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

Huminsulin Profil Iii Kwikpen

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Huminsulin Profil Iii Kwikpen (Insulin Human (Rdna))

Huminsulin Profil Iii Kwikpen is a prefilled KwikPen injectable solution that contains insulin human (rDNA) as its active ingredient. It is supplied in a single‑use, subcutaneous delivery device, marketed in the European Union. The product provides a recombinant human insulin formulation for the management of blood glucose in diabetes. It is a prescription‑only medication and is not classified as a controlled substance and is intended for use under medical supervision.

Manufacturer / TM Owner

Lilly Deutschland Gmbh

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Indications & Clinical Uses

Huminsulin Profil Iii Kwikpen is indicated for the treatment of diabetes mellitus where insulin therapy is required.

  • Type 1 diabetes mellitus in adults and children.
  • Type 2 diabetes mellitus when oral agents do not achieve glycemic targets.
  • Adjunct to diet and exercise for basal insulin replacement.
  • Use during pregnancy or lactation only when benefits outweigh risks (consult healthcare provider).
  • May be employed in insulin pump therapy as a rapid‑acting component if compatible.

How It Works

  • Huminsulin Profil Iii Kwikpen delivers recombinant human insulin that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers autophosphorylation of the insulin receptor substrate, stimulating the phosphatidylinositol‑3‑kinase (PI3‑K) pathway and promoting translocation of GLUT‑4 transporters to the cell membrane, which increases glucose uptake. In the liver, insulin suppresses gluconeogenesis and glycogenolysis, thereby lowering circulating glucose levels and improves metabolic control.

Side Effects

Adverse reactions reported with Huminsulin Profil Iii Kwikpen are generally related to its pharmacologic action and formulation.

Common

  • Hypoglycemia (low blood glucose).
  • Redness, swelling, or pain at the injection site.
  • Lipodystrophy or local tissue changes.
  • Mild weight gain.
  • Transient rash or itching.

Serious

  • Severe hypoglycemia requiring assistance.
  • Anaphylactic or severe allergic reaction.
  • Hypokalemia (low potassium levels).
  • Significant edema or fluid retention.
  • Insulin antibody syndrome causing unpredictable glucose control.

Precautions & Warnings

When prescribing or using Huminsulin Profil Iii Kwikpen, several safety considerations should be observed.

  • Monitor blood glucose levels regularly to avoid hypo‑ or hyperglycemia.
  • Adjust insulin dose in patients with renal or hepatic impairment.
  • Use with caution in individuals with cardiovascular disease or heart failure.
  • Avoid use in patients with known hypersensitivity to human insulin or any excipients in the pen.
  • Consider pregnancy and lactation only if the therapeutic benefit justifies potential risk.
  • Store the pen according to manufacturer instructions, protecting it from extreme temperatures and direct sunlight.

Avoid Interactions

Huminsulin Profil Iii Kwikpen may interact with other medications that affect glucose metabolism or insulin action.

Avoid

  • Simultaneous administration of other insulin products without appropriate dose reduction.
  • Co‑administration with insulin‑like growth factor‑1 (IGF‑1) therapy due to additive hypoglycemic effect.

Use with caution

  • Concomitant sulfonylureas, meglitinides, or other glucose‑lowering agents that increase hypoglycemia risk.
  • Beta‑blockers, which can mask symptoms of hypoglycemia.
  • Corticosteroids, which may raise insulin requirements.
  • Diuretics that alter potassium balance, potentially affecting insulin activity.

Frequently Asked Questions

Huminsulin Profil Iii Kwikpen contains recombinant human insulin produced by rDNA technology.

Yes, the product is marketed and authorized for use within the European Union.

The pen is indicated for insulin therapy in both type 1 diabetes and type 2 diabetes when additional insulin is needed.

It is delivered subcutaneously using the prefilled KwikPen device, following the injection technique recommended by the manufacturer.

Common adverse effects include hypoglycemia, injection‑site reactions such as redness or swelling, mild weight gain, and occasional skin rash.

Serious reactions can include severe hypoglycemia, anaphylaxis, significant edema, hypokalemia, and insulin antibody syndrome.

Dose adjustments may be necessary in renal impairment; patients should work with their healthcare provider to determine the appropriate dose.

Use during pregnancy is permitted only when the expected benefit outweighs potential risks, and it should be decided by a qualified healthcare professional.

Mixing with other insulin formulations is not recommended unless specifically instructed by a clinician, as dose adjustments are required.

Seek immediate medical assistance, administer a rapid source of glucose if the patient is conscious, and inform the prescribing clinician about the event.

Store the pen at controlled room temperature, protect it from direct heat or freezing, and discard after the labeled period once in use.

Yes, concomitant use of sulfonylureas, meglitinides, or other insulin‑secretagogues can increase the risk of hypoglycemia and should be managed carefully.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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