Product image of Humuline 30/70 Patroon (Insulin Human (Rdna)) supplied by GNH India

Humuline 30/70 Patroon

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humuline 30/70 Patroon (Insulin Human (Rdna))

Humuline 30/70 Patroon is a prescription insulin human (rDNA) injection solution formulated as a mixed‑ratio 30% rapid‑acting and 70% intermediate‑acting insulin. It is supplied in a sterile vial for subcutaneous administration and is marketed in the European Union. The product provides basal and prandial glucose control for patients with diabetes requiring insulin therapy, and it is intended for use under medical supervision as part of a comprehensive diabetes management plan.

Manufacturer / TM Owner

Eli Lilly Nederland B.V.

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Indications & Clinical Uses

Humuline 30/70 Patroon is indicated for the management of hyperglycemia in adults with diabetes.

  • Type 1 diabetes mellitus when basal and mealtime insulin are required.
  • Type 2 diabetes mellitus as an adjunct to diet, exercise, and oral agents when insulin therapy is needed.
  • Situations where a single injection can provide both basal and prandial coverage.
  • Patients transitioning from separate rapid‑acting and intermediate‑acting insulin preparations.

How It Works

  • Humuline 30/70 Patroon contains recombinant human insulin that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers the tyrosine‑kinase signaling cascade, promoting translocation of GLUT‑4 transporters and increasing glucose uptake. In the liver, insulin suppresses gluconeogenesis and glycogenolysis, reducing endogenous glucose output. The mixed‑ratio formulation supplies rapid‑acting insulin for post‑prandial glucose and intermediate‑acting insulin for basal control.

Side Effects

Like all insulin products, Humuline 30/70 Patroon may be associated with adverse reactions, ranging from mild to severe.

Common

  • Hypoglycemia (low blood glucose)
  • Injection site redness, swelling or itching
  • Lipodystrophy at the injection site
  • Weight gain

Serious

  • Severe hypoglycemia with loss of consciousness or seizures
  • Allergic reactions such as urticaria, angio‑edema, or anaphylaxis
  • Persistent hyperglycemia indicating possible insulin resistance
  • Edema or heart failure exacerbation

Precautions & Warnings

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

  • Adjust dose during periods of illness, stress, or changes in physical activity.
  • Monitor blood glucose closely when initiating therapy or changing the dose.
  • Use caution in patients with renal or hepatic impairment, as insulin clearance may be reduced.
  • Avoid use in individuals with known hypersensitivity to human insulin or any excipients.
  • Counsel pregnant or breastfeeding women that safety data are limited; use only if benefits outweigh risks.
  • Review concomitant medications that can mask hypoglycemia symptoms.

Avoid Interactions

Humuline 30/70 Patroon can interact with other medicines, affecting glucose levels or insulin action.

Avoid

  • Concurrent use of other insulin products without dose adjustment.
  • High‑dose sulfonylureas or meglitinides that increase hypoglycemia risk.
  • Beta‑blockers that may blunt hypoglycemia warning signs.

Use with caution

  • Oral antihyperglycemics (e.g., metformin, thiazolidinediones) – monitor glucose closely.
  • Corticosteroids, thyroid hormones, or growth hormone – may raise glucose requirements.
  • Diuretics, especially thiazides – can affect electrolyte balance and glucose control.
  • Alcohol – may cause delayed hypoglycemia.

Frequently Asked Questions

Humuline 30/70 Patroon is a recombinant human insulin that combines 30% rapid‑acting and 70% intermediate‑acting components in a single injection.

It is supplied as a sterile injection solution for subcutaneous use, typically injected into the abdomen, thigh, or upper arm.

Yes, it is indicated for adults with either Type 1 or Type 2 diabetes who require insulin to control blood glucose levels.

Unopened vials should be stored in a refrigerator (2‑8 °C). Once in use, they may be kept at room temperature not exceeding 30 °C for up to 28 days.

Insulin promotes glucose uptake and storage, which can lead to increased caloric retention and modest weight gain in some patients.

The mixed‑ratio formulation delivers both prandial and basal insulin in one injection, reducing the number of daily injections compared with using two separate products.

Initial dosing is individualized; clinicians typically start with a low dose and titrate based on self‑monitored blood glucose and clinical response.

Severe hypoglycemia may present with confusion, seizures, loss of consciousness, or inability to self‑treat; emergency medical assistance is required.

Yes, alcohol can impair gluconeogenesis and may cause delayed hypoglycemia, especially when taken with insulin.

Safety data are limited; it should only be used if the potential benefit to the mother outweighs any possible risk to the fetus, under close medical supervision.

Regular self‑monitoring of blood glucose, periodic HbA1c testing, and assessment for hypoglycemia symptoms are recommended.

Patients with renal impairment may have reduced insulin clearance, so dose reductions and close glucose monitoring are advised.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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