Product image of Humulin Regular (Dialytí) Kwikpen (Insulin Human (Rdna)) supplied by GNH India

Humulin Regular (Dialytí) Kwikpen

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin Regular (Dialytí) Kwikpen (Insulin Human (Rdna))

Humulin Regular (Dialytí) Kwikpen is a pre‑filled insulin pen that delivers insulin human (recombinant DNA) as an injectable solution. It contains regular insulin (100 U/mL) for subcutaneous administration. The product is authorized in the European Union and is prescribed by professionals for the management of diabetes mellitus. It provides a rapid onset of action, beginning within 30 minutes after injection, and is used in basal‑bolus insulin regimens.

Manufacturer / TM Owner

Pharmaserve-Lilly Saci

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Indications & Clinical Uses

Humulin Regular Kwikpen is indicated for the control of blood glucose in patients with diabetes requiring short‑acting insulin therapy.

  • Type 1 diabetes mellitus as part of a basal‑bolus regimen.
  • Type 2 diabetes mellitus when rapid glucose reduction is needed.
  • Management of hyperglycemia during illness, surgery, or steroid therapy.
  • Use in pregnant or lactating women only when benefits outweigh risks (under medical supervision).
  • Supplemental insulin for patients transitioning from other rapid‑acting insulin preparations.
  • Adjustment of dose in response to carbohydrate intake and physical activity.

How It Works

  • Humulin Regular contains recombinant human insulin that binds to insulin receptors on muscle, adipose and hepatic cells. Receptor activation triggers autophosphorylation of the β‑subunit and initiates intracellular signaling cascades, primarily the phosphoinositide 3‑kinase (PI3K)/Akt pathway. This promotes translocation of glucose transporter type 4 (GLUT4) to the cell membrane, increasing glucose uptake, while simultaneously suppressing hepatic gluconeogenesis and glycogenolysis, leading to lowered blood glucose levels.

Side Effects

Adverse reactions to Humulin Regular Kwikpen are categorized by frequency and clinical significance.

Common

  • Hypoglycemia, presenting as sweating, tremor, dizziness, or hunger.
  • Redness, swelling, or itching at the injection site.
  • Lipodystrophy, including localized lipoatrophy or lipohypertrophy.
  • Gradual weight gain associated with improved glycemic control.
  • Mild gastrointestinal discomfort such as nausea or abdominal fullness.

Serious

  • Severe hypoglycemia leading to confusion, loss of consciousness, or seizures.
  • Allergic reactions ranging from urticaria and angioedema to anaphylactic shock.
  • Persistent hyperglycemia suggesting possible insulin resistance or dosing error.
  • Fluid retention, peripheral edema, or worsening heart failure in at‑risk individuals.

Precautions & Warnings

Before initiating therapy with Humulin Regular Kwikpen, clinicians and patients should consider several precautionary measures.

  • Assess renal and hepatic function, as impairment may alter insulin clearance.
  • Review history of hypoglycemia unawareness or prior severe episodes.
  • Adjust doses when initiating or discontinuing concomitant glucocorticoids, β‑blockers, or thiazide diuretics.
  • Monitor blood glucose closely during periods of illness, fasting, or changes in physical activity.
  • Educate patients on proper injection technique and rotation of sites to reduce lipodystrophy.
  • Use caution in pregnant or lactating women; benefits must outweigh potential risks.
  • Consider cardiovascular status, especially in patients with known heart failure.

Avoid Interactions

Humulin Regular Kwikpen can interact with other medicines, affecting glucose control or insulin action.

Avoid

  • Concurrent use of other rapid‑acting insulins without dose adjustment.
  • High‑dose β‑blockers that may mask hypoglycemia symptoms.
  • MAO‑A inhibitors combined with sympathomimetic agents, increasing risk of hypertensive crisis.

Use with caution

  • Oral antidiabetic agents (e.g., sulfonylureas, meglitinides) that may potentiate hypoglycemia.
  • Corticosteroids, which can raise blood glucose and require insulin dose increase.
  • Thiazide diuretics and ACE inhibitors, which may affect potassium balance and insulin sensitivity.
  • Alcohol consumption, especially in excess, which can cause delayed hypoglycemia.

Frequently Asked Questions

Humulin Regular Kwikpen contains regular human insulin at a standard concentration of 100 units per milliliter.

The pen should be kept in the refrigerator (2‑8 °C) until first use; after the first injection, it may be stored at room temperature (up to 30 °C) for up to 28 days.

Yes, it may be prescribed for pediatric patients when a short‑acting insulin is required, but dosing must be individualized by a health‑care professional.

Common signs include sweating, trembling, hunger, dizziness, confusion, and rapid heartbeat. Severe hypoglycemia can lead to loss of consciousness or seizures.

Repeated injections into the same spot can cause lipodystrophy. Rotating injection sites on the abdomen, thigh, or upper arm helps minimize this risk.

Humulin Regular is a short‑acting insulin that begins working within 30 minutes and peaks in 2‑4 hours, whereas long‑acting insulins provide a basal level of insulin over 24 hours with no pronounced peak.

If a dose is missed, the patient should follow the guidance of their prescriber, which may include taking the missed dose as soon as possible if it is still within a reasonable time frame, or skipping it if the next scheduled dose is near.

Yes, alcohol can interfere with glucose metabolism and may cause delayed hypoglycemia, especially when taken on an empty stomach.

Insulin is generally preferred for managing diabetes in pregnancy, but the decision to use Humulin Regular should be based on a risk‑benefit assessment by the treating physician.

Frequent self‑monitoring of blood glucose, especially before meals and at bedtime, is recommended to assess the insulin’s effect and adjust dosing as needed.

Some OTC products, such as decongestants containing pseudoephedrine, can raise blood glucose, while others like NSAIDs may affect renal function and insulin clearance; patients should discuss all OTC use with their health‑care provider.

The patient should stop using the product immediately and seek emergency medical attention, as allergic reactions can progress to anaphylaxis.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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