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Humulin Regular

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin Regular (Insulin Human (Rdna))

Humulin Regular is a insulin product containing insulin human (rDNA) at a concentration of 100 U/mL, supplied as a solution for subcutaneous injection. It is a medication marketed in the European Union for the management of blood glucose in diabetes. The formulation mimics human insulin, providing onset of action to help control post‑prandial glucose excursions and is used as part of a diabetes care plan that includes diet, exercise, and monitoring.

Manufacturer / TM Owner

Eli Lilly Sweden Ab

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Indications & Clinical Uses

Humulin Regular is prescribed for patients with diabetes who need a rapid‑acting insulin to lower blood glucose after meals or during acute hyperglycemia.

  • Type 1 diabetes mellitus for basal‑bolus insulin regimens.
  • Type 2 diabetes mellitus when oral agents are insufficient.
  • Correction of post‑prandial hyperglycemia in both types.
  • Use in combination with a long‑acting (basal) insulin.
  • Management of hyperglycemia during illness or surgery.
  • May be used in pregnant women with diabetes when benefits outweigh risks (clinical judgment).

How It Works

  • Humulin Regular contains recombinant human insulin that binds to insulin receptors on muscle, adipose, and hepatic cells. Receptor activation triggers the tyrosine kinase cascade, promoting translocation of GLUT‑4 transporters to the cell surface, which increases glucose uptake. In the liver, insulin suppresses gluconeogenesis and glycogenolysis, reducing endogenous glucose production. The rapid pharmacokinetic profile yields an onset of action within 30 minutes, peaking at 2–4 hours.

Side Effects

Adverse reactions to Humulin Regular are generally related to its pharmacologic activity and injection site.

Common

  • Hypoglycemia (low blood glucose)
  • Pain, redness, or swelling at the injection site
  • Lipodystrophy or lipoatrophy at injection sites
  • Weight gain
  • Mild allergic skin reactions such as rash or itching

Serious

  • Severe hypoglycemia leading to seizures or loss of consciousness
  • Anaphylactic or severe allergic reactions (e.g., urticaria, angioedema)
  • Hypokalemia
  • Insulin‑induced edema
  • Acute bronchospasm in rare cases

Precautions & Warnings

Clinicians should consider several safety factors before initiating Humulin Regular.

  • Perform frequent blood‑glucose monitoring, especially when initiating or adjusting dose.
  • Adjust dose during periods of illness, reduced food intake, or increased physical activity.
  • Use caution in patients with hypoglycemia unawareness or a history of severe hypoglycemia.
  • Monitor renal and hepatic function; impairment may alter insulin clearance.
  • Pregnancy category is unknown; prescribe only if potential benefits justify the risks.
  • Avoid use in individuals with known hypersensitivity to insulin or any excipients.
  • Consider cardiovascular status, as rapid changes in glucose may affect heart disease patients.

Avoid Interactions

Humulin Regular can interact with several medicines that affect blood‑glucose levels or insulin action.

Avoid

  • Co‑administration of other rapid‑acting insulins or high‑dose sulfonylureas without dose adjustment.
  • Meglitinides taken concurrently without careful monitoring.
  • Excessive alcohol consumption, which can potentiate hypoglycemia.
  • Beta‑blockers that may mask hypoglycemia symptoms.

Use with caution

  • ACE inhibitors or ARBs, which may increase insulin sensitivity and risk of hypoglycemia.
  • Thiazide diuretics, which can raise blood glucose and may require dose changes.
  • Corticosteroids, which increase glucose production and may necessitate higher insulin doses.
  • Oral contraceptives or hormone replacement therapy, which can alter insulin requirements.
  • NSAIDs in patients with compromised renal function.

Frequently Asked Questions

Humulin Regular is supplied as a solution containing 100 units of insulin per milliliter (100 U/mL).

It is given by subcutaneous injection, typically into the abdomen, thigh, or upper arm.

Humulin Regular is indicated for both type 1 and type 2 diabetes mellitus when rapid glucose control is needed.

Onset of action occurs within about 30 minutes, with peak activity at 2–4 hours.

The most frequently reported adverse effects are hypoglycemia, injection‑site pain or redness, and mild skin reactions.

Pregnancy category is unknown; it should be used only if the potential benefits outweigh the potential risks and under medical supervision.

Unopened vials should be refrigerated between 2 °C and 8 °C (36 °F–46 °F) and protected from light.

After opening, the vial may be kept at controlled room temperature (up to 30 °C) for up to 28 days, after which it should be discarded.

Seek immediate medical assistance, administer glucagon if available, and follow emergency hypoglycemia protocols.

Sulfonylureas, meglitinides, and beta‑blockers can increase the risk of hypoglycemia and may require dose adjustments.

Excessive alcohol intake can potentiate insulin‑induced hypoglycemia and should be avoided or limited.

Mixing rapid‑acting insulins with other insulin types is not recommended unless specifically instructed by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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