Product image of Inhafort (Formoterol Fumarate Dihydrate) supplied by GNH India

Inhafort

Active Ingredient:
Formoterol Fumarate Dihydrate
Origin:
EU

Inhafort (Formoterol Fumarate Dihydrate)

Formoterol fumarate dihydrate, the active ingredient in Inhafort, is a long‑acting β2‑adrenergic agonist (LABA) presented as an inhalation product for use via inhalation. It provides bronchodilation to help manage chronic airway diseases such as asthma and chronic obstructive pulmonary disease (COPD) in adult patients. The medication is formulated for delivery through a metered‑dose inhaler, allowing rapid onset of action and sustained airway opening over several hours.

GNH India supplies Inhafort as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Mediner Kft.

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Indications & Clinical Uses

  • Inhafort, a long‑acting β2‑adrenergic agonist, is used to treat chronic obstructive airway diseases.
  • Asthma: improves lung function and reduces symptoms when used regularly as maintenance therapy.
  • Chronic obstructive pulmonary disease (COPD): provides sustained bronchodilation to lessen breathlessness and improve exercise tolerance.
  • Exercise‑induced bronchospasm: used as part of a combination regimen to prevent airway narrowing during physical activity.

How It Works

  • Formoterol binds selectively to β2‑adrenergic receptors on airway smooth‑muscle cells, activating adenylate cyclase and increasing intracellular cyclic AMP. The rise in cAMP leads to protein kinase A activation, which phosphorylates target proteins causing relaxation of smooth muscle and inhibition of mediator release. This results in prolonged bronchodilation lasting up to 12 hours after inhalation. The effect is sustained because formoterol has high affinity for the receptor and slow dissociation.

Side Effects

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

Common Side Effects

  • Tremor: mild shaking of the hands or limbs.
  • Headache: transient headache often resolving without treatment.
  • Throat irritation: dryness or irritation in the throat after inhalation.
  • Cough: occasional cough triggered by the inhaled powder.
  • Palpitations: sensation of rapid or irregular heartbeat.
  • Muscle cramps: occasional leg or calf cramps.

Serious or Rare Side Effects

  • Paradoxical bronchospasm: sudden worsening of breathing difficulty requiring immediate care.
  • Cardiac arrhythmia: irregular heart rhythm that may need medical attention.
  • Severe allergic reaction: rash, swelling, or anaphylaxis requiring emergency treatment.

Precautions & Warnings

When prescribing or using Inhafort, several precautions should be observed to ensure safety.

  • Assess cardiovascular status: evaluate for arrhythmias or ischemic heart disease before initiation.
  • Monitor asthma control: ensure patient has a rescue inhaler and review symptoms regularly.
  • Avoid use in known hypersensitivity: discontinue if allergic reactions occur.
  • Use with caution in severe COPD: consider risk of tachycardia and tremor.
  • Review concomitant beta‑blocker therapy: may diminish bronchodilator effect.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Formoterol can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Beta‑blockers: may antagonize the bronchodilator effect of formoterol and can precipitate bronchospasm, especially in patients with reactive airway disease.
  • Monoamine oxidase inhibitors (MAOIs): concurrent use can lead to severe hypertension due to additive sympathomimetic activity.
  • Diuretics: may enhance the risk of hypokalemia, which can exacerbate cardiac arrhythmias when combined with formoterol.

Moderate Interactions (Monitor Closely)

  • Theophylline: formoterol can increase theophylline plasma concentrations, so serum levels should be monitored and dosage adjusted if needed.
  • Corticosteroids: combined use may produce additive bronchodilation and increase the potential for systemic steroid effects; monitor for signs of over‑exposure.
  • Anticholinergic agents: when used together, there may be excessive tachycardia or palpitations; observe heart rate and adjust therapy as appropriate.

Frequently Asked Questions

Inhafort contains the long‑acting β2‑adrenergic agonist formoterol fumarate dihydrate. It is prescribed for the maintenance treatment of asthma and chronic obstructive pulmonary disease (COPD) to provide sustained bronchodilation and improve breathing over a 12‑hour period.

Formoterol selectively stimulates β2‑adrenergic receptors on airway smooth‑muscle cells. This activation raises intracellular cyclic AMP, leading to relaxation of the muscle and inhibition of bronchoconstrictive mediators, which results in prolonged widening of the airways.

The dose of Inhafort is individualized. A qualified prescriber determines the number of inhalations and frequency based on the patient’s severity of asthma or COPD, response to therapy, and clinical guidelines.

Safety data for formoterol in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by the treating physician.

To order Inhafort, 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 any necessary import documentation.

Inhafort’s active ingredient, formoterol, has a rapid onset of action (within minutes) and a duration of up to 12 hours, similar to other LABAs such as salmeterol. Formoterol’s higher receptor affinity may offer slightly more consistent bronchodilation, but clinical choice depends on patient response, device preference and physician judgment.

Inhafort should be stored at room temperature, below 25 °C, in its original packaging. Keep the inhaler away from moisture, heat and direct sunlight. Do not expose it to freezing temperatures, and replace the device according to the manufacturer’s expiry date.

Inhafort is delivered via a metered‑dose inhaler. The patient should exhale fully, place the mouthpiece in the mouth, seal lips, and inhale slowly and deeply while actuating the device. Hold the breath for about 10 seconds, then exhale gently. Follow the specific inhaler instructions provided by the healthcare professional.

Serious risks include paradoxical bronchospasm, which can cause sudden worsening of breathing, cardiac arrhythmias such as irregular heart rhythm, and severe allergic reactions like anaphylaxis. Patients should seek immediate medical attention if they experience these symptoms.

Inhafort should be avoided in individuals with a known hypersensitivity to formoterol or any component of the inhaler. It is also contraindicated in patients who have experienced a severe paradoxical bronchospasm after using a β2‑agonist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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