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Salbutamol/budesonide
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    Salbutamol/budesonide

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    Salbutamol/budesonide
    Combination of
    Salbutamol Beta2-adrenergic agonist
    Budesonide Corticosteroid
    Clinical data
    Trade names Airsupra
    Other names PT027, albuterol/budesonide
    AHFS/Drugs.com Multum Consumer Information
    License data
    Routes of
    administration
    Inhalation
    ATC code
    • None
    Legal status
    Legal status

    Salbutamol/budesonide, sold under the brand name Airsupra, is a fixed-dose combination medication for the treatment of bronchoconstriction and asthma. It is a combination of salbutamol sulfate (albuterol sulfate), a short-acting beta2-adrenergic agonist, and budesonide, an inhaled corticosteroid. It is inhaled using a pressurized metered-dose inhaler.

    The most common side effects include headache, oral candidiasis, cough, and difficulty speaking.

    Salbutamol/budesonide was approved for medical use in the United States in January 2023. It is the first combination of an inhaled corticosteroid and a short-acting beta-agonist to be approved by the US Food and Drug Administration (FDA). It is the first product containing an inhaled corticosteroid to be approved by the FDA as a reliever treatment (rather than as a controller) for asthma.

    Medical uses

    Salbutamol/budesonide is indicated for the as-needed treatment or prevention of bronchoconstriction and to reduce the risk of asthma attacks.

    History

    The efficacy of salbutamol/budesonide to reduce the risk of severe asthma attacks was evaluated in participants with moderate to severe asthma in MANDALA (NCT03769090), a randomized, double-blind, multicenter study.

    Further reading

    External links

    • Clinical trial number NCT03769090 for "A Study to Assess the Efficacy and Safety of Budesonide/Albuterol Metered-dose Inhaler (BDA MDI/PT027) in Adults and Children 4 Years of Age or Older With Asthma (MANDALA)" at ClinicalTrials.gov



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