Product image of Humulin S (Soluble) (Insulin Human (Rdna)) supplied by GNH India

Humulin S (Soluble)

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin S (Soluble) (Insulin Human (Rdna))

Humulin S (Soluble) is a prescription solution for injection that contains insulin human produced by recombinant DNA technology. It is supplied in an unspecified strength and is administered subcutaneously. As a short‑acting insulin analogue, it is used to replace or supplement endogenous insulin in patients with diabetes mellitus. The product is marketed in the European Union and is classified as an antidiabetic therapeutic drug.

Manufacturer / TM Owner

Eli Lilly And Company Limited

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Indications & Clinical Uses

Humulin S (Soluble) is indicated for the management of blood glucose in both adult and pediatric patients with diabetes, and it may be incorporated into various insulin regimens.

  • Type 1 diabetes mellitus (insulin‑dependent)
  • Type 2 diabetes mellitus when oral agents are insufficient
  • To control hyperglycemia during meals (prandial insulin)
  • As part of basal‑bolus insulin regimens
  • For use in hospitalized patients requiring rapid glucose control
  • For use in insulin pump therapy when rapid‑acting insulin is required

How It Works

  • Humulin S (Soluble) contains recombinant human insulin that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers autophosphorylation and downstream signaling through the PI3‑kinase/Akt pathway, promoting translocation of GLUT‑4 transporters to the cell surface, increasing glucose uptake, and suppressing hepatic gluconeogenesis. This effect lowers circulating glucose levels and assists in maintaining target glycemic ranges.

Side Effects

Adverse reactions to Humulin S (Soluble) are reported in clinical practice and can vary in frequency and severity.

Common

  • Mild to moderate hypoglycemia, characterized by shakiness, sweating, or dizziness.
  • Pain, redness, or swelling at the injection site.
  • Localized lipohypertrophy or lipoatrophy with repeated use.
  • Gradual weight increase associated with improved glycemic control.

Serious

  • Severe hypoglycemia with confusion, seizures, or loss of consciousness.
  • Immediate‑type allergic reactions, including hives, swelling of the face or throat, and anaphylaxis.
  • Fluid retention leading to peripheral edema or worsening heart failure.
  • Marked decrease in serum potassium (hypokalemia) that may affect cardiac rhythm.

Precautions & Warnings

When prescribing Humulin S (Soluble), clinicians should consider several precautionary measures to ensure safe use.

  • Assess renal and hepatic function, as impairment may alter insulin clearance.
  • Monitor blood glucose closely during initiation, dose changes, or illness.
  • Use lower initial doses in pediatric patients and in those with low body weight.
  • Educate patients on recognizing and treating hypoglycemia promptly.
  • Review concomitant medications that affect glucose metabolism, such as glucocorticoids.
  • Caution in pregnancy and lactation; benefits must outweigh potential risks.
  • Avoid use in patients with known hypersensitivity to human insulin or excipients.

Avoid Interactions

Humulin S (Soluble) may interact with other agents that influence glucose levels or insulin action.

Avoid

  • Concurrent use of other rapid‑acting insulins without dose adjustment.
  • High‑dose beta‑blockers that mask hypoglycemia symptoms.
  • MAO‑inhibitors combined with sympathomimetic agents causing unpredictable glucose changes.

Use with caution

  • Oral hypoglycemic agents (e.g., sulfonylureas, meglitinides) that increase hypoglycemia risk.
  • Corticosteroids, which may raise blood glucose and require insulin dose increase.
  • Thiazide diuretics, which can affect potassium balance and insulin sensitivity.
  • Alcohol, especially in excess, which can cause delayed hypoglycemia.

Frequently Asked Questions

Humulin S (Soluble) is a short‑acting recombinant human insulin used to control post‑prandial blood glucose.

It is supplied as a solution for injection and is given subcutaneously, typically before meals.

Yes, it may be prescribed for pediatric patients with type 1 or type 2 diabetes, with dosing adjusted for age and weight.

The most frequently reported adverse effects include mild hypoglycemia, injection‑site pain or redness, and localized lipohypertrophy.

Medical attention is needed for severe hypoglycemia, signs of an allergic reaction such as swelling or difficulty breathing, or sudden swelling/edema.

Humulin S (Soluble) is classified as prescription‑only; its use in pregnancy should be based on a risk‑benefit assessment by a healthcare professional.

Humulin S (Soluble) has a rapid onset and short duration, targeting meal‑related glucose spikes, whereas long‑acting insulins provide basal coverage over 24 hours.

Blood glucose levels, signs of hypoglycemia, injection‑site reactions, weight changes, and renal or hepatic function should be regularly monitored.

Yes, excessive alcohol can cause delayed hypoglycemia and may interfere with glucose monitoring, so patients should consume alcohol cautiously.

Concurrent use of other rapid‑acting insulins without dose adjustment, high‑dose beta‑blockers, and certain MAO‑inhibitor combinations should be avoided.

It binds to insulin receptors, activating intracellular pathways that increase glucose uptake into cells and suppress hepatic glucose production.

Unopened vials should be kept refrigerated; after opening, the solution can be stored at room temperature for a limited period as indicated by the manufacturer.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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