Fasenra 30 mg solution for injection in pre-filled pen
Spain
Table of Contents
Patient Information Leaflet
Introduction
Patient Information Leaflet
Fasenra 30mg solution for injection in a prefilled pen
benralizumab
Read the entire leaflet carefully before you start using this medicine because it contains important information for you.
- Keep this leaflet, as you may need to read it again.
- If you have any questions, ask your doctor, pharmacist, or nurse.
- This medicine has been prescribed for you only, and you should not give it to other people, even if they have the same symptoms as you, because it may harm them.
- If you experience any adverse reactions, consult your doctor, pharmacist, or nurse, even if they are adverse reactions not listed in this leaflet. See section 4.
Leaflet Contents
- What Fasenra is and what it is used for
- What you need to know before using Fasenra
- How to use Fasenra Pen
- Possible side effects
- How to store Fasenra Pen
- Contents of the pack and other information
1. What Fasenra is and what it is used for
What Fasenra is
Fasenra contains the active substance benralizumab, which is a monoclonal antibody, that is, a type of protein that recognises and binds to a specific substance in the body. The target of benralizumab is a protein called interleukin-5 receptor, which is found particularly on a type of white blood cell called an eosinophil.
What Fasenra is used for
Asthma
Fasenra is used to treat severe eosinophilic asthma in adults. Eosinophilic asthma is a type of asthma in which patients have too many eosinophils in their blood or lungs.
Fasenra is used in combination with other asthma medications (high-dose "inhaled corticosteroids" plus other anti-asthma medicines) when the disease is not well controlled by these other medicines alone.
Eosinophilic granulomatosis with polyangiitis (EGPA)
Fasenra is used to treat EGPA in adults. EGPA is a disease in which people have too many eosinophils in their blood and tissues and also have some form of vasculitis. This means there is inflammation of the blood vessels. This disease most frequently affects the lungs and paranasal sinuses, but often affects other organs such as the skin, heart, and kidneys.
How Fasenra works
Eosinophils are white blood cells involved in the inflammation of asthma and EGPA. By binding to eosinophils, Fasenra helps reduce their numbers and reduce inflammation.
Benefits of using Fasenra
Asthma
Fasenra may reduce the frequency of asthma attacks you are experiencing, helping you to breathe better and reducing your asthma symptoms. If you are using medicines called "oral corticosteroids", taking Fasenra may also allow you to reduce your daily dose or stop treatment with oral corticosteroids needed to control your asthma.
EGPA
Fasenra may reduce symptoms and prevent flare-ups of EGPA. This medicine may also allow you to reduce your daily dose of oral corticosteroids needed to control symptoms.
2. What you need to know before using Fasenra
Donotuse Fasenra:
- If you are allergic to benralizumab or to any of the other ingredients of this medicine (listed in section 6). Talk to your doctor, nurse, or pharmacist if you think this applies to you.
Warningsand precautions
Talk to your doctor, nurse, or pharmacist before using Fasenra:
- if you have a parasitic infection or live in an area where parasitic infections are common, or if you travel to such regions. This medicine may reduce your ability to fight certain types of parasitic infections.
- if you have ever had an allergic reaction to an injection or medication (see section 4 for symptoms of an allergic reaction).
Also, consult your doctor, pharmacist, or nurse if you are receiving Fasenra:
- if your asthma remains uncontrolled or worsens during treatment with this medicine.
- if you experience any symptoms of an allergic reaction (see section 4). Allergic reactions have occurred in patients receiving this medicine.
Fasenra is not a rescue medicine. Do not use it to treat a sudden asthma attack.
Bewaryof signs of serious allergic reactions
Fasenra may potentially cause serious allergic reactions. You should be alert for signs of such reactions (such as hives, rash, difficulty breathing, fainting, discomfort, feeling dizzy and/or swelling of the face, tongue, or mouth) while receiving Fasenra.
It is important that you discuss with your doctor how to recognize early symptoms of serious allergic reactions and how to manage them if they occur.
To improve traceability of biological medicines, record the name and batch number shown on the outer packaging and on the label of the prefilled pen each time you receive a new pack of Fasenra, and provide this information when reporting any adverse event.
Other medicines for asthma or EGPA
Do not stop abruptly or change the dose of your other medications for your condition when starting Fasenra.
If your response to treatment allows, your doctor may attempt to reduce the dose of some of these medicines, especially those known as "corticosteroids". This should be done gradually and under the direct supervision of your doctor.
Tell your doctor if you are taking, have recently taken, or might need to take any other medicines before using Fasenra.
Children and adolescents
Do not administer this medicine to children under 18 years of age, as the safety and benefits of this medicine are unknown in this population.
Pregnancyand breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor before using this medicine.
Do not use Fasenra during pregnancy unless your doctor tells you otherwise. It is unknown whether Fasenra may affect the fetus.
It is not known whether components of Fasenra pass into breast milk. If you are breastfeeding or plan to breastfeed, talk to your doctor.
Drivingand using machines
It is unlikely that Fasenra will affect your ability to drive or use machines.
Fasenra contains polysorbate 20
This medicine contains 0.06 mg of polysorbate 20 (of plant origin) in each 30 mg prefilled pen. Polysorbates may cause allergic reactions. Inform your doctor if you have any known allergies.
3. How to use Fasenra Pen
Always use this medicine exactly as your doctor has told you. If you are unsure, consult your doctor, nurse, or pharmacist.
Asthma
The recommended dose is one 30 mg injection. The first 3 injections are given every 4 weeks. After that, the injections are 30 mg doses every 8 weeks.
EGPA
The recommended dose is one 30 mg injection every 4 weeks.
Fasenra is administered by injection just under the skin (subcutaneously). You and your doctor or nurse should decide whether you should self-inject Fasenra. You must not self-inject Fasenra if you have not previously received Fasenra, or if you have previously had an allergic reaction to Fasenra.
You or your caregiver must receive training on the correct way to inject Fasenra. Carefully read the 'Instructions for Use' for the pre-filled pen before using Fasenra.
If you forget to use Fasenra
If you forget to inject a dose of Fasenra, speak with your doctor, pharmacist, or nurse as soon as possible.
If you stop treatment with Fasenra
Do not stop treatment with Fasenra unless your doctor advises you to do so. Interrupting or stopping treatment with Fasenra may cause your symptoms to return and asthma exacerbations.
If your asthma symptoms worsen while receiving Fasenra injections, speak with your doctor.
If you have any further questions about the use of this medicine, ask your doctor, pharmacist, or nurse.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Serious allergic reactions
Contact your doctor immediately if you think you may be having an allergic reaction. Such reactions can occur hours or days after the injection.
Frequency not known (cannot be estimated from the available data):
- anaphylaxis
Common symptoms include:
- swelling of the face, tongue or mouth
- breathing problems
- fainting, dizziness, lightheadedness (due to a drop in blood pressure)
Frequent (may affect up to 1 in 10 people):
- hypersensitivity reactions (hives, skin rash)
Other side effects
Frequent (may affect up to 1 in 10 people):
- headache
- pharyngitis (sore throat)
- fever (high temperature)
- reaction at the injection site (for example, pain, redness, itching, swelling near the injection site)
Reporting of side effects
If you experience any side effect, talk to your doctor, pharmacist or nurse, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the national reporting system included in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.
5. Storage of Fasenra Pen
Keep this medicine out of the sight and reach of children.
Fasenra Pen is for single use only.
Do not use this medicine after the expiry date stated on the label and the carton after 'EXP'. The expiry date refers to the last day of the month indicated.
Store in the original packaging to protect from light.
Store in a refrigerator (between 2 °C and 8 °C).
Fasenra Pen may be stored at room temperature up to 25 °C for a maximum of 14 days. After removal from the refrigerator, Fasenra must be used within 14 days or discarded, and the date of disposal should be written on the carton.
Do not shake, freeze, or expose to heat.
Medicines should not be disposed of via wastewater. Ask your pharmacist how to dispose of medicines and packaging that you no longer need. This will help protect the environment.
6. Contents of the pack and other information
Composition of Fasenra Pen
The active substance is benralizumab. One 1 ml pre-filled pen contains 30 mg of benralizumab.
The other components are histidine, histidine monohydrochloride monohydrate, trehalose dihydrate, polysorbate 20 (E 432) and water for injections.
Nature and contents of the container
Fasenra is a solution that varies in colour from colourless to yellow. It may contain particles.
Fasenra is available in a pack containing one pre-filled pen.
Marketing Authorisation Holder
AstraZeneca AB
SE‑151 85 Södertälje
Sweden
Manufacturer
AstraZeneca AB
Gärtunavägen
SE-152 57 Södertälje
Sweden
MedImmune UK Ltd
6 Renaissance Way
Liverpool, L24 9JW
United Kingdom
AstraZeneca Nijmegen B.V., Nijmegen
Lagelandseweg 78
Nijmegen, 6545CG
The Netherlands
For further information on this medicinal product, please contact the local representative of the Marketing Authorisation Holder:
Belgium/Belgium/Belgium AstraZeneca S.A./N.V. Tel: +32 2 370 48 11 | Lithuania UAB AstraZeneca Lietuva Tel: +370 5 2660550 |
| Luxembourg/Luxembourg AstraZeneca S.A./N.V. Tél/Tel: +32 2 370 48 11 |
Czech Republic AstraZeneca Czech Republic s.r.o. Tel: +420 222 807 111 | Hungary AstraZeneca Kft. Tel.: +36 1 883 6500 |
Denmark AstraZeneca A/S Tlf.: +45 43 66 64 62 | Malta Associated Drug Co. Ltd Tel: +356 2277 8000 |
Germany AstraZeneca GmbH Tel: +49 40 809034100 | Netherlands AstraZeneca BV Tel: +31 85 808 9900 |
Estonia AstraZeneca Tel: +372 6549 600 | Norway AstraZeneca AS Tlf: +47 21 00 64 00 |
Greece AstraZeneca A.E. Tel: +30 210 6871500 | Austria AstraZeneca Österreich GmbH Tel: +43 1 711 31 0 |
Spain AstraZeneca Farmacéutica Spain, S.A. Tel: +34 91 301 91 00 | Poland AstraZeneca Pharma Poland Sp. z o.o. Tel.: +48 22 245 73 00 |
France AstraZeneca Tél: +33 1 41 29 40 00 | Portugal AstraZeneca Produtos Farmacêuticos, Lda. Tel: +351 21 434 61 00 |
Croatia AstraZeneca d.o.o. Tel: +385 1 4628 000 | Romania AstraZeneca Pharma SRL Tel: +40 21 317 60 41 |
Ireland AstraZeneca Pharmaceuticals (Ireland) DAC Tel: +353 1609 7100 | Slovenia AstraZeneca UK Limited Tel: +386 1 51 35 600 |
Iceland Vistor hf. Sími: +354 535 7000 | Slovakia AstraZeneca AB, o.z. Tel: +421 2 5737 7777 |
Italy AstraZeneca S.p.A. Tel: +39 02 00704500 | Finland AstraZeneca Oy Puh/Tel: +358 10 23 010 |
Cyprus Alkemion Pharmaceutical Ltd Tel: +357 22490305 | Sweden AstraZeneca AB Tel: +46 8 553 26 000 |
Latvia SIA AstraZeneca Latvija Tel: +371 67377100 | United Kingdom (Northern Ireland) AstraZeneca UK Ltd Tel: +44 1582 836 836 |
Date of the most recent review of this leaflet:
Detailed information on this medicine is available on the European Medicines Agency website: https://www.ema.europa.eu.
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Instructions for Use
Fasenra 30 mg solution for injection in a pre-filled pen
benralizumab
For subcutaneous injection
Single-use pre-filled pen
Before starting to use Fasenra Pen, a healthcare professional must train you or your caregiver on how to use it correctly.
Read these “Instructions for Use” before starting to use Fasenra Pen and each time you need to administer a new injection. There may be new information. This information does not replace a consultation with your healthcare professional regarding your disease or your treatment.
If you or your caregiver has any questions, consult your healthcare professional.
Important information
Store Fasenra in a refrigerator at 2°C to 8°C inside its carton until ready for use. Fasenra may be kept at room temperature up to 25°C for up to 14 days. After removal from the refrigerator, Fasenra must be used within 14 days or be discarded.
Do not use your Fasenra Pen if:
| Do not:
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If any of the above occurs, discard the Fasenra Pen into a puncture-resistant sharps container and use a new pre-filled pen.
Each Fasenra Pen contains 1 dose of Fasenra for single use only.
Keep Fasenra and all medicines out of the sight and reach of children.
Your FasenraPen
Do not remove the cap until you have reached step 6 of these instructions and are ready to inject Fasenra.
| After use |
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Step 1 – Gather the materials
- 1 Fasenra Pen from the refrigerator
- 1 alcohol wipe
- 1 cotton ball or gauze pad
- 1 sharps container
(See step 10 – Dispose of the Fasenra Pen safely)
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Pre-filled pen | Alcohol wipe | Cotton ball or gauze | Sharps container |
Step 2 – Prepare to use your Fasenra Pen | |
Check the expiration date (EXP). Do not use if the expiration date has passed. Before administration, allow the prefilled pen to reach room temperature of 20°C to 25°C by removing it from the refrigerator and letting it sit for approximately 30 minutes. Do not heat the Fasenra Pen in any other way. For example, do not heat it in a microwave, with hot water, or place it near sources of heat. Use Fasenra within 14 days after removing it from the refrigerator. Do not remove the cap until you reach step 6. |
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Step 3 – Check the liquid | |
| Look at the Fasenra Pen liquid through the viewing window. The liquid should be clear and colorless to slightly yellow. It may contain small white particles. Do not inject Fasenra if the liquid is cloudy, discolored, or contains large particles. You may see a small air bubble in the liquid. This is normal. You do not need to do anything about it. |
Step 4 – Choose the injection site | |
| The recommended site for injection is the front part of the thigh. You may also use the lower abdomen. Do not inject:
A caregiver may administer the injection in the upper arm, thigh, or abdomen. Do not attempt to inject yourself in the upper arm. For each injection, select a different site, at least 3 cm away from the previous injection site. |
Step 5 – Clean the injection site | |
| Wash your hands thoroughly with soap and water. Clean the injection site using an alcohol wipe with a circular motion. Allow it to air dry. Do not touch the cleaned area before injecting. Do not fan or blow on the cleaned area. |
Step 6 – Remove the cap | |
| Hold the Fasenra Pen with one hand. Carefully pull the cap off using the other hand. Set the cap aside for disposal later. The green needle cover is now exposed. This is designed to prevent you from touching the needle. Do not attempt to touch the needle or push the needle cover with your finger. Do not try to reattach the cap onto the Fasenra Pen. This could cause premature injection or damage the needle. Proceed to the next steps immediately after removing the cap. |
Step 7 – Inject Fasenra | |
Follow your healthcare provider's instructions on how to inject. You may either gently pinch the injection site or administer the injection without pinching the skin. Inject Fasenra by following the steps shown in figures a, b, c, and d. Keep the Fasenra Pen in place for the complete injection. Do not change the position of the Fasenra Pen once the injection has started.
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Position the Fasenra Pen at the injection site.
Place the Fasenra Pen needle shield straight (at a 90º angle) against your skin. Make sure you can see the viewing window.
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Press down firmly. You will hear a click. A "click" indicates that the injection has started. The green plunger will move downward in the viewing window during the injection. | Continue pressing firmly for 15 seconds. You will hear a second "click". The second click indicates that the injection is complete. The green plunger will completely fill the viewing window. | Lift the Fasenra pen straight upward. The needle shield will slide down and lock into place, covering the needle. |
Step 8 - Check the viewing window | |||
| Check the viewing window to make sure that all the liquid has been injected. If the green plunger does not completely fill the viewing window, you may not have received the full dose. If this occurs or if you have any other concerns, contact your healthcare professional. | ||
Before injection |
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| After injection |
Step 9 – Check the injection site | |
| There may be a small amount of blood or fluid at the injection site. This is normal. Gently press the skin with a cotton ball or gauze until bleeding stops. Do not rub the injection site. If necessary, cover the injection site with a small bandage. |
Step 10 – Safely dispose of the used Fasenra Pen | |
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Do not throw the Fasenra Pen into your household waste. Dispose of the cap and any other used materials in your household waste. |
Disposal guide Dispose of the container as a whole according to the instructions provided by your healthcare professional or pharmacist. Do not recycle your sharps container. |

Before use






















