Tiacil 0.50% W/V Eye Drops, Solution
Revised: 14 September 2009
AN: 02109/2008
SUMMARY OF PRODUCT CHARACTERISTICS |
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1. |
NAME OF THE VETERINARY MEDICINAL PRODUCT |
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Tiacil 0.50% w/v Eye drops, solution |
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2. |
QUALITATIVE AND QUANTITATIVE COMPOSITION |
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Active substance(s) Gentamicin sulphate, (activity 600 IU/mg)………………………… Excipients Parahydroxybenzoic acid……………………………………………. Disodium Edetate…………………………………………………….. |
% w/v 0.50 0.09 0.50 |
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For a full list of excipients, see section 6.1 |
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3. |
PHARMACEUTICAL FORM |
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Eye drops, solution. Sterile, opalescent, aqueous solution. |
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4. |
CLINICAL PARTICULARS |
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4.1 |
Target species |
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Cats, dogs and rabbits |
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4.2 |
Indications for use, specifying the target species |
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For the treatment of blepharitis, conjunctivitis, keratoconjunctivitis (including post-operative keratitis) and anterior uveitis, in dogs, cats and rabbits |
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4.3 |
Contraindications |
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None. |
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4.4 |
Special warnings for each target species |
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None. |
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4.5 |
Special precautions for use |
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i. |
Special precautions for use in animals |
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Official, national and regional antimicrobial policies should be taken into account when the product is used. Where possible, in vitro sensitivity tests should be undertaken prior to treatment. Occular re-examination should be made at frequent intervals during prolonged therapy. Tiacil Ophthalmic solution may be used in case of corneal erosion or superficial ulcer. |
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ii. |
Special precautions for the person administering the veterinary medicinal product to animals |
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People with known allergy (hypersensitivity) to aminoglycosides should avoid contact with this product. Wash hands after use. |
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4.6 |
Adverse reactions (frequency and seriousness) |
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In rare cases, acute irritation and pain may occur. This resloves spontaneously. |
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4.7 |
Use during pregnancy, lactation or lay |
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No special precautions. |
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4.8 |
Interaction with other medicinal products and other forms of interaction |
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None known. |
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4.9 |
Amount(s) to be administered and administration route |
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Apply 1 or 2 drops directly into the conjunctival sac three times a day until control is achieved, which in most cases can be expected after 5 to 7 days. Care should be taken to avoid contamination of the contents during use. Ocular re-examination should be made at frequent intervals during extended therapy. If there is no response to treatment withing 7 to 14 days or the condition worsens, the diagnosis should be re-established |
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4.10 |
Overdose (symptoms, emergency procedures, antidotes), if necessary |
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In cases of severe irritation, the treatment should be stopped immedately and the diagnosis reassessed. |
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4.11 |
Withdrawal period(s) |
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Not for use in rabbits intended for human consumption |
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5. |
PHARMACOLOGICAL PROPERTIES |
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ATC Vet Code: QS01AA11 |
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Tiacil is an ophthalmic solution containing Gentamicin sulphate as active ingredient, an antibiotic of the aminoglycoside family. |
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5.1 |
Pharmacodynamic properties |
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Gentamicin is a broad spectrum bactericidal antibiotic, active against such organisms as Klebsiella and Pseudomonas. Gentamicin is particularly effective on rapidly multiplying organisms. Gentamycin is lethal to susceptible bacteria mainly by binding to bacterial ribosomes and impairing protein synthesis. |
5.2 |
Pharmacokinetic particulars |
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The application of one or two drops to the eye enables the persistence of therapeutic levels for more than 6 hours. |
6. |
PHARMACEUTICAL PARTICULARS |
6.1 |
List of excipients |
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Parahydroxybenzoic Acid Disodium Edetate Hypromellose Povidone K30 Sodium Chloride Sodium Hydroxide (for pH adjustment) Trometamol Water for injection |
6.2 |
Incompatibilities |
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None known. |
6.3 |
Shelf life |
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Shelf life of the veterinary medicinal product as packaged for sale: 2 years Shelf life after opening the immediate packaging: 28 days |
6.4 |
Special precautions for storage |
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Do not store above 25°C Any contents remaining 28 days after the date on which the container was first opened should be discarded. Care should be taken to avoid contamination of the contents during use. Following withdrawal of first dose, use the product within 28 days. |
6.5 |
Nature and composition of immediate packaging |
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5 ml type II amber glass bottles with blue polyethylene low density cap and blue rubber chlorobutyl dropper. |
6.6 |
Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products, if appropriate |
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Any unused product or waste material should be disposed of in accordance with national requirements. |
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MARKETING AUTHORISATION HOLDER |
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Virbac S.A. 1ère avenue , 2065m – LID 06516 Carros Cedex France |
8. |
MARKETING AUTHORISATION NUMBER |
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Vm 05653/4026 |
9. |
DATE OF FIRST AUTHORISATION |
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Date: 29/01/1993 |
10. |
DATE OF REVISION OF THE TEXT |
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Date: September 2009 |
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