Octaplaslg Solution For Infusion
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PACKAGE LEAFLET: INFORMATION FOR THE USER
octaplasLG® 45 - 70 mg/mL solution for infusion
Human plasma proteins
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, ask your doctor.
- This medicine has been prescribed for you. 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 octaplasLG® is and what it is used for
2. Before you use octaplasLG®
3. How to use octaplasLG®
4. Possible side effects
5. How to store octaplasLG®
6. Further information
1. WHAT octaplasLG® IS AND WHAT IT IS USED FOR
octaplasLG® is human plasma pooled and treated for virus inactivation. Human plasma is the fluid part of human blood that carries the cells. It contains human plasma proteins which are important to maintain normal clotting characteristics and is used the same way as normal fresh-frozen plasma (FFP).
octaplasLG® helps in case of complex deficiencies of coagulation factors which can be caused by severe failure of the liver or massive transfusion. octaplasLG® may also be given in emergency situations when a coagulation factor concentrate (such as Factor V or Factor XI) is not available or a necessary laboratory diagnosis is not possible.
It may also be given to rapidly reverse the effects of oral anticoagulants (coumarin or indanedione type), when vitamin K is insufficient due to impaired liver function or in emergency situations.
octaplasLG® can be given to patients who undergo plasma exchange in order to restore the balance of the coagulation factors.
2. BEFORE YOU USE octaplasLG®
Do not use octaplasLG®
- if you are allergic (hypersensitive) to human plasma proteins or any of the other constituents of octaplasLG® (please refer to section 6).
- if you know you have antibodies against the immunoglobulin called IgA.
- if you had previous reactions to any preparation of human plasma or FFP.
- if you know you have a low level of protein S (a Vitamin K dependent protein in your blood).
Take special care with octaplasLG®
- if you have a low level of immunoglobulin A.
- if you had previous reactions to plasma protein including FFP.
- if you are suffering from heart failure or fluid in the lungs (pulmonary oedema).
- if you have known risks for blood clotting (thrombotic) complications because of the potential increased risk of venous thromboembolism (clots forming in your veins).
- in case of increased inhibition of coagulation (fibrinolysis).
- Tell your doctor if you have any other illnesses.
octaplasLG® is not generally recommended for the treatment of von Willebrand's Disease.
Virus safety
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 the 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 the viruses. Despite these measures, when medicines prepared from human blood or plasma are administrated, the possibility of passing on infection cannot be totally excluded. This also applies to any unknown or emerging viruses or other types of infections.
The measures taken are considered effective for enveloped viruses such as human immunodeficiency virus (HIV), hepatitis B virus and hepatitis C virus.
The measures taken may be of limited value against certain non-enveloped viruses such as hepatitis A virus, hepatitis E virus and Parvovirus B19.
It is strongly recommended that every time you receive a dose of octaplasLG® the name and batch number of the product are recorded in order to maintain a record of the batch used.
Your doctor may recommend that you consider vaccination against hepatitis A and B viruses if you regularly/repeatedly receive human plasma-derived products.
Using other medicines
During clinical trials, octaplasLG® has been administered in combination with various other medications, and no interactions have been identified.
octaplasLG® may not be mixed with other intravenous fluids or medicines except red blood cells and blood platelets.
To avoid the possibility of blood clots, solutions containing calcium must not be administered by the same intravenous pathway as octaplasLG®.
There are no known reactions with other drugs.
Please tell your doctor if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.
Using octaplasLG® with food and drink
No effects have been observed.
Pregnancy and breast-feeding
If you are pregnant you must tell your doctor. You will only be given octaplasLG® if your doctor considers it important for you.
Ask your doctor for advice before taking any medicine.
Driving and using machines
No effect has been observed upon the ability to drive or operate machinery. You alone are responsible to decide if you are in a fit condition to drive a motor vehicle or perform other tasks that demand increased concentration.
Important information about some of the ingredients of octaplasLG®
Not applicable. For a list of incredients please refer to section 6.
3. HOW TO USE octaplasLG®
Always use octaplasLG® exactly as your doctor has told you. You should check with your doctor if you are not sure.
- octaplasLG® may be thawed using a water bath or a dry tempering system such as the SAHARA III.
Allow the content of the bag to warm to approximately +37°C before infusion, but the temperature of octaplasLG® must not exceed +37°C.
Using a water bath the thawing procedure should not take more than 30 minutes.
Using a dry tempering system the course of temperature of octaplasLG® should be recorded. The tempering process should be terminated when +37°C is indicated on the display/recorder.
- Before octaplasLG® can be given to you by infusion an ABO-blood group compatibility test must be performed.
- In emergency cases, octaplasLG® blood group AB can be given to all patients.
octaplasLG® is given by an infusion into your veins. It is important that the infusion rate should not exceed 1 mL octaplasLG® per kg of your body weight per minute.
Your dosage depends upon your clinical situation and your body weight. Your doctor will determine the appropriate amount that you should receive.
Special dosage recommendations:
- The dosage for coagulation factor deficiencies is 5 to 20 mL octaplasLG® per kg of your body weight.
- In TTP patients the whole plasma volume exchanged should be replaced with octaplasLG®.
- For the treatment of bleeding within the body (haemorrhages) in intensive plasma exchange procedures your doctor will determine the necessary dosage.
- Calcium gluconate may be given into another vein to minimise the negative effects of the citrate contained in octaplasLG®.
You should be observed during and at least for 20 minutes after the administration in case you develop an allergic reaction (anaphylactic reaction) or shock, in which case the infusion must be stopped immediately.
If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor.
5. HOW TO STORE octaplasLG®
Keep out of sight and out of reach of children.
Store in a freezer at < - 18°C and protect from light.
octaplasLG® has a shelf-life of 4 years starting from the day of manufacturing.
Do not use octaplasLG® after the expiry date which is stated on the label and the carton after the abbreviation EXP. The expiry date refers to the last day of the month.
After thawing octaplasLG® can be stored for up to 8 hours at +4°C or for up to 4 hours at room temperature (+20 to +25°C) before use, provided that the bag has not been opened.
Once the bag has been opened, the product must be used immediately.
Thawed octaplasLG® must not be refrozen. Unused product must be discarded.
Do not use octaplasLG® if you notice that the solution is cloudy or contains deposits.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.
If you use more octaplasLG® than you should
High dosages may lead to fluid overload, fluid in lungs and/or heart problems.
If you forget to use octaplasLG®
Your doctor is responsible to supervise administration and to keep your laboratory values within the specified range.
If you stop using octaplasLG®
Based on laboratory values your doctor decides when to stop administration of octaplasLG® and will assess possible risks.
4. POSSIBLE SIDE EFFECTS
Like all medicines, octaplasLG® can cause side effects, although not everybody gets them.
These may include: fatigue, tingling feelings (paraesthesia), tremor, flushing, chills (shivering with or without fever), nausea, vomiting, local swelling (oedema), fever, abnormal symptoms in the lungs and low calcium levels.
Some patients may have allergic type reactions such as: rash, fever, chills, nausea, vomiting, and abdominal or back pain. Rarely, the infusion of human plasma may cause anaphylactic shock (an immediate serious allergic reaction which produces a flushing of the skin; drop in blood pressure; difficulty in breathing and collapse). High infusion rates may cause circulatory disorders especially in patients with liver function abnormalities.
Rarely, incompatibility between antibodies in octaplasLG® and antigens in your blood can result in haemolytic transfusion reactions; chills; fever; a non-productive cough; difficulty in breathing; rash; and bleeding within the body.
Infusion of octaplasLG® may give rise to specific coagulation factor antibodies.
High dosages or infusion rates may induce increased blood volume; oedema in the lungs and/or cardiac failure.
6. FURTHER INFORMATION
What octaplasLG® contains
- The active substance are human plasma proteins (45 - 70 mg/mL).
- The other ingredients are:
Sodium citrate dihydrate, Sodium dihydrogenphosphate dihydrate and Glycine
octaplasLG® also contains trace amounts of the chemicals tri(n-butyl)phosphate and octoxynol, which are used during manufacturing for viral inactivation.
What octaplasLG® looks like and contents of the pack
octaplasLG® is a solution for infusion.
octaplasLG® is a clear or slightly opalescent yellow solution. octaplasLG® is available in 200 mL blood bags.
Marketing Authorisation Holder:
[To be completed nationally]
Manufacturers:
Octapharma Pharmazeutika Produktionsge.m.b.H Oberlaaer Str. 235 1100 Vienna Austria
Octapharma AB
SE-112 75 Stockholm, Sweden
This leaflet was last approved in: 12/2011
Depending on type and severity of adverse reactions, the infusion rate must be reduced or the administration must be stopped. Appropriate action will be taken by your doctor.
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