Product image of Oxis Turbohaler 6 (Formoterol Fumarate Dihydrate) supplied by GNH India

Oxis Turbohaler 6

Active Ingredient:
Formoterol Fumarate Dihydrate
Origin:
EU

Oxis Turbohaler 6 (Formoterol Fumarate Dihydrate)

Formoterol fumarate dihydrate, the active ingredient in Oxis Turbohaler 6, is a long‑acting β2‑adrenergic agonist presented as a dry‑powder inhaler for inhalation use. It provides bronchodilation for patients with reversible airway obstruction, typically in asthma and chronic obstructive pulmonary disease. GNH India supplies Oxis Turbohaler 6 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

GNH India supplies Oxis Turbohaler 6 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Astrazeneca Ab

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Indications & Clinical Uses

Formoterol fumarate dihydrate is a bronchodilator that acts on the β2‑adrenergic pathway to relax airway smooth muscle.

  • Asthma: improves control of symptoms and reduces the frequency of exacerbations.
  • Chronic obstructive pulmonary disease (COPD): provides sustained bronchodilation and helps decrease dyspnoea during daily activities.
  • Exercise‑induced bronchoconstriction: prevents airway narrowing that can occur with physical exertion.

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 relaxation of smooth‑muscle fibers, producing a rapid and prolonged bronchodilatory effect that improves airflow in obstructive airway diseases.

Side Effects

Formoterol may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Throat irritation: mild discomfort or dryness in the throat after inhalation.
  • Cough: transient coughing immediately after use of the inhaler.
  • Headache: mild to moderate headache not related to other causes.
  • Tremor: fine shaking of the hands, especially at higher doses.
  • Palpitations: sensation of rapid or irregular heartbeat.

Serious or Rare Side Effects

  • Paradoxical bronchospasm: sudden worsening of airway obstruction after inhalation.
  • Cardiac arrhythmia: irregular heart rhythm that may require medical attention.
  • Hypokalaemia: low blood potassium levels, potentially leading to muscle weakness.
  • Severe allergic reaction: rash, itching, swelling, or difficulty breathing.
  • Hyperglycaemia: elevated blood glucose, particularly in patients with diabetes.

Precautions & Warnings

When using Formoterol inhalation therapy, patients and clinicians should observe several safety measures.

  • Assess severity: evaluate the patient’s baseline lung function before initiating therapy.
  • Monitor response: regularly review symptom control and rescue‑inhaler use.
  • Avoid overuse: do not exceed the prescribed number of inhalations per day.
  • Caution in cardiac disease: patients with known arrhythmias or coronary disease should be monitored closely.
  • Pregnancy and lactation: use only if the potential benefit outweighs any risk to the fetus or infant.
  • Store at ambient temperature: keep below 25°C, in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Formoterol may interact with several other medicines, altering its safety or effectiveness. Major Interactions (Avoid):\n- Non‑selective β‑blockers: may diminish bronchodilator response and precipitate bronchospasm.

  • Monoamine oxidase inhibitors (MAOIs): can increase the risk of cardiovascular side effects.

Moderate Interactions (Monitor Closely)

  • Diuretics: may exacerbate hypokalaemia when combined with β2‑agonists.
  • Theophylline: concurrent use can increase the likelihood of tremor and tachycardia.
  • Corticosteroids: may enhance systemic β2‑agonist effects, requiring dose adjustment.
  • Anticholinergics: additive bronchodilation may increase the risk of dry mouth.
  • Certain antidepressants (e.g., SSRIs): may potentiate tachycardia, requiring observation.

Frequently Asked Questions

Oxis Turbohaler 6 contains formoterol fumarate dihydrate, a long‑acting β2‑agonist that is used to maintain bronchodilation in patients with asthma, chronic obstructive pulmonary disease (COPD) and exercise‑induced bronchoconstriction. It is prescribed as a maintenance inhaler to improve airway patency and reduce the frequency of symptoms.

Formoterol selectively stimulates β2‑adrenergic receptors on airway smooth‑muscle cells, activating adenylate cyclase and raising cyclic AMP levels. The increased cAMP causes smooth‑muscle relaxation, leading to rapid and sustained widening of the airways and improved airflow during both resting and exertional periods.

The dose of Oxis Turbohaler 6 is individualized by the prescribing clinician based on the patient’s disease severity, age and response to therapy. The prescriber determines the number of inhalations per day and any adjustments needed over time.

Formoterol is classified as pregnancy category C in many regions, meaning it should only be used when the potential benefit justifies any potential risk to the fetus. Breastfeeding mothers should consult their healthcare provider, as small amounts may be excreted in milk.

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 any required import documentation.

Formoterol offers a rapid onset of action (within minutes) combined with a 12‑hour duration, similar to other long‑acting β2‑agonists such as salmeterol. Compared with anticholinergic bronchodilators, formoterol primarily targets β2 receptors, providing a different mechanism that can be combined for additive effect in severe COPD.

Store the Turbohaler below 25°C in its original packaging, protecting it from moisture and direct sunlight. Do not expose the device to extreme temperatures, as this may affect powder flow and dose consistency.

The patient inhales a single dose of dry‑powder medication by loading the Turbohaler, exhaling fully away from the device, then inhaling forcefully and deeply through the mouthpiece. The inhaler is designed for multiple daily doses as directed by the prescriber.

Serious risks include paradoxical bronchospasm, cardiac arrhythmias, severe hypokalaemia and anaphylactic reactions. Patients should seek immediate medical attention if they experience sudden worsening of breathing, rapid or irregular heartbeat, muscle weakness or signs of an allergic reaction.

Formoterol is contraindicated in patients with a known hypersensitivity to formoterol or any excipients in the Turbohaler, and in individuals who have experienced a severe paradoxical bronchospasm after using a β‑agonist inhaler.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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