Product image of Humulin N (Insulin Human) supplied by GNH India

Humulin N

Active Ingredient:
Insulin Human
Origin:
EU

Humulin N (Insulin Human)

Humulin N is a prescription injectable suspension containing insulin human (NPH) as its active ingredient. It is supplied in a standardized concentration for subcutaneous administration and is marketed in the European Union. As a basal insulin, Humulin N provides prolonged glucose‑lowering activity to help maintain blood‑sugar control in patients with diabetes mellitus. The formulation is designed for dosing and is intended for use under the guidance of a healthcare professional.

Manufacturer / TM Owner

Eli Lilly Nederland B.V.

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Indications & Clinical Uses

Humulin N is indicated for the long‑term management of blood glucose in adults and children with diabetes.

  • Type 1 diabetes mellitus (insulin‑dependent).
  • Type 2 diabetes mellitus when basal insulin is required.
  • Adjunct to rapid‑acting insulin analogues for basal‑bolus regimens.
  • Use during pregnancy only when benefits outweigh risks (under medical supervision).
  • May be employed in patients transitioning from other intermediate‑acting insulins.
  • Part of intensive insulin therapy protocols for hospitalized patients with hyperglycemia.

How It Works

  • Humulin N contains recombinant human insulin that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers the tyrosine kinase pathway, promoting translocation of GLUT‑4 transporters and increasing glucose uptake. In the liver, insulin suppresses gluconeogenesis and glycogenolysis, reducing endogenous glucose production. The NPH formulation releases insulin slowly, providing a basal level of activity for up to 12–18 hours after subcutaneous injection.

Side Effects

Adverse reactions to Humulin N may vary in frequency and severity; they are typically categorized as common or serious.

Common

  • Mild hypoglycemia, especially if meals are delayed or carbohydrate intake is insufficient.
  • Injection site reactions such as redness, swelling, or itching.
  • Lipodystrophy presenting as localized fat accumulation or loss.
  • Transient weight gain related to improved glycemic control.

Serious

  • Severe hypoglycemia with neuroglycopenic symptoms (confusion, seizures, loss of consciousness).
  • Allergic reactions including urticaria, angioedema, or anaphylaxis.
  • Insulin antibody formation leading to unpredictable glucose response.

Precautions & Warnings

When prescribing or using Humulin N, clinicians and patients should consider several precautionary measures to minimize risks.

  • Assess renal and hepatic function, as impairment can prolong insulin action.
  • Adjust dose during periods of illness, stress, or changes in physical activity.
  • Monitor blood glucose closely when initiating therapy or modifying the regimen.
  • Use lower initial doses in elderly patients to reduce hypoglycemia risk.
  • Avoid use in patients with known hypersensitivity to insulin human or any excipients.
  • Counsel patients on proper injection technique to prevent lipohypertrophy.
  • Review pregnancy status; insulin requirements may change during gestation.

Avoid Interactions

Humulin N can interact with other medications that affect glucose metabolism or insulin pharmacodynamics, requiring dose adjustments or monitoring.

Avoid

  • Concurrent use of other insulin products or concentrated insulin formulations without appropriate dose reduction.
  • Co‑administration with sulfonylureas or meglitinides that may precipitate severe hypoglycemia.

Use with caution

  • Beta‑blockers may mask hypoglycemia symptoms; monitor glucose more frequently.
  • Corticosteroids and thiazide diuretics can increase insulin resistance, potentially requiring higher doses.
  • Oral contraceptives or hormone replacement therapy may alter insulin requirements.

Frequently Asked Questions

Humulin N is an intermediate‑acting insulin formulation containing human insulin (NPH) that provides basal glucose control.

Humulin N is typically administered once or twice daily, depending on the individual’s glycemic targets and physician’s recommendation.

Yes, Humulin N is approved for use in pediatric patients with type 1 diabetes when basal insulin therapy is needed.

Mild hypoglycemia may present as shakiness, sweating, hunger, irritability, or a rapid heartbeat.

Humulin N may be used during pregnancy only if the potential benefits outweigh the risks and under close medical supervision.

Humulin N has a slower onset and longer duration, providing basal insulin coverage, whereas rapid‑acting insulins act within minutes to control post‑meal glucose spikes.

If a dose is missed, take it as soon as you remember unless it is close to the time of the next scheduled dose; consult your healthcare provider for specific guidance.

Alcohol can increase the risk of hypoglycemia, especially when combined with insulin; monitor blood glucose closely if you consume alcohol.

Improved glycemic control can lead to modest weight gain due to reduced glucose loss in urine and increased caloric retention.

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

Elderly patients may have reduced renal function and a higher risk of hypoglycemia; lower starting doses and careful monitoring are advised.

Beta‑blockers can mask typical hypoglycemia symptoms such as tachycardia, making it harder to recognize low blood sugar; more frequent glucose checks are recommended.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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