REFACTO AF 1000 IU, POWDER AND SOLVENT FOR INJECTABLE SOLUTION

Introduction

Package Leaflet: Information for the User

ReFacto AF 250 UI powder and solvent for solution for injection

ReFacto AF 500 UI powder and solvent for solution for injection

ReFacto AF 1000 UI powder and solvent for solution for injection

ReFacto AF 2000 UI powder and solvent for solution for injection

moroctocog alfa (recombinant human coagulation factor VIII)

Read all of this leaflet carefully before you start using this medicine because it contains important information for you.

• Keep this leaflet, you may need to read it again.
• If you have any further questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you only. Do not pass it on to others, as it may harm them, even if their symptoms are the same as yours.
• If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

Contents of the pack and other information:

1. What is ReFacto AF and what is it used for
2. What you need to know before you use ReFacto AF
3. How to use ReFacto AF
4. Possible side effects
5. Storing ReFacto AF
6. Contents of the pack and further information

1. What is ReFacto AF and what is it used for

ReFacto AF contains the active substance moroctocog alfa, human coagulation factor VIII. Factor VIII is necessary for blood to clot and stop bleeding. In patients with hemophilia A (congenital factor VIII deficiency), it is either not present or does not work properly.

ReFacto AF is used to treat and prevent (prophylaxis) bleeding episodes in adults and children of all ages (including newborns) with hemophilia A.

2. What you need to know before you use ReFacto AF

Do not use ReFacto AF

• if you are allergic to moroctocog alfa or any of the other ingredients of this medicine (listed in section 6);
• if you are allergic to hamster proteins.

Talk to your doctor if you are unsure.

Warnings and precautions

Talk to your doctor or pharmacist before you start using ReFacto AF

• if you have allergic reactions. Some signs of allergic reactions are difficulty breathing, shortness of breath, swelling, hives, itching, chest tightness, wheezing, and low blood pressure. Anaphylaxis is a severe allergic reaction that causes difficulty swallowing or breathing, redness or swelling of the hands, face, or both. If you experience any of these symptoms, stop the infusion immediately and contact your doctor or seek emergency medical attention immediately. In cases of severe allergic reactions, alternative treatment should be considered.

• the formation of inhibitors (antibodies) is a known complication that can occur during treatment with all factor VIII medicines. These inhibitors, especially at high levels, can prevent the treatment from working properly, so you or your child will be closely monitored for the development of such inhibitors. If your bleeding or your child's bleeding is not being controlled with ReFacto AF, contact your doctor immediately.

• if your bleeding does not stop as expected, contact your doctor or seek emergency medical attention immediately.

Other medicines and ReFacto AF

Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.

Pregnancy, breastfeeding, and fertility

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

Driving and using machines

ReFacto AF has no influence on the ability to drive and use machines.

ReFacto AF contains sodium

After reconstitution, ReFacto AF contains 1.27 mmol (or 29 mg) of sodium (the main component of cooking/table salt) per vial. This is equivalent to 1.5% of the maximum recommended daily intake of sodium for an adult. Depending on your body weight and your dose of ReFacto AF, you may receive multiple vials. This should be taken into account if you are on a low-salt diet.

3. How to use ReFacto AF

Follow the instructions for administration of this medicine exactly as told by your doctor. If you are unsure, consult your doctor or pharmacist again.

Treatment with ReFacto AF should be started by a doctor who has experience in the treatment of patients with hemophilia A. Your doctor will decide the dose of ReFacto AF you should receive. This dose and its duration will depend on your individual needs for factor VIII replacement therapy. ReFacto AF is given by injection into a vein and the injection takes several minutes. Injections of ReFacto AF can be given by patients or their caregivers, provided they have received appropriate training.

During your treatment, your doctor may change the dose of ReFacto AF you receive.

Consult your doctor before traveling. When you travel, you should carry your factor VIII product in sufficient quantity for the planned treatment.

It is recommended that each time you administer ReFacto AF, you record the name on the label and the batch number of the product. You can stick one of the detachable labels found on the vial to document the batch number in your diary or to report any side effects.

Reconstitution and administration

The instructions below are a guide for the reconstitution and administration of ReFacto AF. Patients should follow the specific reconstitution and administration instructions given by their doctors.

For reconstitution, use only the pre-filled syringe provided in the pack. For administration, other sterile disposable syringes can be used.

ReFacto AF is administered by intravenous (IV) infusion after reconstituting the lyophilized powder for injection with the provided syringe of solvent, [a 9 mg/ml (0.9%) sodium chloride injection solution]. Do not mix ReFacto AF with other infusion solutions.

Always wash your hands before performing reconstitution and administration. During the reconstitution procedure, follow aseptic technique (i.e., clean and germ-free).

Reconstitution:

1. Wait for the ReFacto AF lyophilized vial and the pre-filled syringe of solvent to reach room temperature.

1. Remove the plastic cap from the ReFacto AF vial to expose the central part of the rubber stopper.

1. Clean the top of the vial with the provided alcohol swab or another antiseptic solution and wait for it to dry. After cleaning, do not touch the rubber stopper with your hand or let it touch any surface.

1. Remove the cap from the plastic vial adapter package. Do not remove the adapter from the package.

1. Place the vial on a flat surface. While holding the adapter package, place the adapter over the vial and press firmly on the package until the adapter snaps into place on top of the vial and the adapter's spike penetrates the vial's stopper.

1. Remove the adapter package and discard it.

1. Attach the plunger rod to the solvent syringe by inserting the rod into the syringe's cap opening, pressing, and twisting firmly until it is seated in the cap.

1. Remove the plastic tip cap from the solvent syringe by breaking the perforation of the cap. This is done by bending the cap up and down until the perforation breaks. Do not touch the inside of the cap or the tip of the syringe. The cap may need to be put back on (if ReFacto AF reconstituted is not administered immediately), so it should be placed aside on its top.

1. Place the vial on a flat surface. Connect the solvent syringe to the vial adapter by inserting the syringe tip into the adapter opening while pressing and twisting firmly in a clockwise direction until the connection is secure.

1. Slowly push the plunger rod to inject all of the solvent into the ReFacto AF vial.

1. With the syringe still connected to the adapter, gently swirl the vial until the powder is dissolved.

1. Visually inspect the final solution for particles before administration. The solution should appear clear to slightly opalescent and colorless.

Note: If you use more than one vial of ReFacto AF per infusion, each vial must be reconstituted following the above instructions. The solvent syringe should be removed, leaving the vial adapter in place, and another large luer-lock syringe can be used to withdraw the reconstituted contents from each individual vial.

1. Make sure the syringe plunger rod is still fully inserted, turn the vial upside down, and slowly put all of the solution back into the syringe through the vial adapter.

1. Separate the syringe from the vial adapter by pulling the syringe and twisting it counterclockwise. Discard the vial with the adapter.

Note: If the reconstituted solution is not used immediately, the syringe cap should be carefully put back on. Do not touch the syringe tip or the inside of the cap.

ReFacto AF should be used immediately or within 3 hours after reconstitution. Before administration, the reconstituted solution can be stored at room temperature.

Administration (Intravenous Infusion):

ReFacto AF should be administered using the infusion set provided in this pack and the pre-filled syringe of solvent provided or a sterile disposable plastic syringe with a luer-lock connection.

1. Connect the syringe to the luer-lock connection of the infusion set.

1. Apply a tourniquet and prepare the injection site by cleaning the skin well with one of the provided alcohol swabs.

1. Insert the infusion set needle into the vein, following your doctor's instructions, and remove the tourniquet. Remove any air that may be in the infusion set by aspirating it into the syringe. The reconstituted product should be injected intravenously over several minutes. Your doctor may adjust the recommended infusion rate to make it more comfortable.

Discard the unused solution, empty vial(s), and used needles and syringes in an appropriate container for disposing of medical waste, as these materials may harm others if not disposed of properly.

If you use more ReFacto AF than you should

Consult your doctor or pharmacist.

If you stop using ReFacto AF

Do not stop using ReFacto AF without consulting your doctor.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Allergic reactions

If allergic reactions(anaphylactic) sudden, severeoccur, the infusion must be stopped immediately. You should contact your doctor immediatelyif you experience any of the following early symptoms of allergic reactions:

• rash, hives, urticaria, itching
• swelling of lips and tongue
• difficulty breathing, wheezing, chest tightness
• general feeling of being unwell
• dizziness and loss of consciousness

Severe symptoms, such as difficulty breathing and fainting (or near-fainting), require rapid emergency treatment. Anaphylactic reactions, sudden, severe are uncommon (may affect up to 1 in 100 patients)

Development of inhibitors

In children who have not received prior treatment with factor VIII medicines, inhibitor antibodies (see section 2) may occur very commonly (more than 1 in 10 patients); however, in patients who have received prior treatment with factor VIII (more than 150 days of treatment), the risk is uncommon (less than 1 in 100 patients). If this happens, the medicines you or your child are taking may stop working properly, and you or your child may experience persistent bleeding. In this case, contact your doctor immediately.

Very common side effects(may affect more than 1 in 10 patients)

• development of inhibitors in patients who have never been treated before with factor VIII products
• headache
• cough
• joint pain
• fever

Common side effects(may affect up to 1 in 10 patients)

• bleeding
• dizziness
• loss of appetite, diarrhea, vomiting, stomach pain, nausea
• hives, skin rash, itching
• muscle pain
• chills, reaction related to the catheter site
• some blood tests may show an increase in antibodies against factor VIII

Uncommon side effects(may affect up to 1 in 100 patients)

• development of inhibitors in patients who have been treated before with factor VIII products (less than 1 in 100 patients)
• severe allergic reaction
• numbness, drowsiness, altered taste
• chest pain, rapid heartbeat, palpitations
• low blood pressure, pain and redness of the veins related to the presence of blood clots, flushing
• difficulty breathing
• excessive sweating
• weakness, reaction at the injection site (including pain)
• mild increase in cardiac enzymes
• increase in liver enzymes, increase in bilirubin

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 leaflet. You can also report side effects directly through the national reporting system listed in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storing ReFacto AF

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 outer carton and on the label of the vial after EXP. The expiry date refers to the last day of the month shown.

Store and transport refrigerated (2°C-8°C). Do not freeze to prevent damage to the pre-filled syringe containing the solvent.

For your convenience, the medicine can be removed from the refrigerator and stored at room temperature (up to 25°C) for a single period of up to 3 months. At the end of this room temperature storage period, the product should not be returned to the refrigerator, but should be used or discarded. Write the date you removed ReFacto AF from the refrigerator and stored it at room temperature (up to 25°C) on the outer carton. Keep the vial in the outer carton to protect it from light.

The reconstituted product should be used within 3 hours after reconstitution.

The solution will be clear to slightly opalescent and colorless. Do not use this medicine if you notice it is turbid or contains visible particles.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.

6. Container contents and additional information

Composition of ReFacto AF

• The active ingredient is moroctocog alfa (recombinant coagulation factor VIII). Each vial of ReFacto AF nominally contains 250, 500, 1000, or 2000 IU of moroctocog alfa.

• The other components are sucrose, calcium chloride dihydrate, L-histidine, polysorbate 80, and sodium chloride (see section 2 "ReFacto AF contains sodium"). A solvent [sodium chloride injection solution 9 mg/ml (0.9%)] is also provided for reconstitution.

• After reconstitution with the solvent [sodium chloride solution 9 mg/ml (0.9%)], each vial contains 62.5; 125; 250, or 500 IU, respectively (depending on the potency of moroctocog alfa, i.e., 250, 500, 1000, or 2000 IU) of moroctocog alfa per 1 ml of prepared injection solution.

Appearance of the product and container contents

ReFacto AF is a glass vial with powder for injection and a solvent supplied in a pre-filled syringe.

The container contents are:

• a vial of 250, 500, 1000, or 2000 IU of moroctocog alfa powder
• a pre-filled syringe of solvent, 4 ml of sterile sodium chloride injection solution 9 mg/ml (0.9%), with a plunger rod
• a sterile vial adapter device for reconstitution
• a sterile infusion system
• two alcohol swabs
• adhesive tape
• a gauze

Marketing authorization holder

Pfizer Europe MA EEIG

Boulevard de la Plaine 17

1050 Brussels

Belgium

Manufacturer

Wyeth Farma S.A.

Autovía del Norte A-1 Km 23

Desvío Algete Km 1

28700 San Sebastián de los Reyes

Madrid

Spain

For further information on this medicinal product, please contact the local representative of the marketing authorization holder.

Date of last revision of this leaflet:

Detailed information on this medicinal product is available on the European Medicines Agency website: https://www.ema.europa.eu.