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Humulin Regular

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin Regular (Insulin Human (Rdna))

Humulin Regular is a short‑acting insulin human (rDNA) product supplied as a sterile injection solution for subcutaneous use. It contains recombinant human insulin as the active ingredient and is marketed in the European Union as a prescription‑only medication. The formulation is designed to provide rapid glucose‑lowering effects after injection, supporting the management of diabetes mellitus.

Manufacturer / TM Owner

Lilly Portugal - Produtos Farmacêuticos, Lda

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Indications & Clinical Uses

Humulin Regular is indicated for the control of blood glucose in patients with diabetes mellitus. It is used as part of a comprehensive diabetes management plan that may include diet, exercise, and other antidiabetic agents.

  • Treatment of type 1 diabetes mellitus in adults, adolescents, and children.
  • Management of type 2 diabetes mellitus when oral agents are insufficient.
  • Use in hospital settings for rapid correction of hyperglycemia.
  • Adjunct therapy during pregnancy or lactation when insulin is required.
  • Pre‑meal dosing to cover carbohydrate intake and prevent post‑prandial spikes.
  • Adjustment of basal insulin regimens in patients requiring tighter glycemic control.

How It Works

  • Humulin Regular delivers recombinant human insulin that binds to insulin receptors on muscle, fat, and liver cells. This binding activates the receptor’s tyrosine kinase activity, promoting translocation of GLUT‑4 transporters to the cell surface, which increases glucose uptake. In the liver, insulin suppresses gluconeogenesis and glycogenolysis, thereby reducing endogenous glucose production and lowering plasma glucose concentrations.

Side Effects

Humulin Regular may cause a range of adverse reactions, ranging from mild to severe. Awareness of these potential effects helps patients and clinicians monitor therapy safely.

Common

  • Hypoglycemia (low blood glucose)
  • Injection site redness, swelling, or itching
  • Lipodystrophy at the injection site
  • Weight gain
  • Mild nausea or abdominal discomfort

Serious

  • Severe hypoglycemia with loss of consciousness or seizures
  • Allergic reactions such as rash, urticaria, or anaphylaxis
  • Edema or heart failure exacerbation in susceptible individuals
  • Persistent hyperglycemia indicating possible insulin resistance or dosing issues

Precautions & Warnings

Before initiating Humulin Regular, several safety considerations should be reviewed to minimize risk.

  • Assess renal and hepatic function, as impairment can alter insulin clearance.
  • Monitor for signs of hypoglycemia, especially in patients with irregular meals or increased physical activity.
  • Use caution in patients with cardiovascular disease, as rapid glucose shifts may affect cardiac stability.
  • Adjust doses during pregnancy, lactation, or in the elderly, who may have altered insulin sensitivity.
  • Educate patients on proper injection technique to avoid lipohypertrophy.
  • Review concomitant use of other glucose‑lowering agents to prevent additive hypoglycemic effects.

Avoid Interactions

Humulin Regular can interact with various medications, influencing its efficacy or safety profile.

Avoid

  • Other insulin products or concentrated insulin formulations that may cause overlapping dosing.
  • Beta‑blockers, which can mask hypoglycemia symptoms.
  • High‑dose salicylates that may potentiate insulin’s glucose‑lowering effect.

Use with caution

  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that increase hypoglycemia risk.
  • ACE inhibitors or ARBs, which may enhance insulin sensitivity.
  • Corticosteroids, which can raise blood glucose and require dose adjustments.
  • Thiazide diuretics, which may affect glucose metabolism.
  • Alcohol, as it can cause unpredictable glucose fluctuations.

Frequently Asked Questions

Humulin Regular is a short‑acting, recombinant human insulin (rDNA) formulated for subcutaneous injection.

Onset of action typically occurs within 30 minutes after injection, with peak activity around 2–4 hours.

Yes, it is indicated for the treatment of both type 1 and type 2 diabetes mellitus when rapid glucose control is needed.

No, Humulin Regular is a prescription‑only medication in the European Union.

Common adverse effects include hypoglycemia, injection‑site reactions, mild weight gain, and occasional nausea.

Serious reactions such as severe hypoglycemia, allergic responses (rash, anaphylaxis), or sudden swelling/edema should be reported to a healthcare professional promptly.

Unopened vials should be refrigerated (2–8 °C). Once in use, they may be kept at room temperature for up to 28 days, protected from light.

Alcohol can cause unpredictable blood‑glucose changes and may increase the risk of hypoglycemia when combined with insulin.

Humulin Regular is usually administered 30 minutes before meals to match the post‑prandial glucose rise.

Regular blood‑glucose monitoring, including pre‑meal and occasional post‑meal checks, is recommended to guide dose adjustments.

Insulin is generally preferred for diabetes management during pregnancy, but dosing should be individualized and closely supervised by a healthcare provider.

Mixing with other insulin formulations is not recommended unless specifically instructed by a clinician, as it may affect absorption and action profiles.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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