Product image of Huminsulin Profil Iii Patronen (Insulin Human (Rdna)) supplied by GNH India

Huminsulin Profil Iii Patronen

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Huminsulin Profil Iii Patronen (Insulin Human (Rdna))

Huminsulin Profil Iii Patronen is a prescription insulin product containing human insulin (recombinant DNA) for subcutaneous administration. It is supplied in an unspecified strength and dosage form, marketed in the European Union. The medication belongs to the insulin class of antidiabetic agents and is used to regulate blood glucose in patients with diabetes mellitus. It is a biosynthetic analogue of endogenous human insulin and provides a biosynthetic analogue of endogenous human insulin.

Manufacturer / TM Owner

Eli Lilly Ges. M.B.H

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Indications & Clinical Uses

Huminsulin Profil Iii Patronen is prescribed to control elevated blood glucose levels in patients diagnosed with diabetes mellitus.

  • Type 1 diabetes mellitus, as basal or bolus insulin.
  • Type 2 diabetes mellitus when oral agents or other injectables do not achieve target glycaemic control.
  • Adjunct to diet and exercise for overall diabetes management.
  • Use in insulin‑pump (continuous subcutaneous insulin infusion) systems if the formulation is compatible.
  • Treatment of hyperglycaemia during hospitalization, including postoperative or stress‑related elevations.

How It Works

  • Huminsulin Profil Iii Patronen delivers recombinant human insulin that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers autophosphorylation and downstream signaling through the PI3‑K/Akt pathway, promoting translocation of GLUT‑4 transporters and increasing glucose uptake. In the liver, the drug suppresses gluconeogenesis and glycogenolysis, thereby lowering endogenous glucose production.

Side Effects

Adverse reactions to Huminsulin Profil Iii Patronen vary in frequency and severity.

Common

  • Hypoglycaemia (low blood glucose)
  • Injection‑site pain, redness or swelling
  • Lipodystrophy at the injection site
  • Weight gain

Serious

  • Severe hypoglycaemia with loss of consciousness
  • Allergic reactions such as urticaria, angio‑edema or anaphylaxis
  • Edema or fluid retention
  • Hypersensitivity leading to bronchospasm

Precautions & Warnings

Clinicians should consider several safety factors before initiating Huminsulin Profil Iii Patronen.

  • Assess renal and hepatic function, as impairment may alter insulin clearance.
  • Monitor blood glucose closely during dose initiation and titration.
  • Educate patients on recognizing and treating hypoglycaemia.
  • Use caution in pregnant or breastfeeding individuals; benefits must outweigh potential risks.
  • Review any history of allergic reactions to insulin or excipients.
  • Adjust doses during periods of illness, surgery, or changes in physical activity.

Avoid Interactions

Huminsulin Profil Iii Patronen can interact with other medications that affect glucose homeostasis or insulin metabolism.

Avoid

  • Concurrent use of other rapid‑acting or long‑acting insulin products without dose adjustment.
  • Sulfonylureas or meglitinides, which may increase hypoglycaemia risk.
  • Beta‑adrenergic antagonists that mask hypoglycaemia symptoms.

Use with caution

  • Oral antihyperglycaemic agents (e.g., metformin, SGLT2 inhibitors) – monitor glucose levels.
  • Corticosteroids, thiazide diuretics, or growth hormone – may require higher insulin doses.
  • Alcohol consumption – can cause delayed hypoglycaemia.

Frequently Asked Questions

The active ingredient is recombinant human insulin, produced using DNA technology.

It is given by subcutaneous injection, typically into the abdomen, thigh, or upper arm.

Yes, it is indicated for the management of hyperglycaemia in both type 1 and type 2 diabetes when insulin therapy is required.

No, it is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

Common adverse effects include hypoglycaemia, injection‑site pain or redness, lipodystrophy, and modest weight gain.

Severe hypoglycaemia with loss of consciousness, anaphylactic reactions, marked edema, or bronchospasm require urgent care.

Renal impairment can affect insulin clearance, so dose adjustments and close monitoring are recommended.

Combined use may increase the risk of hypoglycaemia, so clinicians often reduce the dose of one or both agents.

Insulin is generally preferred for diabetes in pregnancy, but the decision should be individualized by the treating physician.

If the formulation is compatible with pump devices, it may be used for continuous subcutaneous insulin infusion under medical supervision.

Consume fast‑acting carbohydrates such as glucose tablets or fruit juice, then re‑check blood glucose after 15 minutes.

Patients should follow a balanced diet and coordinate carbohydrate intake with insulin dosing as advised by their healthcare team.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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