Product image of Insuman Comb 15 Solostar (Insulin Human) supplied by GNH India

Insuman Comb 15 Solostar

Active Ingredient:
Insulin Human
Origin:
EU

Insuman Comb 15 Solostar (Insulin Human)

Insulin human, the active ingredient in Insuman Comb 15 Solostar, is a short‑acting insulin presented as a pre‑filled injection pen for subcutaneous administration. It is used to control blood glucose levels in adults and children with type 1 diabetes mellitus and type 2 diabetes mellitus, providing rapid onset of action after injection.

GNH India supplies Insuman Comb 15 Solostar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with distribution across EU and other regulated markets. The company ensures product quality through strict regulatory compliance and cold‑chain logistics.

Manufacturer / TM Owner

Sanofi-Aventis Deutschland Gmbh

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Indications & Clinical Uses

Insuman Comb 15 Solostar, a human insulin formulation, is used in the management of diabetes mellitus by providing rapid glucose control.

  • Type 1 diabetes mellitus: lowers fasting and post‑prandial glucose levels.
  • Type 2 diabetes mellitus: improves glycaemic control when combined with diet, exercise, or other antidiabetic agents.
  • Gestational diabetes mellitus: assists in achieving target glucose levels during pregnancy.

How It Works

  • Insulin human binds to insulin receptors on muscle, adipose and hepatic cells, activating the receptor’s intrinsic tyrosine kinase activity. This triggers downstream signaling cascades that promote translocation of GLUT‑4 transporters to the cell surface, increasing glucose uptake, while also suppressing hepatic gluconeogenesis, enhancing glycogen synthesis and lipogenesis, and inhibiting lipolysis, thereby reducing blood glucose concentrations.

Side Effects

Insuman Comb 15 Solostar may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Hypoglycemia: sweating, tremor, dizziness, or confusion that may require carbohydrate intake.
  • Injection site reactions: redness, swelling, itching, or mild pain at the injection site.
  • Weight gain: modest increase in body weight due to improved glucose utilization and anabolic effects.

Serious or Rare Side Effects

  • Severe hypoglycemia: loss of consciousness, seizures, or need for emergency assistance.
  • Allergic reactions: urticaria, angioedema, or anaphylaxis that may require immediate medical treatment.
  • Lipodystrophy: localized fat loss or accumulation at injection sites, potentially affecting insulin absorption.

Precautions & Warnings

When using Insuman Comb 15 Solostar, several precautions should be observed to ensure safety and efficacy.

  • Dose adjustment: tailor insulin dose based on blood glucose monitoring and carbohydrate intake.
  • Renal impairment: monitor closely as reduced clearance may increase hypoglycemia risk.
  • Hepatic dysfunction: use with caution; altered insulin metabolism may occur.
  • Pregnancy: insulin is category B, but dosing should be individualized by a healthcare professional.
  • Concomitant medications: assess for agents that may potentiate hypoglycemia, such as sulfonylureas.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the pen.

Avoid Interactions

Insuman Comb 15 Solostar can interact with other medicines, affecting glucose control or insulin action.

Major Interactions (Avoid)

  • Beta‑blockers: may mask hypoglycemia symptoms.
  • MAO inhibitors: can potentiate insulin’s glucose‑lowering effect.
  • Corticosteroids: may cause significant hyperglycemia requiring dose increase.

Moderate Interactions (Monitor Closely)

  • Sulfonylureas or meglitinides: additive risk of hypoglycemia.
  • ACE inhibitors: may enhance insulin sensitivity.
  • Thiazide diuretics: can raise blood glucose levels.
  • Oral contraceptives: may slightly increase insulin requirements.

Frequently Asked Questions

Insuman Comb 15 Solostar is a pre‑filled injection pen containing human insulin. It is prescribed to lower elevated blood glucose in individuals with type 1 diabetes mellitus, type 2 diabetes mellitus, and, when indicated, gestational diabetes. The rapid‑acting formulation provides prompt glucose reduction after meals or correction doses, helping patients achieve target glycaemic control as part of a comprehensive diabetes management plan.

Insulin human mimics the action of endogenous pancreatic insulin. After subcutaneous injection it binds to insulin receptors on muscle, fat and liver cells, activating intracellular tyrosine kinase pathways. This promotes translocation of GLUT‑4 transporters to the cell surface, increasing glucose uptake, while simultaneously suppressing hepatic glucose production, glycogenolysis, and lipolysis, thereby lowering circulating blood glucose levels.

The dose of Insuman Comb 15 Solostar is individualized by the prescribing healthcare professional. Dosing is based on factors such as the patient’s current blood glucose readings, carbohydrate intake, body weight, renal and hepatic function, and overall treatment goals. Patients should follow the specific instructions provided by their clinician and adjust the pen’s dose according to regular glucose monitoring.

Insulin human is classified as pregnancy category B, indicating no evidence of risk in animal studies and a lack of well‑controlled human data. It is generally considered safe for use in pregnant women when required to control maternal hyperglycaemia, as uncontrolled diabetes poses greater risk to the fetus. Breastfeeding mothers should also use insulin under medical guidance, as only minimal amounts are transferred into breast milk.

To place an order, visit the product page on gnhindia.com and submit an enquiry specifying the desired quantity of Insuman Comb 15 Solostar. GNH India works with hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials. After confirmation, the sales team provides pricing, availability, shipping details—including cold‑chain logistics if needed—and assists with any required import documentation.

Insuman Comb 15 Solostar contains human insulin, whereas many other rapid‑acting products use insulin analogues such as insulin lispro, aspart or glulisine. Human insulin has a slightly longer onset and duration compared with analogues, which may affect timing of meals and dosing flexibility. However, it provides comparable glucose‑lowering efficacy and is often chosen for its established safety profile and cost considerations in certain markets.

The pen should be stored in a refrigerator at 2 °C to 8 °C (36 °F to 46 °F) and protected from direct light. Do not freeze or shake the device. Once in use, the pen may be kept at controlled room temperature (up to 30 °C) for a maximum of 28 days, but any remaining insulin should be discarded after this period. Always keep the pen in its original packaging.

Insuman Comb 15 Solostar is administered subcutaneously using the pre‑filled pen. The injection site should be rotated among the abdomen, thigh, or upper arm to reduce lipodystrophy risk. The pen is primed according to the manufacturer’s instructions before the first use, and the dose is selected by turning the dose selector to the prescribed units. After injection, the needle is safely disposed of in an approved sharps container.

The most serious risks include severe hypoglycemia, which can lead to loss of consciousness, seizures, or accidents if not promptly treated; allergic reactions ranging from urticaria to anaphylaxis; and lipodystrophy that may impair insulin absorption. Patients should be educated to recognize early signs of hypoglycemia, monitor blood glucose regularly, and seek immediate medical attention for any signs of a severe allergic response.

Insuman Comb 15 Solostar should not be used by individuals with a known hypersensitivity to human insulin or any of the pen’s excipients. It is also contraindicated in patients experiencing hypoglycemia unawareness where they cannot recognize low‑blood‑glucose symptoms, and in those with severe renal or hepatic failure unless dose adjustments are made under close medical supervision. Consultation with a healthcare provider is essential before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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