Avamys Nasal Spray

218.40

Avamys Nasal Spray is used to treat symptoms of allergic rhinitis. This includes nasal congestion, runny, itchy, nose, sneezing and watery, red, itchy eyes. Avamys Nasal Spray contains the medicine fluticasone furoate. This medicine belongs to a group of medicines known as corticosteroids.

 

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Description

Avamys Nasal Spray is used to treat symptoms of allergic rhinitis. This includes nasal congestion, runny, itchy, nose, sneezing and watery, red, itchy eyes. Avamys Nasal Spray contains the medicine fluticasone furoate. This medicine belongs to a group of medicines known as corticosteroids.

Dosage

Adults and adolescents (12 years and over)

The recommended starting dose is two spray actuations (27.5 micrograms of fluticasone furoate per spray actuation) in each nostril once daily (total daily dose, 110 micrograms).

Once adequate control of symptoms is achieved, dose reduction to one spray actuation in each nostril (total daily dose 55 micrograms) may be effective for maintenance.

The dose should be titrated to the lowest dose at which effective control of symptoms is maintained.

Children (6 to 11 years of age)

The recommended starting dose is one spray actuation (27.5 micrograms of fluticasone furoate per spray actuation) in each nostril once daily (total daily dose, 55 micrograms).

Patients not adequately responding to one spray actuation in each nostril once daily (total daily dose, 55 micrograms) may use two spray actuations in each nostril once daily (total daily dose, 110 micrograms).

Once adequate control of symptoms is achieved, dose reduction to one spray actuation in each nostril once daily (total daily dose, 55 micrograms) is recommended.

For full therapeutic benefit regular, scheduled usage is recommended. Onset of action has been observed as early as 8 hours after initial administration. However, it may take several days of treatment to achieve maximum benefit, and the patient should be informed that their symptoms will improve with continuous regular use (see section 5.1). The duration of treatment should be restricted to the period that corresponds to allergenic exposure.

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