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Study drug compliance with study drug was evaluated by counting and comparing the number of tablets dispensed at the baseline visit with the number returned at the final visit.

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Based on these key questions, the eligibility criteria were developed for studies included in this review.

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The clinical safety of Clarinex Oral Solution was documented in three, 15-day, double-blind, placebo-controlled safety studies in pediatric subjects with a documented history of allergic rhinitis, chronic idiopathic urticaria, or subjects who were candidates for antihistamine therapy.

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Finally, in all desloratadine trials involving nasal congestion in SAR (and SAR-asthma), the agent was well tolerated, exhibiting no anticholinergic or sedative effects and incidences of adverse events similar to those seen with placebo.

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Non drowsy Aerius is also indicated for the relief of symptoms associated with year round allergies (perennial allergic rhinitis).

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We designed this study to objectively quantify the impact of indoor environment on higher-order cognitive function, a driver of real-world productivity in office workers.

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