Product image of Nebulgen Adulti (Flunisolide) supplied by GNH India

Nebulgen Adulti

Active Ingredient:
Flunisolide
Origin:
EU

Nebulgen Adulti (Flunisolide)

Flunisolide, the active ingredient in Nebulgen Adulti, is a glucocorticoid presented as an inhalation formulation for inhalation use. It is indicated for the treatment of asthma in adult patients, helping to reduce airway inflammation and improve breathing control.

GNH India supplies Nebulgen Adulti as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to European Union quality standards and provides reliable global distribution.

Manufacturer / TM Owner

I.B.N. Savio S.R.L.

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Indications & Clinical Uses

Flunisolide is an inhaled glucocorticoid that targets airway inflammation in respiratory disorders.

  • Asthma: reduces airway inflammation, improves symptom control, and decreases frequency of exacerbations.
  • Allergic airway inflammation: diminishes inflammatory response to allergens, helping maintain lung function.
  • Bronchial hyperreactivity: lessens airway hyperresponsiveness, contributing to better breathing stability.

How It Works

  • Flunisolide binds to intracellular glucocorticoid receptors, altering gene transcription to suppress pro‑inflammatory cytokines, inhibit eosinophil activation, and reduce airway edema. This anti‑inflammatory action decreases airway hyperresponsiveness and improves pulmonary function in asthma patients.

Side Effects

Flunisolide may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Oral candidiasis: fungal infection of the mouth or throat.
  • Hoarseness: voice changes or hoarseness.
  • Throat irritation: soreness or irritation in the throat.
  • Cough: persistent cough after inhalation.
  • Dysphonia: difficulty speaking due to vocal cord irritation.
  • Dry mouth: reduced salivation leading to discomfort.

Serious or Rare Side Effects

  • Adrenal suppression: reduced cortisol production.
  • Severe allergic reaction: anaphylaxis or angioedema.
  • Pneumonia: lower respiratory tract infection.
  • Immunosuppression: increased susceptibility to infections.
  • Oropharyngeal ulceration: painful lesions in the mouth.
  • Glaucoma or cataract formation: ocular pressure changes with long‑term use.

Precautions & Warnings

When using Nebulgen Adulti, consider the following precautions:

  • Monitor lung function: assess response and adjust therapy as needed.
  • Check for oral thrush: inspect mouth regularly and advise rinsing after use.
  • Evaluate adrenal function: consider in long‑term high‑dose therapy.
  • Use with caution in infections: respiratory infections may worsen.
  • Avoid abrupt discontinuation: taper to prevent adrenal crisis.
  • Store at room temperature: keep in original container, protect from moisture and heat.

Avoid Interactions

Flunisolide may interact with other medicines; awareness of interaction severity helps guide safe use.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase systemic exposure.
  • Systemic corticosteroids: additive immunosuppressive effects.
  • Live vaccines: reduced efficacy and increased infection risk.

Moderate Interactions (Monitor Closely)

  • Beta‑agonists (e.g., albuterol): potential for reduced bronchodilator response.
  • Theophylline: may require serum level monitoring.
  • Antifungal azoles (e.g., fluconazole): may modestly increase flunisolide levels.

Frequently Asked Questions

Nebulgen Adulti contains flunisolide, an inhaled glucocorticoid indicated for the maintenance treatment of asthma in adults. It helps control airway inflammation, reduce symptoms, and prevent asthma exacerbations when used as prescribed.

Flunisolide binds to intracellular glucocorticoid receptors, modulating gene transcription to suppress inflammatory cytokines, inhibit eosinophil activity, and reduce airway edema. This anti‑inflammatory effect diminishes airway hyperresponsiveness and improves breathing.

The prescribed dose of Nebulgen Adulti is determined by the treating physician based on disease severity, patient age, and individual response. Patients should follow the specific dosing instructions provided by their healthcare professional.

Safety data for flunisolide in pregnancy are limited and the product is classified as pregnancy category unknown. It should be used only if the potential benefit justifies the risk, and breastfeeding mothers should consult their physician before use.

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

Compared with other inhaled glucocorticoids such as budesonide or fluticasone, flunisolide offers a similar anti‑inflammatory profile. Differences lie in potency, particle size and device compatibility, which may influence dosing frequency and patient preference.

Nebulgen Adulti should be stored at room temperature, below 25 °C, in its original packaging, protected from moisture, heat and direct sunlight to maintain stability throughout its shelf life.

The medication is delivered via a nebulizer or inhalation device. Patients should inhale the prescribed dose as directed, typically after rinsing the mouth and avoiding swallowing the aerosol to reduce local side effects.

Serious risks include adrenal suppression, severe allergic reactions such as anaphylaxis, and opportunistic infections like pneumonia. Patients should be monitored for signs of these conditions and seek immediate medical attention if they occur.

Nebulgen Adulti is contraindicated in patients with known hypersensitivity to flunisolide or any component of the formulation. It should also be used with caution in individuals with active untreated infections or uncontrolled systemic diseases.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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