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Humulin R

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin R (Insulin Human (Rdna))

Humulin R is a recombinant human insulin (Insulin human) supplied as a 100 U/mL injectable solution for subcutaneous administration. It is a short‑acting insulin indicated for the management of diabetes mellitus and is marketed in the European Union as a prescription‑only product.

Manufacturer / TM Owner

Lilly France

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Indications & Clinical Uses

Humulin R is used to control blood glucose levels in patients with diabetes. It is appropriate for both type 1 and type 2 diabetes and may be employed as part of a basal‑bolus regimen or in combination with other antidiabetic agents.

  • Initiation of insulin therapy in newly diagnosed type 1 diabetes.
  • Supplemental insulin for type 2 diabetes when oral agents are insufficient.
  • Management of hyperglycemia during illness or stress.
  • Adjunctive therapy in diabetic ketoacidosis after initial fluid and electrolyte replacement.
  • Adjustments for meals and physical activity in insulin‑treated patients.

How It Works

  • Humulin R contains recombinant human insulin that binds to insulin receptors on cell membranes, activating the intrinsic tyrosine kinase activity. This triggers downstream signaling pathways, including the PI3‑K/Akt cascade, which enhances glucose transporter (GLUT4) translocation to the cell surface, increases peripheral glucose uptake, suppresses hepatic gluconeogenesis, and promotes glycogen synthesis, thereby lowering plasma glucose concentrations.

Side Effects

Humulin R may cause a range of adverse reactions, ranging from mild to severe. Awareness of common and serious events helps clinicians monitor patients effectively.

Common

  • Hypoglycemia (low blood glucose)
  • Injection‑site pain or erythema
  • Lipodystrophy at the injection site
  • Weight gain
  • Allergic skin reactions such as rash or pruritus

Serious

  • Severe hypoglycemia with neuroglycopenic symptoms
  • Anaphylactic reaction or angioedema
  • Persistent hyperglycemia indicating insulin resistance
  • Edema or congestive heart failure exacerbation
  • Hypersensitivity leading to urticaria or bronchospasm

Precautions & Warnings

When prescribing Humulin R, clinicians should consider patient‑specific factors and monitor for potential complications.

  • Assess renal and hepatic function before initiating therapy.
  • Adjust dose in patients with fluctuating dietary intake or exercise patterns.
  • Use caution in pregnant or breastfeeding women; category B indicates no proven risk.
  • Monitor for signs of hypoglycemia, especially in the elderly or those with impaired awareness.
  • Educate patients on proper injection technique to reduce lipodystrophy.
  • Review concomitant medications that may mask hypoglycemia symptoms.

Avoid Interactions

Humulin R can interact with several drug classes, influencing its efficacy or safety profile.

Avoid

  • Concurrent use of other rapid‑acting insulins without dose adjustment, which may precipitate severe hypoglycemia.
  • Beta‑blockers that can blunt hypoglycemia warning signs.

Use with caution

  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that increase hypoglycemia risk.
  • Corticosteroids, which may raise glucose levels and require dose escalation.
  • Diuretics, especially thiazides, that can affect electrolyte balance and glucose control.
  • ACE inhibitors or ARBs, which may potentiate insulin’s glucose‑lowering effect.
  • Alcohol, as it can cause unpredictable glucose fluctuations.

Frequently Asked Questions

Humulin R is supplied as a 100 U/mL injectable solution for subcutaneous injection.

Humulin R is indicated for both type 1 and type 2 diabetes mellitus as part of insulin therapy.

Humulin R is a short‑acting insulin that peaks within 2–4 hours, whereas long‑acting insulins provide a basal level of insulin over 24 hours.

Humulin R is classified as pregnancy category B, indicating no proven risk in animal studies, but it should be used only if clearly needed.

Common adverse effects include hypoglycemia, injection‑site pain, lipodystrophy, weight gain, and mild skin reactions.

Severe hypoglycemia, anaphylaxis, persistent hyperglycemia, and signs of heart failure or edema should be evaluated promptly.

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

Renal impairment can reduce insulin clearance, increasing hypoglycemia risk; dose adjustments and close monitoring are recommended.

Avoid combining with other rapid‑acting insulins without dose changes. Use caution with beta‑blockers, sulfonylureas, corticosteroids, diuretics, and ACE inhibitors.

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

The ATC classification for Humulin R is A10AB01.

It binds to insulin receptors, activating signaling pathways that increase GLUT4 translocation, enhance peripheral glucose uptake, suppress hepatic glucose production, and promote glycogen storage.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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