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

Humulin N (Nph) Cartridge

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin N (Nph) Cartridge (Insulin Human (Rdna))

Humulin N (Nph) Cartridge contains insulin human produced by recombinant DNA technology. It is supplied as a cartridge for use with an insulin pen, intended for subcutaneous injection. The product is a prescription‑only, EU‑marketed basal insulin formulation that provides intermediate‑acting glucose control for people with diabetes.

Manufacturer / TM Owner

Eli Lilly Čr, S.R.O.

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Indications & Clinical Uses

Humulin N is prescribed to manage blood glucose levels in diabetes mellitus. It is used as part of a comprehensive diabetes treatment plan that may include diet, exercise, and other medications.

  • Long‑acting basal insulin for Type 1 diabetes mellitus.
  • Long‑acting basal insulin for Type 2 diabetes mellitus.
  • Supplemental insulin therapy when rapid‑acting insulin is insufficient.
  • Combination therapy with mealtime insulin analogues.
  • Adjusted dosing for patients requiring stable overnight glucose control.

How It Works

  • Insulin human binds to insulin receptors on cell membranes, activating the intrinsic tyrosine kinase activity of the receptor. This triggers downstream signaling pathways that promote translocation of glucose transporter‑4 (GLUT‑4) to the cell surface, enhancing glucose uptake in muscle and adipose tissue, stimulating glycogen synthesis in the liver, and suppressing hepatic gluconeogenesis, thereby lowering plasma glucose concentrations.

Side Effects

Adverse reactions to Humulin N may vary in frequency and severity.

Common

  • Injection site pain or erythema.
  • Hypoglycemia (low blood glucose).
  • Lipodystrophy at injection sites.
  • Weight gain.
  • Edema or fluid retention.

Serious

  • Severe hypoglycemia leading to loss of consciousness.
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Persistent hyperglycemia indicating possible insulin resistance.
  • Rare cases of insulin antibody formation.

Precautions & Warnings

Before starting Humulin N, patients should be evaluated for factors that may affect insulin therapy.

  • Review history of hypoglycemia unawareness or severe episodes.
  • Assess renal or hepatic impairment, which may alter insulin clearance.
  • Monitor during pregnancy or lactation; adjust dosing as needed.
  • Caution in patients with cardiovascular disease due to potential fluid shifts.
  • Educate on proper injection technique to reduce lipodystrophy.
  • Ensure regular blood glucose monitoring to avoid over‑correction.

Avoid Interactions

Certain drugs can modify the glucose‑lowering effect of Humulin N.

Avoid

  • Concurrent use of other insulin products without dose adjustment.
  • High‑dose sulfonylureas that may precipitate severe hypoglycemia.
  • Beta‑blockers masking hypoglycemia symptoms.

Use with caution

  • Oral antihyperglycemics (e.g., metformin, thiazolidinediones) requiring dose titration.
  • Corticosteroids that increase glucose levels.
  • Diuretics that may affect fluid balance and insulin absorption.
  • ACE inhibitors or ARBs, which can potentiate hypoglycemia in some patients.

Frequently Asked Questions

Humulin N is an intermediate‑acting, recombinant human insulin formulated for subcutaneous delivery via an insulin pen cartridge.

It is inserted into a compatible insulin pen and injected subcutaneously, typically into the abdomen, thigh, or upper arm.

Yes, Humulin N is indicated as a basal insulin component for both Type 1 and Type 2 diabetes management.

Humulin N generally begins to lower glucose within 2–4 hours after injection, peaks around 6–10 hours, and can provide glucose control for up to 18–24 hours.

Rotating injection sites helps reduce the risk of lipodystrophy and should be done with each dose.

Common side effects include mild hypoglycemia, injection‑site pain, redness, and occasional weight gain.

Seek medical attention for severe hypoglycemia, signs of an allergic reaction such as swelling or difficulty breathing, or persistent high blood glucose despite dosing.

Insulin is generally considered safe during pregnancy, but dosing may need adjustment; consult a healthcare professional for individualized guidance.

Store unopened cartridges in a refrigerator (2–8 °C). Once in use, keep at room temperature away from direct heat and light, and discard after the manufacturer’s recommended period.

Avoid combining with other insulin products without dose adjustment and be cautious with high‑dose sulfonylureas, as they can increase the risk of severe hypoglycemia.

Regular self‑monitoring of blood glucose is essential to adjust dosing and prevent hypo‑ or hyperglycemia.

Transitioning should be done under medical supervision, with dose conversion based on individual response and glucose monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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