Product image of Humulin M3 (Mixture 3) (Insulin Human) supplied by GNH India

Humulin M3 (Mixture 3)

Active Ingredient:
Insulin Human
Origin:
EU

Humulin M3 (Mixture 3) (Insulin Human)

Humulin M3 (Mixture 3) is an insulin human product supplied as an injectable solution for intramuscular or subcutaneous use. It contains human insulin as the active ingredient and is marketed in the European Union. The formulation combines short‑acting and intermediate‑acting insulin components to provide rapid onset and prolonged glucose‑lowering effects, supporting diabetes management. Humulin M3 is intended for patients needing a mixed insulin regimen for basal and prandial control.

Manufacturer / TM Owner

Eli Lilly And Company Limited

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Indications & Clinical Uses

Humulin M3 is indicated for the treatment of diabetes mellitus in patients who require both basal and mealtime insulin coverage.

  • Type 1 diabetes mellitus requiring mixed insulin therapy.
  • Type 2 diabetes mellitus when oral agents and basal insulin are insufficient.
  • Adjunct to diet and exercise for glycemic control.
  • Use in patients who benefit from a fixed ratio of rapid‑acting and intermediate‑acting insulin.
  • Situations where a single daily injection simplifies the regimen.
  • Patients transitioning from separate rapid‑acting and intermediate‑acting insulin preparations.

How It Works

  • Humulin M3 binds to insulin receptors on peripheral tissues, activating the receptor’s intrinsic tyrosine kinase activity. This triggers intracellular signaling cascades that promote glucose transporter (GLUT4) translocation to the cell membrane, increasing glucose uptake in muscle and adipose tissue. Simultaneously, hepatic gluconeogenesis and glycogenolysis are suppressed, reducing endogenous glucose production and lowering blood glucose concentrations.

Side Effects

Adverse reactions to Humulin M3 may occur; they are categorized by frequency and severity.

Common

  • Hypoglycemia (low blood glucose).
  • Injection‑site pain, redness, or swelling.
  • Lipodystrophy at injection sites.
  • Weight gain.
  • Allergic skin reactions such as rash or urticaria.

Serious

  • Severe hypoglycemia with loss of consciousness.
  • Anaphylactic or systemic allergic reaction.
  • Edema or exacerbation of heart failure.
  • Persistent hyperglycemia due to insulin resistance.

Precautions & Warnings

When prescribing Humulin M3, clinicians should consider several safety factors to minimize risks.

  • Risk of hypoglycemia; patients need regular glucose monitoring.
  • Adjust dose in renal or hepatic impairment.
  • Use with caution in pregnancy; benefits must outweigh potential risks.
  • Avoid in patients with known hypersensitivity to human insulin or formulation excipients.
  • Store the product according to label to maintain potency.
  • Educate patients on proper injection technique and rotation sites.

Avoid Interactions

Humulin M3 can interact with other medicines, affecting blood glucose levels or insulin action.

Avoid

  • Concurrent use of other insulin products without dose adjustment.
  • Beta‑blockers that may mask hypoglycemia symptoms.
  • Alcohol excess that can precipitate hypoglycemia.
  • MAO‑inhibitors that may potentiate insulin effects.

Use with caution

  • Thiazide or loop diuretics that may raise blood glucose.
  • ACE inhibitors or ARBs that can enhance insulin sensitivity.
  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) requiring dose coordination.
  • Corticosteroids that increase glucose levels.
  • Lipid‑lowering agents (e.g., fibrates) that may affect insulin metabolism.

Frequently Asked Questions

Humulin M3 is a human insulin formulation that combines short‑acting and intermediate‑acting insulin in a single injectable solution, providing both rapid onset and prolonged glucose‑lowering action compared with single‑component insulins.

Humulin M3 is prescribed for both type 1 and type 2 diabetes mellitus when a mixed insulin regimen is needed to cover basal and mealtime glucose control.

The product is given by intramuscular or subcutaneous injection, typically using a sterile needle and syringe or an appropriate insulin pen, following the dosing schedule determined by a healthcare professional.

Humulin M3 already contains a fixed ratio of rapid‑acting and intermediate‑acting insulin; mixing with additional insulin should only be done under medical supervision to avoid dosing errors.

Unopened vials or pens should be stored in a refrigerator (2–8 °C). Once in use, they may be kept at controlled room temperature (up to 30 °C) for a period specified by the manufacturer, usually up to 28 days.

Common signs include sweating, trembling, hunger, confusion, rapid heartbeat, and visual disturbances. Severe hypoglycemia may cause loss of consciousness or seizures and requires immediate treatment.

The pregnancy category for Humulin M3 is listed as unknown. Use during pregnancy should be based on a risk‑benefit assessment by the prescribing clinician.

Alcohol can potentiate the glucose‑lowering effect of insulin and increase the risk of hypoglycemia, especially when consumed on an empty stomach.

Patients should discontinue use and seek immediate medical attention if they develop signs of a systemic allergic reaction such as rash, itching, swelling, dizziness, or difficulty breathing.

Elderly patients may have altered renal or hepatic function and a higher risk of hypoglycemia; dose adjustments and close monitoring of blood glucose are often required.

Yes, it can be combined with oral agents such as metformin or sulfonylureas, but dose coordination is essential to avoid excessive glucose lowering.

Patients should follow the guidance provided by their healthcare professional, which typically involves taking the missed dose as soon as remembered if it is still within a safe time window, or skipping it if it is close to the next scheduled dose.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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