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

Humulin R (Regolare)

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin R (Regolare) (Insulin Human (Rdna))

Humulin R (Regolare) is a human insulin (Rdna) injectable solution supplied at a strength of 100 IU/mL. It is a prescription‑only medication marketed in the European Union for subcutaneous administration to help regulate blood glucose in people with diabetes. The formulation contains recombinant DNA‑derived insulin identical to endogenous human insulin, providing rapid onset of action after injection. It is stored in a vial and must be kept refrigerated until use.

Manufacturer / TM Owner

Eli Lilly Italia S.P.A.

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Indications & Clinical Uses

Humulin R is indicated for the management of hyperglycaemia in adults and children with diabetes mellitus.

  • Initiation of basal‑bolus insulin therapy in type 1 diabetes, typically combined with carbohydrate counting.
  • Supplemental rapid‑acting insulin for mealtime glucose control in type 2 diabetes, often used when oral agents are insufficient.
  • Adjustment of insulin dose during periods of illness, stress, or changes in diet, guided by frequent blood‑glucose monitoring.
  • Use in hospital or outpatient settings where a short‑acting insulin is required for intravenous or subcutaneous administration.
  • Replacement therapy when endogenous insulin production is insufficient, such as after pancreatectomy or in advanced diabetes.

How It Works

  • Humulin R consists of recombinant human insulin that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers autophosphorylation of the β‑subunit, initiating the PI3‑K/Akt signaling cascade that promotes translocation of GLUT‑4 transporters to the cell surface, increasing glucose uptake. In the liver, insulin suppresses gluconeogenesis and glycogenolysis, thereby lowering circulating glucose levels. The rapid onset of action reflects its short absorption time after subcutaneous injection.

Side Effects

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

Common

  • Hypoglycaemia, manifested by sweating, tremor, or confusion.
  • Injection‑site reactions such as redness, swelling, or itching.
  • Lipodystrophy, including lipohypertrophy at repeated injection sites.
  • Mild weight gain associated with improved glycaemic control.
  • Nausea or abdominal discomfort reported occasionally.
  • Transient visual disturbances such as blurred vision during rapid glucose shifts.

Serious

  • Severe hypoglycaemia leading to loss of consciousness or seizures.
  • Allergic reactions ranging from urticaria to anaphylaxis.
  • Edema or heart failure exacerbation in susceptible patients.
  • Persistent hyperglycaemia indicating possible insulin resistance.
  • Severe allergic response presenting as angio‑edema of the face, lips, or tongue.
  • Acute pancreatitis manifested by upper abdominal pain and elevated enzymes.

Precautions & Warnings

When prescribing Humulin R, clinicians should consider several precautionary measures to minimise risks and optimise therapy.

  • Assess renal and hepatic function, as impairment may alter insulin clearance.
  • Adjust dose in patients with fluctuating dietary intake or physical activity.
  • Monitor for hypoglycaemia in elderly, pregnant, or fasting individuals.
  • Educate patients on proper injection technique to avoid lipohypertrophy.
  • Review concomitant medications that may potentiate or mask hypoglycaemia.
  • Use caution in patients with a history of cardiovascular disease or heart failure.
  • Store the product according to label instructions; avoid freezing.

Avoid Interactions

Humulin R may interact with other agents that affect glucose metabolism or insulin action.

Avoid

  • Concurrent use of high‑dose sulfonylureas that can precipitate severe hypoglycaemia.
  • Administration of glucagon or beta‑agonists during an insulin overdose.
  • Mixing Humulin R with other insulin formulations not specifically approved for co‑administration.
  • Use of MAO inhibitors is not recommended as they may interfere with insulin metabolism.

Use with caution

  • Beta‑blockers, which may mask hypoglycaemic symptoms.
  • Corticosteroids, which can increase insulin resistance and require dose adjustments.
  • Diuretics, especially thiazides, that may elevate blood glucose.
  • Oral antidiabetic agents such as metformin, where combined therapy necessitates close monitoring.
  • Alcohol consumption can potentiate insulin’s glucose‑lowering effect and increase hypoglycaemia risk.

Frequently Asked Questions

Humulin R is supplied as an injectable solution containing 100 international units (IU) of insulin per milliliter.

Yes, Humulin R is indicated for the treatment of hyperglycaemia in both type 1 and type 2 diabetes mellitus.

Humulin R is a rapid‑acting insulin that peaks within 2–4 hours after subcutaneous injection, whereas long‑acting insulins provide a basal level of insulin over 24 hours.

Humulin R is administered by subcutaneous injection, typically into the abdomen, thigh, or upper arm.

Common adverse effects include hypoglycaemia, injection‑site reactions such as redness or itching, lipodystrophy, mild weight gain, occasional nausea, and transient visual disturbances.

If symptoms progress to confusion, loss of consciousness, seizures, or do not improve after consuming fast‑acting carbohydrates, emergency medical care should be sought.

Humulin R should be refrigerated (2–8 °C) and protected from light. Do not freeze; if frozen, discard the product.

Reduced renal function can decrease insulin clearance, increasing the risk of hypoglycaemia; dose adjustments and close monitoring are recommended.

Mixing Humulin R with other insulin formulations is not recommended unless the product label specifically permits it.

High‑dose sulfonylureas, glucagon, beta‑agonists, and MAO inhibitors should be avoided. Beta‑blockers, corticosteroids, thiazide diuretics, oral antidiabetics, and alcohol should be used with caution.

The pregnancy category for Humulin R is listed as unknown; treatment decisions should be made by a healthcare professional weighing potential benefits and risks.

Regular self‑monitoring of blood glucose, periodic assessment of HbA1c, and evaluation for signs of hypoglycaemia or adverse reactions are essential.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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