Product image of Huminsulin Basal Durchstechflaschen Humulin Nph Vial (Insulin Human (Rdna)) supplied by GNH India

Huminsulin Basal Durchstechflaschen Humulin Nph Vial

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Huminsulin Basal Durchstechflaschen Humulin Nph Vial (Insulin Human (Rdna))

Huminsulin Basal Durchstechflaschen Humulin Nph Vial is a sterile injection solution containing insulin human (recombinant DNA) intended for subcutaneous or intramuscular administration. It is supplied in a vial format for use with a syringe, and is marketed in the European Union as a prescription‑only product for the long‑acting basal insulin needs of patients with diabetes. The formulation provides a consistent supply of insulin to help regulate blood glucose.

Manufacturer / TM Owner

Eli Lilly Ges. M.B.H

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Indications & Clinical Uses

Huminsulin Basal is indicated for the management of hyperglycemia in adults and children with diabetes when a long‑acting insulin is required.

  • Type 1 diabetes mellitus as part of a basal‑bolus regimen.
  • Type 2 diabetes mellitus when oral agents or short‑acting insulin are insufficient.
  • Adjunct therapy during pregnancy under specialist supervision.
  • Use in patients undergoing bariatric surgery to maintain basal insulin coverage.
  • Replacement therapy for patients with insulin deficiency due to pancreatic disease.

How It Works

  • Insulin human binds to the insulin receptor on cell membranes, activating the intrinsic tyrosine kinase activity of the receptor. This triggers downstream signaling through the PI3‑K/Akt pathway, promoting translocation of GLUT‑4 transporters to the plasma membrane and increasing glucose uptake in muscle and adipose tissue. Simultaneously, hepatic gluconeogenesis and glycogenolysis are suppressed, leading to lower circulating glucose levels.

Side Effects

Like all insulin preparations, Huminsulin Basal may be associated with adverse reactions that vary in frequency and severity.

Common

  • Mild hypoglycemia (blood glucose <70 mg/dL) with symptoms such as shakiness or sweating.
  • Redness, swelling, or itching at the injection site.
  • Small amounts of localized lipodystrophy or skin thickening.
  • Transient weight gain due to fluid retention.

Serious

  • Severe hypoglycemia causing loss of consciousness or seizures.
  • Immediate‑type allergic reactions including anaphylaxis, urticaria, or angio‑edema.
  • Significant hypokalemia resulting from rapid intracellular glucose shift.
  • Development of insulin antibodies that may alter glucose control.

Precautions & Warnings

When prescribing or using Huminsulin Basal, clinicians and patients should observe several precautionary measures to minimize risks and ensure optimal glycemic control.

  • Monitor blood glucose closely during initiation and dose adjustments to avoid hypoglycemia.
  • Adjust doses in renal or hepatic impairment, as insulin clearance may be reduced.
  • Use caution in patients with a history of severe allergic reactions to insulin products.
  • Educate patients on proper injection technique and site rotation to prevent lipodystrophy.
  • Review concomitant medications that can mask hypoglycemia symptoms, such as beta‑blockers.
  • Pregnant or breastfeeding women should use only under specialist guidance.

Avoid Interactions

Huminsulin Basal can interact with other agents that affect glucose metabolism or insulin action.

Avoid

  • Concurrent use of other rapid‑acting insulins without dose reduction may cause severe hypoglycemia.
  • Combining with meglitinides or sulfonylureas without careful monitoring can increase hypoglycemia risk.
  • Co‑administration with growth hormone may antagonize insulin’s glucose‑lowering effect.

Use with caution

  • Beta‑blockers may blunt adrenergic warning signs of hypoglycemia; monitor closely.
  • Corticosteroids and thiazide diuretics can raise blood glucose, requiring insulin dose adjustments.
  • Alcohol intake can cause delayed hypoglycemia, especially when insulin levels are high.
  • Exercise increases insulin sensitivity; patients should adjust insulin or carbohydrate intake accordingly.

Frequently Asked Questions

It contains insulin human (recombinant DNA) formulated as a long‑acting basal insulin for subcutaneous or intramuscular injection.

Yes, Huminsulin Basal is classified as a prescription‑only medication in the European Union.

The product is indicated for both adult and pediatric patients with type 1 or type 2 diabetes when basal insulin therapy is needed.

Store the unopened vial in a refrigerator (2‑8 °C). Do not freeze. After first use, keep at room temperature (up to 30 °C) and discard after 28 days.

Inject subcutaneously into the abdomen, thigh, or upper arm, rotating sites to reduce the risk of lipodystrophy.

Huminsulin Basal provides a prolonged, steady release of insulin over 12‑24 hours, whereas rapid‑acting insulins act within minutes and are used for mealtime glucose control.

Common signs include shakiness, sweating, hunger, irritability, rapid heartbeat, and blurred vision. Check blood glucose promptly if symptoms appear.

Patients with renal impairment may require lower insulin doses because insulin clearance is reduced; dose adjustments should be made under medical supervision.

Yes, alcohol can potentiate insulin’s glucose‑lowering effect and increase the risk of delayed hypoglycemia, especially when taken on an empty stomach.

Use only under specialist guidance; insulin is the preferred glucose‑lowering therapy in pregnancy, but dose and monitoring must be individualized.

Stop the injection immediately and seek medical attention. Anaphylaxis requires emergency treatment with epinephrine and supportive care.

Frequent monitoring (e.g., before meals and at bedtime) is recommended during initiation and any dose changes to avoid hypoglycemia and achieve target glucose levels.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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