Most AEs in this study were of mild to moderate intensity and comparable to placebo. The most common AEs reported were: epistaxis, headache, nasopharyngitis, laryngopharyngeal pain. 1
*Global, randomised, double-blind, placebo-controlled, 6-week study evaluating the efficacy and tolerability of intranasal FF in patients ≥12 years of age (n=302) with perennial AR. The primary efficacy measure was mean change from baseline over the 6-week treatment period in daily reflective TNSS.
AR: allergic rhinitis; FF: fluticasone furoate; TNSS: total nasal symptom score.
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