Product image of Insulatard (Insulin Human) supplied by GNH India

Insulatard

Active Ingredient:
Insulin Human
Origin:
EU

Insulatard (Insulin Human)

Insulin Human, the active ingredient in Insulatard, is an insulin presented as a suspension for injection for subcutaneous use. It provides basal insulin coverage to manage blood glucose in individuals with type 1 or type 2 diabetes mellitus.

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

Manufacturer / TM Owner

Novo Nordisk A/S

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Indications & Clinical Uses

Insulatard is used to provide basal insulin therapy in the management of diabetes mellitus.

  • Type 1 diabetes mellitus: supplies long‑acting insulin to control fasting glucose and reduce hyperglycaemia.
  • Type 2 diabetes mellitus: adds basal insulin to supplement endogenous secretion and improve overall glycaemic control.

How It Works

  • Insulin Human binds to insulin receptors on muscle, adipose and hepatic cells, activating the receptor’s intrinsic tyrosine kinase activity. This triggers intracellular signaling cascades that promote translocation of GLUT‑4 transporters, increasing glucose uptake, and suppresses hepatic gluconeogenesis, thereby lowering circulating blood glucose levels. The intermediate‑acting formulation releases insulin gradually after subcutaneous injection, providing a prolonged basal effect.

Side Effects

Insulatard may be associated with a range of adverse reactions, which are classified by frequency and severity.

Common Side Effects

  • Hypoglycaemia: low blood glucose episodes, especially if meals are missed or dosing is excessive.
  • Injection‑site pain or erythema: mild discomfort or redness at the injection site.
  • Lipodystrophy: localized thickening or loss of subcutaneous fat with repeated injections.
  • Weight gain: modest increase in body weight over time.
  • Edema: mild fluid retention, often in the lower extremities.
  • Allergic skin reaction: itching or rash at the site.

Serious or Rare Side Effects

  • Severe hypoglycaemia: profound low glucose requiring assistance.
  • Anaphylactic reaction: life‑threatening systemic allergy with airway compromise.
  • Insulin antibodies: formation of antibodies that may alter insulin action.
  • Hypokalemia: low potassium levels secondary to rapid glucose shift.

Precautions & Warnings

When using Insulatard, several precautions should be observed to ensure safe and effective therapy.

  • Dose titration: adjust the dose gradually based on self‑monitored blood glucose and clinical response.
  • Hypoglycaemia risk: educate patients to recognise and treat low glucose promptly.
  • Renal or hepatic impairment: monitor closely and consider dose reduction in severe dysfunction.
  • Pregnancy and lactation: use only if the potential benefit outweighs uncertain risk, as safety data are limited.
  • Concomitant medications: review other glucose‑lowering agents to avoid additive hypoglycaemic effect.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the suspension.

Avoid Interactions

Insulatard can interact with other medicines, influencing glucose control or insulin action.

Major Interactions (Avoid)

  • Sulfonylureas or meglitinides: combined use markedly increases risk of severe hypoglycaemia.
  • Beta‑blockers: may mask typical hypoglycaemia symptoms such as tachycardia.
  • MAO‑inhibitors: rare reports of potentiated insulin effect leading to hypoglycaemia.

Moderate Interactions (Monitor Closely)

  • Oral hypoglycaemic agents (e.g., metformin, DPP‑4 inhibitors): additive glucose‑lowering effect may require dose adjustment.
  • Corticosteroids: can raise blood glucose, potentially necessitating higher insulin doses.
  • Thiazide diuretics: may cause modest hyperglycaemia, requiring closer monitoring.

Frequently Asked Questions

Insulatard is an intermediate‑acting insulin formulation used to provide basal insulin coverage in patients with type 1 or type 2 diabetes mellitus. It helps maintain stable fasting blood glucose levels and reduces overall hyperglycaemia when used as part of a comprehensive diabetes management plan.

Insulin Human mimics the action of natural human insulin by binding to insulin receptors on muscle, fat and liver cells. This activates intracellular pathways that increase glucose uptake, promote glycogen synthesis, and suppress hepatic glucose production, thereby lowering circulating blood glucose concentrations.

The dose of Insulatard is individualized. A qualified prescriber determines the appropriate amount based on the patient’s blood‑glucose monitoring results, body weight, diet, activity level and overall treatment goals. Patients should follow the dosing instructions provided by their healthcare professional.

Safety data for Insulatard in pregnancy and lactation are limited. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant. Healthcare providers will assess each case and may prefer alternative insulin regimens with more established safety profiles.

To order Insulatard, submit an enquiry on the product page at gnhindia.com indicating the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide. After verification of trade or institutional credentials, the sales team will respond with pricing, availability, shipping details (including cold‑chain handling) and any required import documentation.

Insulatard is an intermediate‑acting insulin human suspension, providing a gradual onset and duration of action that differs from long‑acting analogues such as glargine or detemir. While analogues offer a more predictable profile and less variability, Insulatard remains a cost‑effective option for many patients and is suitable when a slightly shorter basal coverage is desired.

Insulatard must be stored refrigerated at 2‑8 °C. Keep the vial in its original container, protect it from light, and avoid freezing or shaking the suspension. If needed for short‑term use, it may be kept at room temperature for up to 28 days, but it should be returned to refrigeration as soon as possible.

Insulatard is administered by subcutaneous injection, typically into the abdomen, thigh or upper arm. The injection should be given once or twice daily, depending on the prescriber’s regimen. Patients should rotate injection sites to minimise lipodystrophy and follow aseptic technique for each dose.

The most serious risks include severe hypoglycaemia, which can cause loss of consciousness or seizures, and anaphylactic reactions that may threaten airway patency. Patients should be educated to recognise early signs of low blood glucose and allergic responses, and seek immediate medical attention if they occur.

Insulatard should not be used by individuals with a known hypersensitivity to insulin human or any excipients in the formulation. It is also contraindicated in patients experiencing hypoglycaemia until the condition is corrected, and in those with severe insulin resistance where alternative therapeutic strategies are more appropriate.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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