Product image of Liprolog Mix50 (Insulin Lispro) supplied by GNH India

Liprolog Mix50

Active Ingredient:
Insulin Lispro
Origin:
EU

Liprolog Mix50 (Insulin Lispro)

Insulin lispro, the active ingredient in Liprolog Mix50, is a rapid‑acting insulin analog presented as a subcutaneous injectable formulation for subcutaneous use. It is used to control blood glucose in adults and children with type 1 or type 2 diabetes mellitus. The product is manufactured for the European Union market and meets EU regulatory standards.

GNH India supplies Liprolog Mix50 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eli Lilly Nederland B.V.

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Indications & Clinical Uses

Liprolog Mix50, a rapid‑acting insulin analog, is used to manage hyperglycaemia in diabetes mellitus.

  • Type 1 diabetes mellitus: improves post‑prandial glucose control and reduces risk of hyperglycaemic episodes.
  • Type 2 diabetes mellitus: assists in achieving glycaemic targets when combined with oral agents or basal insulin.

How It Works

  • Insulin lispro binds to insulin receptors on muscle and adipose cells, activating the receptor’s tyrosine kinase activity. This triggers intracellular signaling that moves GLUT‑4 transporters to the cell surface, increasing glucose uptake. In the liver it suppresses gluconeogenesis and glycogenolysis, lowering circulating glucose. Its rapid dissociation from hexameric complexes provides a quicker onset of action than regular human insulin.

Side Effects

Liprolog Mix50 may be associated with a range of adverse reactions, which are classified by frequency and severity.

Common Side Effects

  • Hypoglycaemia: low blood glucose levels, often presenting with sweating, tremor, or confusion.
  • Injection site reactions: redness, swelling, or itching at the injection site.
  • Lipodystrophy: localized changes in subcutaneous fat tissue.
  • Weight gain: modest increase in body weight over time.

Serious or Rare Side Effects

  • Severe hypoglycaemia: prolonged loss of consciousness or seizures.
  • Allergic reactions: urticaria, angioedema, or anaphylaxis.
  • Lipohypertrophy with repeated injections causing large fatty deposits.

Precautions & Warnings

When prescribing Liprolog Mix50, clinicians should consider several safety measures to minimise risks.

  • Dose adjustment: tailor the insulin dose to individual carbohydrate intake and blood glucose monitoring.
  • Hypoglycaemia risk: educate patients on recognising and treating low blood glucose promptly.
  • Renal impairment: monitor kidney function and adjust dose if necessary.
  • Pregnancy and lactation: use only if benefits outweigh potential risks, as safety data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Insulin lispro can interact with other medicines, altering its glucose‑lowering effect or increasing adverse events.

Major Interactions (Avoid)

  • Beta‑blockers: may mask hypoglycaemia symptoms, requiring closer monitoring.
  • MAO‑B inhibitors (e.g., selegiline): can potentiate insulin’s hypoglycaemic effect.

Moderate Interactions (Monitor Closely)

  • Oral hypoglycaemic agents (e.g., sulfonylureas, meglitinides): additive glucose‑lowering effect may increase hypoglycaemia risk.
  • Corticosteroids: may raise blood glucose, necessitating dose adjustments.
  • Thiazide diuretics: can impair glucose tolerance, requiring closer glucose monitoring.

Frequently Asked Questions

Liprolog Mix50 is a rapid‑acting insulin analog indicated for the management of blood glucose in patients with type 1 or type 2 diabetes mellitus, helping to control post‑meal hyperglycaemia.

Insulin lispro binds to insulin receptors, activates tyrosine kinase signalling, promotes GLUT‑4 translocation to the cell surface, increases peripheral glucose uptake, and suppresses hepatic glucose production, resulting in a rapid reduction of plasma glucose after meals.

The dose is individualized; a qualified prescriber determines the amount and timing based on the patient’s carbohydrate intake, blood‑glucose targets, and overall treatment plan.

Safety data are limited; it should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by the treating physician.

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 (including cold‑chain if needed) and import documentation.

Insulin lispro has a faster onset and shorter duration than regular human insulin and is comparable to other rapid‑acting analogs such as insulin aspart and insulin glulisine, allowing flexible mealtime dosing.

Store the product at 2‑8 °C in a refrigerator, protect it from light, and do not freeze or shake the vial or pen. Keep it in the original packaging until use.

It is injected subcutaneously into the abdomen, thigh, or upper arm using a sterile needle or pen device, preferably within 15 minutes before a meal.

The most critical risks are severe hypoglycaemia, which can lead to loss of consciousness or seizures, and rare allergic reactions such as anaphylaxis; patients should be educated to recognise symptoms and seek immediate medical attention.

Individuals with known hypersensitivity to insulin lispro or any component of the formulation, and patients experiencing severe hypoglycaemia unresponsive to treatment, should avoid using this product; suitability must be evaluated by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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