Land: Nederland
Taal: Nederlands
Bron: CBG-MEB (College ter Beoordeling van Geneesmiddelen)
TRAVOPROST
Stada Arzneimittel AG Stadastrasse 2-18 61118 BAD VILBEL (DUITSLAND)
S01EE04
TRAVOPROST
Oogdruppels, oplossing
BOORZUUR (E 284) ; MACROGOLGLYCEROLHYDROXYSTEARAAT ; MANNITOL (D-) (E 421) ; NATRIUMCHLORIDE ; NATRIUMHYDROXIDE (E 524) ; POLYQUATERNIUM-1 ; PROPYLEENGLYCOL (E 1520) 7,5 mg/ml ; WATER, GEZUIVERD ; ZOUTZUUR (E 507),
Oculair gebruik
Travoprost
Hulpstoffen: BOORZUUR (E 284); MACROGOLGLYCEROLHYDROXYSTEARAAT; MANNITOL (D-) (E 421); NATRIUMCHLORIDE; NATRIUMHYDROXIDE (E 524); POLYQUATERNIUM-1; PROPYLEENGLYCOL (E 1520) 7,5 mg/ml; WATER, GEZUIVERD; ZOUTZUUR (E 507);
2015-02-21
Travoprost STADA, NL3029 2020-08-17 1 PACKAGE LEAFLET: INFORMATION FOR THE USER Travoprost STADA 40 microgram/ml oogdruppels, oplossing Travoprost READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING THIS MEDICINE BECAUSE IT CONTAINS IMPORTANT INFORMATION FOR YOU. - Keep this leaflet. You may need to read it again. - If you have any further questions, ask your doctor or pharmacist. - This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. - If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET 1. What Travoprost STADA is and what it is used for 2. What you need to know before you use Travoprost STADA 3. How to use Travoprost STADA 4. Possible side effects 5. How to store Travoprost STADA 6. Contents of the pack and other information 1. WHAT TRAVOPROST STADA IS AND WHAT IT IS USED FOR TRAVOPROST STADA CONTAINS TRAVOPROST , one of a group of medicines called PROSTAGLANDIN ANALOGUES . It works by reducing the pressure in the eye. It may be used on its own or with other drops e.g. beta-blockers, which also reduce pressure. TRAVOPROST STADA IS USED TO REDUCE HIGH PRESSURE IN THE EYE IN ADULTS. This pressure can lead to an illness called glaucoma. 2. WHAT YOU NEED TO KNOW BEFORE YOU USE TRAVOPROST STADA DO NOT USE TRAVOPROST STADA • IF YOU ARE ALLERGIC to Travoprost STADA or any of the other ingredients of this medicine (listed in section 6). Ask your doctor for advice if this applies to you. WARNINGS AND PRECAUTIONS Talk to your doctor or, pharmacist before using Travoprost STADA: • Travoprost STADA MAY INCREASE the length, thickness, colour and/or number of your EYELASHES . Changes in the eyelids including unusual hair growth or in the tissues around the eye have also been observed. • Travoprost STADA may CHANGE THE COLOUR OF YOUR IRIS (the coloured part of your eye). This change may be permanent. A Lees het volledige document
Travoprost SmPC, NL3029, 2020-08-17 SUMMARY OF PRODUCT CHARACTERISTICS Travoprost SmPC, NL3029, 2020-08-17 1. NAME OF THE MEDICINAL PRODUCT Travoprost STADA 40 microgram/ml oogdruppels, oplossing 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each mL of solution contains 40 micrograms of travoprost. Excipient(s) with known effect: Each mL of solution contains 2 mg of macrogolglycerol hydroxystearate 40. For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Eye drops, solution. (Eye drops) Clear, colourless solution. pH 6.3 to 7.3; osmolality 265 - 320 mOsmol/kg 4. CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Decrease of elevated intraocular pressure in adult patients with ocular hypertension or open-angle glaucoma (see section 5.1). 4.2 POSOLOGY AND METHOD OF ADMINISTRATION _Posology _ Use in adults, including elderly population The dose is one drop of Travoprost STADA in the conjunctival sac of the affected eye(s) once daily. Optimal effect is obtained if the dose is administered in the evening. Nasolacrimal occlusion or gently closing the eyelid after administration is recommended. This may reduce the systemic absorption of medicinal products administered via the ocular route and result in a decrease in systemic adverse reactions. If more than one topical ophthalmic medicinal product is being used, the medicinal products must be administered at least 5 minutes apart (see section 4.5). If a dose is missed, treatment should be continued with the next dose as planned. The dose should not exceed one drop in the affected eye(s) daily. When substituting another ophthalmic antiglaucoma medicinal product with travoprost eye drops, the other medicinal product should be discontinued and travoprost eye drops should be started the following day. Travoprost SmPC, NL3029, 2020-08-17 Patients with hepatic and renal impairment Travoprost has been studied in patients with mild to severe hepatic impairment and in patients with mild to severe renal impairment (creatinine clearance as low as 14 ml/min). No dosa Lees het volledige document