Buy Advair Diskus
Advair Diskus

106.55
Advair Diskus (Salmeterol, Fluticasone Propionate) is a combination inhaler used for the long-term management of asthma and COPD. It contains a corticosteroid for reducing inflammation and a long-acting beta-agonist to relax the airways. By addressing dual aspects of respiratory distress, Advair Diskus helps maintain consistent, improved airflow for patients.


Availability
In Stock
Delivery Time
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Active Ingredient(s)
Salmeterol, Fluticasone
Reference Brand
Seretide Accuhaler
Manufacturer
GlaxoSmithKline
Product Form
Dry Powder Inhaler
Regulatory Classification
Rx
Primary Category
Asthma Control, COPD Management
Product Category
Respiratory system, Drugs for obstructive airway diseases, Adrenergics in combination with corticosteroids
Pharmacological Class
Long-acting beta2-agonist (LABA), Inhaled corticosteroid (ICS)
Manufacturer Description
A preventer inhaler used daily to control long-term symptoms of asthma and COPD.
Mechanism of Action
Fluticasone reduces inflammation and swelling in the airways, while Salmeterol works by relaxing the airway muscles to keep them open for longer. Together, they prevent shortness of breath and wheezing.
Route of Administration
Inhalation
Onset Time
Up to 30-60 minutes (not for acute relief)
Duration
12 hours
Contraindications
Acute asthma attack (not a rescue inhaler), Severe milk protein allergy, Hypersensitivity to components
Severe Adverse Events
Paradoxical bronchospasm, Pneumonia (in COPD patients), Reduced bone density (long-term use), Glaucoma or cataracts
Common Side Effects
Hoarseness, Throat irritation, Headache
Uncommon Side Effects
Oral thrush (candidiasis), Muscle cramps, Palpitations
Drug Interactions
Beta-blockers, Ritonavir, Ketoconazole, Diuretics
Pregnancy Safety Warnings
Use only if benefit outweighs risk; consult a doctor.
Age Restrictions
Approved for children 4 years and older (strength dependent)
Storage Guidelines
Store in a dry place at room temperature
Related Products
Symbicort, Seretide, AirFluSal Forspiro

Advair Diskus FAQ

Can I use Advair Diskus while traveling internationally?

Yes, the inhaler can be taken on flights and in most countries, but you should carry it in your hand luggage and keep the original packaging to demonstrate it is a prescribed medication. Check the destination country's regulations for inhaled steroids, as some require a prescription copy or a doctor’s note.

What should I look for on the Advair Diskus label to confirm the dose?

Each Diskus inhaler is embossed with an alphanumeric code indicating the strength (e.g., “100/50 µg”). The foil wrapper also displays the dose and expiry date. Verify that the code matches the prescription before use.

Does smoking affect the efficacy of Advair Diskus?

Smoking can reduce the anti-inflammatory benefits of the inhaled corticosteroid and may increase airway irritation, potentially lowering overall treatment effectiveness. Patients are advised to quit smoking to achieve optimal control of asthma or COPD.

Are there any special considerations for athletes subject to drug testing?

Both salmeterol and fluticasone are permitted under World Anti-Doping Agency (WADA) rules when used via inhalation at therapeutic doses. Athletes should retain a copy of the prescription and the medication label in case of a therapeutic use exemption (TUE) request.

How does Advair Diskus differ from separate salmeterol and fluticasone inhalers?

The combination inhaler delivers both medications in a single actuation, improving convenience and adherence. Separate inhalers require two separate inhalations, which can increase the risk of missed doses or incorrect timing.

What is the typical shelf-life of an unopened Advair Diskus inhaler?

Unopened inhalers generally retain their potency for 24 months from the date of manufacture, provided they are stored at room temperature and protected from moisture. The exact expiry date is printed on the foil pouch.

Can I use a spacer device with the Diskus inhaler?

The Diskus is a dry-powder inhaler designed for direct inhalation and does not require a spacer. Using a spacer may interfere with dose delivery and is not recommended.

Why does Advair Diskus have a “black box” warning in some regions?

The warning highlights the increased risk of asthma-related death when LABA therapy is used without an accompanying inhaled corticosteroid. Advair Diskus combines both agents, which mitigates this specific risk, but patients must still adhere to prescribed dosing.

What factors influence the cost of Advair Diskus in the UK?

Pricing depends on the dosage strength, NHS prescribing policies, and whether a branded or generic version is supplied. Patent expiries and the availability of biosimilar alternatives can also affect cost.

Is there a recycling programme for used Advair Diskus inhalers?

Many NHS pharmacies participate in medication return schemes that accept empty inhaler devices for environmentally responsible disposal. Check with your local pharmacy for specific return options.

Advair Diskus: Combination Inhaler Overview

Advair Diskus is a prescription inhaler that combines two active ingredients: salmeterol, a long-acting β2-adrenergic agonist (LABA), and fluticasone propionate, an inhaled corticosteroid (ICS). The product is marketed in the United Kingdom and regulated by the Medicines and Healthcare products Regulatory Agency (MHRA). It is available in three fixed-dose strengths-100 µg/50 µg, 250 µg/50 µg, and 500 µg/50 µg of salmeterol and fluticasone respectively-delivered via a breath-actuated Diskus inhaler.

The combination is indicated for maintenance therapy in adults and adolescents (≥12 years) with asthma, and for chronic obstructive pulmonary disease (COPD) in patients with a history of exacerbations. It is not intended for the relief of acute bronchospasm.

How Advair Diskus Works in the Body

Pharmacology of Salmeterol

  • Salmeterol selectively stimulates β2-adrenergic receptors on airway smooth muscle, leading to relaxation and bronchodilation.
  • Its long-acting profile (≈12 hours) provides sustained airway opening, reducing the frequency of symptoms.

Pharmacology of Fluticasone Propionate

  • Fluticasone is a potent glucocorticoid that binds intracellular glucocorticoid receptors, modulating gene transcription to suppress airway inflammation.
  • The anti-inflammatory effect reduces mucus production, edema, and eosinophilic infiltration, improving overall airway stability.

Combined Effect

  • The LABA component rapidly improves airflow, while the corticosteroid component addresses the underlying inflammatory process.
  • By delivering both agents in a single inhalation, adherence improves and the risk of LABA monotherapy-related adverse events (e.g., asthma-related death) is minimized.

Conditions Treated by Advair Diskus

Asthma Maintenance Therapy

  • Recommended for patients whose asthma is not adequately controlled with an inhaled corticosteroid alone.
  • Helps decrease the frequency of daytime symptoms, night-time awakenings, and need for rescue bronchodilators.

COPD Management

  • Indicated for COPD patients with a history of exacerbations who require additional bronchodilation and anti-inflammatory therapy.
  • Aims to reduce exacerbation rates, improve lung function, and enhance health-related quality of life.

Patient Suitability and Contraindications

Who Should Use Advair Diskus?

  • Adults and adolescents (≥12 years) with a confirmed diagnosis of asthma or COPD who need regular, twice-daily maintenance therapy.
  • Patients who can demonstrate correct inhaler technique and are able to coordinate inhalation with device activation.

Absolute Contraindications

  • Known hypersensitivity to salmeterol, fluticasone propionate, or any excipients in the Diskus device.
  • Patients experiencing an acute asthma attack or requiring immediate bronchodilator relief.
  • Concomitant use of non-selective β-blockers (e.g., propranolol) in asthma patients.

Relative Contraindications / Cautions

  • Severe cardiovascular disorders (e.g., arrhythmias, uncontrolled hypertension).
  • Thyroid disorders, especially hyperthyroidism.
  • Pregnancy (Category B in the UK) - use only if the clinical benefit outweighs potential risk.
  • Lactation - fluticasone appears in low concentrations in breast milk; weigh benefits against possible effects on the infant.

Special Populations

  • Elderly: May have reduced β2-receptor sensitivity; start at the lowest effective dose.
  • Renal/Hepatic Impairment: No dose adjustment required for mild to moderate impairment, but monitor for systemic corticosteroid effects.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Hoarseness, throat irritation, or dry mouth (often mitigated by rinsing the mouth after inhalation).
  • Oral candidiasis (thrush) - usually prevented by proper oral hygiene.
  • Headache, mild tremor, or transient increased heart rate.

Serious Adverse Events

  • Paradoxical bronchospasm immediately after inhalation - discontinue and seek urgent medical attention.
  • Adrenal suppression, especially with high-dose or prolonged use of the corticosteroid component.
  • Decreased bone mineral density with long-term high-dose therapy; consider calcium and vitamin D supplementation.

Drug Interactions

  • Major Interactions

  • Non-selective β-blockers may diminish bronchodilator effect and increase risk of bronchospasm.

  • Moderate Interactions

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir) can raise systemic fluticasone levels, heightening steroid-related side effects.

  • Diuretics or antihypertensives may potentiate salmeterol-induced tachycardia; monitor blood pressure.

  • Pharmacodynamic Interactions

  • Concurrent use of other inhaled or systemic corticosteroids increases risk of systemic glucocorticoid effects.

Food and Lifestyle Interactions

  • No significant food interactions; however, inhalation should be performed after a normal breath, not immediately after a heavy meal that may alter breathing pattern.
  • Alcohol consumption does not directly affect the inhaler, but excessive intake may impair coordination with device use.
  • Driving: Patients should ensure adequate symptom control before operating machinery; sudden bronchospasm could impair ability to drive safely.

How to Take Advair Diskus

Standard Dosing (once daily)

  • 100 µg/50 µg strength - one inhalation daily, typically in the morning.
  • 250 µg/50 µg strength - one inhalation daily, usually in the morning.
  • 500 µg/50 µg strength - one inhalation daily, preferably in the morning.

Dose selection is guided by disease severity and prior response to inhaled corticosteroids. The prescribing clinician will determine the appropriate strength.

Administration Technique

  1. Open the Diskus by sliding the two halves apart until a “click” is heard.
  2. Exhale fully away from the device (do not inhale through the mouthpiece).
  3. Place the mouthpiece between the lips, creating a tight seal.
  4. Inhale rapidly and deeply through the mouthpiece; the dose is delivered automatically.
  5. Hold breath for 5-10 seconds, then exhale slowly.
  6. Close the device after each use to protect the dose from moisture.

Missed Dose

  • If a dose is missed, take it as soon as remembered unless it is within 12 hours of the next scheduled dose; in that case, skip the missed dose and resume the regular schedule. Do not double the dose.

Overdose Management

  • Symptoms may include severe tremor, palpitations, or paradoxical bronchospasm.
  • Seek urgent medical care; supportive measures (e.g., supplemental oxygen, bronchodilators) are indicated.

Discontinuation

  • For asthma, abrupt cessation is acceptable because the LABA component is long-acting; however, continuous corticosteroid therapy is recommended to avoid loss of anti-inflammatory control.
  • In COPD, tapering is generally not required, but clinicians may reassess the need for ongoing combination therapy during routine reviews.

Monitoring and Follow-Up

  • Pulmonary Function Tests (spirometry) at baseline and every 3-6 months to assess forced expiratory volume (FEV₁) and peak expiratory flow.
  • Symptom Diary - record rescue inhaler use, night-time awakenings, and activity limitation.
  • Adrenal Function - consider morning serum cortisol measurement in patients on high-dose fluticasone for >3 months.
  • Bone Health - periodic bone mineral density testing for long-term high-dose users, especially post-menopausal women.

Patients should contact their healthcare provider if they experience persistent hoarseness, oral candidiasis, worsening breathlessness, or signs of systemic corticosteroid excess.

Storage and Handling

  • Store the Diskus at room temperature (15-30 °C) away from direct sunlight and moisture.
  • Keep the inhaler in its original foil pouch until first use; discard the device after 6 weeks of opening, even if doses remain.
  • Do not expose the inhaler to freezing temperatures.
  • For safe disposal, return the empty device to a pharmacy or follow local NHS waste guidelines for medical devices.

Medication-Specific Glossary

Long-acting β2-agonist (LABA)
A class of bronchodilators that provide sustained relaxation of airway smooth muscle for up to 12 hours, reducing bronchospasm frequency.
Inhaled corticosteroid (ICS)
A steroid formulated for direct delivery to the lungs, exerting anti-inflammatory effects locally while minimizing systemic exposure.
Diskus Device
A dry-powder inhaler (DPI) that releases a precise dose of medication when the patient inhales forcefully through the mouthpiece.

Medical Disclaimer

This article provides educational information about Advair Diskus and is not a substitute for professional medical advice. Treatment decisions, including the choice of dose or the use of the medication for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Information for Advair Diskus is sourced from established medical standards and updated frequently. It is provided for general guidance and should be confirmed with a healthcare professional before use.
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