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Humulin I (Isophane)

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin I (Isophane) (Insulin Human (Rdna))

Humulin I (Isophane) is a prescription insulin product that contains recombinant human insulin (isophane) as its active ingredient. It is supplied as an injectable suspension for subcutaneous or intramuscular administration. The formulation is designed for prolonged absorption, providing basal insulin coverage. Humulin I is marketed in the European Union and is classified as a short‑acting intermediate‑acting insulin analog used in diabetes management therapy for patients worldwide.

Manufacturer / TM Owner

Eli Lilly Nederland B.V.

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Indications & Clinical Uses

Humulin I (Isophane) is indicated for the management of blood glucose in adults with diabetes.

  • Used in type 1 diabetes mellitus as part of a basal insulin regimen.
  • Used in type 2 diabetes mellitus when basal insulin is required.
  • Adjunct to oral antidiabetic agents in patients whose glucose is inadequately controlled.
  • Combined with rapid‑acting insulin analogues for basal‑bolus therapy.
  • May be employed during pregnancy when benefits outweigh risks, under medical supervision.

How It Works

  • Humulin I (Isophane) consists of recombinant human insulin that forms microprecipitates after injection, creating a depot that releases insulin slowly. The insulin molecules bind to insulin receptors on muscle and adipose cells, activating the receptor’s tyrosine kinase pathway. This promotes translocation of GLUT‑4 transporters, increasing glucose uptake, and suppresses hepatic gluconeogenesis, thereby lowering circulating blood glucose levels. The prolonged action helps maintain basal insulin levels between meals and overnight.

Side Effects

Adverse reactions to Humulin I (Isophane) can vary in frequency and severity.

Common

  • Mild hypoglycemia (low blood sugar).
  • Injection site redness, swelling, or itching.
  • Lipodystrophy at the injection site.
  • Weight gain associated with improved glycemic control.

Serious

  • Severe hypoglycemia with neurological symptoms.
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Edema or heart failure exacerbation.
  • Hypersensitivity leading to bronchospasm.

Precautions & Warnings

When prescribing or using Humulin I (Isophane), clinicians should consider several precautionary measures to ensure safe therapy.

  • Assess renal and hepatic function before initiation.
  • Monitor blood glucose regularly to adjust dose and prevent hypoglycemia.
  • Use caution in patients with cardiovascular disease or heart failure.
  • Evaluate for signs of allergic reactions during the first weeks of therapy.
  • Adjust dose during pregnancy, lactation, or in elderly patients.
  • Avoid abrupt discontinuation without medical guidance.

Avoid Interactions

Humulin I (Isophane) may interact with other medicines, affecting glucose control or insulin activity.

Avoid

  • Concurrent use of other insulin products without dose adjustment.
  • Beta‑blockers that mask hypoglycemia symptoms.
  • MAO‑inhibitors that can potentiate insulin’s glucose‑lowering effect.

Use with caution

  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that increase hypoglycemia risk.
  • Corticosteroids, which may raise blood glucose and require higher insulin doses.
  • Thyroid hormones, as hyperthyroidism can enhance insulin clearance.

Frequently Asked Questions

Humulin I (Isophane) is a recombinant human insulin formulated as an intermediate‑acting injectable suspension, classified as a basal insulin used to provide long‑lasting glucose control.

Yes, Humulin I is indicated for adults with type 1 diabetes as part of a basal regimen and for type 2 diabetes when basal insulin supplementation is needed.

Humulin I is administered by subcutaneous injection, and in some clinical situations it may be given intramuscularly, following the prescribing information.

After injection, the insulin forms microprecipitates that dissolve slowly, releasing insulin over several hours to maintain a steady basal level of glucose control.

Common adverse effects include mild hypoglycemia, injection‑site reactions such as redness or swelling, lipodystrophy, and modest weight gain.

Severe hypoglycemia can occur if the dose is too high, meals are missed, or if the patient engages in vigorous exercise without adjusting insulin or carbohydrate intake.

Patients should avoid using other insulin products without dose adjustment, beta‑blockers that mask hypoglycemia symptoms, and MAO‑inhibitors that may amplify insulin’s glucose‑lowering effect.

Unopened vials should be stored in a refrigerator (2‑8 °C). After opening, they may be kept at room temperature for up to 28 days, protecting them from light.

Dose may need adjustment during pregnancy; clinicians should balance maternal glucose control with fetal safety and monitor closely.

Regular self‑monitoring of blood glucose, periodic HbA1c testing, and clinical assessment of renal, hepatic, and cardiovascular status are recommended.

Yes, it is often combined with rapid‑acting insulin analogues in a basal‑bolus regimen to cover both basal and prandial glucose needs.

The patient should stop the injection immediately, seek medical attention, and inform their healthcare provider about the reaction for alternative therapy consideration.

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GNH India Pharmaceuticals Limited

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