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In the 12-month, open-label, active-controlled, long-term safety trial in adults and adolescents 12 years of age and older, 404 patients with perennial allergic rhinitis or vasomotor rhinitis were treated with DYMISTA 1 spray per nostril twice daily and 207 patients were treated with fluticasone propionate nasal spray, 2 sprays per nostril once daily. Overall, adverse reactions were 47% in the DYMISTA treatment group and 44% in the fluticasone propionate nasal spray group. The most frequently reported adverse reactions ( ≥ 2%) with DYMISTA were headache, pyrexia, cough, nasal congestion, rhinitis, dysgeusia, viral infection, upper respiratory tract infection, pharyngitis, pain, diarrhea, and epistaxis. In the DYMISTA treatment group, 7 patients (2%) had mild epistaxis and 1 patient ( < 1%) had moderate epistaxis. In the fluticasone propionate nasal spray treatment group 1 patient ( < 1%) had mild epistaxis. No patients had reports of severe epistaxis. Focused nasal examinations were performed and no nasal ulcerations or septal perforations were observed. Eleven of 404 patients (3%) treated with DYMISTA and 6 of 207 patients (3%) treated with fluticasone propionate nasal spray discontinued from the trial due to adverse events.

Este medicamento es sólo para uso externo. No lo ingiera por vía oral. Siga las instrucciones de la etiqueta del medicamento. Lávese las manos antes y después de usarlo. Aplique una pequeña capa sobre las zonas afectadas. No la cubra con un vendaje o apósito a menos que se lo indique su médico o su profesional de la salud. Evite que el medicamento entre en contacto con sus ojos. Si esto ocurre, enjuáguelos con abundante agua fría del grifo. Es importante que no utilice más medicamento que lo indicado. No utilice su medicamento con una frecuencia mayor a la indicada. Si lo hace aumentarán las probabilidades de sufrir efectos secundarios.

Propionate injection

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