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

Humulin I (Isophane)

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

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

Humulin I is a recombinant human insulin (isophane) formulated as a 100 U/mL injectable suspension. It is an intermediate‑acting insulin approved in the European Union for prescription use. The product is supplied for subcutaneous or intramuscular injection and is used to help regulate blood glucose levels in people with diabetes.

Manufacturer / TM Owner

Eli Lilly And Company Limited

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Indications & Clinical Uses

Humulin I is indicated for the management of diabetes mellitus when basal insulin coverage is required. It is commonly used as part of a comprehensive diabetes treatment plan that may include diet, exercise, and other medications.

  • Type 1 diabetes mellitus requiring basal insulin support.
  • Type 2 diabetes mellitus inadequately controlled with oral agents alone.
  • Gestational diabetes mellitus when insulin therapy is indicated.
  • Adjunct to rapid‑acting insulin for basal‑bolus regimens.
  • Situations where a steady, intermediate‑acting insulin profile is preferred.

How It Works

  • Humulin I contains insulin human (isophane), which binds to insulin receptors on muscle, adipose, and hepatic cells. Receptor activation triggers intracellular signaling cascades that promote glucose uptake into peripheral tissues and suppress hepatic gluconeogenesis, resulting in a gradual and prolonged reduction of plasma glucose concentrations characteristic of intermediate‑acting insulin preparations.

Side Effects

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

Common

  • Injection site redness, swelling, or itching.
  • Mild hypoglycemia (low blood sugar).
  • Weight gain.
  • Lipodystrophy at the injection site.
  • Transient headache.

Serious

  • Severe hypoglycemia leading to loss of consciousness.
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Persistent hypoglycemia requiring medical intervention.
  • Edema or heart failure exacerbation in susceptible patients.

Precautions & Warnings

When prescribing Humulin I, clinicians should consider several safety factors. Patients should be educated on proper injection technique and glucose monitoring.

  • Adjust dose during periods of illness, stress, or changes in physical activity.
  • Use caution in patients with renal or hepatic impairment.
  • Monitor for signs of hypoglycemia, especially in the elderly or those with irregular meals.
  • Evaluate cardiovascular status, as fluid retention may worsen heart failure.
  • Pregnancy category B; benefits should outweigh potential risks.
  • Store the suspension according to label instructions to maintain potency.

Avoid Interactions

Humulin I may interact with other agents that affect blood glucose or insulin metabolism.

Avoid

  • Concurrent use of other insulin products without dose adjustment.
  • Beta‑blockers that mask hypoglycemia symptoms.
  • High‑dose corticosteroids that increase glucose levels.

Use with caution

  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that can potentiate hypoglycemia.
  • Alcohol, which may cause unpredictable glucose fluctuations.
  • Thyroid hormones, as hyperthyroidism can enhance insulin clearance.
  • Certain diuretics that may affect electrolyte balance and glucose control.

Frequently Asked Questions

Humulin I is an intermediate‑acting insulin (isophane) that provides glucose control for approximately 12‑18 hours after injection.

Humulin I is classified as pregnancy category B in the EU, indicating that it may be used when the expected benefit justifies any potential risk to the fetus.

Unopened vials should be stored in a refrigerator (2‑8 °C). After opening, the suspension can be kept at room temperature (up to 30 °C) for up to 28 days, protected from light.

Common signs include sweating, shaking, rapid heartbeat, hunger, confusion, and in severe cases, loss of consciousness or seizures.

Yes, rotating injection sites helps reduce lipodystrophy and improves insulin absorption.

Humulin I should not be mixed with other insulin types in the same syringe; separate injections are recommended to maintain predictable absorption.

If a dose is missed, administer it as soon as remembered unless it is close to the time of the next scheduled dose; do not double the dose.

Alcohol can cause unpredictable changes in blood glucose, potentially increasing the risk of hypoglycemia when using Humulin I.

Elderly patients may have a higher risk of hypoglycemia and may require lower starting doses and more frequent glucose monitoring.

Humulin I has a slower onset and longer duration of action compared with short‑acting insulins, making it suitable for basal glucose control rather than mealtime spikes.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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