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

Humulin R

Active Ingredient:
Insulin Human
Origin:
EU

Humulin R (Insulin Human)

Humulin R is a short‑acting insulin product that contains the active ingredient insulin human. It is supplied as a solution for subcutaneous injection, typically in standard concentrations (e.g., 100 U/mL) approved for use in the European Union. The medication is prescribed to replace or supplement endogenous insulin in adults and children who need rapid insulin to control glucose spikes through the day.

Manufacturer / TM Owner

Eli Lilly Hrvatska D.O.O.

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Indications & Clinical Uses

Humulin R is indicated for the management of blood glucose in patients with diabetes mellitus.

  • Type 1 diabetes mellitus (insulin‑dependent)
  • Type 2 diabetes mellitus when oral agents or other injectables do not achieve target glycaemic control
  • Prandial (mealtime) glucose control to reduce post‑meal hyperglycaemia
  • Correction of acute hyperglycaemia as a supplemental (correction) dose
  • Use in pediatric patients as directed by a qualified healthcare professional
  • Adjunct therapy during pregnancy when insulin is required and other agents are contraindicated

How It Works

  • Humulin R provides insulin identical to human endogenous insulin. After subcutaneous injection, it is absorbed into the bloodstream where it binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers the tyrosine kinase pathway, promoting translocation of GLUT‑4 transporters to the cell surface, increasing glucose uptake, and suppressing hepatic gluconeogenesis, thereby lowering plasma glucose concentrations effectively in the body.

Side Effects

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

Common

  • Hypoglycaemia, presenting as sweating, tremor, dizziness, or confusion, especially if meals are missed or dose is excessive.
  • Injection‑site reactions such as pain, redness, swelling, or bruising that usually resolve spontaneously.
  • Lipodystrophy, including lipohypertrophy or lipoatrophy, at repeated injection sites.
  • Gradual weight gain associated with improved glycaemic control.

Serious

  • Anaphylactic reaction, characterized by difficulty breathing, throat swelling, or sudden drop in blood pressure.
  • Severe hypersensitivity manifesting as widespread rash, urticaria, or angio‑edema requiring immediate medical attention.
  • Persistent hyperglycaemia or ketoacidosis despite appropriate dosing, suggesting possible insulin resistance or dosing error.

Precautions & Warnings

When using Humulin R, certain precautions and warnings should be considered to minimise risk and ensure safe therapy.

  • Verify blood glucose before each injection and adjust dose according to current levels.
  • Avoid using Humulin R in patients with known hypersensitivity to human insulin or any excipients.
  • Monitor for hypoglycaemia, especially in elderly, children, or those with renal/hepatic impairment.
  • Use caution during pregnancy and lactation; insulin needs may change and require close supervision.
  • Store the product according to label instructions; discard after the indicated in‑use period.
  • Teach proper injection technique and site rotation to avoid lipodystrophy.

Avoid Interactions

Humulin R may interact with other medicines, affecting glucose control or increasing the risk of adverse events.

Avoid

  • Concurrent use of other rapid‑acting insulins without dose adjustment, which can cause severe hypoglycaemia.
  • Beta‑blockers that mask hypoglycaemia symptoms.
  • MAO‑A inhibitors that may potentiate insulin’s glucose‑lowering effect.

Use with caution

  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that increase hypoglycaemia risk; dose may need adjustment.
  • Corticosteroids, which raise blood glucose and may require higher insulin doses.
  • Thyroid hormones or thyroid replacement therapy, which can alter insulin requirements.

Frequently Asked Questions

Humulin R is a short‑acting, regular insulin that begins to work within 30 minutes after injection and peaks in 2–4 hours, unlike long‑acting insulins that provide a basal level of insulin over 24 hours.

Yes, Humulin R is prescribed for patients with type 1 diabetes and for type 2 diabetes when additional insulin is needed to achieve glycaemic targets.

Unopened vials should be refrigerated (2–8 °C). Once opened, the solution may be kept at room temperature not exceeding 30 °C for up to 28 days, after which any remaining insulin should be discarded.

Common signs include sweating, trembling, rapid heartbeat, hunger, dizziness, confusion, and irritability. Severe hypoglycaemia can cause loss of consciousness or seizures.

Repeated injections into the same spot can cause lipodystrophy. Rotating injection sites on the abdomen, thigh, or upper arm helps maintain consistent absorption and reduces tissue changes.

Humulin R is typically administered 30 minutes before a meal to match the rise in post‑prandial blood glucose, but exact timing should follow the prescribing clinician’s instructions.

Alcohol can increase the risk of hypoglycaemia, especially when taken on an empty stomach, and may mask its symptoms. Patients should consume alcohol with food and monitor glucose closely.

If a dose is missed and blood glucose is still elevated, the missed dose can usually be taken as soon as remembered, provided there is enough time before the next scheduled dose. If unsure, consult a healthcare professional.

Insulin is the preferred medication for managing diabetes in pregnancy, but dose requirements may change. Close monitoring and dose adjustments by a qualified provider are essential.

Beta‑blockers can blunt the typical adrenergic symptoms of hypoglycaemia (such as rapid heartbeat), making low blood glucose harder to recognise. Patients on both should monitor glucose more frequently.

Humulin R is available in both vial and pre‑filled pen formats. The choice depends on patient preference and prescribing guidelines.

Regular self‑monitoring of blood glucose, periodic HbA1c testing, and occasional renal or hepatic function tests are recommended to assess effectiveness and safety.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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