Quest for the right Drug
אוקטאניין F 1000 יח' בינ"ל OCTANINE F 1000 IU (COAGULATION FACTOR IX (HUMAN), FACTOR IX)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תוך-ורידי : I.V
צורת מינון:
אבקה וממס להכנת תמיסה להזרקה : POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
עלון לרופא
מינוניםPosology התוויות
Indications תופעות לוואי
Adverse reactions התוויות נגד
Contraindications אינטראקציות
Interactions מינון יתר
Overdose הריון/הנקה
Pregnancy & Lactation אוכלוסיות מיוחדות
Special populations תכונות פרמקולוגיות
Pharmacological properties מידע רוקחי
Pharmaceutical particulars אזהרת שימוש
Special Warning עלון לרופא
Physicians Leaflet
Pharmacological properties : תכונות פרמקולוגיות
Pharmacodynamic Properties
5.1 Pharmacodynamic properties Pharmacotherapeutic group: antihemorrhagics: blood coagulation factor IX ATC-code: B02BD04 Factor IX is a single chain glycoprotein with a molecular mass of about 68,000 Dalton. It is a vitamin-K dependent coagulation factor and it is synthesised in the liver. Factor IX is activated by factor XIa in the intrinsic coagulation pathway, and by the factor VII/tissue factor complex in the extrinsic pathway. Activated factor IX, in combination with activated factor VIII, activates factor X. Activated factor X converts prothrombin into thrombin. Thrombin then converts fibrinogen into fibrin and a clot is formed. Haemophilia B is a sex-linked hereditary disorder of blood coagulation due to decreased levels of factor IX and results in profuse bleeding into joints, muscles or internal organs, either spontaneously or as a result of accidental or surgical trauma. By replacement therapy the plasma levels of factor IX is increased, thereby enabling a temporary correction of the factor deficiency and correction of the bleeding tendencies. Paedriatric population A study in 25 children below 6 years of age was conducted. Thereof, 6 patients were previously untreated. The recovery after administration of >25 IU of OCTANINE F/kg body weight was investigated during the first 3 months of treatment and after 12-24 months. The incremental recovery (geometric mean ± s.d., one-stage assay, actual potency) was calculated to be 0.8±1.4 and 0.9±1.3 %/IU/kg at the 1st and the 2nd assessment, respectively.
Pharmacokinetic Properties
5.2 Pharmacokinetic properties For OCTANINE F the following results were achieved in one pharmacokinetic study with 13 Haemophilia B patients over 12 years of age (mean age 28 years, range 12-61 years): N=13 Median Mean SD* Minimum Maximum Incremental Recovery 1.2 1.3 0.5 0.8 2.4 [IU/dl]/[IU/kg] AUC*norm 32.4 37.7 13.0 24.5 64.0 (IU x dl-1 x h x IU-1 x kg) Half-life (h) 27.8 29.1 5.2 22.0 36.8 MRT* (h) 39.4 40.0 7.3 30.2 51.6 Clearance (ml x h-1 x kg) 3.1 2.9 0.9 1.6 4.1 *AUC = area under the curve *MRT = mean residence time *SD = standard deviation The incremental recovery was also tested in a second study. The meta-analysis of all recovery assessments (n=19) resulted in a mean recovery of 1.1 [IU/dl]/[IU/kg].
שימוש לפי פנקס קופ''ח כללית 1994
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תאריך הכללה מקורי בסל
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הגבלות
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רישום
150 35 33831 00
מחיר
0 ₪
מידע נוסף
עלון מידע לרופא
23.08.17 - עלון לרופאעלון מידע לצרכן
לתרופה במאגר משרד הבריאות
אוקטאניין F 1000 יח' בינ"ל