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Package Leaflet: Information for the User


REPLENINE®-VF 250 IU, 500 IU, 1000 IU
Please read all of this leaflet carefully before you start using this medicine.
• Keep this leaflet. You may need to read it again.
• If you have any further questions, please ask your doctor.
• This medicine has been prescribed for you personally. Do not pass it on to others. It may harm them, even if their
symptoms are the same as yours.
• If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor.
In this leaflet:
1. What Replenine-VF is and what it is used for
2. Before you use Replenine-VF
3. How to use Replenine-VF
4. Possible side effects
5. How to store Replenine-VF
6. Further information

Replenine-VF is a high purity factor IX from human blood plasma obtained from screened donors. It is a white sterile powder,
supplied with sterile water (Sterilised Water for Injections).
Replenine-VF is given by injection into a vein (intravenously) and is used to prevent and treat bleeding in patients with
haemophilia B (an inherited shortage of factor IX in the blood). Your doctor will explain further why this medicine has been
given to you.

DO NOT USE this medicine if you:
• are allergic (hypersensitive) to factor IX or to any of the other ingredients (See Section 6 ‘Further information’).
­Take special care with Replenine-VF if you:
• suddenly have unusual bruising and feeling very unwell, which may need specialist medical attention
• have heart or liver disease, which may need specialist medical attention
• have a risk of blood clotting
• have had surgery
• have a high level of antibodies to factor IX (Your doctor may give you an alternative treatment. He/she will check the level
of factor IX and antibodies in your blood before and after treatment, especially for your first injections).
When injecting, take special care to keep all needles sterile.
If you develop an allergic reaction (see Section 4 ‘Possible side effects’ for a list of these) stop the treatment and tell your
doctor immediately.
Your doctor will advise you about any vaccinations you may need as a routine precaution when using a blood plasma
Your doctor will be extremely careful about using Replenine-VF in new-born infants.
Taking other medicines
Please tell your doctor if you are taking, or have recently taken, any other medicines, including those obtained without a
These injections must not be mixed with other medicinal products.

Pregnancy and breast-feeding

If you are pregnant, think you may be pregnant or are breast-feeding, tell your doctor. Your doctor will tell you if this product
is necessary for you to take at this time.

Driving and using machines

There are no known effects of this product on your ability to drive or operate machinery.
Please note
When medicines are made from human blood or plasma, certain measures are put in place to prevent infections being passed on to patients.
These include careful selection of blood and plasma donors to make sure those at risk of carrying infections are excluded, and the testing of
each donation and pools of plasma for signs of virus/infections. Manufacturers of these products also include steps in the processing of the
blood or plasma that can inactivate or remove viruses. Despite these measures, when medicines prepared from human blood or plasma are
administered, the possibility of passing on infection cannot be totally excluded. This also applies to any unknown or emerging viruses or other
types of infection.
The measures taken are considered effective for enveloped viruses such as human immunodeficiency virus (HIV), hepatitis B virus and hepatitis
C virus and for the non-enveloped hepatitis A and parvovirus B19 viruses.
It is strongly recommended that every time you recieve a dose of Replenine-VF the name and batch number of the product are recorded in order
to maintain a record of the batches used.

Always use this medicine exactly as your doctor has told you. You should check with your doctor if you are not sure.
Replenine-VF should be administered directly into a vein. Use only the recommended injection equipment.
• Your doctor will explain how much you should use.
• The dose, especially the first dose, should be given slowly (approximately 3 mL per minute).
• After reconstitution, the injection should be completed within one hour and the solution must not be stored.
• If further treatment is needed, doses may be repeated at intervals of 8 to 24 hours, as required. Your doctor will advise you if
this is necessary.
The table gives the approximate doses of factor IX which are needed to stop bleeding in various conditions:
Initial dose of Replenine-VF
(IU/kg body weight)

Minor spontaneous bleeding in joints and muscles.

17 to 34

Severe bleeding in joints and muscles, bruising,
minor surgery, e.g. tooth extraction, cartilage repair.

25 to 51

Life-threatening bleeding, major surgery.*

51 to 85

Table 1- factor IX dosing instructions
* In major surgery Replenine-VF may be given either as individual injections or by continuous infusion over several days (see
also section: How much is given before, during and after major surgery?).
Your doctor will recommend the appropriate dose for young children. Generally the calculation of doses for children should follow
that for adults.
When to inject Replenine-VF

The medicine should be injected when the first sign of bleeding occurs.
The injection should be repeated as necessary to stop the bleeding.
Each individual bleed should be judged on its own severity.
Replenine-VF can also be injected as part of treatment to prevent bleeding starting.
If you are using this product for the first time, your doctor will supervise you.

Dissolving your medicine before use
Vial of Replenine-VF

Quantity of Water supplied

Quantity of Water for Half Volume

250 IU

5 mL

2.5 mL

500 IU

10 mL

5 mL

1000 IU

20 mL

10 mL

Table 2 - details of sterile water quantities

1. Replenine-VF must only be dissolved in the sterile water provided with the product.
2. Before you remove the “flip-off” top, make sure that the vial of Replenine-VF and the container of water supplied with it
are both at room temperature (between 20°C and 30°C).
3. Sterile water for use with Replenine-VF is provided in a glass vial with a stopper.
4. Replenine-VF is supplied with the amount of sterile water as shown on the table.
5. Your doctor will tell you if you can dissolve Replenine-VF in half the normal volume of sterile water.
How to Dissolve Replenine-VF
You can dissolve your product in two ways using the Transfer Device called Mix2VialTM:
(A) Dissolving in Full Volume or
(B) Dissolving with Half Volume
A) Dissolving in Full Volume
The Mix2VialTM Transfer Device is provided with your product for needle-free, easy and safe use.
Step 1
• Remove the cap from the product
vial and clean the top of the
stopper with an alcohol swab.
• Repeat this step with the sterile
water vial.
• Peel back the top of the Transfer
Device package but leave the
device in the package.

Step 4
• The sterile water will be pulled
into the product vial by the
vacuum contained within it.
• Gently swirl the vial to make sure
the product is thoroughly mixed.
Do not shake the vial.
• A clear or slightly pearl-like
solution should be obtained,
usually in about 2 to 21/2 minutes
(5 minutes maximum).

Step 2
• Place the blue end of the Transfer
Device on the water vial and push
straight down until the spike
penetrates the rubber stopper and
snaps into place.
• Remove the plastic outer packaging
from the Transfer Device and discard
it, taking care not to touch the
exposed end of the device.

Step 5
• Separate the empty water vial and
blue part from the clear part by
unscrewing anti-clockwise.
• Draw air into the syringe by pulling
the plunger to the required volume of
water added.
• Connect the syringe to the white filter.
• Push the air in the syringe into the

Step 3
• Turn the water vial upside down
with the device still attached.
• Place the clear end of the Transfer
Device on the product vial and
push straight down until the spike
penetrates the rubber stopper and
snaps into place.

Step 6
• Immediately invert the vial of
solution which will be drawn into
the syringe.
• Disconnect the filled syringe from
the device.
• The product is now ready for
administration. Follow the normal
safety practices for administration.

Note: If you have to use more than one vial to make up your required dose, repeat Steps 1 to 6 withdrawing the solution in the vial into the
same syringe.
The Transfer Device supplied with your product is sterile and cannot be used more than once. When the reconstitution process is complete
dispose of in your ‘sharps box’.

B) Dissolving with Half Volume
T o use the Transfer Device when dissolving Replenine-VF in half volumes, it is first necessary to remove and discard half the
volume of water from the vial of sterile water.
• Remove the “flip-off”cover from the vial of sterile water and clean the top of the stopper with an alcohol swab.
• Pierce the stopper of the vial of sterile water with a needle and syringe and draw up half the volume of sterile water.
• Check that the correct amount is withdrawn. The needle and syringe can now be safely disposed of (in your ‘sharps box’).
• The remaining sterile water in the vial will be used for reconstitution (half the original volume). See Table 2 for quantities of
To complete the dissolving process follow steps 1-6 in Section A above. The product is then ready for administration.
Do not use this medicine if:
• the water is not pulled into the product vial with either method of reconstitution (this indicates a loss of vacuum in the vial,
so the product must not be used).
• the dissolved product and Sterilised Water for Injections form a gel or a clot (if this happens, please tell Bio Products
Laboratory, reporting the batch number printed on the vial).
Do not use solutions which are cloudy or have bits in them.
Administration User Kit
This additional carton can be provided upon request from Bio Products Laboratory, which will include:
Alcohol swabs: one is used to clean the vial stoppers after flipping off the caps. The other should be used to disinfect
your skin at the injection site.
Winged Infusion set: a butterfly No. 23 needle for administration of the product.
20 mL syringe: the dissolved solution is withdrawn into the syringe. This size of syringe is provided to enable more than
one vial to be administered using one syringe.
to stick on the injection site after administration.
Injecting the Medicine
After the medicine is dissolved:
• To inject the medicine, attach a suitable needle to the syringe.
• The dose, especially your first dose, should be given slowly (no more than 3 mL per minute) into your vein.
– the solution must not be stored after reconstitution.
– you must finish injecting the dose into a vein within one hour of dissolving the medicine.
– the solution must not be added to any other fluids, blood or any other medicine.
– you should only use the sterile water supplied to make up the solution, never inject the water on its own, without first
dissolving the powder in it.
How much is given before, during and after major surgery?
(See also the Table 1 on Page 2)
Before: Major surgery should only be performed when levels of factor IX and factor IX inhibitors (antibodies) in your blood can
be tested.
If antibodies are not present, a dose is given before the operation to increase the level in your blood to between 80 and 100
IU/dL, usually about 65-85 IU per kg of body weight.
After: During the first few days after the operation, the plasma factor IX concentration will be checked at regular periods. A dose of
Replenine-VF (factor IX) is usually given every 8 to 24 hours, as needed.
After the first few days, the number of doses may be reduced.
Treatment is usually continued for 7 days or longer, depending on the type of operation.

I f the factor IX concentration does not reach the expected level (this will be tested by your doctor), or if it decreases faster
than expected (within 12 hours), an inhibitor of factor IX may be present which stops it from working properly. Your doctor will
arrange for the appropriate laboratory tests to see if there is such an inhibitor present.
If you use more Replenine-VF than you should
If you think you may be using too much, stop the injection and tell your doctor.
If you know you have used too much, tell your doctor as soon as possible.
If you forget to use Replenine-VF
Do not use a double dose to make up for a forgotten dose.
If you stop using Replenine-VF
Always consult your doctor before deciding to stop your treatment.

As with all medicines, Replenine-VF may cause side effects, although not everybody gets them.
Hypersensitivity or allergic reactions have been observed infrequently in patients treated with factor IX containing products.
If you get any of the following symptoms, stop the infusion and tell your doctor immediately:
• swelling around the face and throat
• nettle-rash (urticaria)
• restlessness
• burning and stinging at the infusion site
• hives
• rapid heart beat
• chills
• low blood pressure
• tightness of the chest or wheezing
• flushing
• lethargy
• tingling
• nausea or vomiting
 idney problems (such as nephrotic syndrome) have been reported in some haemophilia B patients who have inhibitors
(antibodies) to factor IX and a history of allergic reaction to factor IX containing products.
Inhibitors (antibodies) may develop to factor IX during treatment. This could mean that the treatment does not work properly.
If bleeding does not stop after an injection, then speak to your doctor.
On rare occasions, fever has been observed (in fewer than 1 in 1,000 people).
The use of low purity factor IX products has been associated with heart attack, thrombosis and blood coagulation. The use of
high purity factor IX, such as Replenine-VF, is rarely associated with such side effects.
In clinical trials with Replenine-VF, the following side effects have been reported in fewer than 1 in 10 people.
• Reaction at the injection site, e.g. irritation, inflammation.
• Headache.
If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor.

• Keep out of the reach and sight of children.

• You should store the powder in its container and carton, in the dark in the refrigerator. Do not freeze. Short periods of
storage at room temperature, in the dark, will not damage the product.
• The vial of sterilised water that comes with the medicine should also be stored in the refrigerator. Do not freeze.
• Do not use the medicine or the sterilised water after the expiry date, which is stated as “EXPIRY” on the containers. The
expiry date refers to the last day of that month.
• Do not use the sterilised water if any small bits can be seen in it.
• Once reconstituted, Replenine-VF must be used within one hour.
After injection of the correct dose, dispose of any solution that remains, along with used syringes, needles and containers. Ask
your doctor for a special container (‘sharps box’) for this purpose and take it back to the doctor or pharmacist when full.
Medicines should not be disposed of via wastewater or household waste.

What Replenine-VF contains
The active substance is human coagulation factor IX.
The other ingredients are: protein, glycine, lysine, sodium, citrate, phosphate and chloride.
What Replenine-VF looks like and the contents of the pack
Replenine-VF is a white, crumbly, sterile powder and is packed in quantities of 250 International Units (IU), 500 IU or 1000 IU
in glass vials. These vials are closed with a synthetic rubber stopper under vacuum, held on by a tamper-evident cap.
Replenine-VF should only be reconstituted with Sterilised Water for Injections which is supplied with Replenine-VF in clear
glass bottles.
Provided with the product is a Transfer Device called Mix2VialTM to enable needle-free, easy and safe reconstitution.
An Administration User Kit can be provided upon request which contains: a sterile 20 mL plastic syringe, a single winged
infusion set (butterfly needle), alcohol swabs and a sterile plastic dressing.
Marketing Authorisation Holder and manufacturer
Bio Products Laboratory Limited, Dagger Lane, Elstree, Herts. WD6 3BX, United Kingdom
Marketing Authorisation Number
PL 08801/0028
This leaflet was last approved in
November 2012
For further information or if you have any questions about the use of this product, please contact BPL via the Marketing
Department at the address above or through

Bio Products Laboratory Limited,
Dagger Lane, Elstree, Herts. WD6 3BX, U.K.
Tel: +44 (0)20 8957 2200


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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.