The main pharmaco-therapeutic effects: Hemostatic aurally . Side effects  and complications in the use of drugs: inhibition of factor VIII; unusual taste  in the mouth, nausea, injection site reactions, AR, dizziness, itching, rash,  changes JSC. The main pharmaco-therapeutic effects: Hemostatic. Method of  production of drugs: lyophilized powder for injection, Mr 250, 500 or 1000 IU.  Dosing and Administration of Maximum  Voluntary Ventilation for / v input by direct syringe injection or drip  infusion, should be taken within 3 h after dilution, increase the percentage of  factor VIII can be calculated by multiplying factor on the dose antyhemofilnoho  kg (IU / kg) at 2% dosage necessary to aurally hemostasis depends on the extent  and severity Anterior Superior Iliac  Spine bleeding, according to the Lower  Respiratory Tract Infection general settings: treatment for weak  (superficial early) bleeding here  10 IU / kg, the therapy should not be repeated, unless there were signs further  bleeding (therapeutic level of 20% required). Dosing and Administration of  drugs: pryznachatsya / v during 3 h after dilution; Kodzhyneyt FS dose necessary  to restore hemostasis, should be chosen individually based on individual patient  needs and intensity of the deficit, the intensity of bleeding, presence of  inhibitors and desired levels of FVIII; often critical value has aurally FVIII  levels during therapy, clinical effectiveness factor VIII is the most important  element in evaluating the effectiveness of treatment to achieve satisfactory  clinical results may be necessary to appoint more FVIII, than calculated, if the  calculated dose can not achieve the expected concentration of FVIII or control  bleeding in patients should suspect the presence of circulating inhibitor to  FVII (its presence and quantity Disaster  should confirm the appropriate laboratory tests) to inhibitors of factor VIII  required dose can vary considerably for different patients and the optimal  scheme of aurally is determined only on the basis of aurally response, some  patients with low titers of inhibitors (less than 10 BU) can be successfully  treated without drugs FVIII inhibitor titer anamnestic increase, to ensure  aurally response should aurally checked FVIII level and clinical response to  treatment for patients with anamnestic response to FVIII treatment and / or  higher titers of inhibitors may be necessary to use alternative medicines, such  as concentrated complex factor IX, aurally Antyhemofilnyy (pigs), recombinant  factor VIIa complex, or coagulants antyinhibitornyy; percentage increase FVIII  FE vivo can be estimated by multiplying the dose Antyhemofilnoho factor  (rekombinatnoho) Kodzhyneyt FS per kg (IU / kg) at 2% / IU / kg, this  calculation method is based on clinical results obtained with the use of plasma  and recombinant factor Antyhemofilnoho preparations, with mild bleeding  (superficial hemorrhages, early bleeding, bleeding in joints) - 10-20 FVIII  plasma / kg, if the bleeding does not stop aurally re-enter the dose  (therapeutic level of activity required in plasma FVIII 20% - 40%), bleeding or  medium severe Papanicolaou  Stain in the muscle, bleeding in mouth, expressed hemartroz, trauma),  surgery (a small surgical procedure) - 15 30 IU / kg, repeat as necessary input  in the same dose through 12-24 hr (therapeutically necessary level of FVIII  activity in plasma of 30% - 60%), severe bleeding and such that is life  threatening (intracranial bleeding, bleeding into the abdominal or chest cavity,  gastrointestinal bleeding, bleeding, bleeding in the CNS, bleeding in  retrofarynhialnyy space or cap. The main pharmaco-therapeutic effects:  Hemostatic. zduhvynno-psoas, fractures, head trauma - initial dose: 40 -50 IU /  kg, repeat dose of 20 -25 IU / kg every 12.8 hours (the required level of  therapeutic FVIII activity in plasma of 80% - 100%), radical surgery -  preoperative dose: 50 IU / kg, ~ 100% check activity before surgery, repeat the  dose, if necessary, first After 6-12 h, and then - within 10-14 days to healing  aurally required level of therapeutic FVIII activity in plasma of ~ 100%).  Coagulation factors. Contraindications to the use of drugs: known intolerance or  AR on the components of the drug to mice or hamster proteins.  
 
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