Product image of Humulin M3 (30/70) Cartridge (Insulin Human (Rdna)) supplied by GNH India

Humulin M3 (30/70) Cartridge

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin M3 (30/70) Cartridge (Insulin Human (Rdna))

Humulin M3 (30/70) Cartridge contains insulin human (recombinant DNA) at 100 U/mL, supplied in a cartridge for use with an insulin pen. It combines 30% rapid‑acting and 70% intermediate‑acting insulin in a single preparation approved in the European Union for prescription use. The product is indicated for subcutaneous administration in patients who need both mealtime and background insulin in one daily injection as part of their therapy.

Manufacturer / TM Owner

Eli Lilly Čr, S.R.O.

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Indications & Clinical Uses

Humulin M3 (30/70) is prescribed for adults and children with diabetes who require a combined basal and bolus insulin regimen.

  • Management of type 1 diabetes mellitus when multiple daily injections are part of the treatment plan.
  • Adjunct therapy for type 2 diabetes mellitus inadequately controlled with oral agents or basal insulin alone.
  • Simplification of insulin therapy by providing both rapid‑acting and intermediate‑acting components in a single cartridge.
  • Use in hospital or outpatient settings where a premixed insulin can reduce injection frequency.

How It Works

  • Insulin human (30/70) binds to insulin receptors on muscle, adipose and hepatic cells, activating the receptor tyrosine kinase pathway. This triggers downstream signaling that promotes translocation of GLUT‑4 transporters to the cell membrane, increasing glucose uptake, while simultaneously suppressing hepatic gluconeogenesis. The rapid‑acting fraction initiates glucose disposal within minutes, and the intermediate‑acting fraction sustains basal insulin activity for up to 24 hours.

Side Effects

Like all insulin products, Humulin M3 may cause adverse reactions. Reported events are grouped by frequency and severity.

Common

  • Mild hypoglycemia with sweating, tremor, or brief confusion.
  • Injection‑site redness, swelling, itching or mild pain.
  • Lipohypertrophy at repeatedly used injection sites.
  • Nausea or abdominal discomfort after injection.
  • Transient headache occurring shortly after injection.

Serious

  • Severe hypoglycemia needing assistance or medical treatment.
  • Allergic reaction ranging from urticaria to anaphylaxis.
  • Fluid retention, edema, or worsening heart failure.
  • Persistent hyperglycemia suggesting dosing error or resistance.
  • Serum‑sickness‑like hypersensitivity reaction with fever and joint pain.
  • Unexplained weight gain indicating possible fluid overload.

Precautions & Warnings

When prescribing Humulin M3, clinicians should consider several precautionary measures to ensure safe use.

  • Assess renal and hepatic function, as impairment may alter insulin clearance.
  • Monitor blood glucose closely during initiation, dose changes, or periods of illness.
  • Adjust doses in patients prone to hypoglycemia, such as the elderly or those with irregular meals.
  • Counsel patients on proper injection technique and site rotation to reduce lipodystrophy.
  • Review concomitant medications that can mask hypoglycemia symptoms.
  • Use caution in pregnancy; although category B, glycemic targets should be individualized.
  • Evaluate cardiovascular status, as fluid retention may exacerbate heart failure.

Avoid Interactions

Humulin M3 can interact with other agents that affect glucose levels or insulin action.

Avoid

  • Concurrent use of other rapid‑acting insulins without dose adjustment.
  • Beta‑blockers that may mask hypoglycemia symptoms.
  • High‑dose corticosteroids that increase insulin resistance.
  • MAO‑inhibitors combined with sympathomimetic agents causing unpredictable glucose changes.

Use with caution

  • Oral antidiabetic drugs (e.g., sulfonylureas, meglitinides) that may potentiate hypoglycemia.
  • ACE inhibitors or ARBs, which can enhance insulin sensitivity.
  • Thiazide diuretics that may raise blood glucose.
  • Alcohol consumption, which can cause delayed hypoglycemia.

Frequently Asked Questions

Humulin M3 contains recombinant human insulin formulated as a premixed solution with 30% rapid‑acting and 70% intermediate‑acting insulin at a concentration of 100 U/mL, supplied in a cartridge for insulin pens.

The 30% rapid‑acting component lowers post‑prandial glucose quickly, while the 70% intermediate‑acting component provides basal coverage for several hours, together offering both mealtime and background insulin effects.

It is prescribed for individuals with type 1 or type 2 diabetes who require a combined basal‑bolus regimen and prefer a single premixed injection to reduce the number of daily doses.

Store the unopened cartridge in a refrigerator (2–8 °C). Once in use, keep it at room temperature not exceeding 30 °C and discard after 28 days, even if there is remaining insulin.

Humulin M3 is classified as pregnancy category B in the EU, indicating no evidence of risk in animal studies. Use only if the potential benefit justifies the potential risk, and glycemic targets should be individualized.

Common signs include sweating, tremor, palpitations, visual disturbances, confusion, dizziness, and in severe cases, loss of consciousness or seizures.

Rotate injection sites with each dose, using different areas of the abdomen, thigh, or upper arm to minimize lipodystrophy and ensure consistent absorption.

If a dose is missed and the next scheduled dose is more than an hour away, administer the missed dose as soon as remembered. If it is close to the next dose, skip the missed dose and continue with the regular schedule. Do not double the dose.

Elderly patients may have reduced renal function and altered insulin sensitivity, increasing hypoglycemia risk. Start with lower doses, monitor glucose closely, and provide education on recognizing hypoglycemia.

Oral agents such as sulfonylureas or meglitinides can enhance the glucose‑lowering effect of Humulin M3, increasing the risk of hypoglycemia. Dose adjustments and close monitoring are recommended.

Used cartridges should be placed in a puncture‑resistant sharps container and disposed of according to local regulations for medical waste.

Alcohol can impair hepatic glucose production and may cause delayed hypoglycemia, especially when taken with insulin. Patients should consume alcohol in moderation and monitor blood glucose closely.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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