Package Leaflet: Information for the Patient
Avancort Duo 137 micrograms/50 micrograms/dose nasal spray suspension
azelastine hydrochloride / fluticasone propionate
Read this package leaflet carefully before you start using this medicine, because it contains important information for you.
Contents of the package leaflet
Avancort Duo contains two active substances: azelastine hydrochloride and fluticasone propionate.
This medicine is used to relieve the symptoms of moderate to severe seasonal allergic rhinitis and perennial allergic rhinitis, if treatment with an antihistamine or intranasal corticosteroid alone is considered insufficient.
Seasonal or perennial allergic rhinitis are allergic reactions to substances such as pollen (hay fever), house dust mites, molds, dust, or domestic animals.
This medicine relieves the symptoms of allergies, such as: runny nose, postnasal drip, sneezing, itching, or nasal congestion.
Do not use Avancort Duo
Warnings and precautions
Talk to your doctor or pharmacist before you start using this medicine if:
In these cases, your doctor will decide whether you can use this medicine:
It is important that you take the dose indicated in section 3 or the dose indicated by your doctor. Treatment with higher doses of nasal corticosteroids than recommended may lead to adrenal suppression, which can cause weight loss, fatigue, muscle weakness, low blood sugar levels, salt craving, joint pain, depression, and skin darkening. If you experience any of these side effects, your doctor may recommend another medicine during periods of stress or elective surgery.
To avoid adrenal suppression, your doctor will advise you to take the lowest dose that maintains effective control of your rhinitis symptoms.
The use of nasal corticosteroids (such as this medicine) may cause slower growth in children and adolescents when used for a long time. The doctor will regularly check the growth of children and ensure that they take the lowest effective dose possible.
Contact your doctor if you experience blurred vision or other visual disturbances.
If you are not sure if you are in any of the above situations, talk to your doctor or pharmacist before using this medicine.
Children
This medicine is not recommended for use in children under 12 years of age.
Other medicines and Avancort Duo
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, including those obtained without a prescription.
Some medicines may increase the effects of this medicine, so your doctor will monitor you closely if you are taking these medicines (including some for HIV: ritonavir, cobicistat, and medicines for the treatment of fungal infections: ketoconazole).
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.
Driving and using machines
This medicine has a minimal influence on the ability to drive and use machines.
Very rarely, you may experience fatigue or dizziness due to the disease itself or during the use of this medicine. In these cases, do not drive or operate machinery. Note that alcohol consumption may enhance these effects.
Avancort Duo contains benzalkonium chloride
This medicine contains 0.014 mg of benzalkonium chloride per application.
Benzalkonium chloride may cause irritation or inflammation inside the nose, especially when used for long-term treatment.
Follow the instructions for administration of this medicine exactly as indicated by your doctor. If you are unsure, consult your doctor or pharmacist again.
It is essential that the use of this medicine is regular for the therapeutic benefit to be complete.
Avoid contact with the eyes.
Adults and adolescents (over 12 years of age)
Use in children under 12 years of age
Use in case of renal and hepatic insufficiency
There are no data available in patients with renal and hepatic insufficiency.
Method of administration
Nasal route.
Read the following instructions carefully and use the product only as indicated.
INSTRUCTIONS FOR USE
Preparation of the spray
Figure 1
Figure 2
Method of spraying
Figure 3
Figure 4
Duration of treatment
This medicine is suitable for long-term use. The duration of treatment corresponds to the period during which you experience allergic symptoms.
If you use more Avancort Duo than you should
If you apply more of this medicine to your nose than you should, it is unlikely that you will have any problems.
If you are unsure, or if you have used a higher dose than recommended for a long time, talk to your doctor.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to use Avancort Duo
Use the nasal spray as soon as you remember, and then take your next dose at the usual time. Do not take a double dose to make up for forgotten doses.
If you stop using Avancort Duo
Do not stop treatment without consulting your doctor, as this may put your treatment at risk.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Very common side effects (may affect more than 1 in 10 people):
Common side effects (may affect up to 1 in 10 people):
Uncommon side effects (may affect up to 1 in 100 people):
Rare side effects (may affect up to 1 in 1,000 people):
Very rare side effects (may affect up to 1 in 10,000 people):
Seek immediate medical attention if you develop any of the following symptoms:
Side effects with unknown frequency (frequency cannot be estimated from the available data)
When this medicine is administered at high doses for a prolonged period, systemic side effects (side effects that affect the whole body) may occur. The likelihood of these effects is much lower if a nasal corticosteroid spray is used instead of oral corticosteroids. These effects may vary between individual patients and between different corticosteroid preparations (see section 2).
Corticosteroid nasal sprays may affect the normal production of hormones in your body, especially if they are used at high doses for a long time. In children and adolescents, this side effect may cause slower growth.
In rare cases, a reduction in bone density (osteoporosis) may occur when corticosteroids are administered nasally for a long period.
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this package leaflet. You can also report side effects directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the bottle and carton after “EXP”. The expiry date is the last day of the month shown.
This medicine does not require any special storage conditions. Do not refrigerate or freeze.
Shelf life after opening: Discard any unused medicine 6 months after first opening the nasal spray.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Avancort Duo
The active substances are: azelastine hydrochloride and fluticasone propionate. Each gram of suspension contains 1,000 micrograms of azelastine hydrochloride and 365 micrograms of fluticasone propionate.
Each application (0.14 g) delivers 137 micrograms of azelastine hydrochloride (= 125 micrograms of azelastine) and 50 micrograms of fluticasone propionate.
The other ingredients (excipients) are: disodium edetate, glycerol (E-422), microcrystalline cellulose and sodium carmellose, polysorbate 80, benzalkonium chloride, phenylethyl alcohol, and purified water.
Appearance of the product and pack contents
Avancort Duo is a homogeneous white suspension.
Avancort Duo is presented in a Type I amber glass bottle, equipped with a spray pump, a nasal applicator made of polypropylene (actuator), and a dust protective cap, containing 23 g (at least 120 applications) of suspension.
Pack size:
One bottle with 23 g of suspension in a 25 ml bottle (at least 120 applications).
Marketing authorisation holder and manufacturer
Marketing authorisation holder
Laboratorios Cinfa, S.A.
Carretera Olaz-Chipi, 10. Polígono Industrial Areta
31620 Huarte (Navarra) – Spain
Manufacturer
ELPEN Pharmaceutical Co Inc.
Marathonos Avenue, 95, Pikermi
19009, Greece
or
Laboratorios Cinfa, S.A.
Carretera Olaz-Chipi, 10. Polígono Industrial Areta
31620 Huarte (Navarra) – Spain
Date of last revision of this package leaflet: April 2025
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/)
You can access detailed and up-to-date information about this medicine by scanning the QR code included in the package leaflet and carton with your smartphone. You can also access this information at the following internet address:
https://cima.aemps.es/cima/dochtml/p/90298/P_90298.html
QR code to: https://cima.aemps.es/cima/dochtml/p/90298/P_90298.html