Product image of Humulina Regular (Insulin Human (Rdna)) supplied by GNH India

Humulina Regular

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulina Regular (Insulin Human (Rdna))

Humulina Regular is a recombinant human insulin (Insulin human, rDNA) supplied as a 100 units/mL injectable solution for subcutaneous, intramuscular, or intravenous administration. It is a prescription‑only antidiabetic agent marketed in the European Union. The product is used to replace or supplement endogenous insulin in patients with diabetes mellitus and is also employed in acute care settings such as diabetic ketoacidosis under medical supervision and individualized dosing.

Manufacturer / TM Owner

Lilly, S.A. (Spain)

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Indications & Clinical Uses

Humulina Regular is indicated for several clinical situations where insulin replacement is required.

  • Management of type 1 diabetes mellitus
  • Management of type 2 diabetes mellitus
  • Intravenous treatment of diabetic ketoacidosis
  • Use in gestational diabetes when other options are unsuitable
  • Perioperative glucose control in surgical patients
  • Control of hyperglycemia in critically ill patients

How It Works

  • Humulina Regular contains 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 membrane, increasing glucose uptake. In the liver, insulin suppresses gluconeogenesis and glycogenolysis, thereby reducing endogenous glucose production and lowering plasma glucose concentrations.

Side Effects

Like all insulin preparations, Humulina Regular may be associated with adverse reactions that vary in frequency and severity.

Common

  • Hypoglycemia (low blood glucose)
  • Injection‑site pain, erythema, or lipohypertrophy
  • Weight gain
  • Peripheral edema

Serious

  • Severe hypoglycemia leading to loss of consciousness or seizures
  • Allergic reactions including anaphylaxis or urticaria
  • Hypokalemia (low potassium levels)
  • Development of insulin antibodies that may alter insulin action

Precautions & Warnings

Clinicians should consider several precautionary measures when prescribing Humulina Regular to ensure safe and effective use.

  • Assess renal and hepatic function before initiation and adjust therapy as needed
  • Use lower initial doses in elderly or frail patients
  • Monitor blood glucose closely during illness, stress, or changes in diet
  • Counsel patients on proper injection technique to avoid lipohypertrophy
  • Avoid use in individuals with known hypersensitivity to human insulin
  • Review pregnancy status; although category B, insulin therapy requires medical supervision
  • Educate patients on recognizing and managing hypoglycemia

Avoid Interactions

Humulina Regular can interact with other medicines, altering its glucose‑lowering effect or increasing the risk of adverse events.

Avoid

  • Sulfonylureas or meglitinides (increased risk of hypoglycemia)
  • Beta‑blockers (may mask hypoglycemia symptoms)
  • MAO‑A inhibitors (potentiated hypoglycemia)
  • High‑dose corticosteroids (counteract insulin effect)

Use with caution

  • ACE inhibitors or ARBs (may enhance insulin sensitivity)
  • Thiazide diuretics (may raise blood glucose)
  • Alcohol (unpredictable glucose changes)
  • Certain antidepressants such as SSRIs (potential glucose variability)
  • Concomitant use of other antidiabetic agents (requires dose adjustments)

Frequently Asked Questions

Humulina Regular is a recombinant human insulin (Insulin human, rDNA) provided as a sterile injectable solution containing 100 units per milliliter. It is available for subcutaneous, intramuscular, or intravenous administration and is prescribed for diabetes management.

Humulina Regular has a slower onset of action and a longer duration compared with rapid‑acting insulin analogues. It typically begins to lower blood glucose within 30 minutes, peaks at 2–4 hours, and can last up to 6–8 hours, making it suitable for basal coverage or intravenous use in emergencies.

Humulina Regular is prescribed for both type 1 and type 2 diabetes mellitus when insulin therapy is required. It is also used intravenously for the treatment of diabetic ketoacidosis.

Yes, Humulina Regular is approved for intravenous administration in the acute management of diabetic ketoacidosis under close medical supervision.

The most frequently reported adverse effects include hypoglycemia, injection‑site reactions such as pain or redness, weight gain, and peripheral edema.

Serious reactions that need urgent care are severe hypoglycemia with loss of consciousness or seizures, allergic responses such as anaphylaxis or urticaria, significant hypokalemia, and the development of insulin antibodies that affect glucose control.

Unopened vials or pens should be refrigerated (2 °C–8 °C) and protected from light. After opening, the product may be kept at controlled room temperature for a limited period as specified by the manufacturer, but should not be frozen.

Humulina Regular is classified as pregnancy category B, indicating no evidence of risk in animal studies. It may be used during pregnancy when the benefits outweigh potential risks, but therapy should be guided by a healthcare professional.

Medications that can potentiate hypoglycemia include sulfonylureas, meglitinides, beta‑blockers (which may mask symptoms), and MAO‑A inhibitors.

Reduced renal function can decrease insulin clearance, increasing the risk of hypoglycemia. Dose adjustments and more frequent glucose monitoring are recommended for patients with moderate to severe renal impairment.

Humulina Regular is administered subcutaneously for routine diabetes management, intramuscularly when rapid absorption is needed, and intravenously in hospital settings for conditions such as diabetic ketoacidosis.

Insulin therapy, including Humulina Regular, can be associated with modest weight gain due to its anabolic effects and improved glucose utilization.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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