Quest for the right Drug
ניטיר (ניטיזינון ) 5 מ"ג NITYR ( NITISINONE) 5 MG (NITISINONE)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
פומי : PER OS
צורת מינון:
טבליה : TABLETS
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
Special Warning : אזהרת שימוש
4.4 Special warnings and precautions for use Monitoring of plasma tyrosine levels It is recommended that a slit-lamp examination of the eyes is performed before initiation of NITYR tablets treatment and thereafter regularly, at least once a year. A patient displaying visual disorders during treatment with NITYR tablets should without delay be examined by an ophthalmologist. It should be established that the patient is adhering to his dietary regimen and the plasma tyrosine concentration should be measured. A more restricted tyrosine and phenylalanine diet should be implemented in case the plasma tyrosine level is above 500 micromol/l. It is not recommended to lower the plasma tyrosine concentration by reduction or discontinuation of NITYR tablets, since the metabolic defect may result in deterioration of the patient's clinical condition. Liver monitoring The liver function should be monitored regularly by liver function tests and liver imaging. It is recommended also to monitor serum alpha-fetoprotein concentration. Increase in serum alpha- fetoprotein concentration may be a sign of inadequate treatment. Patients with increasing alpha-fetoprotein or signs of nodules in the liver should always be evaluated for hepatic malignancy. Platelet and white blood cell (WBC) monitoring Leukopenia and/or thrombocytopenia have been reported; may improve with dose reduction. May be due to underlying liver disease rather than drug-related (McKiernan 2006). Monitor platelets and WBC regularly during therapy. Monitoring visits should be performed every 6 months;shorter intervals between visits are recommended in case of adverse events. Concomitant use with other medicinal products NITYR tablet is a moderate CYP2C9 inhibitor. NITYR tablets treatment may therefore result in increased plasma concentrations of co-administered medicinal products metabolized primarily via CYP2C9. NITYR tablets treated patients who are concomitantly treated with medicinal products with a narrow therapeutic window metabolized through CYP2C9, such as warfarin and phenytoin, should be carefully monitored. Dose- adjustment of these co-administered medicinal products may be needed (see section 4.5).
Effects on Driving
4.7 Effects on ability to drive and use machines NITYR tablets has minor influence on the ability to drive and use machines. Adverse reactions involving the eyes (see section 4.8) can affect the vision. If the vision is affected the patient should not drive or use machines until the event has subsided.
פרטי מסגרת הכללה בסל
התרופה תינתן לטיפול בטירוזינמיה תורשתית מסוג I.
שימוש לפי פנקס קופ''ח כללית 1994
לא צוין
תאריך הכללה מקורי בסל
10/01/2012
הגבלות
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