Fasenra 30 mg solution for injection in pre-filled pen

Spain
Brand name Fasenra 30 mg solution for injection in pre-filled pen
Form solution for injection in pre-filled pen
Active substance / Dosage
Prescription type Hospital Diagnosis
Registration number 1171252002
Manufacturer Astrazeneca Ab
Fasenra 30 mg solution for injection in pre-filled pen solution for injection in pre-filled pen

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

  1. What Fasenra is and what it is used for
  2. What you need to know before using Fasenra
  3. How to use Fasenra Pen
  4. Possible side effects
  5. How to store Fasenra Pen
  6. 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

Text in Cyrillic characters stating Bulgaria, AstraZeneca Bulgaria EOOD, and the phone number +359 24455000

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:

  • it has been frozen
  • it has been dropped or damaged
  • the safety seal on the carton is broken
  • the expiry date (EXP) has passed

Do not:

  • shake your Fasenra Pen
  • share or reuse your Fasenra Pen

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.

Black text on white background reading 'Viewing window' arranged over two linesBefore use

After use

Pen-shaped medical device with a blue cap on the left, a transparent central body with a viewing window, and a dark purple end

Black text on white background reading 'Liquid medication' arranged over two linesBlack text on white background with the Spanish phrase 'Etiqueta con fecha de caducidad' meaning 'Expiry date label'

Pen-shaped medical device with a green tip, a white central body with a transparent viewing window, and a dark purple end section

Black text on white background stating 'Green plunger'Black text on white background with the Spanish phrase 'Protector de la aguja' arranged over two lines, meaning 'Needle protector'

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)

Two square white blister packs overlapped, with dark edges and a recessed center to hold medications or tablets

Stylized black and white drawing of three rounded, irregular pills placed close together on a neutral background

Red biological waste container with a black biohazard symbol in the center and a white lid on top

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.

Stylized icon of a stopwatch with the right half colored blue and black text '30 min' in the center of the white dial

Step 3 – Check the liquid

A hand holding horizontally a medical injection pen with a white body, a purple upper section, and a transparent viewing window

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

Black text on white background with the Spanish phrase 'lugar exclusivo para el cuidador' arranged over four separate lines, meaning 'exclusive space for the caregiver'Front-view diagram of the human body with gray areas indicating injection sites on the arms, thighs

The recommended site for injection is the front part of the thigh. You may also use the lower abdomen.

Do not inject:

  • within 5 cm around the navel
  • where the skin is softened, burned, peeling, or hardened
  • in scars or damaged skin
  • through clothing

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

A hand holding a white tissue to clean or dab a smooth, light-colored area of skin

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

Two hands separating a medical device composed of a transparent cylinder and a main body in white and green, with a gray arrow pointing to the left

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.

A hand holding a purple and silver cylindrical medical device, preparing to inject it at a 90-degree angle into the skin of the body held by another hand

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.

A hand holding a purple and white injection pen while another hand prepares the injection site

A hand holding a vertical injection pen against the skin of the thigh while a stopwatch displays a 15-second timer

A hand holding a vertical injection device and moving it toward the skin of the abdomen

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

A hand holding horizontally an injection pen with a white body, a green viewing window, and a transparent section

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

White cylindrical medical device with a rectangular transparent window showing the liquid level and a dosage indicator

White cylindrical medical device with a turquoise rectangular indicator at the bottom

After injection

Step 9 – Check the injection site

A hand gently pressing a white cotton ball onto the surface of light-colored skin

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

A hand holding a magenta and white injection pen above a red biological waste container with a biohazard symbol

  • Each Fasenra Pen contains a single dose of Fasenra and cannot be reused.
  • Place your used Fasenra Pen immediately into a puncture-resistant sharps container after use.

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.