Product image of Nanogam (Human Normal Immunoglobulin) supplied by GNH India

Nanogam

Active Ingredient:
Human Normal Immunoglobulin
Origin:
EU

Nanogam (Human Normal Immunoglobulin)

Human Normal Immunoglobulin, the active ingredient in Nanogam, is a Immunoglobulin (human normal) presented as a solution for intravenous infusion for intravenous use. It treats primary and secondary immunodeficiency diseases by providing passive immunity.
GNH India supplies Nanogam as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Prothya Biosolutions Netherlands B.V.

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Indications & Clinical Uses

Nanogam is used to replace deficient antibodies in patients with primary or secondary immunodeficiency conditions.

  • Primary immunodeficiency diseases (e.g., common variable immunodeficiency): provides IgG antibodies to reduce infection frequency.
  • Secondary immunodeficiency (e.g., post‑bone marrow transplant, chemotherapy): supplies passive immunity to protect against opportunistic pathogens.
  • Prophylaxis of infections in antibody‑deficient patients: maintains protective antibody levels to prevent bacterial and viral infections.

How It Works

  • Human Normal Immunoglobulin in Nanogam consists of pooled IgG antibodies derived from screened donors. After intravenous infusion, the IgG distributes throughout the vascular and extravascular compartments, binding to pathogens, toxins, and complement components. This neutralizes microbes, facilitates opsonization, and modulates immune cell activity, thereby restoring humoral immunity in individuals lacking adequate antibody production.

Side Effects

Nanogam may be associated with infusion‑related reactions and immune‑mediated events.

Common Side Effects

  • Headache: mild to moderate discomfort during or after infusion.
  • Fever or chills: transient elevation of body temperature.
  • Nausea: mild gastrointestinal upset.
  • Fatigue: temporary feeling of tiredness.
  • Injection site erythema: redness at the infusion site.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Thromboembolic events: blood clots such as deep vein thrombosis.
  • Renal impairment: acute kidney injury, especially with high infusion rates.
  • Hemolysis: destruction of red blood cells.
  • Aseptic meningitis: inflammation of meninges without infection.

Precautions & Warnings

When using Nanogam, clinicians should consider several safety and handling precautions.

  • Patient assessment: evaluate history of IgA deficiency or allergic reactions to blood products.
  • Infusion rate: start slowly and increase gradually to reduce adverse reactions.
  • Hydration status: ensure adequate fluid intake to support renal function.
  • Monitoring: observe vital signs during infusion and for at least 30 minutes after.
  • Concomitant immunosuppressants: assess increased infection risk when combined.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Nanogam can interact with certain medications and clinical conditions.

Major Interactions (Avoid)

  • Live vaccines: may reduce vaccine efficacy or increase risk of infection.
  • High‑dose aspirin or NSAIDs: increase risk of bleeding due to platelet inhibition.
  • Immunoglobulin‑A deficiency with anti‑IgA antibodies: risk of severe anaphylaxis.

Moderate Interactions (Monitor Closely)

  • Corticosteroids: may alter immune response, requiring dose adjustment.
  • Anticoagulants (e.g., warfarin): monitor coagulation parameters.
  • Diuretics: monitor renal function and fluid balance.

Frequently Asked Questions

Nanogam is indicated for patients with primary immunodeficiency diseases such as common variable immunodeficiency, for secondary immunodeficiency following bone‑marrow transplantation or chemotherapy, and for prophylaxis of infections in individuals who lack adequate antibody production.

The pooled IgG antibodies in Nanogam provide passive immunity by binding to a broad range of pathogens and toxins, enhancing opsonization and complement activation, and modulating immune cell functions, thereby compensating for the patient’s deficient antibody response.

The dose of Nanogam is individualized; the prescribing clinician determines the appropriate volume and infusion rate based on the patient’s weight, clinical condition, and laboratory parameters.

Safety data for Nanogam in pregnancy and lactation are limited. The product should be used only if the potential benefit to the mother outweighs any potential risk to the fetus or infant, and the decision should be made by the treating physician.

To order Nanogam, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details, and necessary import documentation.

Nanogam is a standard human normal immunoglobulin preparation similar to other IVIG products in composition and clinical use. Differences may exist in manufacturing processes, donor screening, and stabilizers, but therapeutic efficacy and safety profiles are generally comparable when used according to prescribing information.

Nanogam must be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze the solution or shake the container vigorously, as this can affect product stability.

Nanogam is given as an intravenous infusion. The infusion should be started at a low rate and gradually increased, with continuous monitoring of vital signs and observation for any adverse reactions during and after the infusion.

Serious risks include anaphylactic reactions, thromboembolic events, acute renal impairment, hemolysis, and aseptic meningitis. Prompt recognition and management of these events are essential, and patients should be monitored closely during and after infusion.

Nanogam is contraindicated in patients with known severe IgA deficiency who have anti‑IgA antibodies, and in individuals who have experienced a severe hypersensitivity reaction to immunoglobulin products. Caution is also advised for patients with uncontrolled hypercoagulable states.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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