Quest for the right Drug
זופרן טבליות 8 מ"ג ZOFRAN TABLETS 8 MG (ONDANSETRON AS HYDROCHLORIDE DIHYDRATE)
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
Posology : מינונים
4.2 Posology and Method of Administration Posology Chemotherapy and radiotherapy induced nausea and vomiting (CINV and RINV). Adults The emetogenic potential of cancer treatment varies according to the doses and combinations of chemotherapy and radiotherapy regimens used. The selection of dose regimen should be determined by the severity of the emetogenic challenge. Emetogenic Chemotherapy and Radiotherapy: Zofran can be given either by oral (tablets), intravenous or intramuscular administration. The recomended oral dose is: 8 mg taken 1 to 2 hours before chemotherapy or radiation treatment, followed by 8mg every 12 hours for a maximum of 5 days to protect against delayed or prolonged emesis. For highly emetogenic chemotherapy To protect against delayed or prolonged emesis after the first 24 hours, oral treatment with Zofran may be continued for up to 5 days after a course of treatment. The recommended dose for oral administration is 8mg to be taken twice daily. Paediatric Population Ondansetron may be administered as a single intravenous dose of 5 mg/m2 immediately before chemotherapy, followed by 4 mg orally twelve hours later. 4 mg orally twice daily can be continued for up to 5 days after a course of treatment. Elderly Zofran is well tolerated by patients over 65 years. No alteration of oral dose or frequency of administration is required. Patients with Renal Impairment No alteration of daily dosage or frequency of dosing, or route of administration are required. Patients with Hepatic Impairment Clearance of Zofran is significantly reduced and serum half-life significantly prolonged in subjects with moderate or severe impairment of hepatic function. In such patients a total daily dose of 8mg should not be exceeded. Patients with Poor Sparteine/Debrisoquine Metabolism The elimination half-life of ondansetron is not altered in subjects classified as poor metabolisers of sparteine and debrisoquine. Consequently in such patients repeat dosing will give drug exposure levels no different from those of the general population. No alteration of daily dosage or frequency of dosing is required. Post operative nausea and vomiting (PONV): Adults For the prevention of PONV: ondansetron can be administered orally or by intravenous or intramuscular injection. The recommended oral dose is 16mg taken one hour prior to anaesthesia. For the treatment of established PONV, intravenous or intramuscular administration is recommended. Children and Adolescents aged 2 years and over No studies have been conducted on the use of orally administered ondansetron in the prevention or treatment of post operative nausea and vomiting; slow i.v. injection is recommended for this purpose. Elderly There is limited experience in the use of Zofran in the prevention and treatment of post-operative nausea and vomiting in the elderly, however Zofran is well tolerated in patients over 65 years receiving chemotherapy. Patients with Renal impairment No alteration of daily dosage or frequency of dosing, or route of administration are required. Patients with Hepatic impairment Clearance of Zofran is significantly reduced and serum half life significantly prolonged in subjects with moderate or severe impairment of hepatic function. In such patients a total daily dose of 8mg should not be exceeded. Patients with poor Sparteine/Debrisoquine Metabolism The elimination half-life of ondansetron is not altered in subjects classified as poor metabolisers of sparteine and debrisoquine. Consequently in such patients repeat dosing will give drug exposure levels no different from those of the general population. No alteration of daily dosage or frequency of dosing is required. Method of Administration The tablets should be swallowed whole with liquid.
שימוש לפי פנקס קופ''ח כללית 1994
Nausea and vomiting induced by cytotoxic chemotherapy and radiotherapy. יירשם ע"י רופא אונקולוג לחולים אונקולוגיים בלבד
תאריך הכללה מקורי בסל
01/01/1995
הגבלות
תרופה מוגבלת לרישום ע'י רופא מומחה או הגבלה אחרת
מידע נוסף