Monday 13 August 2012

Liquifilm Tears Preservative Free





1. Name Of The Medicinal Product



Liquifilm® Tears Preservative Free



or



Refresh OphthalmicTM


2. Qualitative And Quantitative Composition



Polyvinyl alcohol 1.4% w/v.



3. Pharmaceutical Form



Eye drops, solution



4. Clinical Particulars



4.1 Therapeutic Indications



Symptomatic relief of dry eye and symptomatic relief of eye irritation associated with deficient tear production.



4.2 Posology And Method Of Administration



Ensure container is intact. Twist off tab and apply eyedrops.



Dosage schedule: Apply one or two drops in each eye as needed, or as directed. No special dosage for the elderly or for children.



Route of administration: Ocular instillation.



4.3 Contraindications



Hypersensitivity to the active substance polyvinyl alcohol or any of the other excipients.



4.4 Special Warnings And Precautions For Use



If irritation, pain, redness and changes in vision occur or worsen, treatment should be discontinued and a new assessment considered.



To avoid contamination, the dropper tip should not be allowed to touch the eye or any other surface.



Contact lenses should be removed before each application and may be reinserted after 15 minutes.



Concomitant ocular medication should be administered 15 minutes prior to the instillation of Liquifilm Tears Preservative Free or Refresh Ophthalmic.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



No interaction studies have been performed.



4.6 Pregnancy And Lactation



The constituents of Liquifilm Tears Preservative Free or Refresh Ophthalmic have been used as pharmaceutical agents for many years with no untoward effects. No special precautions are necessary for the use of Liquifilm Tears Preservative Free or Refresh Ophthalmic in pregnancy and lactation.



4.7 Effects On Ability To Drive And Use Machines



Liquifilm Tears Preservative Free or Refresh Ophthalmic has minor or moderate influence on the ability to drive and use machines as it may cause transient blurring of vision. Do not drive or use hazardous machinery unless vision is clear.



4.8 Undesirable Effects



Liquifilm Tears Preservative Free or Refresh Ophthalmic may cause transient stinging or irritation on instillation.



The frequency of the following undesirable effects is not known (cannot be estimated from the available data).



Eye disorders



• Eye irritation



• Eye pain



• Ocular hyperaemia



• Vision blurred



• Eye pruritus



• Foreign body sensation



• Eye discharge



• Hypersensitivity



4.9 Overdose



No case of overdose has been reported. Accidental overdose will not present any hazard.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Liquifilm® Tears Preservative Free / or Refresh OphthalmicTM exerts a mechanical, not a pharmacological action. The viscosity enhancing agent is polyvinyl alcohol and the lubricating-enhancing agent is povidone.



5.2 Pharmacokinetic Properties



Not applicable



5.3 Preclinical Safety Data



The constituents of Liquifilm® Tears Preservative Free / or Refresh OphthalmicTM have been used safely in pharmaceutical products for many years. Topical administration in animals studies showed no untoward effects.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Povidone



Sodium chloride



Sodium hydroxide or hydrochloric acid (to adjust pH)



Purified water



6.2 Incompatibilities



None known.



6.3 Shelf Life



24 months (unopened).



Do not store opened container.



6.4 Special Precautions For Storage



Store at 25ºC or below.



6.5 Nature And Contents Of Container



Low density polyethylene unit dose vials containing 0.4 ml of Liquifilm® Tears Preservative Free / or Refresh OphthalmicTM.



Cartons contain 2, 5, 10, 15, 30 or 50 units per pack.



6.6 Special Precautions For Disposal And Other Handling



Ensure container is intact. Twist off tab and apply eyedrops.



7. Marketing Authorisation Holder



Allergan Limited



Marlow International



The Parkway



Marlow



Bucks, SL7 1YL



UK



8. Marketing Authorisation Number(S)



PL 00426/0063



9. Date Of First Authorisation/Renewal Of The Authorisation



14th August 2003



10. Date Of Revision Of The Text



23rd July 2008




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