HIZENTRA 200 mg/mL Subcutaneous Injectable Solution

2. What you need to know before you use Hizentra

DO NOTinfuse Hizentra:

• If you are allergic to human immunoglobulins, polysorbate 80, or L-proline.
• Tell your doctor or healthcare professional before treatment if you have previously experienced intolerance to any of these components.
• If you have hyperprolinemia (a genetic disorder caused by high levels of the amino acid proline in the blood).

Into blood vessels.

Warnings and precautions

• Consult your doctor, pharmacist, or nurse before using Hizentra.

You may be allergic (hypersensitive) to immunoglobulins without knowing it. However, true allergic reactions are rare. They can occur even if you have previously received human immunoglobulins and tolerated them well. This can happen especially if you do not have enough immunoglobulin A (IgA) in your blood (IgA deficiency).

• Tell your doctor or healthcare professional if you have an IgA deficiency before starting treatment. Hizentra contains residual amounts of IgA that can cause allergic reactions.

In these rare cases, allergic reactions can occur, such as a sudden drop in blood pressure or shock(see also section 4 "Possible side effects").

• If you notice symptoms of this type during the infusion of Hizentra, stop the infusion and contact your doctor or go to the nearest hospital immediately.

• Tell your doctor if you have a history of heart or vascular disease, or if you have had blood clots, have thick blood, or have been immobilized for a period. These factors can increase your risk of developing a blood clot after taking Hizentra. Also, tell your doctor what medications you are taking, as some contain estrogens (a hormone found, for example, in birth control pills) that can increase your risk of developing a blood clot. Contact your doctor immediately if you experience signs and symptoms such as difficulty breathing, chest pain, pain and swelling of a limb, weakness, or numbness of one side of the body after taking Hizentra.

• Contact your doctor if you experience the following signs and symptoms: severe headache, stiff neck, drowsiness, fever, photophobia, nausea, and vomiting after taking Hizentra. Your doctor will decide if further tests are needed and if you should continue treatment with Hizentra.

Your healthcare professional will avoid possible complications by checking that:

• You are not sensitive to human normal immunoglobulin.

The product must be injected at a slow initial rate. The recommended injection rate in section 3 "How to use Hizentra" must be strictly followed.

• Any symptoms are closely monitored during the entire infusion period, especially if:

this is the first time you receive human normal immunoglobulin

• you have changed from another treatment
• a prolonged period (more than 8 weeks) has passed since your last infusion.

In these cases, you should be observed during the first infusion and for one hour after. If the above points do not apply to you, it is recommended that you be observed for at least 20 minutes after administration.

Interaction of Hizentra with other medicines

• Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
• Do not mix Hizentra with other medicines.
• Before vaccination, tell your doctor about your treatment with Hizentra.

Hizentra may alter the effect of some live virus vaccines such as measles, mumps, rubella, and varicella vaccine. Therefore, after administration of these medicines, you should wait at least 3 months before receiving a live attenuated vaccine. In the case of the measles vaccine, this alteration may persist for up to 1 year.

Pregnancy, breastfeeding, and fertility

• If you are pregnant or breastfeeding, or think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist. Your doctor will decide whether you can receive Hizentra during pregnancy or while breastfeeding.

No studies have been conducted with Hizentra in pregnant women. However, medicines containing immunoglobulin have been used in pregnant or breastfeeding women for years, and no adverse effects have been observed in the course of pregnancy or in the baby.

If you are breastfeeding and receive Hizentra, the immunoglobulins in the medicine may also be found in breast milk. Therefore, your baby may be protected against some infections.

Driving and using machines

During treatment with Hizentra, patients may experience effects such as dizziness or nausea that could affect the ability to drive and use machines. If this happens, do not drive or use machines until these effects have disappeared.

Hizentra contains proline

Do not take this medicine if you have hyperprolinemia (see also section 2 "What you need to know before you use Hizentra"). Tell your doctor before treatment.

Other important information about Hizentra

Blood tests

After receiving Hizentra, the results of some blood tests (serological tests) may be altered for some time.

• Before having any blood tests, tell your doctor about your treatment with Hizentra.

Information about the components of Hizentra

Hizentra is made from human blood plasma (the liquid part of the blood). When medicines are made from blood or plasma, certain measures are taken to prevent the transmission of infections to patients. These measures include:

• careful selection of blood or plasma donors to ensure the exclusion of potential carriers of infections, and
• testing of each donation and plasma pools for the absence of signs of viruses or infections.

Manufacturers of these medicines also include steps in the processing of blood or plasma that can inactivate or remove viruses. Despite these measures, when administering medicines prepared from human blood or plasma, the possibility of transmitting an infection cannot be completely excluded. This is also true for any unknown or emerging virus or other type of infection.

The measures taken are considered effective for enveloped viruses such as human immunodeficiency virus (HIV, the AIDS virus), hepatitis B virus, and hepatitis C virus (inflammation of the liver), and for non-enveloped viruses such as hepatitis A virus and parvovirus B19.

• It is strongly recommended that, each time you receive a dose of Hizentra, you note the name and batch number of the product, in order to maintain a record of the batches used (see section 3, "How to use Hizentra").

Hizentra contains sodium

This medicine contains less than 23 mg of sodium (1 mmol) per vial/syringe; i.e., it is essentially "sodium-free".

3. How to use Hizentra

Follow your doctor's administration instructions for this medication exactly. Consult your doctor if you have any doubts.

Dose

Your doctor will decide how much Hizentra you will receive, based on your weight and response to treatment.

The dose or administration interval should not be changed without consulting your doctor.

If you think you should receive Hizentra more or less frequently, please consult your doctor. If you think you have missed a dose, talk to your doctor as soon as possible.

Substitution therapy

Your doctor will determine if you need a loading dose (for adults and children) of at least 1 to 2.5 ml/kg of body weight divided over several days. After that, maintenance doses will be administered at repeated intervals, from once a day to once every two weeks, to achieve a cumulative monthly dose of between 2 and 4 ml/kg of body weight. Your healthcare professional may adjust the dose based on your response to treatment.

Immunomodulatory therapy

Your doctor will start Hizentra therapy one week after your last intravenous infusion of immunoglobulin, administering it subcutaneously with a weekly dose of 1.0 to 2.0 ml/kg of body weight. Your doctor will determine your weekly dose of Hizentra. The weekly maintenance doses can be divided into smaller doses and administered as frequently as required during the week. For bi-weekly regimens, your doctor will double the weekly dose of Hizentra. Your healthcare professional may adjust the dose based on your response to treatment.

Form and route of administration

In the case of home treatment, this must be initiated by a healthcare professional with experience in the treatment of immunodeficiency/SCID with SCIG and in instructing patients for home treatment.

You will be instructed and trained in:

• aseptic infusion techniques,
• maintaining a treatment diary, and
• measures to take in case of serious adverse effects.

Infusion site(s)

• Administer Hizentra only by the subcutaneous route.
• You can infuse Hizentra at sites such as the abdomen, thigh, arm, and lateral hip. In the case of high doses (> 50 ml), administer at multiple sites.
• You can use an unlimited number of injection sites simultaneously. The sites where injections are applied must be at least 5 cm apart.
• If you use the assisted infusion device technique (e.g., pump-assisted infusion), you can use more than one infusion device simultaneously.
• If you use the manual push technique with a syringe, you can only use one infusion site per syringe. If you need to administer an additional syringe of Hizentra, you must use a new sterile needle and change the infusion site.
• The volume of product infused at a given site may vary.

Infusion rate(s)

Your doctor will determine the appropriate infusion technique and infusion rate for you, taking into account your individual dose, dosing frequency, and product tolerability.

Device-assisted infusion:

The recommended initial infusion rate is up to 20 ml/hour per site. If well tolerated, the infusion rate can be gradually increased to 35 ml/hour per site for the next two infusions. From then on, the infusion rate can be increased according to your tolerability.

Manual push:

The recommended initial infusion rate is up to 0.5 ml/minute per site (30 ml/hour per site). If well tolerated, the infusion rate can be increased up to 2.0 ml/minute per site (120 ml/hour per site) for subsequent infusions. From then on, the infusion rate can be increased further according to your tolerability.

Instructions for use

If you have any doubts about using this product, consult your doctor, pharmacist, or nurse.

If you use more Hizentra than you should

Inform your doctor as soon as possible if you think you have received too much Hizentra.

If you miss a dose of Hizentra

Inform your doctor as soon as possible if you think you have missed a dose.

4. Possible side effects

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

• In isolated cases, you may be allergic (hypersensitive) to immunoglobulins and may experience allergic reactions such as a sudden drop in blood pressure or shock (e.g., you may feel dizzy or lightheaded, feel dizzy when standing up, have cold hands and feet, an unusual heart rhythm or chest pain, or have blurred vision).
• In isolated cases, you may experience pain and/or swelling of an arm or leg with heat in the affected area, discoloration of an arm or leg, unexplained shortness of breath, chest pain or discomfort that worsens with deep breathing, rapid heartbeat, or numbness or weakness on one side of the body, sudden confusion or difficulty speaking or understanding, which could be signs of a blood clot.
• In isolated cases, you may have a severe headache with nausea, vomiting, stiffness in the neck, fever, and sensitivity to light, which could be signs of aseptic meningitis syndrome (AMS), a temporary, reversible, non-infectious inflammation of the membranes surrounding the brain and spinal cord.

• If you notice such signs during Hizentra infusion, interrupt the infusion and go to the nearest hospital immediately.

See also section 2 of this leaflet on the risk of allergic reactions, blood clots, and AMS.

The side effects observed in controlled clinical trials are presented in decreasing order of frequency. The side effects observed post-marketing are of unknown frequency:

The following side effects are very common(affect more than 1 in 10 patients):

• Headache
• Rash
• Infusion site reactions

The following side effects are common(affect between 1 and 10 patients in 100):

• Dizziness
• Migraine
• Increased blood pressure (hypertension)
• Diarrhea
• Abdominal pain
• General discomfort (nausea)
• Vomiting
• Itching (pruritus)
• Hives (urticaria)
• Musculoskeletal pain (musculoskeletal pain)
• Fever
• Joint pain (arthralgia)
• Fatigue (fatigue), including malaise (general discomfort)
• Chest pain
• Flu-like symptoms
• Pain

The following side effects are uncommon(affect between 1 and 10 patients in 1,000):

• Hypersensitivity
• Involuntary movement disorders in one or more parts of the body (tremors, including psychomotor hyperactivity)
• Rapid heartbeat (tachycardia)
• Redness
• Muscle spasms
• Muscle weakness
• Chills, including low body temperature
• Abnormal blood test results that may indicate liver and kidney function disorders

In isolated cases, an ulcer may occur at the infusion site or a burning sensation.

• You can reduce possible side effects if you infuse Hizentra slowly.

These side effects may occur even if you have previously received human immunoglobulins and tolerated them well.

Also, consult section 2 "What you need to know before you start using Hizentra", where you will find additional information on factors that may increase the risk of side effects.

Reporting of side effects

If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet. You can also report them directly through the Spanish Medicines Surveillance System for Human Use: www.notificaRAM.es.

By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of Hizentra

• Keep this medicine out of the sight and reach of children.
• Do not use this medicine after the expiration date stated on the carton and label of the vial after EXP.
• You must use/infuse this medicine as soon as possible after opening the vial. Do not use Hizentra if the vial is open or defective.
• Do not store above 25 °C.
• Do not freeze.
• Keep the vial in the outer packaging to protect it from light.
• Do not throw away medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. This will help protect the environment.

6. Package contents and additional information

Composition of Hizentra

• The active substanceis normal human immunoglobulin. One ml contains 200 mg of normal human immunoglobulin, of which at least 98% is immunoglobulin G (IgG).

The approximate percentage of IgG subclasses is as follows:

IgG1 .................................. 69%

IgG2 .................................. 26%

IgG3 .................................. 3%

IgG4 .................................. 2%

This medicine contains traces of IgA (no more than 50 micrograms/ml).

• The other ingredients(excipients) are L-proline, polysorbate 80, and water for injectable preparations.

Appearance of Hizentra and package contents

Hizentra is a subcutaneous injectable solution (200 mg/ml). The color may vary from pale yellow to light brown.

Hizentra is available in vials of 5, 10, 20, or 50 ml.

Hizentra is also available in pre-filled syringes of 5, 10, 20, and 50 ml.

Package sizes

Packs of 1, 10, or 20 vials.

Hizentra is also available in packs of 1 (for 5, 10, 20, 50 ml) or 10 (for 5, 10, 20 ml) or 20 (for 10, 20 ml) pre-filled syringes.

Please note that this package does not contain alcohol swabs, needles, or other accessories or equipment.

Not all package sizes may be marketed.

Marketing authorization holder and manufacturer

CSL Behring GmbH

Emil-von-Behring-Strasse 76

D-35041 Marburg

Germany

You can request more information about this medicine from the local representative of the marketing authorization holder:

Date of last revision of this leaflet:

Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu/.

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