GNH USA

Europe — EMA

Humulin M3 (30/70) Kwikpen

Humulin M3 (30/70) Kwikpen is a premixed human insulin pen for Type 1 and Type 2 diabetes, detailing uses, mechanism, side effects, and precautions.

Insulin Human

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What is Insulin Human?

Humulin M3 (30/70) Kwikpen is a pre‑filled, disposable insulin pen that contains human insulin in a premixed formulation of 30 % soluble (regular) insulin and 70 % intermediate‑acting NPH insulin. The product is supplied in the European market and is prescribed for subcutaneous injection to help manage blood glucose levels in patients with diabetes, allowing individualized dosing.

What is Insulin Human used for?

Humulin M3 (30/70) Kwikpen is indicated for the treatment of diabetes mellitus in adults and children who require a combination of rapid‑acting and intermediate‑acting insulin.

- Control of fasting and post‑prandial blood glucose in Type 1 diabetes. - Control of fasting and post‑prandial blood glucose in Type 2 diabetes. - Basal‑bolus insulin regimens where a premixed insulin simplifies dosing. - Patients who prefer a pre‑filled pen device for ease of administration. - Adjunct to diet and exercise in patients unable to achieve targets with oral agents alone.

What are the side effects of Insulin Human?

Adverse reactions to Humulin M3 (30/70) Kwikpen are reported in clinical use and may vary in frequency and severity.

Common: - Hypoglycemia, especially if meals are missed or activity is increased. - Injection‑site pain, redness, or swelling. - Lipodystrophy or lipoatrophy at the injection site. - Weight gain associated with improved glycemic control. - Mild allergic skin reactions such as rash or urticaria.

Serious: - Severe hypoglycemia requiring assistance. - Anaphylactic reaction or angioedema. - Hypokalemia due to rapid intracellular shift of potassium. - Diabetic ketoacidosis if insulin therapy is abruptly discontinued. - Acute insulin allergy with systemic symptoms.

What precautions apply to Insulin Human?

When prescribing or using Humulin M3 (30/70) Kwikpen, clinicians should consider several safety considerations to reduce risk.

- Monitor closely for hypoglycemia, especially during dose adjustments or changes in diet. - Adjust doses in patients with renal or hepatic impairment. - Use with caution during pregnancy and lactation; evaluate benefit‑risk balance. - Observe for signs of allergic reactions, particularly in patients with known insulin sensitivities. - Avoid use in individuals with documented hypersensitivity to human insulin or any excipients. - Assess cardiovascular status, as insulin may influence fluid retention and blood pressure.

What does Insulin Human interact with?

Humulin M3 (30/70) can interact with other medicines, altering glucose control or increasing adverse event risk.

Avoid: - Concurrent use of additional insulin products without appropriate dose reduction. - Beta‑blockers that may mask hypoglycemia symptoms. - Monoamine oxidase inhibitors, which can potentiate insulin‑induced hypoglycemia.

Use with caution: - Oral antidiabetic agents such as sulfonylureas or meglitinides, which increase hypoglycemia risk. - Corticosteroids, thiazide diuretics, and sympathomimetic drugs that may raise blood glucose, requiring dose adjustments. - Alcohol consumption, which can enhance insulin’s glucose‑lowering effect.

Frequently asked questions

What type of insulin is contained in Humulin M3 (30/70) Kwikpen?+
Humulin M3 (30/70) Kwikpen contains human insulin in a premixed formulation of 30 % soluble (regular) insulin and 70 % intermediate‑acting NPH insulin.
How is Humulin M3 (30/70) Kwikpen administered?+
The medication is delivered subcutaneously using the pre‑filled Kwikpen device, which allows the user to dial the prescribed dose and inject into the abdomen, thigh, or upper arm.
For which patients is Humulin M3 (30/70) Kwikpen indicated?+
It is indicated for adults and children with Type 1 or Type 2 diabetes who need both rapid‑acting and intermediate‑acting insulin to control fasting and post‑prandial glucose levels.
Can Humulin M3 (30/70) Kwikpen be used during pregnancy?+
Insulin is generally considered the treatment of choice for diabetes in pregnancy, but the decision to use Humulin M3 (30/70) should be made by a healthcare professional after weighing potential benefits and risks.
What are the most common side effects of Humulin M3 (30/70) Kwikpen?+
Common adverse effects include hypoglycemia, injection‑site reactions such as pain or redness, lipodystrophy, mild weight gain, and occasional skin rash or urticaria.
How does Humulin M3 (30/70) Kwikpen differ from a basal‑only insulin?+
Humulin M3 combines a rapid‑acting component that lowers post‑meal glucose with an intermediate‑acting component that provides basal coverage, whereas basal‑only insulins supply only long‑acting background insulin.
What should I do if I experience severe hypoglycemia while using Humulin M3 (30/70)?+
Seek immediate medical assistance, consume fast‑acting carbohydrates if you are able, and inform your healthcare provider to adjust your insulin regimen.
Are there any foods or beverages that should be avoided with Humulin M3 (30/70)?+
Alcohol can enhance insulin’s glucose‑lowering effect and increase hypoglycemia risk; it should be consumed in moderation and with food while monitoring blood glucose.
Can other medications interfere with the action of Humulin M3 (30/70)?+
Yes, drugs such as beta‑blockers, MAO inhibitors, sulfonylureas, corticosteroids, thiazide diuretics, and sympathomimetics can affect glucose control and may require dose adjustments.
How should the Kwikpen be stored before and after opening?+
Before use, store the pen in a refrigerator (2‑8 °C) away from direct heat. After the first use, it may be kept at room temperature (up to 30 °C) for up to 28 days, protecting it from light.
Is it safe to share a Humulin M3 (30/70) Kwikpen with another person?+
No. Insulin pens are prescribed for individual use only; sharing can increase the risk of dosing errors and transmission of infections.
What should I do if the Kwikpen does not appear to be working properly?+
Check that the pen is not expired, that the dose dial is set correctly, and that the needle is properly attached. If problems persist, contact a pharmacist or healthcare provider for replacement.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Insulin Human
Route
Subcutaneous Use
Manufacturer
Eli Lilly Čr, S.R.O.
Origin
EU

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