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 (Miscela) is a prescription insulin human injection solution that combines 30% rapid‑acting insulin with 70% intermediate‑acting insulin. It is supplied as a premixed formulation for subcutaneous or intramuscular administration and is marketed in the European Union. The product provides both mealtime and basal glucose control for people with diabetes and is used under the supervision of a healthcare professional through individualized dosing and regular monitoring.

Manufacturer / TM Owner

Eli Lilly Italia S.P.A.

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Indications & Clinical Uses

Humulin 30/70 is indicated for the management of blood glucose in patients with diabetes mellitus.

  • Type 1 diabetes mellitus requiring basal and mealtime insulin.
  • Type 2 diabetes mellitus when combined basal and prandial coverage is needed.
  • Adults and children (≥2 years) who can safely handle premixed insulin.
  • Situations where a single daily injection simplifies the regimen.
  • Use as part of a comprehensive diabetes care plan that includes diet, exercise, and glucose monitoring.

How It Works

  • Humulin 30/70 contains human insulin molecules that bind to insulin receptors on muscle, adipose, and hepatic cells. Receptor activation triggers the tyrosine kinase pathway, promoting translocation of GLUT‑4 transporters to the cell surface, which increases glucose uptake. The rapid‑acting component reduces post‑prandial glucose, while the intermediate‑acting component suppresses hepatic glucose production, providing basal insulin coverage. The combined formulation yields a biphasic insulin profile that aligns with typical meal patterns and overnight basal needs.

Side Effects

Like all insulin preparations, Humulin 30/70 may be associated with adverse reactions. Reported events range from mild and transient to rare but serious.

Common

  • Mild to moderate hypoglycemia, characterized by shakiness, sweating, or hunger.
  • Localized redness, swelling, itching, or bruising at the injection site.
  • Lipodystrophy, presenting as small areas of fat loss or accumulation under the skin.
  • Gradual weight increase, often related to improved glycemic control.

Serious

  • Severe hypoglycemia leading to confusion, loss of consciousness, or seizures.
  • Allergic reactions such as widespread rash, urticaria, angio‑edema, or anaphylactic shock.
  • Fluid retention or peripheral edema that may worsen heart failure.

Precautions & Warnings

Before initiating Humulin 30/70, certain precautions should be considered to minimize risks and ensure safe use.

  • Assess renal and hepatic function, as impairment may alter insulin clearance.
  • Review history of hypoglycemia unawareness or frequent low glucose episodes.
  • Adjust dose when starting or stopping concomitant glucocorticoids, beta‑blockers, or other agents affecting glucose.
  • Use caution in pregnant or breastfeeding individuals; discuss risks with a healthcare provider.
  • Monitor for signs of cardiovascular disease, especially in patients with edema or heart failure.
  • Educate patients on proper injection technique and site rotation.
  • Ensure regular blood glucose monitoring and dose adjustments as needed.

Avoid Interactions

Humulin 30/70 can interact with several medications, affecting glucose levels or insulin action.

Avoid

  • Concurrent use of other rapid‑acting insulins or insulin analogues without dose adjustment.
  • MAO‑B inhibitors (e.g., selegiline) that may potentiate hypoglycemia.

Use with caution

  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Corticosteroids, which can increase insulin requirements.
  • Thiazide diuretics, which may raise blood glucose.
  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that increase hypoglycemia risk.
  • Alcohol, which can cause delayed hypoglycemia.

Frequently Asked Questions

Humulin 30/70 is a premixed human insulin that contains 30% rapid‑acting insulin and 70% intermediate‑acting insulin in a single injection solution.

It is prescribed for adults and children (usually ≥2 years) with type 1 or type 2 diabetes who need both basal and mealtime insulin coverage.

Humulin 30/70 is usually given once daily, often before the main meal, but dosing frequency may be adjusted by a healthcare professional based on individual needs.

Pregnancy safety has not been fully established; clinicians should weigh potential benefits and risks and discuss them with the patient.

Common signs include shakiness, sweating, hunger, irritability, blurred vision, and in severe cases, confusion, loss of consciousness, or seizures.

Unopened vials should be stored in a refrigerator (2‑8 °C). After opening, they may be kept at room temperature (up to 30 °C) for a limited period, typically 28 days, as specified by the manufacturer.

Recommended sites include the abdomen, thigh, or upper arm, rotating the injection location to reduce the risk of lipodystrophy.

Alcohol can increase the risk of delayed hypoglycemia, especially when taken without food, so patients should consume alcohol cautiously and monitor glucose levels.

If a dose is missed, the patient should follow their healthcare provider’s instructions, which often involve taking the missed dose as soon as remembered unless it is close to the next scheduled dose.

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

Humulin 30/70 combines both basal and rapid‑acting components in one vial, simplifying the regimen to a single daily injection, whereas separate insulins require multiple injections.

Regular self‑monitoring of blood glucose, periodic HbA1c testing, and routine clinical reviews are essential to ensure effective and safe therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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