Product image of Humulin I Kwikpen (Isophane) (Insulin Human (Rdna)) supplied by GNH India

Humulin I Kwikpen (Isophane)

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin I Kwikpen (Isophane) (Insulin Human (Rdna))

Humulin I Kwikpen is a pre‑filled pen suspension containing insulin human (isophane) at a concentration of 100 U/mL. It is a recombinant DNA (rDNA) product approved in the EU for subcutaneous or intramuscular injection, and it is available by prescription. The device delivers intermediate‑acting insulin to help regulate blood glucose in people with diabetes. It provides a convenient, ready‑to‑use delivery system that can be stored at room temperature after opening.

Manufacturer / TM Owner

Eli Lilly Nederland B.V.

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Indications & Clinical Uses

Humulin I Kwikpen is indicated for the management of blood glucose in adults and children with diabetes mellitus. It is used as part of a basal insulin regimen to provide intermediate‑acting coverage.

  • Type 1 diabetes mellitus as part of basal insulin therapy.
  • Type 2 diabetes mellitus when intermediate‑acting insulin is required.
  • Adjunct to rapid‑acting insulin analogues for mixed‑dose regimens.
  • Use during pregnancy (category B) when basal insulin is needed.
  • May be employed in insulin‑pump transition periods if prescribed.

How It Works

  • Humulin I Kwikpen contains insulin human (isophane), an intermediate‑acting insulin analogue that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers the tyrosine‑kinase pathway, promoting translocation of GLUT‑4 transporters and enhancing glucose uptake. In the liver, the signal suppresses gluconeogenesis and glycogenolysis, thereby lowering circulating glucose levels. The protamine component delays absorption, providing a prolonged pharmacodynamic profile.

Side Effects

Like all insulin preparations, Humulin I Kwikpen can cause adverse reactions, most of which are related to its pharmacologic action or formulation.

Common

  • Hypoglycemia, especially if meals are missed or activity is increased.
  • Mild injection‑site reactions such as redness, swelling, or itching.
  • Lipodystrophy or localized fat atrophy at repeated injection sites.
  • Transient weight gain due to fluid retention.
  • Peripheral edema.

Serious

  • Severe hypoglycemia leading to loss of consciousness or seizures.
  • Allergic reactions ranging from urticaria to anaphylaxis.
  • Hypokalemia associated with rapid glucose shifts.
  • Development of insulin antibodies that may alter drug efficacy.
  • Acute pancreatitis (rare).

Precautions & Warnings

When prescribing or using Humulin I Kwikpen, clinicians and patients should observe several safety considerations to minimize risk.

  • Monitor blood glucose regularly to avoid hypoglycemia.
  • Adjust dose during illness, surgery, or changes in physical activity.
  • Use caution in patients with renal or hepatic impairment.
  • Do not mix with other insulin products in the same pen.
  • Store the pen according to label; discard after the recommended in‑use period.
  • Educate patients on proper injection technique and site rotation.

Avoid Interactions

Humulin I Kwikpen may interact with other medicines that affect glucose metabolism or insulin action.

Avoid

  • Concurrent use of other intermediate‑acting insulins, which increases overdose risk.
  • Beta‑blockers that can mask typical hypoglycemia symptoms.
  • Monoamine oxidase (MAO) inhibitors that may potentiate insulin’s glucose‑lowering effect.

Use with caution

  • Oral hypoglycemic agents (e.g., sulfonylureas, meglitinides) may increase hypoglycemia risk.
  • Corticosteroids, thiazide diuretics, and sympathomimetics can raise blood glucose, requiring dose adjustment.
  • Alcohol consumption can cause delayed hypoglycemia, especially after a dose.

Frequently Asked Questions

Humulin I Kwikpen is a pre‑filled, disposable pen that delivers a fixed concentration of 100 U/mL, whereas vials require a separate syringe and needle for each dose. The pen offers convenience and dose‑setting accuracy, while vials may be preferred for larger volume needs.

The pen is designed for subcutaneous or intramuscular injection. After priming, the user selects the prescribed number of units, inserts the needle into the chosen injection site, and presses the dose button. The device automatically retracts the needle after delivery.

Humulin I Kwikpen is classified as pregnancy category B, indicating that animal studies have not shown risk and there are no adequate human studies. It may be used when the potential benefit justifies the potential risk, under medical supervision.

Common adverse reactions include hypoglycemia, mild injection‑site redness or swelling, lipodystrophy, transient weight gain, and peripheral edema.

After the first use, the pen should be stored at room temperature (15‑30 °C) and protected from direct heat or sunlight. It must be discarded after the period specified on the label, typically 28 days, even if insulin remains.

Rotate sites within the same anatomical region (e.g., abdomen, thigh, upper arm) each injection to reduce the risk of lipodystrophy and improve absorption. Avoid injecting into scar tissue, bruised areas, or sites with visible lipohypertrophy.

Protamine binds to insulin molecules, forming a complex that slows absorption from the injection site. This creates a prolonged, intermediate‑acting insulin profile lasting up to 12–18 hours.

Consume 15–20 g of fast‑acting carbohydrate (e.g., glucose tablets, juice). Re‑check blood glucose after 15 minutes and repeat if still low. If the person is unable to swallow, seek emergency medical assistance.

Concurrent use of other intermediate‑acting insulins should be avoided due to overdose risk. Beta‑blockers can mask hypoglycemia symptoms and should be used with caution.

No. Humulin I Kwikpen should not be mixed with other insulin formulations in the same pen, as this can alter the intended pharmacokinetic profile and increase the risk of dosing errors.

Blood glucose should be monitored before meals, at bedtime, and whenever symptoms of hypo‑ or hyperglycemia occur. Additional checks may be needed during dose adjustments, illness, or changes in activity level.

Serious reactions may include rash, itching, swelling of the face or throat, difficulty breathing, or anaphylaxis. If any of these occur, seek immediate medical attention.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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