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SINGULAIR is indicated for prophylaxis and chronic treatment of asthma in patients aged 12 months and older.
SELECTED SAFETY INFORMATION
- Neuropsychiatric events have been reported in patients taking SINGULAIR. These events included agitation, aggressive behavior or hostility, anxiousness, depression, disorientation, dream abnormalities, hallucinations, insomnia, irritability, restlessness, somnambulism, suicidal thinking and behavior (including suicide), and tremor. The clinical details of some postmarketing reports appear consistent with a drug-induced effect. Patients should be advised to report any neuropsychiatric events.
- SINGULAIR is contraindicated in patients with hypersensitivity to any component of this product.
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Asthma Therapy Assessment Questionnaire (ATAQ)
The NIH guidelines recommend scientifically validated self-assessment tools such as ATAQ to help monitor asthma control.
View more than a dozen asthma presentations— live and interactive, or archived.
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SELECTED SAFETY INFORMATION (continued)
- SINGULAIR should not be used as rescue medication to treat acute asthma attacks. Patients should be advised to have appropriate rescue medication available.
- While the dose of inhaled corticosteroid may be reduced gradually under medical supervision, SINGULAIR should not be abruptly substituted for inhaled or oral corticosteroids.
- Patients receiving SINGULAIR should not decrease the dose or stop taking any other antiasthma medications unless instructed by a physician.
- The most common adverse reactions with an incidence >5% and greater than placebo in controlled clinical trials were upper respiratory infection, fever, headache, pharyngitis, cough, abdominal pain, diarrhea, otitis media, influenza, rhinorrhea, sinusitis, and otitis.
Please see Selected Safety Information about SINGULAIR.
Before prescribing SINGULAIR, please read the Prescribing Information.
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