SALMETEROL XINAFOATe (sal-me'ter-ol xin'a-fo-ate) Serevent Classifications: beta2-adrenergic agonist; bronchodilator; respiratory smooth muscle relaxant; Therapeutic: bronchodilator; smooth muscle relaxant Prototype: Albuterol Pregnancy Category: C |
25 mcg aerosol; 50 mcg powder diskus for inhalation
Long-acting beta2-adrenoreceptor agonist and an analog of albuterol. Stimulation of beta2-adrenoreceptors relaxes bronchospasm and increases ciliary motility, thus facilitating expectoration. Inhibits the release of mediators (i.e., histamine) from mast cells, macrophages, and eosinophils.
Relaxes bronchospasm and increases ciliary motility, thus facilitating expectoration of pulmonary secretions. Salmeterol also decreases airway reaction to allergens.
Maintenance therapy for asthma or bronchospasm. Prevention of exercise-induced bronchospasm. Do not use to treat acute bronchospasm.
Hypersensitivity to salmeterol; other long-acting beta2-adrenergic agonists; primary treatment of status asthmaticus; acute bronchospasm; MAOI therapy; pregnancy (category C); safety and efficacy in children <4 y not established.
Cardiovascular disorders, cardiac arrhythmias, hypertension; history of seizures or thyrotoxicosis; liver and renal impairment, older adults, diabetes mellitus, sensitivity to other beta-adrenergic agonists; women in labor; lactation.
Asthma or Bronchospasm Adult/Child (≥4 y): Inhalation 2 inhalations of aerosol (42 mcg) or 1 powder diskus (50 mcg) b.i.d. approximately 12 h apart Prevention of Exercise-Induced Bronchospasm Adult/Child (≥4 y): Inhaled 2 inhalations of aerosol (42 mcg) or 1 powder diskus (50 mcg) 3060 min before exercise |
Assessment & Drug Effects
Patient & Family Education