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
Pharmacological properties : תכונות פרמקולוגיות
Pharmacodynamic Properties
5.1 Pharmacodynamic properties Pharmacotherapeutic group: Ophtalmologicals, antiglaucoma preparations and miotics, betablocking agents, ATC code: S01ED01. Machanism of action Timolol maleate is a non-selective beta-adrenergic receptor blocking agent that does not have significant intrinsic sympathomimetic, direct myocardial depressant, or local anaesthetic activity. Timolol maleate combines reversibly with the beta-adrenergic receptor, and this inhibits the usual biologic response that would occur with stimulation of that receptor. This specific competitive antagonism blocks stimulation of the beta-adrenergic stimulating (agonist) activity, whether these originate from an endogenous or exogenous source. Reversal of this blockade can be accomplished by increasing the concentration of the agonist which will restore the usual biological response. Clinical Efficacy and Safety Unlike miotics, ‘Tiloptic’ reduces IOP with little or no effect on accommodation or pupil size. In patients with cataracts, the inability to see around lenticular opacities when the pupil is constricted is avoided. When changing patients from miotics to ‘Tiloptic’ a refraction might be necessary when the effects of the miotic have passed. Diminished response after prolonged therapy with ‘Tiloptic’ has been reported in some patients.
Pharmacokinetic Properties
5.2 Pharmacokinetic properties The onset of reduction in intra-ocular pressure can be detected within one-half hour after a single dose. The maximum effect occurs in one or two hours; significant lowering of IOP can be maintained for as long as 24 hours with a single dose.
שימוש לפי פנקס קופ''ח כללית 1994
Chronic open angle glaucoma, aphakic glaucoma, secondary glaucoma, ocular hypertension
תאריך הכללה מקורי בסל
01/01/1995
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