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Spiriva

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Spiriva (tiotropium bromide) is a long-acting bronchodilator used for the maintenance treatment of chronic obstructive pulmonary disease (COPD) and asthma. It works by relaxing the muscles in the airways and increasing airflow to the lungs, helping patients maintain consistent respiratory function throughout the day.


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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)
Tiotropium Bromide
Reference Brand
Spiriva HandiHaler / Respimat
Manufacturer
Boehringer Ingelheim
Product Form
Inhalation Powder (Capsule), Inhalation Solution
Regulatory Classification
Rx
Primary Category
COPD Treatment, Asthma Management
Product Category
Respiratory system, Drugs for obstructive airway diseases, Anticholinergics
Pharmacological Class
Long-acting muscarinic antagonist (LAMA)
Manufacturer Description
A long-acting maintenance inhaler used to prevent shortness of breath in people with COPD and asthma.
Mechanism of Action
Tiotropium is a long-acting bronchodilator that blocks muscarinic receptors in the airway muscles. This action causes the muscles to relax, widening the airways and making breathing easier for patients with chronic lung conditions.
Route of Administration
Inhalation
Onset Time
30 minutes to full effect in 1-2 weeks
Duration
24 hours
Contraindications
Hypersensitivity to tiotropium or atropine, Acute bronchospasm (as rescue therapy)
Severe Adverse Events
Urinary retention, Acute narrow-angle glaucoma, Irregular heartbeat (atrial fibrillation), Severe hypersensitivity
Common Side Effects
Dry mouth, Sore throat, Cough
Uncommon Side Effects
Constipation, Sinusitis, Dizziness
Drug Interactions
Other anticholinergics (e.g., Ipratropium), Cimetidine
Pregnancy Safety Warnings
Limited data; use only if clearly needed.
Age Restrictions
Adults for COPD; over 6 years for asthma
Storage Guidelines
Do not store capsules in a humid environment; use device as directed
Related Products
Incruse, Seebri, Eklira

Spiriva FAQ

What is the correct way to store a Spiriva inhaler?

Store Spiriva at room temperature, away from heat, moisture, and direct sunlight. Keep it out of reach of children and do not refrigerate the device.

Can Spiriva be used as a rescue inhaler for sudden breathlessness?

No. Spiriva is a maintenance medication with a slow onset of action. For acute episodes, a short-acting bronchodilator such as salbutamol should be used as prescribed.

How does the 9 µg dose of Spiriva compare to other inhaled bronchodilators?

The 9 µg dose delivers a once-daily amount of tiotropium that provides 24-hour bronchodilation, whereas short-acting β₂-agonists are typically administered multiple times per day at higher peak concentrations but shorter durations.

Are there any special instructions for using Spiriva with other inhalers?

Yes. Use Spiriva first, then follow with any rescue inhaler after a short interval (usually 30 seconds) to ensure optimal drug deposition. Always clean the mouthpiece according to the manufacturer’s guidance.

Does smoking affect the effectiveness of Spiriva?

Smoking can reduce overall lung function and may diminish the perceived benefit of any inhaled therapy. Patients are strongly encouraged to quit smoking to maximize the efficacy of Spiriva and other respiratory medications.

Can pregnant women take Spiriva?

Tiotropium is classified as Pregnancy Category B3 in the UK. It should only be used if the potential benefit outweighs the potential risk to the fetus, after a careful discussion with a healthcare professional.

What should I do if I accidentally swallow a Spiriva capsule?

Swallowing a capsule is unlikely to cause systemic toxicity because tiotropium is designed for inhalation. However, if you experience any unusual symptoms, seek medical advice promptly.

Is Spiriva covered by the NHS, and how can I obtain it?

Spiriva is listed on the NHS formulary for eligible patients with COPD or uncontrolled asthma. It can be prescribed by a GP or respiratory specialist and dispensed at a community pharmacy.

Will using Spiriva affect my ability to drive or operate machinery?

Spiriva does not typically impair cognition or motor skills. However, if you experience dizziness, severe anticholinergic side effects, or an asthma exacerbation, you should avoid driving until symptoms resolve.

How often should I have my lung function tested while on Spiriva?

Routine spirometry is recommended at baseline, then annually, or sooner if you notice worsening symptoms. Regular testing helps assess the medication’s effectiveness and guides any needed adjustments.

What is Spiriva?

Spiriva is a prescription inhaler used to help keep the airways open in people with chronic respiratory conditions. The active ingredient is tiotropium bromide, a long-acting anticholinergic that belongs to the LAMA (Long-acting Muscarine Antagonist) class of bronchodilators.

  • Medication form: inhaler (HandiHaler or Respimat)
  • Available dosage: each inhalation delivers 9 micrograms (µg) of tiotropium bromide
  • Regulatory status in the UK: Prescription-only medicine (POM) authorised by the Medicines and Healthcare products Regulatory Agency (MHRA) and listed on the NHS formulary.
  • Manufacturer: Boehringer Ingelheim (UK subsidiary)

Spiriva is intended for regular, maintenance use and is not a rescue medication for sudden breathing problems.

How Spiriva Works in the Body

Tiotropium bromide blocks muscarinic (M3) receptors on the smooth muscle lining the airways. By preventing acetylcholine-a chemical that normally causes the muscles to contract-from binding to these receptors, Spiriva produces a bronchodilatory effect that relaxes the airway muscles and widens the passages for air flow.

Key pharmacologic points:

  • Onset of action: within 30 minutes after inhalation
  • Peak effect: 2-3 hours
  • Duration: up to 24 hours, allowing once-daily dosing
  • Bioavailability: minimal systemic absorption; the drug acts primarily in the lungs and is cleared unchanged through the kidneys

The sustained blockade of M3 receptors reduces airway resistance, improves lung function, and helps control symptoms such as breathlessness and wheeze.

Conditions Treated by Spiriva

Spiriva is approved by the MHRA (and the European Medicines Agency) for the following indications in the United Kingdom:

  • Chronic Obstructive Pulmonary Disease (COPD) - maintenance treatment of patients with moderate to severe COPD, including chronic bronchitis and emphysema.
  • Asthma - as an add-on maintenance therapy for adults whose asthma remains uncontrolled despite inhaled corticosteroids (ICS) ± long-acting β₂-agonists (LABA).

The medication is meant for regular, long-term use and should be part of a broader disease-management plan that may include inhaled steroids, rescue bronchodilators, pulmonary rehabilitation, and smoking cessation where relevant.

Investigational Uses Under Study

Research has explored additional therapeutic roles for tiotropium bromide, though these applications have not received regulatory approval in the UK:

  • Bronchiectasis: Small-scale trials suggest that tiotropium may improve lung function and reduce exacerbation frequency when added to standard therapy.
  • Chronic cough: Early studies indicate a potential benefit in reducing cough frequency in patients with refractory cough, likely through airway smooth-muscle relaxation.

These investigations are ongoing, and any off-label use should only occur under close supervision of a qualified respiratory specialist.

Disclaimer: Off-label use requires medical supervision and individualized risk assessment.

Evaluating Spiriva for Your Health Profile

Who Might Benefit

  • Adults with a confirmed diagnosis of COPD or asthma who need additional bronchodilation beyond a short-acting inhaler.
  • Patients who prefer once-daily dosing for convenience and adherence.

Absolute Contraindications

  • Known hypersensitivity to tiotropium bromide or any component of the inhaler device.
  • Severe renal impairment (creatinine clearance < 30 mL/min) - tiotropium is cleared unchanged by the kidneys, and accumulation can increase the risk of anticholinergic side effects.

Relative Contraindications & Cautions

  • Pregnancy and lactation: Tiotropium is classified as Pregnancy Category B3 in the UK; animal studies have shown some adverse effects, but human data are limited. Use only if the potential benefit justifies the risk.
  • Elderly patients: Renal function often declines with age; dose adjustment is not recommended, but clinical monitoring is advised.
  • Narrow-angle glaucoma or urinary retention: Anticholinergic activity may exacerbate these conditions.

Patients with any of the above conditions should discuss risks and alternatives with their prescriber before starting Spiriva.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Dry mouth (most frequently reported)
  • Sore throat or irritation after inhalation
  • Constipation
  • Cough immediately following inhaler use

These events are usually mild and tend to improve with continued therapy or proper inhaler technique.

Serious Adverse Events

  • Urinary retention - may require medical evaluation, especially in men with prostate enlargement.
  • Narrow-angle glaucoma exacerbation - seek urgent ophthalmologic care if eye pain or visual changes occur.
  • Angioedema or severe allergic reactions - characterized by swelling of the face, lips, tongue, or throat; emergency treatment is required.
  • Paradoxical bronchospasm - sudden worsening of breathlessness after inhalation; discontinue use and contact a healthcare professional immediately.

Health-care providers may issue a black-box warning for severe anticholinergic effects in patients with pre-existing urinary or ocular conditions.

Drug Interactions

Tiotropium undergoes minimal hepatic metabolism and is not a substrate of cytochrome-P450 enzymes, so clinically significant pharmacokinetic interactions are rare. However, consider the following:

  • Concurrent anticholinergic agents (e.g., other inhaled LAMAs, oral antihistamines with strong anticholinergic properties) may increase the overall anticholinergic burden, leading to dry mouth, constipation, or cognitive effects, especially in the elderly.
  • β₂-agonists (short-acting or long-acting) are generally safe to use together; combination therapy is common in COPD and asthma management.

Patients should always provide a complete medication list-including prescription drugs, over-the-counter products, and herbal supplements-to their prescriber.

Food and Lifestyle Interactions

  • No known food-drug interactions; Spiriva can be taken with or without meals.
  • Alcohol does not affect the pharmacology of tiotropium, but excessive drinking may worsen respiratory symptoms.
  • Operating heavy machinery is not restricted, but patients experiencing dizziness or severe anticholinergic side effects should exercise caution.

How to Take Spiriva

  • Standard dosing: One inhalation delivering 9 µg of tiotropium bromide once daily, preferably at the same time each day.
  • Inhaler technique (HandiHaler example):
  1. Open the inhaler and insert a capsule.
  2. Pierce the capsule by pressing the button.
  3. Breathe out completely, away from the device.
  4. Seal your lips around the mouthpiece and inhale deep and steady.
  5. Hold breath for about 10 seconds, then exhale slowly.
  6. Close the inhaler and discard the used capsule.
  • Special populations: No dose reduction is recommended for elderly patients. Individuals with moderate renal impairment (CrCl 30-50 mL/min) should be monitored closely; severe impairment is a contraindication.
  • Missed dose: If a dose is forgotten, take it as soon as remembered provided there is at least 8 hours before the next scheduled dose. Do not double the dose.
  • Overdose: Symptoms may include severe dry mouth, facial flushing, rapid heart rate, and urinary retention. Management is supportive-ensure airway patency, monitor vital signs, and seek immediate medical attention. No specific antidote exists.
  • Discontinuation: Spiriva can be stopped abruptly, but patients should discuss any change in therapy with their prescriber, especially if they rely on it for symptom control.

Monitoring and Follow-Up

  • Baseline assessment: Spirometry (FEV₁), assessment of symptom control (e.g., CAT score for COPD, ACT score for asthma), and renal function tests.
  • Routine follow-up: Review inhaler technique and symptom relief every 3-6 months; repeat spirometry annually or sooner if the clinical status changes.
  • Renal monitoring: Periodic measurement of serum creatinine is advisable, particularly in patients over 70 years or with known kidney disease.

Regular clinical review helps ensure optimal dosing, detects adverse effects early, and reinforces proper inhaler use.

Storage and Handling

  • Store the inhaler at room temperature (15-30 °C) away from direct heat and moisture.
  • Keep the device out of reach of children and pets.
  • Do not refrigerate or expose to extreme cold, as this may affect capsule integrity.
  • Replace the inhaler according to the manufacturer’s expiration date; discarded inhalers should be disposed of via a pharmacy take-back program or according to local hazardous-waste guidelines.

Medication-Specific Glossary

Long-acting Muscarinic Antagonist (LAMA)
A class of bronchodilators that block muscarinic receptors in the airway smooth muscle for ≥ 24 hours, providing sustained relief from bronchoconstriction.
Bronchodilation
The relaxation of airway smooth-muscle fibers, leading to widened airways and improved airflow.
Inhaler Technique
The series of steps a patient follows to ensure the medication is delivered effectively to the lungs, including proper breathing pattern and device handling.
Renal Clearance
The process by which the kidneys eliminate a drug unchanged from the bloodstream; for tiotropium, it accounts for the majority of drug elimination.
Anticholinergic Burden
The cumulative effect of multiple medications with anticholinergic activity, which can increase the risk of dry mouth, constipation, confusion, and urinary retention, especially in older adults.

Medical Disclaimer

This article provides educational information about Spiriva and is not a substitute for professional medical advice. Treatment decisions, including the use of 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 Spiriva 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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