Background pattern

Amaira 50 microgramos/100 microgramos/inhalacion, polvo para inhalacion (unidosis)

About the medication

Introduction

Leaflet: information for the user

Amaira 50micrograms/100micrograms/ inhalation, powder for inhalation (single dose)

Amaira 50micrograms/250micrograms/ inhalation, powder for inhalation (single dose)

salmeterol/fluticasone propionate

Read this leaflet carefully before starting to use this medicine, as it contains important information for you.

  • Keep this leaflet, as you may need to read it again.
  • If you have any doubts, consult your doctor or pharmacist.
  • This medicine has been prescribed for you only, and you must not give it to others even if they have the same symptoms as you, as it may harm them.
  • If you experience any adverse effects, consult your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.

1. What isAmairaand what it is used for

2. What you need to know before starting to use Amaira

3. How to use Amaira

4. Possible adverse effects

5. Storage of Amaira

6. Contents of the pack and additional information

1. What is Amaira and what is it used for

Amaira contains two active ingredients, salmeterol and fluticasone propionate:

  • Salmeterol is a long-acting bronchodilator. Bronchodilators help keep the airways in the lungs open, making it easier for air to enter and leave. The effects last for at least 12hours.
  • Fluticasone propionate is a corticosteroid that reduces inflammation and irritation in the lungs.

This medication is used to treat adults and adolescents 12 years of age and older.

Your doctor has prescribed this medication to help prevent respiratory problems such as:

  • Asthma

You must use Amaira every day as recommended by your doctor. This will ensure the medication works correctly to control your asthma.

Salmeterol/fluticasone helps prevent shortness of breath and wheezing. However, Amaira should not be used to relieve a sudden attack of shortness of breath or wheezing. In such a case, you must use your quick-relief medication, such as salbutamol. You should always carry your quick-relief medication with you.

2. What you need to know before starting to use Amaira

No use Amaira

If you are allergic to salmeterol, fluticasone propionate or to any other component, lactose monohydrate.

Warnings and precautions

Consult your doctor or pharmacist before starting treatment with salmeterol/fluticasone if you have:

  • Cardiac alterations including rapid or irregular heartbeat
  • Hyperthyroidism
  • High blood pressure
  • Diabetes mellitus (Salmeterol/fluticasone may increase blood sugar levels)
  • Low levels of potassium in the blood
  • Tuberculosis (TB) now or in the past or other lung infections

Contact your doctor if you experience blurred vision or other visual disturbances.

  • Children
  • This medication should not be used in children under 12 years of age.

Use of Amaira with other medications

Inform your doctor or pharmacist if you are using, have used recently or may need to use any other medication. The reason is that, in some cases,salmeterol/fluticasoneis not suitable for administration with other medications.

Inform your doctor if you take any of the following medications, before starting to usesalmeterol/fluticasone:

  • Beta blockers (such as atenolol, propranolol and sotalol). Beta blockers are used mainly to treat hypertension or other cardiac conditions, such as angina pectoris.
  • Medications to treat infections (such as ketoconazole, itraconazole and erythromycin) including some HIV medications (such as ritonavir, medications containing cobicistat). Some of these medications may increase the amount of fluticasone propionate or salmeterol in your body. This may increase your risk of experiencing adverse effects with Amaira, including irregular heartbeat, or may worsen the adverse effects, so your doctor will perform close monitoring if you are taking these medications.
  • Corticosteroids (oral or injectable). If you have taken these medications recently, you may increase the risk ofsalmeterol/fluticasoneaffecting your adrenal glands.
  • Diuretics, also known as medications to urinate, used to treat high blood pressure.
  • Other bronchodilators (such as salbutamol).
  • Medications containing xanthine, such as aminophylline or theophylline. They are often used to treat asthma.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, or if you think you may be pregnant or plan to become pregnant, consult your doctor or pharmacist before using this medication.

Driving and operating machines

It is unlikely thatsalmeterol/fluticasonewill affect your ability to drive or operate machines.

Amaira contains lactose

Amaira contains approximately 13milligrams of lactose in each dose.This amount normally does not cause problems in people with lactose intolerance. Lactose may contain milk proteins that cancause allergic reactions in patients with a milk protein allergy.

3. How to Use Amaira

Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

  • Use Amaira every day, until your doctor tells you to stop. Do not take more than the recommended dose. If in doubt, consult your doctor or pharmacist.
  • Do not stop takingthis medicationor reduce your dose without talking to your doctor first.
  • Salmeterol/fluticasonamust be inhaled through the mouth into the lungs.

The recommended dose is:

Adults and adolescents 12years of age and older

  • Amaira50/100One inhalation twice a day
  • Amaira 50/250One inhalation twice a day

Your symptoms may be well controlled usingthis medicationtwice a day. If so, your doctor may decide to reduce your dose to once a day. The dose may change to:

  • once at night if you have nocturnal symptomssymptoms,
  • once in the morning if you have diurnal symptomssymptoms.

It is very important that you follow your doctor's instructions on how many applications and how often you should take your medication.

If you are using Amaira to treat asthma, your doctor will want to monitor your symptoms regularly.

If your asthma worsens or you have greater difficulty breathing, see your doctor immediately. You may notice more wheezing or a sensation of choking more often or that you need to use your rescue medication more frequently. If any of these things happen, you should continue usingsalmeterol/fluticasona, but do not increase the number of applications. Respiratory disease can worsen and you could become seriously ill. See your doctor, as you may need additional treatment.

Instructions for use

  • Amaira may be different from the inhalers you have used in the past, so it is very important that you use it properly.Your doctor, nurse, or pharmacist should teach you how to use your inhaler. This training is important to ensure that you receive the dose you need. If you have not received this training, ask your doctor, nurse, or pharmacist to show you how to use the inhaler properly, especially if it is the first time you use it.

Periodically, they should check how you use it to ensure that you are using the device properly as prescribed. Not using Amaira properly or as prescribed may result in your asthma not improving as it should.

  • This device contains alveoli that containsalmeterol/propionato de fluticasonain powder.
  • There is a dose counter on the top of the device that indicates how many doses are left. Counts back to 0. The numbers 5 to 0 will appear in red to warn you that there are few doses left. Once the counter marks 0, your inhaler is empty.

Using your inhaler

  1. To open the inhaler, hold it with one hand in a horizontal flat position. Press the red button with your thumb (see figure 1) and slide the pink mouthpiece cover (for 50/100micrograms) or pink (for 50/250micrograms) away from you as far as possible with your thumb of the other hand until you hear a "click" (see figure 2). This will open a small hole in the mouthpiece, and place a dose of medication in the mouthpiece.

Figure1Figure2

Be aware that each time you open the mouthpiece cover with a "click", an alveolus opens and the powder is prepared to be inhaled.Therefore,do not open the mouthpiece cover if you do not need to take the medicine, as the alveoli open and the medicine is wasted.

  1. Keep the inhaler away from your mouth. Breathe out as much as possible. Do not breathe into the inhaler.
  1. Place the mouthpiece in your lips(see figure 3).Breathe in deeply and intensely through the inhaler,not through your nose.

Remove the inhaler from your mouth.

Hold your breath for 10seconds or as long as possible.

Breathe out slowly.

Figure3

The inhaler releases your dose of medication in the form of very fine powder. You may not be able to taste or feel the powder.Do not use an additional dose of the inhaler if you do not taste or feel the medication.

  1. Close the inhaler to keep it clean, sliding the pink mouthpiece cover (for 50/100micrograms), or pink (for 50/250micrograms) of the mouthpiece towards you as far as possible. You will hear a "click" (seefigure4). The mouthpiece cover returns to its original position and is reset. The inhaler is now ready for you to take your next scheduled dose.

5.After rinse your mouth with water and spit it out, or brush your teeth. This may help prevent mouth ulcers and sore throat.

Figure4

Cleaning your inhaler

Keep your inhaler clean and dry.

To clean it, pass a dry cloth over the mouthpiece of the inhaler.

If you use more Amaira than you should

It is very important to use the inhaler as instructed. If you accidentally take more doses than recommended, consult your doctor or pharmacist. You may notice that your heart beats faster than normal and feel tremors. You may also have dizziness, headache, muscle weakness, and joint pain.

If you have used large doses of salmeterol/fluticasona for long periods of time, you should ask your doctor or pharmacist for advice. This is because using high concentrations ofthis medicationmay reduce the amount of steroid hormones produced by the adrenal glands.

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 medication and the amount ingested.

If you forget to use Amaira

Do not take a double dose to compensate for the missed doses. Take the next dose at the usual time.

If you interrupt treatment with Amaira

It is very important to usesalmeterol/fluticasonaevery day as instructed.Continue taking it until your doctor tells you to stop. Do not interrupt or abruptly reduce your treatment withsalmeterol/fluticasona.This could make your breathing worse.

Additionally, if you stop takingsalmeterol/fluticasonaabruptly or reduce your dose, you may (very rarely) cause problems with your adrenal glands (adrenal insufficiency), which sometimes causes adverse effects.

These adverse effects may include any of the following:

  • Abdominal pain
  • Fatigue and loss of appetite, feeling unwell
  • Discomfort and diarrhea
  • Weight loss
  • Headache or drowsiness
  • Low blood sugar levels
  • Hypotension and convulsions (seizures)

When your body is under stress such as fever, trauma (e.g. a car accident or injury), infection, or surgery, adrenal insufficiency can worsen and you may experience any of the adverse effects listed above.

Consult your doctor or pharmacist if you have any adverse effects. To prevent these symptoms, your doctor may prescribe an additional dose of corticosteroids in tablets (such as prednisolone).

Consult your doctor, pharmacist, or nurse if you have any other questions about the use of this medication.

4. Possible Adverse Effects

Like all medicines, this medicine may cause side effects, although not everyone will experience them. To reduce the occurrence of side effects, your doctor will prescribe the lowest dose of this combination of medicines that controls your asthma.

Allergic reactions: you may notice that your breathing suddenly worsens immediately after using Amaira.You may experience wheezing and coughing or shortness of breath. You may also notice itching, hives (urticaria), and swelling (usually of the face, lips, tongue, or throat). You may also feel, suddenly, that your heart is beating very fast, feel like you're losing consciousness, and dizziness (which can lead to collapse or loss of consciousness).If you experience any of these side effects or if they appear suddenly after using Amaira, stop taking this medicineand inform your doctor immediately. Allergic reactions to Amaira are rare (they can affect up to 1 in 100 people).

Very common (may affect more than 1 in 10 people)

  • Headache, which usually improves as treatment continues.

Common (may affect up to 1 in 10 people)

  • Candidiasis (itching, appearance of yellowish cream-colored ulcers) in the mouth and throat. Also, tongue pain, hoarse voice, and throat irritation. Rinsing the mouth with water and spitting it out and/or brushing your teeth immediately after each dose of medicine may help. Your doctor may prescribe antifungal medication (for the treatment of fungal infections) for the treatment of candidiasis.
  • Joint pain and inflammation, and muscle pain.
  • Muscle cramps.

Rare (may affect up to 1 in 100 people)

  • Increased blood sugar levels (hyperglycemia). If you have diabetes, you will need to monitor your blood sugar levels more frequently and adjust your usual diabetes treatment as needed.
  • Cataracts (opacity of the crystalline lens of the eye).
  • Very fast heart rate (tachycardia).
  • Feeling tremors and a fast or irregular heart rhythm (palpitations). These side effects are usually harmless and decrease as treatment continues.
  • Chest pain.
  • Feeling anxious (mainly occurs in children).
  • Sleep disturbances.
  • Allergic skin eruption.

Rare (may affect up to 1 in 1,000 people)

  • Difficulty breathing or wheezing that worsens immediately after using Amaira. Ifthis happens, stop using the Amaira inhaler. Use your rescue inhaler with quick action to improve your breathingand inform your doctor immediately.
  • Salmeterol/fluticasona may increase the normal production of steroid hormones, particularly if you have been taking high doses for long periods of time. The effects include:
    • Delayed growth in children and adolescents
    • Decreased bone mineral density
    • Glaucoma
    • Weight gain
    • Rounded face (moon face) (Cushing's syndrome).

Your doctor will regularly monitor you for the occurrence of any of these side effects and ensure that you are taking the lowest dose of this combination of medicines to control your asthma.

  • Changes in behavior, such as hyperactivity and irritability (although these effects occur mainly in children).
  • Irregular or irregular heartbeats or that the heart has extra beats (arrhythmias). Consult your doctor, but do not stop taking Amaira unless your doctor tells you to.
  • Fungal infection of the esophagus (throat), which can cause difficulty swallowing.

Unknown frequency, but may also occur:

  • Depression or aggression (is more likely to occur in children).
  • Blurred vision

Reporting of side effects

If you experience any type of side effect, consult your doctor, pharmacist, or nurse,even if it's a possible side effect that doesn't appear in this prospectus.You can also report them directly through the Spanish System for the Pharmacovigilance of Medicines for Human Use:www.notificaram.es.By reporting side effects, you can contribute to providing more information on the safety of this medicine.

5. Conservation of Amaira

  • Keep this medication out of the sight and reach of children.
  • Do not use Amaira after the expiration date that appears on the packaging and on the label of your inhaler after CAD. The expiration date is the last day of the month indicated.
  • Do not store at a temperature above 30°C.
  • Medicines should not be disposed of through drains or in the trash. Dispose of the containers and medicines you no longer need at the SIGRE collection pointof the pharmacy. If in doubt, ask your pharmacist how to dispose of the containers and medicines you no longer need. By doing so, you will help protect the environment.

6. Contents of the packaging and additional information

Composition of Amaira

The active principles are salmeterol and fluticasone propionate.

Amaira 50micrograms/100micrograms

Each individual inhalation provides a released dose (the dose that comes out of the mouthpiece) of 47micrograms of salmeterol (as xinafoate) and 92micrograms of fluticasone propionate. This corresponds to a pre-dispensed dose of 50micrograms of salmeterol (as xinafoate) and 100micrograms of fluticasone propionate.

Amaira 50micrograms/250micrograms

Each individual inhalation provides a released dose (the dose that comes out of the mouthpiece) of 45micrograms of salmeterol (as xinafoate) and 229micrograms of fluticasone propionate. This corresponds to a pre-dispensed dose of 50micrograms of salmeterol (as xinafoate) and 250 of fluticasone propionate.

The other component is lactose monohydrate(see section2 in “Amaira contains lactose”)(contains milk proteins).

Appearance of the product and contents of the package

  • Amairacontains a strip of alveoli filled with white to off-white powder. The aluminum paper protects the inhalation powder from atmospheric effects.
  • Each dose is pre-dispensed.
  • The white plastic devices with a pink clear mouthpiece (for 50/100micrograms), or pink (for 50/250micrograms) are found in packages of:

1, 2, 3 or 10×inhalers with60inhalations each.

Only some package sizes may be commercially available.

Marketing Authorization Holder:

Zentiva k.s.

U Kabelovny 130

102 37 Prague 10

Czech Republic

Responsible for manufacturing:

Oy Medfiles Ltd

Volttikatu 5, Volttikatu 8

Kuopio, 70700

Finland

Further information on this medicinal product can be obtained by contacting the local representative of the marketing authorization holder:
Zentiva Spain S.L.U.

Avenida de Europa, 19, Edificio 3, Planta 1.

28224 Pozuelo de Alarcón, Madrid

Spain

This medicinal product is authorized in the Member States of the European Economic Area with the following names:

Austria

Everio Airmaster

Belgium

Brecur Airmaster 50 microgram/100 microgram/ dose, inhalatiepoeder, voorverdeeld

Brecur Airmaster 50 microgram/250 microgram/ dose, inhalatiepoeder, voorverdeeld

Brecur Airmaster 50 microgrammes/100 microgrammes/dose, poudre pour inhalation en récipient unidose

Brecur Airmaster 50 microgrammes/250 microgrammes/dose, poudre pour inhalation en récipient unidose

Brecur Airmaster 50 Mikrogramm/100 mikrogramm einzeldosiertes Pulver zur Inhalation

Brecur Airmaster 50 Mikrogramm/250 Mikrogramm einzeldosiertes Pulver zur Inhalation

Bulgaria

?????? ?????????50 ??????????/100 ??????????/???? ???? ?? ?????????, ????????????? ???????

?????? ?????????50 ??????????/250 ??????????/???? ???? ?? ?????????, ????????????? ???????

Slovakia

EverioAirmaster 50 mikrogramov/100 mikrogramov

EverioAirmaster50 mikrogramov/250 mikrogramov

Spain

Amaira50micrograms/100micrograms/ inhalation, powder for inhalation (single-dose)

Amaira50micrograms/250micrograms/ inhalation, powder for inhalation (single-dose)

Estonia

Everio Airmaster

France

PROPIONATE DE FLUTICASONE/SALMETEROL ZENTIVA 100 microgrammes/50 microgrammes/dose, poudre pour inhalationen récipient unidose

PROPIONATEDE FLUTICASONE/SALMETEROL ZENTIVA 250 microgrammes/50 microgrammes/dose, poudre pour inhalationen récipient unidose

Hungary

Fluzalto Airmaster 50 mikrogramm/100 mikrogramm/adag adagolt inhalációs por

Fluzalto Airmaster 50 mikrogramm/250 mikrogramm/adagadagolt inhalációs por

Ireland

Bronx Airmaster

Lithuania

EverioAirmaster 50/100 mikrogramu/dozeje dozuoti ikvepiamieji milteliai

Everio Airmaster 50/250 mikrogramu/dozeje dozuoti ikvepiamieji milteliai.

Poland

Neuair Airmaster

Czech Republic

Everio Airmaster

Romania

Everio Airmaster 50 micrograme /100 micrograme pulbere de inhalat unidoza

Everio Airmaster 50 micrograme /250 micrograme pulbere de inhalat unidoza

Sweden

Neuair Airmaster

Last review date of this leaflet:November 2021

Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.es/.

Country of registration
Prescription required
Yes
Manufacturer
Composition
Lactosa monohidrato (13,127 mg mg)
This information is for reference only and does not constitute medical advice. Always consult a licensed doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.

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