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Am J Ther ; 5(4): 245-51, 1998 Jul.
Article in English | MEDLINE | ID: mdl-10099066

ABSTRACT

The objective of this study was to compare the efficacy and safety of Claritin-D 24 Hour (once daily) with that of Claritin-D 12 Hour (twice daily) and placebo in the treatment of patients with seasonal allergic rhinitis (SAR). In this double-blind, placebo-controlled, multicenter study, 469 patients with moderate-to-severe SAR symptoms were treated for 2 weeks with one of the following: Claritin-D 24 Hour (a combination tablet formulation of loratadine 10 mg in the coating and pseudoephedrine sulfate 240 mg in an extended-release core), Claritin-D 12 Hour (a combination tablet formulation of loratadine 5 mg in the tablet coating and 120 mg pseudoephedrine sulfate, 60 mg in the coating and 60 mg in the core), or placebo. Claritin-D 24 Hour and Claritin-D 12 Hour were consistently superior to placebo (P < 0.01) in reducing total, nasal, and nonnasal symptom scores. Patients in the Claritin-D 24 Hour and Claritin-D 12 Hour groups also had significantly greater (P

Subject(s)
Anti-Allergic Agents/administration & dosage , Ephedrine/administration & dosage , Loratadine/administration & dosage , Rhinitis, Allergic, Seasonal/drug therapy , Vasoconstrictor Agents/administration & dosage , Adolescent , Adult , Aged , Analysis of Variance , Anti-Allergic Agents/adverse effects , Child , Delayed-Action Preparations , Double-Blind Method , Drug Administration Schedule , Drug Combinations , Ephedrine/adverse effects , Female , Humans , Loratadine/adverse effects , Male , Middle Aged , Tablets , Treatment Outcome , United States , Vasoconstrictor Agents/adverse effects
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