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Requiring treatments judged by the investigator subinvestigator at the time of enrollment to randomization Patients with a complication of infection or systemic mycosis for which no effective antibiotics are available Patients with uncured nasal septal ulcer, operated nose or nasal trauma.

Patients with a history of hypersensitivity to steroids and any ingredients of the study drugs Pregnant, lactating metaspray nasal spray dosage possibly pregnant patients or the patients who themselves or whose partners wish to become pregnant during the study Patients with severe hepatic or renal disorder, heart or blood disease, diabetes mellitus, metaspray nasal spray dosage, or other serious complication, suffering from problems metaspray nasal spray dosage systemic metaspray nasal spray dosage who have pollens as multiple allergens and the period from 7 days before enrollment to randomization to completion of the treatment period coincides with the period of scattering of relevant pollens Patients with a complication of vasomotor rhinitis or eosinophilic rhinitis Patients with a complication of a nasal disease infectious sinusitis, hypertrophic rhinitis, acute or chronic rhinitis, nasal polyps, or septal deviation which may interfere with efficacy evaluation of the study drugs Patients with a complication of a disease acute upper respiratory tract inflammation, acute laryngitis or acute tonsillitis, etc.

Patients with symptoms of perennial allergic rhinitis, the severity of which is moderate or severer according to the severity grading provided in the Guidelines for the Management of Allergic Rhinitis in Japan partly modified with the 4-nasal symptom score of 4 or over at informed consent and during the pre-treatment observation period Patients with positive reaction to the eosinophil count in nasal discharge metaspray nasal spray dosage nasal challenge test in addition to the skin test or specific IgE antibody test Patients or their legal representatives in case of patients aged under 20 years capable of giving written informed consent Patients with a complication of tuberculous diseases or lower respiratory tract infections, and those with a complication of otorhinolaryngeal infection acute upper respiratory tract inflammation, acute laryngopharyngitis, acute tonsillitis, etc.

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No individualmometasone furoate-treated patient was noted to have developed a significant elevation in intraocular pressure or cataracts in this 12-week study.

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Responsibility for the content of the site - edicaid is establishing a lock-in requiring use of a single pharmacy for beneficiaries with high utilization of multiple prescriptions. The Department will phase in the PDL by sets of drug classes. Notes: HHS had taken no action on the waiver as of.

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