Product image of Humulin 30/70 (Miscela) (Insulin Human) supplied by GNH India

Humulin 30/70 (Miscela)

Active Ingredient:
Insulin Human
Origin:
EU

Humulin 30/70 (Miscela) (Insulin Human)

Humulin 30/70 is a premixed insulin injection solution that contains human insulin at 100 IU/mL, composed of 30 % soluble (regular) insulin and 70 % intermediate‑acting NPH insulin. It is supplied in a sterile vial for subcutaneous use and is marketed in the European Union as a prescription‑only (Rx) product for the treatment of diabetes mellitus in adults and children who need a combined basal‑prandial insulin daily regimen therapy.

Manufacturer / TM Owner

Eli Lilly Italia S.P.A.

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Indications & Clinical Uses

Humulin 30/70 is indicated for the glycemic control of patients with diabetes mellitus when a mixed insulin formulation is appropriate.

  • Type 1 diabetes mellitus requiring both basal and prandial insulin coverage.
  • Type 2 diabetes mellitus inadequately controlled with oral agents alone.
  • Adults and pediatric patients who prefer fewer daily injections compared with separate basal and rapid‑acting insulins.
  • Situations where a predictable 30/70 ratio simplifies dose titration.
  • Use in combination with diet, exercise, and other antidiabetic medications as part of a comprehensive management plan.

How It Works

  • Humulin 30/70 delivers two insulin components that act on the same insulin receptor. The soluble fraction begins to bind receptors within 30 minutes, promoting rapid glucose uptake in muscle and adipose tissue and suppressing hepatic glucose output. The NPH fraction releases more slowly, maintaining receptor activation for up to 24 hours and providing basal insulin coverage. Together they lower circulating blood glucose by enhancing peripheral utilization and reducing hepatic production.

Side Effects

Adverse reactions to Humulin 30/70 may vary in frequency and severity.

Common

  • Mild hypoglycemia, especially if meals are missed or delayed.
  • Injection‑site redness, swelling, or itching.
  • Lipodystrophy presenting as localized thickening or thinning of subcutaneous tissue.
  • Transient weight gain due to fluid retention.

Serious

  • Severe hypoglycemia with neuroglycopenic symptoms (confusion, seizures, loss of consciousness).
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Persistent or worsening edema and heart failure exacerbation.

Precautions & Warnings

Clinicians should consider several precautions when prescribing Humulin 30/70 to ensure safe and effective use.

  • Assess renal and hepatic function, as impairment can prolong insulin action and increase hypoglycemia risk.
  • Adjust doses during periods of illness, reduced food intake, or increased physical activity.
  • Monitor blood glucose closely during pregnancy; insulin requirements may change rapidly.
  • Avoid use in patients with known hypersensitivity to human insulin or any excipients in the formulation.
  • Educate patients on proper injection technique and rotation of sites to prevent lipohypertrophy.
  • Review concomitant medications that may mask hypoglycemia symptoms, such as beta‑blockers.

Avoid Interactions

Humulin 30/70 can interact with other drugs, affecting glucose control or insulin pharmacodynamics.

Avoid

  • Concurrent use of other rapid‑acting insulins or concentrated insulin formulations without dose adjustment.
  • MAO‑B inhibitors that may potentiate hypoglycemic episodes.

Use with caution

  • Beta‑blockers, which can blunt hypoglycemia warning signs.
  • Thiazide diuretics and corticosteroids, which may raise blood glucose and require insulin dose increases.
  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that increase hypoglycemia risk when combined with premixed insulin.
  • Alcohol, especially in excess, because it can cause delayed hypoglycemia.

Frequently Asked Questions

The soluble (regular) insulin component acts quickly, lowering blood glucose within 30 minutes, while the NPH component provides a slower, longer‑lasting effect that maintains basal insulin levels for up to 24 hours.

Yes, Humulin 30/70 is approved for use in both adults and pediatric patients who require a combined basal‑prandial insulin regimen, but dosing must be individualized by a healthcare professional.

Humulin 30/70 is typically administered twice daily, before breakfast and before dinner, to provide coverage for meals and basal insulin needs.

Mild hypoglycemia may present as shakiness, sweating, hunger, irritability, or a rapid heartbeat. Prompt carbohydrate intake can correct these symptoms.

Yes, rotating injection sites within the abdomen, thigh, or upper arm helps prevent lipodystrophy and ensures consistent insulin absorption.

Insulin is generally considered the preferred treatment for diabetes in pregnancy, but Humulin 30/70 should be used only under close medical supervision with frequent glucose monitoring.

Alcohol can cause delayed hypoglycemia, especially when consumed on an empty stomach, so patients should monitor glucose levels closely and limit alcohol intake.

Yes, beta‑blockers may blunt typical warning signs such as rapid heartbeat, making it harder to recognize low blood glucose; patients should check glucose levels regularly.

Stop the injection immediately and seek medical attention. Symptoms may include rash, swelling, itching, or difficulty breathing, which require prompt treatment.

Humulin 30/70 should be stored in a refrigerator (2–8 °C) before opening. Once in use, it can be kept at room temperature for up to 28 days, protected from light.

When combined with sulfonylureas, the risk of hypoglycemia increases, so dose adjustments and close glucose monitoring are recommended.

Patients should perform regular self‑monitoring of blood glucose, especially before meals and at bedtime, and adjust doses based on healthcare provider guidance.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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