Dymista nasal spray is used to relieve the symptoms of moderate to severe seasonal and perennial allergic rhinitis.
Seasonal and perennial allergic rhinitis are allergic reactions to substances such as pollen (hayfever), house mites, moulds, dust or pets.
To read the patient information leaflet for this product click here https://www.medicines.org.uk/emc/files/pil.9450.pdf
Adults ( over 18s): ONE spray into EACH nostril morning and night
The active substances are: azelastine hydrochloride
and fluticasone propionate.
Each g of suspension contains 1000 micrograms
azelastine hydrochloride and 365 micrograms
fluticasone propionate.
Each actuation (0.14 g) delivers 137 micrograms
azelastine hydrochloride (= 125 micrograms azelas
tine) and 50 micrograms fluticasone propionate.
The other ingredients are: Disodium edetate,
glycerol, microcrystalline cellulose, carmellose
sodium, polysorbate 80, benzalkonium chloride ,
phenylethyl alcohol and purified water.
~Do not use Dymista Nasal Spray:
• If you are allergic to azelastine hydrochloride or
fluticasone propionate or any of the other ingredients of this medicine (listed in section 6).
Warnings and precautions
Talk to your doctor or pharmacist before using
Dymista Nasal Spray if:
• You had a recent operation on your nose.
• You have an infection in your nose. Infections of
the nasal airways should be treated with antibacterial or antifungal medication. If you are
given medication for an infection in your nose you
can continue to use Dymista Nasal Spray to treat
your allergies.
• You have tuberculosis or an untreated infection.
• You have a change in vision or a history of increased ocular pressure, glaucoma and/or
cataracts. If this applies to you, you will be closely
monitored whilst using Dymista Nasal Spray.
• You suffer from impaired adrenal function. Care
must be taken when transferring from systemic
steroid treatment to Dymista Nasal Spray.
• You suffer from a severe liver disease. Your risk of
suffering from systemic side effects is increased.