GNH USA

Europe — EMA

Humulin I (Isophane)

Humulin I Isophane – detailed overview of uses, mechanism, side effects, precautions, interactions, and FAQs for this EU‑market insulin injection.

Insulin Human (Rdna)

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What is Insulin Human (Rdna)?

Humulin I (Isophane) is a prescription insulin product that contains recombinant human insulin (isophane) as its active ingredient. It is supplied as an injectable suspension for subcutaneous or intramuscular administration. The formulation is designed for prolonged absorption, providing basal insulin coverage. Humulin I is marketed in the European Union and is classified as a short‑acting intermediate‑acting insulin analog used in diabetes management therapy for patients worldwide.

What is Insulin Human (Rdna) used for?

Humulin I (Isophane) is indicated for the management of blood glucose in adults with diabetes.

- Used in type 1 diabetes mellitus as part of a basal insulin regimen. - Used in type 2 diabetes mellitus when basal insulin is required. - Adjunct to oral antidiabetic agents in patients whose glucose is inadequately controlled. - Combined with rapid‑acting insulin analogues for basal‑bolus therapy. - May be employed during pregnancy when benefits outweigh risks, under medical supervision.

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

Adverse reactions to Humulin I (Isophane) can vary in frequency and severity.

Common: - Mild hypoglycemia (low blood sugar). - Injection site redness, swelling, or itching. - Lipodystrophy at the injection site. - Weight gain associated with improved glycemic control.

Serious: - Severe hypoglycemia with neurological symptoms. - Allergic reactions such as urticaria, angioedema, or anaphylaxis. - Edema or heart failure exacerbation. - Hypersensitivity leading to bronchospasm.

What precautions apply to Insulin Human (Rdna)?

When prescribing or using Humulin I (Isophane), clinicians should consider several precautionary measures to ensure safe therapy.

- Assess renal and hepatic function before initiation. - Monitor blood glucose regularly to adjust dose and prevent hypoglycemia. - Use caution in patients with cardiovascular disease or heart failure. - Evaluate for signs of allergic reactions during the first weeks of therapy. - Adjust dose during pregnancy, lactation, or in elderly patients. - Avoid abrupt discontinuation without medical guidance.

What does Insulin Human (Rdna) interact with?

Humulin I (Isophane) may interact with other medicines, affecting glucose control or insulin activity.

Avoid: - Concurrent use of other insulin products without dose adjustment. - Beta‑blockers that mask hypoglycemia symptoms. - MAO‑inhibitors that can potentiate insulin’s glucose‑lowering effect.

Use with caution: - Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that increase hypoglycemia risk. - Corticosteroids, which may raise blood glucose and require higher insulin doses. - Thyroid hormones, as hyperthyroidism can enhance insulin clearance.

Frequently asked questions

What type of insulin is Humulin I (Isophane) and how is it classified?+
Humulin I (Isophane) is a recombinant human insulin formulated as an intermediate‑acting injectable suspension, classified as a basal insulin used to provide long‑lasting glucose control.
Can Humulin I (Isophane) be used in both type 1 and type 2 diabetes?+
Yes, Humulin I is indicated for adults with type 1 diabetes as part of a basal regimen and for type 2 diabetes when basal insulin supplementation is needed.
What routes of administration are approved for Humulin I (Isophane)?+
Humulin I is administered by subcutaneous injection, and in some clinical situations it may be given intramuscularly, following the prescribing information.
How does Humulin I (Isophane) provide basal insulin coverage?+
After injection, the insulin forms microprecipitates that dissolve slowly, releasing insulin over several hours to maintain a steady basal level of glucose control.
What are the most common side effects of Humulin I (Isophane)?+
Common adverse effects include mild hypoglycemia, injection‑site reactions such as redness or swelling, lipodystrophy, and modest weight gain.
When is severe hypoglycemia most likely to occur with Humulin I?+
Severe hypoglycemia can occur if the dose is too high, meals are missed, or if the patient engages in vigorous exercise without adjusting insulin or carbohydrate intake.
Should patients on Humulin I avoid any specific medications?+
Patients should avoid using other insulin products without dose adjustment, beta‑blockers that mask hypoglycemia symptoms, and MAO‑inhibitors that may amplify insulin’s glucose‑lowering effect.
How should Humulin I be stored before and after opening?+
Unopened vials should be stored in a refrigerator (2‑8 °C). After opening, they may be kept at room temperature for up to 28 days, protecting them from light.
Is dose adjustment needed for Humulin I during pregnancy?+
Dose may need adjustment during pregnancy; clinicians should balance maternal glucose control with fetal safety and monitor closely.
What monitoring is recommended for patients using Humulin I (Isophane)?+
Regular self‑monitoring of blood glucose, periodic HbA1c testing, and clinical assessment of renal, hepatic, and cardiovascular status are recommended.
Can Humulin I be used in combination with rapid‑acting insulin analogues?+
Yes, it is often combined with rapid‑acting insulin analogues in a basal‑bolus regimen to cover both basal and prandial glucose needs.
What should a patient do if they experience an allergic reaction to Humulin I?+
The patient should stop the injection immediately, seek medical attention, and inform their healthcare provider about the reaction for alternative therapy consideration.
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
Intramuscular Use , Subcutaneous Use
Manufacturer
Eli Lilly Nederland B.V.
Origin
EU

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