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

Humulin I (Isofano)

Active Ingredient:
Insulin Human
Origin:
EU

Humulin I (Isofano) (Insulin Human)

Humulin I (Isofano) is a pharmaceutical product containing the active ingredient insulin human, supplied as a sterile injectable solution for intramuscular or subcutaneous administration. It is a biosynthetic form of human insulin, marketed in the European Union and available by prescription for the management of blood glucose levels in diabetes. The preparation is intended for use under the guidance of a healthcare professional and conforms to EU pharmaceutical standards.

Manufacturer / TM Owner

Eli Lilly Italia S.P.A.

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Indications & Clinical Uses

Humulin I (Isofano) is used as a short‑acting insulin to help control hyperglycemia in patients with diabetes mellitus.

  • To lower elevated blood glucose in type 1 diabetes when administered at mealtimes.
  • To provide supplemental insulin coverage for type 2 diabetes patients who require additional glycemic control.
  • To be used in insulin‑pump therapy or as a correction dose in conjunction with basal insulin regimens.
  • To assist in managing glucose levels during periods of stress, illness, or surgery when insulin requirements may increase.

How It Works

  • Insulin human binds to the insulin receptor, a transmembrane tyrosine kinase, on muscle, adipose and hepatic cells. Receptor activation triggers autophosphorylation and downstream signaling through the PI3K‑Akt pathway, promoting translocation of GLUT‑4 transporters to the cell surface, increasing glucose uptake, and inhibiting hepatic gluconeogenesis. The net effect is a rapid reduction in circulating glucose concentrations. Additionally, insulin suppresses lipolysis and protein catabolism, contributing to overall metabolic regulation.

Side Effects

Like other insulin preparations, Humulin I (Isofano) may be associated with adverse reactions that vary in frequency and severity.

Common

  • Injection site pain, redness or swelling.
  • Mild hypoglycemia presenting as shakiness, sweating, or hunger.
  • Weight gain associated with improved glycemic control.
  • Lipodystrophy or skin thickening at repeated injection sites.

Serious

  • Severe hypoglycemia leading to loss of consciousness or seizures.
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Persistent hypokalemia or electrolyte disturbances.

Precautions & Warnings

Healthcare providers should consider several precautionary measures when prescribing Humulin I (Isofano) to ensure safe and effective use.

  • Verify patient’s diagnosis and insulin requirements before initiating therapy.
  • Monitor blood glucose regularly to adjust dose and avoid hypoglycemia.
  • Use caution in patients with renal or hepatic impairment, as insulin clearance may be reduced.
  • Assess for a history of allergic reactions to insulin or excipients.
  • Educate patients on proper injection technique and rotation of sites.
  • Consider pregnancy status; insulin requirements may change during gestation.
  • Review concomitant medications that can mask hypoglycemia symptoms.

Avoid Interactions

Humulin I (Isofano) can interact with other medicines, affecting glucose control or insulin action.

Avoid

  • Concurrent use of other rapid‑acting insulins or insulin analogues without dose adjustment.
  • Beta‑blockers that may blunt hypoglycemia warning signs.
  • MAO‑inhibitors or certain antidepressants that can potentiate insulin’s glucose‑lowering effect.

Use with caution

  • Oral hypoglycemic agents (e.g., sulfonylureas, meglitinides) may increase risk of hypoglycemia.
  • Corticosteroids, thiazide diuretics, or growth hormone can raise blood glucose, requiring dose changes.
  • Alcohol consumption can cause delayed hypoglycemia, especially when combined with insulin.

Frequently Asked Questions

Humulin I (Isofano) contains insulin human, a short‑acting, biosynthetic form of human insulin used to lower blood glucose.

It is supplied as a sterile solution for injection and can be given either intramuscularly or subcutaneously, according to clinical guidance.

Yes, it may be prescribed for patients with type 1 diabetes and for type 2 diabetes when additional rapid‑acting insulin is needed.

Common adverse reactions include injection‑site discomfort, mild hypoglycemia, weight gain, and localized lipodystrophy.

Medical attention is warranted for signs of severe hypoglycemia, allergic reactions such as swelling or difficulty breathing, or persistent electrolyte abnormalities.

Insulin is generally considered the preferred treatment for diabetes in pregnancy, but dosing may need adjustment; patients should discuss use with their obstetric and diabetes care team.

Alcohol can potentiate insulin’s glucose‑lowering effect and may cause delayed hypoglycemia, especially when taken with insulin.

Regular self‑monitoring of blood glucose, periodic assessment of HbA1c, and observation for signs of hypoglycemia are recommended.

Mixing insulins should only be done under professional supervision, as dose adjustments are required to avoid unpredictable glucose control.

Patients should follow their healthcare provider’s instructions, which typically involve administering the missed dose as soon as possible if it is still within a reasonable time frame, or skipping it if it is close to the next scheduled dose.

The product should be stored in a refrigerator (2‑8 °C) before use and may be kept at room temperature for a limited period after opening, as indicated on the label.

The Anatomical Therapeutic Chemical (ATC) classification code for insulin human is A10AB01.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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