Quest for the right Drug
טילופטיק % 0.5 TILOPTIC 0.5 % (TIMOLOL AS MALEATE)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
עיני : OCULAR
צורת מינון:
טיפות עיניים : EYE DROPS, SOLUTION
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 Recommended therapy is one drop in the affected eye twice a day. If needed, ‘Tiloptic’ may be used with other agent(s) for lowering intra-ocular pressure. The use of two topical beta-adrenergic blocking agents is not recommended (see 4.4 ‘Special warnings and precautions for use’). Intra-ocular pressure should be reassessed approximately four weeks after starting treatment because response to ‘Tiloptic’ may take a few weeks to stabilise. Provided that the intra-ocular pressure is maintained at satisfactory levels, many patients can then be placed on once-a-day therapy. When using nasolacrimal occlusion or closing the eyelids for 2 minutes, the systemic absorption is reduced. This may result in a decrease in systemic side effects and an increase in local activity. Transfer from other agents When another topical beta-blocking agent is being used, discontinue its use after a full day of therapy and start treatment the next day with one drop of ‘Tiloptic’ in each affected eye twice a day. When transferring a patient from a single anti-glaucoma agent other than a topical beta-blocking agent, continue the agent and add one drop of ‘Tiloptic’ in each affected eye twice a day. On the following day, discontinue the previous agent completely, and continue with the ‘Tiloptic’. Use in the elderly: there has been wide experience with the use of timolol maleate in elderly patients. The dosage recommendations given above reflect the clinical data derived from this experience. Paediatric Population: Safety and effectiveness in pediatric patients have not been established.
שימוש לפי פנקס קופ''ח כללית 1994
Chronic open angle glaucoma, aphakic glaucoma, secondary glaucoma, ocular hypertension
תאריך הכללה מקורי בסל
01/01/1995
הגבלות
תרופה שאושרה לשימוש כללי בקופ'ח
מידע נוסף