Ventolin in asthma care
Understand the appropriate use of Ventolin when implementing the 2024 BTS/NICE/SIGN Asthma Guidelines
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The role of Ventolin inhalers (salbutamol) in asthma care today
The use of Ventolin on this page refers to Ventolin inhalers (Accuhaler - Evohaler) only.
Ventolin (Salbutamol) pMDI/DPIs are indicated in adults, adolescents and children aged 4 to 11 years for use in the management of bronchospasm and/or reversible airways obstruction and also used for the relief of asthma symptoms. Ventolin should be used to relieve symptoms when they occur, and to prevent them in those circumstances recognised by the patient to precipitate an asthma attack (e.g. before exercise or unavoidable allergen exposure).1,2
In asthma, short acting beta-2 agonists (SABAs) including Ventolin Accuhaler/Evohaler should not be the main or only treatment. It is encouraged that SABAs should be prescribed with concomitant inhaled corticosteroid (anti-inflammatory).1,2
For babies and children under 4 years of age, see sections 4.2 and 5.1 of Ventolin Evohaler SmPC.1
Please refer to the SmPCs for full indications, contra-indications and other details.
When is Ventolin an appropriate reliever option for people with asthma?
Ventolin remains an established reliever option when prescribed with concomitant inhaled corticosteroid (ICS) for appropriate patients in the following groups:3
Please refer to the NICE/BTS/SIGN 2024 Guidelines (NG245) for details before prescribing.
How does the BTS/NICE/SIGN guideline support personalised care?
In November 2024, a collaborative guideline developed jointly by the BTS, NICE and SIGN was published, which updated and replaced previous guidance from these bodies on the diagnosis, treatment and monitoring of asthma.3
The combined BTS/NICE/SIGN asthma guideline NG245 emphasises personalised care, with age-specific recommendations for people aged 12 and over, children aged 5 to 11, and children under 5, as well as newly diagnosed patients.3
While the BTS/NICE/SIGN guideline recommends MART or AIR for the majority of asthma patients, there is still a need and recommendation for prescribing SABAs in certain patient groups (listed above).3
Patients of any age with an existing asthma diagnosis who are stable on an appropriate regimen (such as those comprising an ICS or ICS/long-acting beta agonist (LABA) plus Ventolin as needed) do not have to switch treatment.3
Monitor asthma control at every review to identify patients who can remain on an existing treatment regimen such as Ventolin, and those for whom alternative therapies should be considered.
Symptoms are important, but they may not provide a full picture of asthma control.
✔️ In addition to asking about symptoms, check for other signs to determine whether the patient's asthma is uncontrolled and may warrant a change in treatment:3
Use a validated symptom questionnaire, such as the Asthma Control Test (ACT) or Asthma Control Questionnaire (ACQ) to support your assessment.4,5
✔️ If a patient appears to have poorly controlled asthma, the guidelines emphasise assessment before adjusting medication.3
Review and address the possible reasons for uncontrolled asthma before changing an individual's asthma treatment.
Confirm the diagnosis, and review modifiable risk factors and triggers that may be impacting control, such as:3
STEP 1: IS ASTHAMA WELL CONTROLLED?
Consider using questionnaires, e.g., the Asthma Control test (ACT) or
Asthma Control Questionnaire (ACQ) to help quantify asthma control.
If not using ACT/ACQ, examples of questions that can help establish
whether the patient's asthma is controlled are:
STEP 2: CHECK POSSIBLE CAUSES OF LACK OF CONTROL
Take into account and try to address the possible reasons for uncontrolled
asthma before starting or adjusting medicines for asthma:
Issues found? → Fix first → Reassess
Still uncontrolled? → STEP 3
STEP 3: CONSIDER TREATMENT CHANGE
Follow age-specific guideline algorithm to determine next step
In patients of any age, ensure:
Shared-decision-making, education on new inhaler, follow-up review
Consistency of inhaler device is very important for people with asthma. Changing from a regular, familiar device, particularly without adequate patient training or consultation, may negatively impact asthma control and patient outcomes.6 In part, this is because using any inhaler incorrectly can substantially reduce the amount of dose delivered to the lung.7 Furthermore, adherence is negatively impacted by changing treatments without consultation.6
Prescribing of Ventolin by brand may support your patients by ensuring they receive the inhaler they know how to use and prefer.6,8,9,10
To help reduce confusion and anxiety and ensure patients receive the inhaler they have been given training for, the brand and inhaler device should be specified when prescribing.9 Generic prescribing of inhalers is not encouraged, as it risks people being given an unfamiliar device at the point of dispensing.10
Important: Ventolin must always be prescribed with a concomitant ICS.3,11
Please refer to the Ventolin Accuhaler and Ventolin Evohaler SmPCs for full prescribing information, including the list of adverse reactions.1,2
Common adverse reactions include tremor, headache and tachycardia. Contraindications include hypersensitivity to the active substance or any of the excipients listed in 6.1 of the SmPCs. Non-IV formulations of salbutamol must not be used to arrest uncomplicated premature labour or threatened abortion.1,2 Ventolin Accuhaler is also contraindicated in patients with severe milk-protein allergy.2
Abbreviations
ACQ, Asthma Control Questionnaire; ACT, Asthma Control Test; AIR, anti-inflammatory reliever; BTS, British Thoracic Society; DPI, dry powder inhaler; ICS, inhaled corticosteroid; LABA, long-acting beta agonist; MART, maintenance and reliever therapy; NICE, National Institute for Health and Care Excellence; SABA, short acting beta-agonist; SIGN, Scottish Intercollegiate Guidelines Network.
References
Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/ or search for MHRA Yellowcard in the Google Play or Apple App Store.
Adverse events should also be reported to GSK on 0800 221 441 or UKSafety@gsk.com.
July 2026 | PM-GB-SLB-WCNT-260001 (V2.0)