Friday, September 16, 2016

Minims Fluorescein Sodium





1. Name Of The Medicinal Product



Minims Fluorescein Sodium 2%


2. Qualitative And Quantitative Composition



2% w/v solution of Fluorescein Sodium PhEur.



3. Pharmaceutical Form



Single-use, sterile eye drops.



4. Clinical Particulars



4.1 Therapeutic Indications



As a diagnostic stain.



Fluorescein does not stain a normal cornea but conjunctival abrasions are stained yellow or orange, corneal abrasions or ulcers are stained a bright green and foreign bodies are surrounded by a green ring.



Fluorescein can be used in diagnostic examinations including Goldmann tonometry and in the fitting of hard contact lenses.



4.2 Posology And Method Of Administration



Adults, Children and the Elderly



Instil dropwise into the eye.



Sufficient solution should be applied to stain the damaged areas. Excess may be washed away with sterile saline solution.



4.3 Contraindications



Not to be used with soft contact lenses.



4.4 Special Warnings And Precautions For Use



Special care should be taken to avoid microbial contamination. Pseudomonas aeruginosa grows well in fluorescein solutions, therefore, a single dose solution is preferred. Each Minims unit should be discarded after a single use.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



None known.



4.6 Pregnancy And Lactation



Safety for use in pregnancy and lactation has not been established, therefore use only when considered essential by the physician.



4.7 Effects On Ability To Drive And Use Machines



May cause transient blurring of vision on instillation. Warn patients not to drive or operate hazardous machinery until vision is clear.



4.8 Undesirable Effects



ADRs are very rare(<1/10,000),including isolated reports.



Symptoms of allergic-type reactions and anaphylaxis have been reported following topical ophthalmic administration of Fluorescein sodium and may manifest as:



Eye disorders: allergic conjunctivitis, peri-orbital oedema



Immune system disorders: anaphylactic reaction



Skin and subcutaneous tissue disorders: urticaria, rash



4.9 Overdose



Overdose following the recommended use is unlikely.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Fluorescein acts as a diagnostic stain.



5.2 Pharmacokinetic Properties



Fluorescein will resist penetration of a normal cornea and most excess solution will, therefore, be carried with the tear film away from the conjunctival sac. The majority will be lost through the naso-lacrimal ducts and absorbed via the gastro-intestinal tract from where it is converted rapidly to its glucuronide and excreted via the urine.



If fluorescein crosses the cornea it will enter the Bowman's membrane, stroma and possibly the anterior chamber. Aqueous flow and diffusion into the blood in the anterior chamber finally removes fluorescein from the eye and it is excreted unchanged in the urine.



5.3 Preclinical Safety Data



There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of this SPC.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Purified Water



6.2 Incompatibilities



None known.



6.3 Shelf Life



Unopened: 15 months.



6.4 Special Precautions For Storage



Store below 25°C. Do not freeze. Protect from light.



6.5 Nature And Contents Of Container



A sealed conical shaped polypropylene container fitted with a twist and pull off cap. Each Minims unit contains approximately 0.5ml of solution. Each unit is overwrapped in a polypropylene/paper pouch. 20 units are packed into a suitable carton.



6.6 Special Precautions For Disposal And Other Handling



Each Minims unit should be discarded after use.



7. Marketing Authorisation Holder



Chauvin Pharmaceuticals Ltd



106 London Road



Kingston-upon-Thames



Surrey



KT2 6TN



8. Marketing Authorisation Number(S)



PL 0033/5008R



9. Date Of First Authorisation/Renewal Of The Authorisation



Date of first Authorisation: 23 April 1987



Date of renewal of Authorisation: 18 February 1992



10. Date Of Revision Of The Text



June 2007




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