Product image of Mixtard 30 (Insulin Human) supplied by GNH India

Mixtard 30

Active Ingredient:
Insulin Human
Origin:
EU

Mixtard 30 (Insulin Human)

Insulin human, the active ingredient in Mixtard 30, is a short‑acting insulin presented as an injectable solution for subcutaneous administration. It is used to lower elevated blood glucose levels in patients with diabetes mellitus, including both type 1 and type 2, and is marketed in the European Union.

GNH India supplies Mixtard 30 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing regulatory‑approved batches that meet EU quality standards and supporting global procurement for diabetes care programs.

Manufacturer / TM Owner

Novo Nordisk A/S

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Indications & Clinical Uses

Mixtard 30 is a human insulin formulation indicated for the management of hyperglycaemia in diabetes mellitus, providing both basal and rapid‑acting coverage.

  • Type 1 diabetes mellitus: supplies both basal and mealtime insulin to achieve target glycaemic levels and reduce risk of ketoacidosis.
  • Type 2 diabetes mellitus: adds exogenous insulin to improve glucose control when diet, exercise, and oral agents are inadequate.
  • Hyperglycaemic crisis (e.g., diabetic ketoacidosis): can be used under medical supervision to rapidly lower plasma glucose while other therapies are initiated.

How It Works

  • Insulin human binds to insulin receptors on muscle, adipose and hepatic cells, activating the receptor tyrosine kinase pathway. This stimulates translocation of GLUT‑4 transporters, enhancing glucose uptake, promotes glycogen synthesis, and suppresses hepatic gluconeogenesis, thereby lowering circulating blood glucose concentrations.

Side Effects

Common Side Effects

  • Hypoglycaemia: low blood sugar episodes, especially if meals are missed or dose is excessive.
  • Injection site reactions: redness, swelling, or itching at the injection site.
  • Weight gain: increased adipose tissue due to improved glucose utilization.
  • Lipodystrophy: localized fat accumulation or loss with repeated injections.
  • Edema: mild fluid retention, particularly in the lower extremities.
  • Headache: transient mild headache after injection.

Serious or Rare Side Effects

  • Severe hypoglycaemia leading to seizures or loss of consciousness.
  • Anaphylactic reaction: hives, difficulty breathing, or swelling of the face.
  • Insulin allergy: systemic rash or urticaria.
  • Hypokalemia: low potassium levels, potentially causing cardiac arrhythmia.
  • Insulin antibodies: may alter insulin action or cause immune complex reactions.

Precautions & Warnings

Before using Mixtard 30, patients should be aware of the following precautions:

  • Blood glucose monitoring: check levels regularly to adjust dose appropriately.
  • Dose adjustments: modify insulin dose when initiating, changing diet, or during illness.
  • Renal impairment: use caution as reduced clearance may increase hypoglycaemia risk.
  • Known hypersensitivity: avoid if allergic reactions to human insulin have occurred.
  • Pregnancy category B: use only if the potential benefit justifies the potential risk to the fetus.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mixtard 30 may interact with other medicines as follows:

Major Interactions (Avoid)

  • Sulfonylureas: combined effect can cause severe hypoglycaemia.
  • Beta‑blockers: may mask typical hypoglycaemia symptoms such as tachycardia.
  • Glucocorticoids: can reduce insulin effectiveness, requiring dose increase.

Moderate Interactions (Monitor Closely):\n- ACE inhibitors: may enhance insulin sensitivity, increasing hypoglycaemia risk.

  • Thiazide diuretics: can raise blood glucose, potentially necessitating higher insulin doses.
  • Alcohol: may potentiate hypoglycaemia, especially with missed meals.

Frequently Asked Questions

Mixtard 30 is a human insulin preparation used to control high blood glucose in patients with diabetes mellitus, including both type 1 and type 2. It provides both basal and rapid‑acting insulin to help achieve target glycaemic levels and prevent complications associated with chronic hyperglycaemia.

Insulin human binds to insulin receptors on muscle, fat and liver cells, activating intracellular pathways that increase glucose uptake, promote glycogen storage, and suppress hepatic glucose production. This coordinated action lowers circulating blood glucose and facilitates its utilization for energy.

The dose of Mixtard 30 is individualized and determined by a qualified healthcare professional based on the patient’s blood glucose readings, diet, activity level and overall treatment plan. Patients should follow the prescriber’s instructions and not adjust the dose without medical guidance.

Mixtard 30 is classified as pregnancy category B, indicating that animal studies have not shown risk but there are limited human data. It may be used during pregnancy or lactation only if the potential benefit outweighs any possible risk, and under close medical supervision.

To order Mixtard 30, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain handling) and necessary import documentation.

Mixtard 30 contains human insulin, providing a predictable pharmacokinetic profile similar to other short‑acting insulin analogues. Compared with rapid‑acting insulin analogues, it may have a slightly longer onset but offers a cost‑effective option for basal‑bolus regimens, especially in markets where biosimilar human insulin is preferred.

Mixtard 30 should be stored in a refrigerator at 2‑8 °C, protected from light, and must not be frozen or shaken. Once in use, the vial can be kept at room temperature for up to 28 days, but any unused solution should be discarded after this period.

Mixtard 30 is administered by subcutaneous injection into the abdomen, thigh or upper arm. The injection site should be rotated to reduce the risk of lipodystrophy. Patients should be trained by a healthcare professional on proper injection technique and dose measurement.

The most serious risks include severe hypoglycaemia, which can lead to seizures or loss of consciousness, and allergic reactions such as anaphylaxis. Patients should be educated to recognize early signs of low blood sugar and to seek immediate medical attention for any severe allergic symptoms.

Mixtard 30 should not be used by individuals with a known hypersensitivity to human insulin or any of the product’s excipients. It is also contraindicated in patients with hypoglycaemia unawareness who cannot safely monitor and respond to low blood glucose levels.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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