Flunisolide
A to Z Drug Facts
Flunisolide |
(flew-NIH-sole-ide) |
AeroBid |
Aerosol: » 250 mcg per actuation |
AeroBid-M |
Aerosol: » 250 mcg per actuation |
Nasalide |
Solution, spray: 0.025% (each actuation delivers » 25 mcg flunisolide) |
Nasarel |
Solution, spray: 0.025% (each actuation delivers » 25 mcg flunisolide) |
Bronalide |
Class: Corticosteroid |
Action Has local anti-inflammatory activity on lung or nasal mucosa with minimal systemic effect. May decrease number and activity of cells involved in inflammatory response and enhance effect of other drugs or endogenous substances that aid in bronchodilation.
Inhalation: Control of bronchial asthma and related bronchospastic states for patients requiring chronic treatment with corticosteroids.
Intranasal: Symptoms of perennial or seasonal rhinitis. Unlabeled use(s): Treatment of serous otitis media in children and treatment of polyps.
Contraindications Primary treatment of status asthmaticus or acute asthma when intensive measures are required; systemic fungal infections; persistently positive Candida albicans sputum culture; untreated local infection of the nasal mucosa (intranasal use).
ADULTS AND CHILDREN 6 TO 15 YR: Inhalation 2 inhalations (500 mcg) bid. ADULTS: Do not exceed 4 inhalations bid (2 mg/day). CHILDREN: Do not exceed 2 inhalations bid. ADULTS: Intranasal Initial dose: 2 sprays (50 mcg) in each nostril bid. Max: 8 sprays in each nostril daily. CHILDREN 6 TO 14 YR: Initial dose: 1 spray (25 mcg) in each nostril tid or 2 sprays in each nostril bid. Max: 4 sprays in each nostril daily.
Interactions None well documented.
Fluticasone: Use caution when coadministering ketoconazole and other known cytochrome P450 inhibitors.
CNS: Headache, lightheadedness (inhalation, intranasal). DERM: Rash, facial edema (inhalation). GI: Dry mouth. META: Suppression of hypothalamic-pituitary-adrenal (HPA) function (inhalation). RESP: Throat irritation, hoarseness, dysphonia, coughing, wheezing, pharyngeal fungal infections, pulmonary infiltrates (inhalation); nasopharyngeal irritation, burning, stinging, rebound congestion, bronchial asthma, sneezing, rhinorrhea (intranasal). OTHER: Hypersensitivity reaction (eg, urticaria, angioedema, rash, bronchospasm, edema of face and tongue, pruritus, wheezing, dyspnea).
Pregnancy: Category C. Lactation: Undetermined. Because other corticosteroids are excreted in human milk, use caution. Children: Safety and efficacy in children less than 6 yr not established. Oral corticosteroids may suppress growth in children and adolescents, particularly with higher doses over extended periods. Acute asthma: Not indicated for rapid relief of bronchospasm. Fungal infections: Antifungal therapy and discontinuance of steroid may be necessary. Hypersensitivity: Immediate and delayed reactions have occurred. Immunology: Patients receiving immunosuppressant agents are more susceptible to infections than healthy adults. If a patient is exposed to measles or chickenpox, appropiate prophylaxis and treatment may be indicated. Route change: Particular caution is needed when transferring patient from systemically active corticosteroids to flunisolide inhaler because deaths caused by adrenal insufficiency have occurred in asthmatic patients during and after transfer from systemic to aerosol corticosteroids. Systemic effects: Use cautiously in patients taking alternate-day prednisone; may increase likelihood of HPA suppression. Exceeding recommended dose may cause systemic effects.
PATIENT CARE CONSIDERATIONS |
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Copyright © 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts