GNH USA

Europe — EMA

Humuline 30/70 Cartridge

Learn about Humuline 30/70 Cartridge – a human insulin mix for subcutaneous use in diabetes, its uses, side effects, precautions, and drug interactions.

Insulin Human (Rdna)

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What is Insulin Human (Rdna)?

Humuline 30/70 Cartridge is a prescription insulin product that contains human insulin produced by recombinant DNA technology. It is supplied in a cartridge format designed for use with compatible insulin pens, allowing subcutaneous administration. The formulation provides a mixture of 30% rapid‑acting and 70% intermediate‑acting insulin, facilitating basal and prandial glucose control in patients with diabetes. It is marketed in the European Union and surrounding markets.

What is Insulin Human (Rdna) used for?

Humuline 30/70 Cartridge is indicated for the management of blood glucose in adults with diabetes mellitus.

- Type 1 diabetes mellitus as part of a basal‑bolus insulin regimen. - Type 2 diabetes mellitus when oral agents and lifestyle measures do not achieve target glycaemia. - Adjunct therapy during periods of increased insulin demand, such as illness or surgery. - Use in combination with rapid‑acting insulin analogues for flexible mealtime coverage. - Pediatric patients with type 1 diabetes when weight‑based dosing is appropriate. - Patients requiring a fixed proportion of rapid and intermediate insulin to simplify dosing schedules.

What are the side effects of Insulin Human (Rdna)?

Adverse reactions to Humuline 30/70 may occur; they are categorized by frequency and clinical significance.

Common: - Mild hypoglycemia, especially if meals are delayed or carbohydrate intake is insufficient. - Injection site reactions such as redness, swelling, or itching. - Lipodystrophy presenting as localized thickening or loss of subcutaneous fat at repeated injection sites. - Weight gain associated with increased insulin dosing.

Serious: - Severe hypoglycemia with neuroglycopenic symptoms (confusion, seizures, loss of consciousness). - Allergic reactions ranging from urticaria to anaphylaxis. - Edema or heart failure exacerbation in susceptible patients. - Hypersensitivity leading to serum sickness–like reaction.

What precautions apply to Insulin Human (Rdna)?

When prescribing or using Humuline 30/70, clinicians and patients should consider several precautionary measures to minimize risk.

- Adjust dose during reduced food intake, increased activity, or illness to avoid hypoglycemia. - Monitor blood glucose frequently when initiating therapy or changing insulin‑to‑carbohydrate ratios. - Use caution in renal or hepatic impairment because insulin clearance may be decreased. - Assess for cardiovascular disease; rapid fluid shifts can worsen heart failure. - Avoid use in patients with known hypersensitivity to human insulin or cartridge components.

What does Insulin Human (Rdna) interact with?

Humuline 30/70 may interact with other medications; understanding these interactions helps maintain glycemic control and safety.

Avoid: - Concurrent use of other rapid‑acting insulins or insulin analogues without dose adjustment, which can cause severe hypoglycemia. - Beta‑blockers that mask hypoglycemia symptoms, potentially delaying treatment.

Use with caution: - Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that increase insulin secretion, requiring careful glucose monitoring. - Corticosteroids, thiazide diuretics, or sympathomimetics that raise blood glucose, possibly necessitating higher insulin doses. - Alcohol intake, especially in excess, which can cause unpredictable glucose fluctuations.

Frequently asked questions

What type of insulin is contained in Humuline 30/70 Cartridge?+
Humuline 30/70 Cartridge contains recombinant human insulin that is a mixture of 30% rapid‑acting and 70% intermediate‑acting insulin.
How is Humuline 30/70 Cartridge administered?+
It is supplied as a cartridge for use with compatible insulin pens and is administered by subcutaneous injection.
Which patients are typical candidates for Humuline 30/70 Cartridge?+
It is commonly prescribed for adults with type 1 or type 2 diabetes who need both basal and prandial insulin coverage.
Can Humuline 30/70 be used in children with diabetes?+
Pediatric use may be considered under medical supervision, especially for type 1 diabetes where weight‑based dosing is appropriate.
What are the most common side effects of Humuline 30/70?+
Common adverse effects include mild hypoglycemia, injection‑site reactions such as redness or itching, and lipodystrophy at repeated sites.
What serious adverse reactions should be reported?+
Serious reactions include severe hypoglycemia with neurological symptoms, allergic responses up to anaphylaxis, and worsening of edema or heart failure.
How should the dose be adjusted during illness or reduced food intake?+
Dose reductions are often needed to prevent hypoglycemia; patients should monitor glucose closely and consult their healthcare provider.
Are there any drug interactions that can increase the risk of low blood sugar?+
Yes, using other rapid‑acting insulins or insulin analogues without dose adjustment, as well as beta‑blockers that mask hypoglycemia symptoms, can increase risk.
What medications may require caution when taken with Humuline 30/70?+
Oral antidiabetic agents, corticosteroids, thiazide diuretics, sympathomimetics, and excessive alcohol may require dose adjustments or closer monitoring.
Is Humuline 30/70 safe for pregnant or breastfeeding women?+
Pregnant or nursing patients should discuss insulin needs with their healthcare provider, as requirements may change during these periods.
How should Humuline 30/70 be stored before use?+
The cartridge should be kept in its original packaging, protected from light, and stored at controlled room temperature; do not freeze.
When should a patient discard an unused Humuline 30/70 cartridge?+
Cartridges should be discarded after the expiration date or if the insulin appears discolored, cloudy, or contains particles.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Insulin Human (Rdna)
Route
Subcutaneous Use
Manufacturer
S.A. Eli Lilly Benelux N.V.
Origin
EU

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