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Humulin N

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin N (Insulin Human (Rdna))

Humulin N is a recombinant human insulin (rDNA) supplied as a solution for injection. It is provided in the standard concentration for subcutaneous use and is marketed in the European Union as a prescription‑only antidiabetic agent. Humulin N is indicated for basal insulin therapy in both type 1 and type 2 diabetes, helping to maintain steady glucose levels between meals and overnight. It is supplied in single‑dose vials for convenient administration.

Manufacturer / TM Owner

Eli Lilly Farmacevtska Družba

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Indications & Clinical Uses

Humulin N is used as a basal (long‑acting) insulin to control blood glucose in diabetes.

  • Type 1 diabetes mellitus as part of a basal‑bolus regimen.
  • Type 2 diabetes mellitus when oral agents are insufficient.
  • Adjunct therapy for patients requiring stable overnight glucose control.
  • Combination with rapid‑acting insulin for full‑day coverage.
  • May be used during pregnancy only under specialist supervision if indicated.

How It Works

  • Humulin N contains recombinant human insulin that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers autophosphorylation and downstream signaling through the PI3‑K/Akt pathway, promoting translocation of GLUT‑4 transporters and increasing glucose uptake. In the liver, insulin suppresses gluconeogenesis and glycogenolysis, thereby lowering endogenous glucose production and contributing to overall glycemic control.

Side Effects

Like other insulin preparations, Humulin N may cause injection‑site reactions and systemic effects related to hypoglycemia.

Common

  • Low blood sugar (hypoglycemia) presenting as sweating, tremor, or confusion.
  • Redness, swelling, or itching at the injection site.
  • Weight gain associated with improved glucose utilization.
  • Lipodystrophy (localized fat accumulation or loss) at repeated injection sites.
  • Bruising or bleeding at injection site.

Serious

  • Severe hypoglycemia leading to loss of consciousness or seizures.
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Persistent hyperglycemia indicating possible insulin resistance or dosing error.
  • Hypokalemia secondary to insulin‑driven cellular uptake of potassium.
  • Anaphylactic shock requiring immediate medical attention.

Precautions & Warnings

Before initiating Humulin N, clinicians should evaluate patient history and monitor several clinical parameters to reduce risk.

  • Assess renal and hepatic function, as impairment may alter insulin clearance.
  • Review history of hypoglycemia unawareness or severe episodes.
  • Adjust dose when starting or stopping concomitant glucocorticoids, beta‑blockers, or diuretics.
  • Educate patients on proper injection technique and rotation of sites.
  • Advise regular blood glucose monitoring, especially during illness or changes in diet.
  • Consider pregnancy status; insulin is the preferred agent but requires specialist guidance.

Avoid Interactions

Humulin N can interact with several medications that affect glucose metabolism or insulin pharmacodynamics.

Avoid

  • Concurrent use of other rapid‑acting insulins without dose adjustment, which may cause severe hypoglycemia.
  • MAO‑B inhibitors (e.g., selegiline) that potentiate insulin’s glucose‑lowering effect.
  • High‑dose salicylates that may increase insulin sensitivity and risk of hypoglycemia.

Use with caution

  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Corticosteroids, which can raise blood glucose and require higher insulin doses.
  • Thiazide diuretics, which may increase serum potassium shifts and affect glucose control.

Frequently Asked Questions

Humulin N is a recombinant human insulin (rDNA) formulated as a solution for subcutaneous injection and classified as a basal, long‑acting insulin.

It is prescribed for adults and children with type 1 or type 2 diabetes who need basal insulin to maintain stable glucose levels between meals and overnight.

Humulin N has a prolonged onset and duration, providing steady insulin levels for up to 24 hours, whereas rapid‑acting insulins act within minutes to cover meals.

Insulin is generally preferred for diabetes in pregnancy, but Humulin N should only be used under specialist supervision and after a risk‑benefit assessment.

Common reactions include redness, swelling, itching, bruising, or mild pain at the site of injection.

Unopened vials should be kept refrigerated (2‑8 °C). Once opened, they may be stored at room temperature not exceeding 30 °C for up to 28 days.

Symptoms can include sweating, tremor, hunger, confusion, irritability, or blurred vision. Severe cases may lead to loss of consciousness.

Yes, glucocorticoids can raise blood glucose, often requiring an increase in the insulin dose; dose adjustments should be made under medical guidance.

Humulin N is typically administered alone as a basal dose; mixing with other insulins is not recommended without specific instructions from a healthcare professional.

Regular self‑monitoring of blood glucose, periodic HbA1c testing, and routine assessment of renal and hepatic function are recommended.

Alcohol can increase the risk of hypoglycemia, especially when taken without food; patients should consume alcohol cautiously and monitor glucose levels closely.

If a dose is missed, take it as soon as remembered unless it is close to the time of the next scheduled dose; avoid double‑dosing and consult a healthcare provider for guidance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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