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

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

Manufacturer / TM Owner

Astrazeneca Uk Limited

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Indications & Clinical Uses

Formoterol fumarate dihydrate is a bronchodilator that acts on the airway smooth‑muscle pathway to improve airflow in chronic respiratory disease.

  • Asthma: improves symptom control and reduces the frequency of exacerbations.
  • Chronic obstructive pulmonary disease (COPD): enhances bronchodilation and supports maintenance therapy.
  • Exercise‑induced bronchoconstriction: prevents 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 relaxation of smooth‑muscle fibers, producing sustained bronchodilation and improved airflow during the respiratory cycle.

Side Effects

Formoterol may cause a range of adverse reactions, most of which are mild to moderate in severity.

Common Side Effects

  • Tremor: mild, transient shaking of the hands or limbs.
  • Headache: dull or throbbing discomfort, often resolving without intervention.
  • Throat irritation: mild soreness or dryness after inhalation.
  • Cough: brief episodes triggered by the inhaled powder.
  • Palpitations: sensation of rapid or irregular heartbeat, usually transient.
  • Nasal congestion: mild blockage or runny nose.

Serious or Rare Side Effects

  • Paradoxical bronchospasm: sudden worsening of airway obstruction requiring immediate medical attention.
  • Cardiac arrhythmias: irregular heart rhythms that may be life‑threatening.
  • Hypokalemia: low blood potassium levels that can affect muscle function.
  • Severe allergic reaction: rash, swelling, or difficulty breathing indicating anaphylaxis.

Precautions & Warnings

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

  • Assess baseline lung function: perform spirometry before initiating therapy.
  • Monitor for cardiovascular effects: watch for tachycardia, palpitations, or hypertension.
  • Avoid abrupt discontinuation: taper under medical supervision to prevent rebound bronchoconstriction.
  • Use with a rescue inhaler: maintain a short‑acting bronchodilator for acute symptoms.
  • Educate on inhaler technique: ensure correct use to maximize drug delivery and minimize oral deposition.
  • Store at ambient temperature: keep below 25°C, in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Formoterol can interact with several drug classes, altering its safety profile or efficacy.

Major Interactions (Avoid)

  • Non‑selective β‑blockers: may diminish bronchodilator response and precipitate bronchospasm.
  • Monoamine oxidase inhibitors (MAOIs): increase the risk of cardiovascular side effects.
  • Diuretics (especially loop diuretics): may exacerbate hypokalemia when combined with Formoterol.

Moderate Interactions (Monitor Closely)

  • Other β2‑agonists: additive bronchodilator effect can raise the risk of tachycardia.
  • Theophylline: may increase plasma concentrations of Formoterol.
  • Anticholinergics: combined use may enhance bronchodilation but requires monitoring for dry mouth and urinary retention.

Frequently Asked Questions

Oxis Turbohaler 6 contains formoterol fumarate dihydrate, a long‑acting β2‑agonist indicated for maintenance treatment of asthma and chronic obstructive pulmonary disease (COPD). It helps keep airways open, reducing symptoms such as wheezing, shortness of breath, and the need for rescue medication.

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 sustained bronchodilation and improved airflow throughout the breathing cycle.

The prescribed dose of Oxis Turbohaler 6 is determined by a qualified healthcare professional based on the patient’s condition, age, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose without medical advice.

Formoterol is classified as pregnancy category C in many regions, meaning risk cannot be ruled out. It should only be used if the potential benefit justifies the potential risk to the fetus. Breastfeeding mothers should consult their physician, as the drug may pass into breast milk.

To place an order, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details and import documentation.

Formoterol offers a rapid onset of action (within minutes) and a duration of effect up to 12 hours, similar to other long‑acting β2‑agonists such as salmeterol. Choice between agents often depends on inhaler device preference, dosing schedule, and individual patient response.

Store the inhaler at ambient temperature, below 25 °C, in its original packaging. Keep it away from moisture, direct sunlight and extreme heat to maintain drug potency and device functionality.

The device is a dry‑powder inhaler. The patient inhales sharply through the mouthpiece after loading a dose, ensuring a deep, steady breath to deliver the medication to the lower airways. Proper technique should be reviewed with a healthcare professional.

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

Formoterol is contraindicated in patients with a known hypersensitivity to formoterol or any excipients in the inhaler, and in individuals who have experienced a severe paradoxical bronchospasm with β2‑agonists. Caution is also advised for patients with uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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