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HSA Approval

TRAVATAN C EYE DROP SOLUTION 30MCG/ML

SIN15206P

TRAVATAN C EYE DROP SOLUTION 30MCG/ML

TRAVATAN C EYE DROP SOLUTION 30MCG/ML

April 10, 2017

NOVARTIS (SINGAPORE) PTE LTD

NOVARTIS (SINGAPORE) PTE LTD

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantNOVARTIS (SINGAPORE) PTE LTD
Licence HolderNOVARTIS (SINGAPORE) PTE LTD

Product Classification

D
Drug Type
Therapeutic
F
Forensic Class
Prescription Only
HSA Singapore Classification

Formulation Information

SOLUTION, STERILE

**4.2 Posology and method of administration** **Posology** Use in adults, including elderly patients The dose is 1 drop of TRAVATAN C eye drops in the conjunctival sac of the affected eye(s) once daily. Optimal effect is obtained if the dose is administered in the evening. TRAVATAN C eye drops may be used concomitantly with other topical ophthalmic drug products to lower intraocular pressure. Use in patients with renal impairment Travoprost 30 mcg/ml has not been studied in patients with renal impairment. However, travoprost 40 mcg/ml has been studied in patients with mild to severe renal impairment (creatinine clearance as low as 14 ml/min). No dosage adjustment is necessary in these patients (see section 5.2 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). Therefore, no need for dose adjustment at the lower concentration of active ingredient is anticipated. Use in patients with hepatic impairment Travoprost 30 mcg/ml has not been studied in patients with hepatic. However, travoprost 40 mcg/ml has been studied in patients with mild to severe hepatic impairment.No dosage adjustment is necessary in these patients (see section 5.2 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). Therefore, no need for dose adjustment at the lower concentration of active ingredient is anticipated. Use in children and adolescents The safety and efficacy of TRAVATAN C eye drops in children and adolescents below the age of 18 years has not been established. No data are available. **Method of administration** For ocular use. For patients who wear contact lenses, please refer to section 4.4 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_. The patient should remove the protective overwrap immediately prior to initial use. To prevent contamination of the dropper tip and solution, care must be taken not to touch the eyelids, surrounding areas or other surfaces with the dropper tip of the bottle. Keep the bottle tightly closed when not in use. The dropper tip should also not come into contact with the eye as this may cause injury to the eye. Nasolacrimal occlusion or gently closing the eyelid(s) for 2 minutes 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 a dose is missed, treatment should be continued with the next dose as planned. The dose should not exceed 1 drop in the affected eye(s) daily. Since it has been shown that more frequent administration of prostaglandin analogs may decrease the IOP lowering effect. When substituting another ophthalmic antiglaucoma medicinal product with TRAVATAN C eye drops, the other medicinal product should be discontinued and TRAVATAN C eye drops should be started the following day. If more than one topical ophthalmic medicinal product is being used, the medicinal products must be administered at least 5 minutes apart. Eye ointments should be administered last.

OPHTHALMIC

Medical Information

**4.1 Therapeutic indications** TRAVATAN C® eye drops contains travoprost, a prostaglandin analogue. TRAVATAN C eye drops is indicated for the decrease of elevated intraocular pressure in adult patients with ocular hypertension or open-angle glaucoma (see section 5.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).

**4.3 Contraindications** Hypersensitivity to the active substance or to any of the excipients listed in section 6.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_.

S01EE04

travoprost

Manufacturer Information

NOVARTIS (SINGAPORE) PTE LTD

S.A. Alcon-Couvreur N.V.

Alcon Laboratories Inc - ASPEX

Active Ingredients

Travoprost

0.03 mg/ml

Travoprost

Documents

Package Inserts

Travatan C eye drop solution PI.pdf

Approved: November 17, 2022

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TRAVATAN C EYE DROP SOLUTION 30MCG/ML - HSA Approval | MedPath