sulfonylureas.
  • Pancreatitis: acute inflammation of the pancreas.
  • Bone fracture: increased risk of femoral fractures in susceptible patients.

Precautions & Warnings

When prescribing Incresync, clinicians should consider several precautionary measures to minimise risk.

  • Liver function monitoring: assess hepatic enzymes before initiation and periodically during therapy.
  • Heart failure assessment: avoid in patients with active or uncontrolled congestive heart failure.
  • Edema evaluation: monitor for peripheral swelling, particularly in the ankles.
  • Bladder cancer history: use with caution in patients with a history of bladder carcinoma.
  • Renal function: adjust use in moderate renal impairment and monitor creatinine.
  • Pregnancy and lactation: safety not established; avoid unless benefits outweigh potential risks.
  • Store at ambient temperature: keep tablets in the original container, protect from moisture and heat.

Avoid Interactions

Incresync can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Concomitant insulin or sulfonylureas: increased risk of hypoglycaemia.
  • Strong CYP2C8 inhibitors (e.g., gemfibrozil): raise pioglitazone plasma concentrations.
  • Co‑administration with another DPP‑4 inhibitor: additive inhibition of DPP‑4, not recommended.

Moderate Interactions (Monitor Closely)

  • Diuretics: may mask pioglitazone‑induced fluid retention.
  • ACE inhibitors or ARBs: monitor renal function and electrolytes.
  • Warfarin: possible alteration of INR, requiring closer coagulation monitoring.
  • NSAIDs: may increase risk of renal impairment when combined.

Frequently Asked Questions

Incresync is prescribed for the treatment of type 2 diabetes mellitus in adult patients when diet, exercise, and single‑agent therapy do not achieve adequate glycaemic control. The combination of pioglitazone and alogliptin targets both insulin resistance and impaired insulin secretion to help lower blood glucose levels.

Pioglitazone activates the nuclear receptor PPARγ, which regulates genes involved in glucose and lipid metabolism. Activation increases insulin sensitivity in muscle and adipose tissue, enhances glucose uptake, and reduces hepatic glucose production, thereby contributing to overall blood‑sugar reduction.

The dose of Incresync is individualized by the prescribing healthcare professional based on the patient’s clinical condition, response to therapy, and any concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose without medical guidance.

Safety of Incresync 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 this decision must be made by a qualified healthcare provider.

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

Incresync combines two mechanisms—PPARγ activation and DPP‑4 inhibition—offering both improved insulin sensitivity and enhanced incretin effect. This dual approach can be advantageous over monotherapy agents that target only one pathway, but the choice of therapy should be individualized based on efficacy, safety profile, comorbidities and patient preference.

Incresync tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the container tightly closed and out of reach of children.

Incresync is taken orally, usually once daily with or without food, as directed by the prescribing clinician. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically advised.

Serious risks include worsening of congestive heart failure, hepatic injury, severe hypoglycaemia (especially when combined with insulin or sulfonylureas), pancreatitis, and increased risk of bone fractures. Patients should be educated to report symptoms such as rapid weight gain, shortness of breath, jaundice, severe abdominal pain, or unexplained fractures promptly.

Incresync is contraindicated in patients with known hypersensitivity to pioglitazone, alogliptin, or any excipients, as well as in individuals with active or uncontrolled congestive heart failure. Caution is also advised for patients with a history of bladder cancer, severe liver disease, or renal impairment, and the drug should be avoided in pregnancy unless clearly justified.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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