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Humulin Regular

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin Regular (Insulin Human (Rdna))

Humulin Regular is a recombinant human insulin (Insulin human, rDNA) supplied as an injectable solution for subcutaneous or intravenous administration. It is marketed in the European Union and is available only by prescription. The product contains a standard strength of insulin, though specific unit concentration may vary by formulation. Humulin Regular is used to replace or supplement endogenous insulin in patients with diabetes mellitus and to help achieve glycemic control.

Manufacturer / TM Owner

Eli Lilly Danmark A/S

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Indications & Clinical Uses

Humulin Regular is indicated for the management of blood glucose in adults and children with diabetes.

  • Type 1 diabetes mellitus, as basal or mealtime insulin replacement.
  • Type 2 diabetes mellitus, when oral agents are insufficient to maintain target glucose levels.
  • Gestational diabetes, under specialist supervision, to control hyperglycemia.
  • Hospitalized patients requiring rapid‑acting insulin via intravenous infusion for surgical or critical care settings.
  • Use in pediatric patients when individualized dosing is required.

How It Works

  • Humulin Regular is a recombinant form of human insulin that binds to insulin receptors on the surface of muscle, adipose and hepatic cells. Receptor activation triggers autophosphorylation of the β‑subunit, initiating the intracellular PI3‑kinase/Akt signaling cascade. This cascade promotes translocation of glucose‑transporters (GLUT‑4) to the cell membrane, enhancing glucose uptake, and suppresses hepatic gluconeogenesis, thereby lowering plasma glucose concentrations in the bloodstream.

Side Effects

Like all insulin preparations, Humulin Regular may cause adverse reactions, most of which are related to its glucose‑lowering effect or injection site.

Common

  • Hypoglycemia (low blood glucose), presenting with sweating, tremor, hunger, or confusion.
  • Injection‑site reactions such as redness, swelling, or mild pain.
  • Lipodystrophy, including lipohypertrophy at repeated injection sites.

Serious

  • Severe hypoglycemia leading to loss of consciousness or seizures.
  • Allergic reactions ranging from urticaria to anaphylaxis.
  • Edema or fluid retention, especially in patients with cardiac or renal impairment.

Precautions & Warnings

Healthcare providers should assess individual risk factors before initiating Humulin Regular and monitor patients regularly during therapy.

  • Avoid use in patients with known hypersensitivity to recombinant human insulin or any excipients.
  • Adjust dose in renal or hepatic impairment, as insulin clearance may be reduced.
  • Caution in pregnant or breastfeeding women; benefits must outweigh potential risks.
  • Monitor for signs of hypoglycemia, especially when combined with other glucose‑lowering agents.
  • Educate patients on proper injection technique to prevent lipohypertrophy and dosing errors.
  • Consider cardiovascular status, as rapid glucose shifts can affect heart function.

Avoid Interactions

Humulin Regular can interact with several medications, altering glucose control or increasing adverse event risk.

Avoid

  • Concurrent use with sulfonylureas or meglitinides without dose adjustment may cause severe hypoglycemia.
  • Beta‑blockers can mask hypoglycemia symptoms, making detection difficult.

Use with caution

  • Concurrent corticosteroids may increase insulin requirements.
  • Thiazide diuretics can raise blood glucose levels, necessitating dose changes.
  • ACE inhibitors may enhance insulin sensitivity, potentially leading to hypoglycemia.
  • Alcohol intake can potentiate insulin’s glucose‑lowering effect and precipitate hypoglycemia.
  • Growth hormone therapy may antagonize insulin action, requiring higher doses.
  • Certain antipsychotics may affect glucose metabolism, warranting closer monitoring.

Frequently Asked Questions

Humulin Regular is a short‑acting, recombinant human insulin (rDNA) that mimics the action of naturally occurring insulin.

It is supplied as an injectable solution and can be given subcutaneously for routine dosing or intravenously in hospital settings for rapid glucose control.

It is prescribed for individuals with type 1 or type 2 diabetes who need insulin replacement, as well as for certain pregnant women with gestational diabetes under specialist care.

Yes, pediatric patients may receive Humulin Regular when individualized dosing and monitoring are provided by a qualified healthcare professional.

Common signs include sweating, shaking, hunger, confusion, irritability, and rapid heartbeat; severe cases may cause loss of consciousness or seizures.

Patients should rotate injections among the abdomen, thigh, and upper arm, avoiding areas of lipohypertrophy, to reduce local reactions and ensure consistent absorption.

Humulin Regular can be used during pregnancy when the benefits outweigh potential risks, but treatment should be supervised by an obstetrician‑diabetologist.

Blood glucose levels, signs of hypoglycemia, renal and hepatic function, and any injection‑site reactions should be regularly assessed.

Alcohol can enhance insulin’s glucose‑lowering effect and increase the risk of hypoglycemia, so patients should consume alcohol cautiously.

Unopened vials should be stored in a refrigerator (2‑8 °C). Once opened, they may be kept at room temperature not exceeding 30 °C for up to 28 days, depending on the manufacturer’s instructions.

Reduced renal function can decrease insulin clearance, so dose adjustments and closer glucose monitoring are recommended for patients with renal impairment.

The patient should contact their healthcare provider for guidance; generally, a missed dose is taken as soon as remembered unless the next scheduled dose is near, in which case the missed dose may be skipped to avoid hypoglycemia.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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