The shelf-life of unopened vials of Biofactor Streptokinase 1 500 000 is 3 years.
Contraindications to treatment with Biofactor Streptokinase, because of the increased risk of haemorrhage under thrombolytic therapy, include:
- existing or recent internal haemorrhage
- all forms of reduced blood coagulability, in particular spontaneous fibrinolysis and extensive clotting disorders
- recent cerebrovascular accident, intracranial or intraspinal surgery
- intracranial neoplasm
- recent head trauma
- arteriovenous malformation or aneurysm
- known neoplasm with risk of haemorrhage
- acute pancreatitis
- uncontrollable hypertension with systolic values over 200 mm Hg and/or diastolic values over 100 mm Hg or hypertensive retinal changes Grades III/IV
- recent implantation of a vessel prosthesis
- simultaneous or recent treatment with oral anticoagulants (INR >1.3)
- severe liver or kidney damage
- endocarditis or pericarditis. Isolated cases of pericarditis, misdiagnosed as acute myocardial infarction and treated with streptokinase, have resulted in pericardial effusions including tamponade
- known haemorrhagic diathesis
- recent major operations (6th to 10th post-operative day, depending on the extent of the procedure)
- invasive operations, e.g. recent organ biopsy, long-term (traumatic) closed chest cardiac massage
No incompatibilities have been reported when Biofactor Streptokinase is used as recommended. This medicinal product must not be mixed with other medicinal products.
Human albumin, Aminoacetic acid (glycine), Mannitol
Powder for solution for infusion.
White to slightly yellow powder.
The following adverse reactions are based on clinical trial and post-marketing experience. The following standard categories are used:
| Very common | more than1/10 |
| Common | more than 1/100; less than 1/10 |
| Uncommon | more than 1/1000; less than 1/100 |
| Rare | more than 1/10,000; less than 1/1000 |
| Very Rare | less than 1/10,000 (including isolated cases) |
Blood and lymphatic system disorders
Common: haemorrhage at the injection site, ecchymoses, gastrointestinal bleeding, genitourinary bleeding, epistaxis
Uncommon: cerebral haemorrhages with their complications and possible fatal outcome, retinal haemorrhages, severe haemorrhages (also with fatal outcome), liver haemorrhages, retroperitoneal bleeding, bleeding into joints, splenic rupture. Blood transfusions are rarely required.
Very rare: haemorrhage into the pericardium including myocardial rupture during thrombolytic treatment of acute myocardial infarction
In serious haemorrhagic complications, streptokinase therapy should be discontinued and a proteinase inhibitor, e.g., aprotinin, should be given as follows. Initially 500 000 KIU (Kallikrein Inactivator Unit) up to one million KIU by slow intravenous injection or infusion. If necessary this should be followed by 200,000 KIU every four hours by intravenous drip until the bleeding stops. In addition, combination with synthetic antifibrinolytics is recommended. If necessary, clotting factors can be substituted. Additional administration of synthetic antifibrinolytics has been reported to be efficient in single cases of bleeding episodes.
Immune system disorders
Very Common: development of antistreptokinase antibodies (see also 4.4)
Common: allergic anaphylactic reactions, e.g. rash, flushing, itching, urticaria, angioneurotic oedema, dyspnoea, bronchospasm, hypotension
Very Rare: delayed allergic reactions, e.g. serum sickness, arthritis, vasculitis, nephritis, neuroallergic symptoms (polyneuropathy, e.g. Guillain Barré syndrome), severe allergic reactions up to shock including respiratory arrest.
Allergic reactions can largely be avoided by giving the infusion slowly. Moderate or mild allergic reactions can be managed with concomitant antihistamine and/or corticosteroid therapy. If a severe allergic reaction occurs the infusion of streptokinase should be discontinued immediately and the patient given the appropriate treatment. The current medical standards for shock treatment should be observed. Lysis therapy should be continued with homologous fibrinolytics, such as Urokinase or tPA.
Nervous system disorders
Rare: neurologic symptoms (e.g. dizziness, confusion, paralysis, hemiparesis, agitation, convulsion) in the context of cerebral haemorrhages or cardiovascular disorders with hypoperfusion of the brain
Eye disorders
Very rare: iritis/uveitis/iridocyclitis
Cardiac and vascular disorders
Common: at the start of therapy, hypotension, tachycardia, bradycardia
Very rare: crystal cholesterol embolism
During fibrinolytic therapy with streptokinase in patients with myocardial infarction, the following events have been reported as complications of myocardial infarction and/or symptoms of reperfusion:
Very common: hypotension, heart rate and rhythm disorders, angina pectoris
Common: recurrent ischaemia, heart failure, reinfarction, cardiogenic shock, pericarditis, pulmonary oedema
Uncommon: cardiac arrest (leading to respiratory arrest), mitral insufficiency, pericardial effusion, cardiac tamponade, myocardial rupture, pulmonary or peripheral embolism
These cardiovascular complications can be life-threatening and may lead to death.
During local lysis of peripheral arteries, distal embolization cannot be excluded.
Respiratory Disorders
Very rare: non-cardiogenic pulmonary oedema after intracoronary thrombolytic therapy in patients with extensive myocardial infarction
Gastrointestinal disorders
Common: nausea, diarrhoea, epigastric pain, vomiting
General disorders and administration site conditions
Common: headache, back pain, musculoskeletal pain, chills, fever, asthenia, malaise
Testing
Common: Transient elevations of serum transaminases and bilirubin
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard.
In an Ames Test on Biofactor Streptokinase, no evidence of mutagenic potential was found. No other preclinical safety studies have been performed on Biofactor Streptokinase.
Biofactor Streptokinase is indicated in adults.
Acute myocardial infarction: within 12 hours of onset with persistent ST-segment elevation or recent left bundle-branch block. Note: No statement on therapy outcome can be made for administration beyond the time window indicated above.
Pharmacotherapeutic group: Streptokinase (antithrombotic agents, enzymes)
ATC code: B01A D01
Biofactor Streptokinase is a highly purified streptokinase derived from β haemolytic streptococci of Lancefield group C. The activation of the endogenous fibrinolytic system is initiated by the formation of a streptokinase-plasminogen complex.
This complex possesses activator properties and converts plasminogen into the proteolytic and fibrinolytic active plasmin. The more plasminogen that is bound within this activator complex, the less plasminogen is left to be converted into its enzymatically active form. Therefore, high doses of streptokinase are associated with a lower bleeding risk and vice versa.
After intravenous administration and neutralisation of the individual antistreptokinase-antibody titre, streptokinase is immediately available systemically for activation of the fibrinolytic system.
Streptokinase has a very short half-life. The first rapid clearance from the plasma is due to the formation of the complex between streptokinase and streptokinase antibody. This complex is biochemically inert and is cleared rapidly from the circulation. Once the antibody has been neutralised, the streptokinase activates the plasminogen as described above.
The elimination kinetics of streptokinase follows a biphasic course. A small proportion of the dose is bound to anti-streptokinase antibodies and metabolised with a half-life of 18 minutes while most of it forms a streptokinase-plasminogen activator complex and is biotransformed with a half-life of about 80 minutes.
Peak fibrinolytic activity is found in the blood about 20 minutes after dosing.
Like other proteins, streptokinase is metabolised proteolytically in the liver and eliminated via the kidneys. Animal data suggest that streptokinase may also be excreted unchanged in the bile.
01 July 2015
Biofactor Streptokinase 1 500 000
Biofactor GmbH
Rudolf-Huch-Str. 14, D-38667 Bad Harzburg, Germany
Fax: +49 5322 960516 Email: [email protected]
Do not store above +25°C and do not freeze.
Do not store the reconstituted solution for more than 24 hours in a refrigerator at +2°C to +8°C.
Biofactor Streptokinase 1 500 000 is supplied in glass vials with rubber closures and aluminium seal with plastic flip-top caps.
Biofactor Streptokinase 1 500 000 is available in packages containing one vial.
PL 29723/0004
Biofactor Streptokinase is contraindicated in pregnancy. There is no evidence of the drug's safety in pregnancy, nor is there evidence from animal work that it is free from hazard. Bleeding and anaphylactic reactions might cause abortion and foetal death, especially when streptokinase is given within the first 18 weeks of pregnancy. Use only when there is no safer alternative.
It is unknown whether streptokinase is excreted in human milk. Breast milk should be discarded during the first 24 hours following thrombolytic therapy.
Biofactor Streptokinase 1 500 000 is presented as a powder for solution in vials containing 1.5 million International Units (IU) of purified streptokinase as the active ingredient.
Highly purified streptokinase is extracted from the culture filtrate of certain strains of the streptococcus group C. It is presented as a white to slightly yellow powder and contains stabilisers.
The following conditions would normally be considered contraindications to streptokinase therapy, but in certain situations the benefits could outweigh the potential risks:
- recent severe gastrointestinal bleeding, e.g. active peptic ulcer
- risk of severe local haemorrhage, e.g. in case of translumbar aortography
- recent trauma and cardiopulmonary resuscitation
- invasive operations, e.g. recent intubation
- puncture of non-compressible vessels, intramuscular injections, large arteries
- recent abortion or delivery
- pregnancy
- diseases of the urogenital tract with existing or potential sources of bleeding (implanted bladder catheter)
- known septic thrombotic disease
- severe arteriosclerotic vessel degeneration, cerebrovascular diseases
- cavernous pulmonary diseases, e.g. open tuberculosis or severe bronchitis
- mitral valve defects or atrial fibrilation
- aortic dissection
- diabetic retinopathy increase risk of local bleeding
Antistreptokinase
Repeat treatment with streptokinase administered more than 5 days and less than 12 months after initial treatment may not be effective. This is because of the increased likelihood of resistance due to antistreptokinase antibodies.
Also, the therapeutic effect may be reduced in patients with recent streptococcal infections such as streptococcal pharyngitis, acute rheumatic fever and acute glomerulonephritis.
Infusion rate and corticosteroid prophylaxis
At the beginning of therapy, a fall in blood pressure, tachycardia or bradycardia (in individual cases going as far a shock) are commonly observed. Therefore, at the beginning of therapy the infusion should be performed slowly.
Corticosteroids can be administered prophylactically to reduce the likelihood of infusion-related allergic reactions.
Pre-treatment with heparin or coumarin derivatives
If the patient is under active heparinization, it should be neutralised by administering protamine sulphate before the start of the thrombolytic therapy. The thrombin time should not be more than twice the normal control value before thrombolytic therapy is started. In patients previously treated with coumarin derivatives, the INR (International Normalized Ratio) must be less than 1.3 before starting the streptokinase infusion.
Simultaneous treatment with acetylsalicylic acid
Recent evidence indicates that controlled-dose adjuvant acetylsalicyclic therapy in combination with streptokinase is capable of improving the response in the management of acute myocardial infarction.
Streptokinase is not indicated for restoration of patency of intravenous catheters.
Not relevant.
Posology
Paediatric population
The safety and efficacy of Biofactor Streptokinase have not been sufficiently established in children. Due to low levels of plasminogen in newborns and in children with acquired plasminogen deficiency and due to the potential of streptokinase for allergic/anaphylactic reactions, it is not recommended in neonates, infants and children.
Adults
Systemic administration: A single dose of 1.5 million IU streptokinase should be infused intravenously over one hour.
Local intracoronary administration: A bolus of 20,000 IU streptokinase should be followed by a maintenance infusion of 2,000 IU to 4,000 IU per minute over 30 to 90 minutes depending on the achievement of coronary artery patency.
Method of Administration
Upon reconstitution with physiological saline a clear solution, colourless to yellowish, is obtained.
Note: When thrombolytic therapy is necessary and a high antibody concentration against streptokinase is present or when recent streptokinase therapy has been given (more than 5 days and less than one year previously), homologous fibrinolytics should be used.
Adjuvant treatment
Treatment with aspirin (150 mg daily) for at least 4 weeks is recommended for prophylaxis after streptokinase therapy for acute myocardial infarction. The first dose should be given as soon as possible after the myocardial infarction.
The contents should be dissolved in 4-5 ml of physiological saline or water for injection. The solution should be swirled gently to facilitate quick reconstitution, but care should be taken to avoid foaming.
Biofactor Streptokinase may be given by intravenous infusion in 50-200 ml of physiological saline, 5% glucose solution, 5% fructose solution, or Ringer-lactate solution.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
26 June 1998 / 15 May 2009
There is an increased risk of haemorrhage in patients who are receiving or who have recently been treated with anticoagulants, e.g. heparin or drugs which inhibit platelet formation or function, e.g. platelet aggregation inhibitors, dextrans.
