Product image of Insuman Basal (Insulin Human) supplied by GNH India

Insuman Basal

Active Ingredient:
Insulin Human
Origin:
EU

Insuman Basal (Insulin Human)

Insulin human, the active ingredient in Insuman Basal, is an insulin presented as a solution for injection for subcutaneous use. It treats hyperglycaemia in patients with Type 1 and Type 2 diabetes mellitus.
GNH India supplies Insuman Basal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sanofi-Aventis Deutschland Gmbh

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Indications & Clinical Uses

Insuman Basal provides basal insulin therapy for diabetes management.

  • Type 1 diabetes mellitus: supplies long‑acting insulin to maintain fasting glucose levels.
  • Type 2 diabetes mellitus: supplements endogenous insulin to improve overall glycaemic control.
  • Diabetes requiring basal insulin supplementation: offers steady insulin coverage when oral agents are insufficient.

How It Works

  • Insulin human binds to insulin receptors on muscle, adipose and hepatic cells, activating the receptor’s tyrosine kinase activity. This triggers intracellular signaling that promotes glucose uptake, glycogen synthesis and inhibition of hepatic glucose production, thereby lowering circulating blood glucose concentrations.

Side Effects

Insuman Basal may cause adverse reactions typical of insulin therapy.

Common Side Effects

  • Hypoglycaemia: low blood glucose episodes, especially if dosing is excessive.
  • Injection site reactions: redness, swelling or itching at the injection site.
  • Weight gain: increased adipose tissue due to improved glucose utilisation.
  • Lipodystrophy: localized changes in subcutaneous fat with repeated injections.
  • Edema: mild fluid retention in extremities.

Serious or Rare Side Effects

  • Severe hypoglycaemia: neuroglycopenic symptoms requiring immediate assistance.
  • Allergic reactions: urticaria, rash, or anaphylaxis.
  • Insulin antibodies: may alter insulin effectiveness.
  • Acute metabolic acidosis: rare but serious metabolic disturbance.
  • Stevens‑Johnson syndrome: severe skin reaction, though extremely uncommon.

Precautions & Warnings

When using Insuman Basal, consider the following safety measures.

  • Dose individualisation: adjust dose based on regular blood glucose monitoring.
  • Hypoglycaemia risk: educate patients on recognising and treating low blood sugar.
  • Concomitant illnesses: modify therapy during infection, surgery or renal/hepatic impairment.
  • Pregnancy and lactation: use only if benefits outweigh potential risks; category not established.
  • Hypersensitivity: discontinue if signs of allergic reaction appear.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Insuman Basal can interact with several drug classes.

Major Interactions (Avoid)

  • Other insulin products: additive hypoglycaemic effect.
  • Meglitinides (e.g., repaglinide): increased risk of severe hypoglycaemia.
  • Beta‑blockers: may mask hypoglycaemia symptoms.

Moderate Interactions (Monitor Closely)

  • Oral antidiabetic agents (metformin, sulfonylureas): may potentiate glucose‑lowering effect.
  • ACE inhibitors and ARBs: can enhance insulin sensitivity.
  • Diuretics: may affect potassium levels influencing insulin action.
  • Corticosteroids: may increase insulin requirements.
  • Alcohol: can cause unpredictable glucose fluctuations.

Frequently Asked Questions

Insuman Basal is a basal insulin formulation used to provide long‑acting glucose control in patients with Type 1 or Type 2 diabetes mellitus. It is prescribed when consistent insulin coverage is needed to maintain fasting and basal blood‑glucose levels.

Insulin human mimics the natural hormone insulin. It binds to insulin receptors on muscle, fat and liver cells, activating pathways that increase glucose uptake, promote glycogen storage and suppress hepatic glucose production, thereby lowering blood‑sugar concentrations.

The dose of Insuman Basal is individualized. A qualified prescriber determines the appropriate amount based on the patient’s blood‑glucose readings, body weight, diet, activity level and other medications. Patients should follow the dosing instructions provided by their healthcare professional.

The pregnancy category for Insuman Basal is not definitively established. It should only be used during pregnancy or lactation if the prescriber judges that the potential benefits outweigh any possible risks to the mother or infant.

To order, submit an enquiry on the product page at gnhindia.com indicating the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping (including cold‑chain where required) and any necessary import documentation.

Insuman Basal contains human insulin, whereas many newer basal insulins use insulin analogues with altered pharmacokinetics. Human insulin has a well‑characterised safety profile and is generally less expensive, but analogue insulins may offer more predictable absorption and lower nocturnal hypoglycaemia rates in some patients.

Insuman Basal should be stored at 2‑8 °C (refrigerated) in its original carton, protected from light. Do not freeze or shake the vial. Once in use, it may be kept at room temperature (up to 30 °C) for a maximum of 28 days, after which any remaining solution should be discarded.

Insuman Basal is administered by subcutaneous injection, typically once daily at the same time each day. Injection sites include the abdomen, thigh or upper arm. Patients should rotate sites to minimise lipodystrophy and follow aseptic technique as instructed by their healthcare provider.

The most serious risks are severe hypoglycaemia, which can cause loss of consciousness or seizures, and allergic reactions ranging from rash to anaphylaxis. Prompt recognition and treatment of low blood‑glucose symptoms and any signs of hypersensitivity are essential.

Insuman Basal should be avoided in individuals with a known hypersensitivity to human insulin or any excipients in the formulation. It is also contraindicated in patients with severe hypoglycaemia unresponsive to treatment until the underlying cause is resolved.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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