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Humulin M3 (30/70)

Active Ingredient:
Insulin Human
Origin:
EU

Humulin M3 (30/70) (Insulin Human)

Humulin M3 (30/70) is an injectable suspension of insulin human, a short‑acting and intermediate‑acting insulin mixture used in the European market. It contains recombinant human insulin at a 30% rapid‑acting and 70% protamine‑crystallized proportion, providing both immediate and prolonged glucose‑lowering effects. The product is prescription‑only and administered subcutaneously. It is supplied in vials for use with a syringe, and it is intended for patients requiring basal‑bolus insulin therapy.

Manufacturer / TM Owner

Eli Lilly Nederland B.V.

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Indications & Clinical Uses

Humulin M3 (30/70) is prescribed to help control blood glucose levels in adults and children with diabetes.

  • For both type 1 and type 2 diabetes mellitus when a mixed insulin regimen is appropriate.
  • As the basal (long‑acting) component of a basal‑bolus insulin therapy plan.
  • In patients who require a predictable overnight and fasting glucose control.
  • When combined with rapid‑acting insulin analogues to cover mealtime carbohydrate intake.
  • As an adjunct to oral antidiabetic drugs in type 2 diabetes when additional glucose lowering is needed.

How It Works

  • Insulin human binds to the insulin receptor on cell membranes, triggering autophosphorylation of the receptor’s β‑subunit. This activates the intracellular PI3‑K/Akt signaling cascade, which promotes translocation of GLUT‑4 transporters to the plasma membrane, increasing glucose uptake in muscle and adipose tissue. Concurrently, hepatic gluconeogenesis and glycogenolysis are suppressed, facilitating storage of glucose as glycogen and lowering blood glucose concentrations in the bloodstream.

Side Effects

The most frequently reported adverse reactions to Humulin M3 (30/70) are related to its glucose‑lowering action and injection site.

Common

  • Hypoglycemia, presenting as sweating, tremor, hunger, or confusion.
  • Redness, swelling, or itching at the injection site.
  • Transient weight gain due to increased glucose storage.
  • Lipodystrophy, such as localized lipoatrophy or lipohypertrophy.
  • Mild peripheral edema.

Serious

  • Severe hypoglycemia with loss of consciousness or seizures.
  • Immediate hypersensitivity reactions, including urticaria or angioedema.
  • Anaphylactic shock, a life‑threatening allergic response.
  • Development of insulin antibodies that may alter insulin action.
  • Significant electrolyte disturbances such as hypokalemia.

Precautions & Warnings

Before initiating therapy with Humulin M3 (30/70), several safety considerations should be reviewed to minimize risk.

  • Verify blood glucose levels and adjust dose to avoid hypoglycemia.
  • Use caution in patients with renal or hepatic impairment, as insulin clearance may be reduced.
  • Monitor pregnant or breastfeeding women closely; insulin requirements often change during these periods.
  • Assess for a history of allergic reactions to human insulin or excipients.
  • Educate patients on proper injection technique and rotation of sites to prevent lipodystrophy.
  • Consider dose adjustments during periods of illness, surgery, or changes in physical activity.
  • Review concomitant medications that may mask hypoglycemia symptoms.

Avoid Interactions

Humulin M3 (30/70) can interact with other medicines, affecting blood glucose control or insulin action.

Avoid

  • Concurrent use of other rapid‑acting insulin analogues without dose adjustment, which may cause severe hypoglycemia.
  • Beta‑blockers that blunt hypoglycemia warning signs.

Use with caution

  • Oral antidiabetic agents such as sulfonylureas or meglitinides, which increase hypoglycemia risk.
  • Corticosteroids, which raise blood glucose and may require higher insulin doses.
  • Diuretics, especially thiazides, that can affect potassium levels and insulin sensitivity.
  • ACE inhibitors or ARBs, which may potentiate insulin’s glucose‑lowering effect.
  • Alcohol, which can cause delayed hypoglycemia after insulin administration.

Frequently Asked Questions

Humulin M3 (30/70) contains recombinant human insulin in a suspension where 30% is rapid‑acting insulin and 70% is protamine‑crystallized insulin, providing both short‑acting and intermediate‑acting effects.

It is given by subcutaneous injection, typically using a syringe or an insulin pen, into the abdomen, thigh, buttock, or upper arm.

Humulin M3 (30/70) is indicated for both type 1 and type 2 diabetes mellitus when a mixed insulin regimen is appropriate.

The 30% rapid‑acting component lowers post‑prandial glucose, while the 70% protamine‑crystallized component provides basal coverage, helping to maintain stable glucose levels throughout the day and night.

Typical symptoms include sweating, trembling, hunger, confusion, irritability, and rapid heartbeat. Prompt treatment with fast‑acting carbohydrate is recommended.

The pregnancy category is listed as unknown; clinicians should weigh potential benefits against risks and monitor glucose closely if it is prescribed to pregnant patients.

Rotate injections within the same anatomical region (e.g., abdomen) and avoid using the same spot repeatedly to reduce the risk of lipodystrophy.

Stop the injection immediately, seek medical attention, and inform the healthcare provider about the reaction for possible alternative therapy.

Patients should coordinate carbohydrate intake with insulin timing and monitor blood glucose to adjust meals or snacks as needed.

Frequent monitoring is advised, especially before meals, at bedtime, and when symptoms of hypo‑ or hyperglycemia occur, to guide dose adjustments.

Store unopened vials in a refrigerator (2–8 °C). Once in use, keep at room temperature, away from direct heat or light, and discard after the labeled in‑use period.

Mixing with other insulin formulations is not routinely recommended without specific guidance from a healthcare professional, as it may alter the intended pharmacokinetic profile.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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