SEREVENT DISKUS (SALMETEROL XINAFOATE)
SEREVENT DISKUS (SALMETEROL XINAFOATE) is one of 8,063 medications in the MedPlain dataset. Key details — Brand name: SEREVENT DISKUS; Generic name: SALMETEROL XINAFOATE; Manufacturer: GlaxoSmithKline LLC.
| Brand name | SEREVENT DISKUS |
|---|---|
| Generic name | SALMETEROL XINAFOATE |
| Manufacturer | GlaxoSmithKline LLC |
| Used for | 1 INDICATIONS AND USAGE SEREVENT DISKUS is a LABA indicated for: • Treatment of asthma in patients aged 4 years and older with an ICS. ( 1.1 ) • Prevention of exercise-induced bronchospasm (EIB) in patients aged 4 years and older. ( 1.2 ) • Maintenance treatment of bronchospasm associated with chronic obstructive pulmonary disease (COPD). ( 1.3 ) Important limitation of use: Not indicated for relief of acute bronchospasm. ( 1.1 , 1.3 ) 1.1 Treatment of Asthma SEREVENT DISKUS is indicated for the treatment of asthma and in the prevention of bronchospasm only as concomitant therapy with an ICS in patients aged 4 years and older with reversible obstructive airway disease, including patients wit |
| Dosage | 2 DOSAGE AND ADMINISTRATION SEREVENT DISKUS should be administered by the orally inhaled route only. More frequent administration or a greater number of inhalations (more than 1 inhalation twice daily) is not recommended as some patients are more likely to experience adverse effects. Patients using SEREVENT DISKUS should not use additional LABA for any reason. [See Warnings and Precautions ( 5.4 , 5.6 ).] • For oral inhalation only. ( 2 ) • Treatment of asthma in patients aged 4 years and older: |
| Warnings | WARNING: ASTHMA-RELATED DEATH Long-acting beta 2 -adrenergic agonists (LABA), such as salmeterol, the active ingredient in SEREVENT DISKUS, as monotherapy (without inhaled corticosteroids [ICS]) increase the risk of asthma-related death. Data from a large placebo-controlled U.S. trial that compared the safety of salmeterol with placebo added to usual asthma therapy showed an increase in asthma-related deaths in subjects receiving salmeterol (13 deaths out of 13,176 subjects treated for 28 weeks |
| Active ingredient(s) | SALMETEROL XINAFOATE |
| Route | ORAL |
| Official label | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=12d9728e-6b5c-4aee-bfb0-745e542ed2e4 |