NUWIQ 1500 IU POWDER AND SOLVENT FOR INJECTABLE SOLUTION

2. What you need to know before you use Nuwiq

Do not use Nuwiq:

• if you are allergic to the active substance turoctocog alfa or any of the other ingredients of this medicine (listed in section 6).

If you are not sure, ask your doctor.

Warnings and precautions

Talk to your doctor before you start using Nuwiq.

There is a rare possibility that you may experience an allergic reaction (a sudden severe allergic reaction) to Nuwiq. You should be able to recognise the early signs of allergic reactions, which are listed in section 4 "Allergic reactions".

If any of these symptoms occur, stop the injection immediately and contact your doctor.

The formation of inhibitors (antibodies) is a known complication that can occur during treatment with all factor VIII medicines. These inhibitors, especially in large quantities, can prevent the treatment from working properly, so you and your child will be carefully monitored for the development of such inhibitors. If your bleeding or your child's bleeding is not controlled with Nuwiq, contact your doctor immediately.

Cardiovascular events

In patients with cardiovascular risk factors, replacement therapy with FVIII may increase the risk of cardiovascular events.

Complications associated with catheters

If you require a central venous access device (CVAD), the risk of CVAD-associated complications, including localised infections, bacteria in the blood, and thrombosis at the catheter implantation site, should be considered.

It is important to keep a record of the batch number of Nuwiq. Therefore, each time you receive a new pack of Nuwiq, note the date and batch number (indicated on the pack after Batch) and keep this information in a safe place.

Other medicines and Nuwiq

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

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before using this medicine.

Driving and using machines

Nuwiq does not affect the ability to drive and use machines.

Nuwiq contains sodium

This medicine contains 18.4 mg of sodium (a major component of cooking/table salt) in each vial. This is equivalent to 0.92% of the maximum recommended daily intake of sodium for an adult.

3. How to use Nuwiq

Treatment with Nuwiq will be started by a doctor who has experience in the care of patients with haemophilia A. Follow exactly the instructions for administration of this medicine given by your doctor or nurse. If you are unsure, ask your doctor or nurse again.

Nuwiq is usually injected into a vein (intravenously) by your doctor or a nurse with experience in the care of patients with haemophilia A. You or another person may also inject Nuwiq, but only after you have received appropriate training.

Your doctor will calculate your dose of Nuwiq (in International Units = IU) based on your condition and body weight and whether it is being used for prevention or treatment of bleeding. How often you need an injection will depend on how well Nuwiq works for you. Normally, treatment of haemophilia A is lifelong.

Prevention of bleeding

The usual dose of Nuwiq is 20 to 40 IU per kg body weight, administered every 2 to 3 days. However, in some cases, especially in younger patients, more frequent injections or higher doses may be needed.

Treatment of bleeding

The dose of Nuwiq is calculated based on your body weight and the factor VIII levels that need to be achieved. The target factor VIII levels will depend on the severity and location of the bleeding.

If you think that the effect of Nuwiq is too weak, talk to your doctor. Your doctor will do the relevant laboratory tests to make sure you have adequate factor VIII levels. This is especially important if you are going to have major surgery.

Patients who develop factor VIII inhibitors

If your plasma factor VIII level does not reach the expected level with Nuwiq, or if bleeding is not adequately controlled, it may be due to the development of factor VIII inhibitors. Your doctor will check this. You may need a higher dose of Nuwiq or a different product to control bleeding. Do not increase the total dose of Nuwiq to control your bleeding without talking to your doctor.

Use in children and adolescents

The way Nuwiq is used in children and adolescents does not differ from the way it is used in adults. Since it may be necessary to administer factor VIII medicines more frequently in children and adolescents, a central venous access device (CVAD) may be needed. A CVAD is an external connector that allows access to the bloodstream through a catheter without injection through the skin.

If you use more Nuwiq than you should

No symptoms of overdose have been reported. If you have injected more Nuwiq than you should, talk to your doctor.

If you forget to use Nuwiq

Do not take a double dose to make up for forgotten doses. Proceed with the next dose as planned and follow your doctor's recommendations.

If you stop using Nuwiq

Do not stop using Nuwiq without talking to your doctor.

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

4. Possible side effects

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

Stop using this medicine and seek urgent medical attention if:

• you notice symptoms of allergic reactions

Allergic reactions can include skin rash, hives, itching (urticaria), including generalised urticaria, swelling of the lips and tongue, difficulty breathing, wheezing, chest tightness, vomiting, agitation, low blood pressure, and dizziness. These symptoms can be early signs of anaphylactic shock. If severe allergic reactions (anaphylactic reactions) (very rare: may affect up to 1 in 10,000 people) occur, stop the injection immediately and contact your doctor. Severe symptoms require urgent emergency treatment.

• you notice that the medicine is not working properly (bleeding does not stop or becomes frequent)

In children and adolescents who have not been treated previously with factor VIII medicines, inhibitory antibodies (see section 2) may occur very frequently (more than 1 in 10 patients).

However, in patients who have been treated previously 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.

Common side effects that may affect up to 1 in 10 people

Hypersensitivity, fever.

Uncommon side effects that may affect up to 1 in 100 people

Tingling or numbness (paraesthesia), headache, dizziness, vertigo, shortness of breath, dry mouth, back pain, swelling and/or pain at the injection site, a vague feeling of being unwell (malaise), haemorrhagic anaemia, positive test results for non-neutralising antibody formation (in previously treated patients).

Reporting of side effects

If you experience any side effects, talk to your doctor. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via 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. Storage of Nuwiq

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 carton and on the label of the vial after EXP. The expiry date is the last day of the month stated.

Store in a refrigerator (2°C to 8°C). Do not freeze. Keep the vial in the outer carton in order to protect from light.

Before Nuwiq powder is reconstituted, it can be stored at room temperature (up to 25°C) for a single period not exceeding 1 month. Note the date when you start storing Nuwiq at room temperature on the carton. Do not store Nuwiq in the refrigerator again after it has been stored at room temperature.

Use the reconstituted solution immediately after reconstitution.

Warnings regarding visible signs of deterioration

Do not use this medicine if you notice visible signs of deterioration of the pack, especially the syringe and/or the vial.

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

Nuwiq Composition

Powder:

• The active ingredient is human recombinant coagulation factor VIII (simoctocog alfa).

Each powder vial contains 250, 500, 1000, 1500, 2000, 2500, 3000, or 4000 IU of simoctocog alfa. Each reconstituted solution contains approximately 100, 200, 400, 600, 800, 1000, 1200, or 1600 IU/mL of simoctocog alfa.

• The other components are sucrose, sodium chloride, calcium chloride dihydrate, arginine hydrochloride, sodium citrate dihydrate, and poloxamer 188. See section 2, "Nuwiq contains sodium".

Solvent:

Water for injections

Product Appearance and Container Contents

Nuwiq is supplied as a powder and solvent for solution for injection. The powder is white or almost white in a glass vial. The solvent is water for injections in a pre-filled glass syringe.

After reconstitution, the solution is clear, colorless, and free from foreign particles.

Each Nuwiq container contains:

• 1 vial of powder with 250, 500, 1000, 1500, 2000, 2500, 3000, or 4000 IU of simoctocog alfa
• 1 pre-filled syringe with 2.5 mL of water for injections
• 1 vial adapter
• 1 butterfly needle
• 2 alcohol swabs

Marketing Authorization Holder and Manufacturer

Octapharma AB, Lars Forssells gata 23, 112 75 Stockholm, Sweden

For further information about 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: http://www.ema.europa.eu.

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This information is intended for healthcare professionals only:

On-demand treatment

The dose to be administered and the frequency of administration should always be oriented towards clinical efficacy in each individual case.

In the case of the following hemorrhagic episodes, factor VIII activity should not be below the given plasma activity level (as a percentage of normal or IU/dL) during the corresponding period. The following table can be used as a dosing guide in surgery and hemorrhagic episodes.

INSTRUCTIONS FOR PREPARATION AND ADMINISTRATION

1. Allow the solvent syringe (water for injections) and the powder to reach room temperature in the closed vial. You can do this by holding them in your hands until they reach the same temperature as your hands. Do not heat the vial and pre-filled syringe in any other way. This temperature should be maintained during reconstitution.
2. Remove the flip-off plastic cap from the powder vial to expose the central part of the rubber stopper. Do not remove the gray stopper or the metal ring surrounding the top of the vial.

1. Clean the top of the vial with an alcohol swab. Let the alcohol dry.
2. Remove the paper cover from the vial adapter package. Do not remove the adapter from its package.

1. Place the powder vial on a flat surface and hold it. Take the adapter package and place the vial adapter over the center of the rubber stopper of the powder vial. Press the adapter package firmly downwards until the adapter spike penetrates the rubber stopper. The adapter will be secured to the vial when done.

1. Remove the paper cover from the pre-filled syringe package. Hold the plunger rod by the end and do not touch the shaft. Attach the threaded end of the plunger rod to the syringe plunger. Turn the plunger rod clockwise until you feel a slight resistance.

1. Break the plastic protective tip of the solvent syringe by snapping the perforation of the flip-off cap. Do not touch the inside of the flip-off cap or the tip of the syringe. If you do not use the solution immediately, close the filled syringe with the plastic protective tip for storage.

1. Remove the adapter packaging and discard it.
2. Firmly attach the solvent syringe to the vial adapter by turning it clockwise until you feel a slight resistance.

1. Slowly inject all of the solvent into the powder vial by pressing the plunger rod downwards.

1. Without removing the syringe, gently swirl or rotate the vial a few times to dissolve the powder. Do not shake. Wait until all of the powder is completely dissolved.
2. Check the final solution for particles before administering. The solution should be clear and colorless, practically free from visible particles. Do not use cloudy or sedimented solutions.
3. Turn the vial attached to the syringe upside down, and slowly withdraw the solution into the syringe. Make sure to transfer all of the vial contents into the syringe.

1. Separate the filled syringe from the vial adapter by turning it counterclockwise and discard the empty vial.
2. The solution is now ready for immediate use. Do not refrigerate.
3. Clean the chosen injection site with one of the provided alcohol swabs.
4. Attach the provided injection kit to the syringe. Insert the injection kit needle into the chosen vein. If you have used a tourniquet to make the vein more visible, it should be released before starting to inject the solution. Blood should not enter the syringe due to the risk of fibrin clot formation.
5. Inject the solution into the vein slowly, no faster than 4 mL per minute.

If you use more than one vial of powder for a treatment, you can use the same needle again. The vial adapter and syringe are for single use only.