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The Rhinocort Aqua Nasal Spray 32 mcg bottle has been filled with an excess to accommodate the priming activity. Further support comes from a clinical study of patients with perennial allergic rhinitis which demonstrated a statistically significant improvement in nasal symptoms for both Rhinocort Aqua Nasal Spray and for the active comparator (mometasone furoate) compared to placebo by 8 hours. Therefore, larger than recommended doses of Rhinocort Aqua Nasal Spray should be avoided and the minimal effective dose for the patient should be used (see DOSAGE AND ADMINISTRATION). In a four-week clinical trial, 61 adult patients who received 256 mcg daily of Rhinocort Aqua Nasal Spray demonstrated no significant differences from patients receiving placebo in plasma cortisol levels measured before and 60 minutes after 0. The table below describes adverse events occurring at an incidence of 2% or greater and more common among Rhinocort Aqua Nasal Spray-treated patients than in placebo-treated patients in controlled clinical trials. The clinical activity of Rhinocort Aqua Nasal Spray is therefore believed to be due to the parent drug, budesonide.
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