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Amdipharm Plc

Regency House, Miles Gray Road, Basildon, Essex, SS14 3AF
Telephone: +44 (0)870 777 7675
Fax: +44 (0)870 777 7875
Medical Information Direct Line: +44 (0)1268 823 049
Medical Information e-mail: medinfo@amdipharm.com
Medical Information Fax: +44 (0)1268 535 287

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Summary of Product Characteristics last updated on the eMC: 04/01/2011
SPC Genticin Eye/Ear Drops


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1. NAME OF THE MEDICINAL PRODUCT

Genticin eye/ear drops.


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2. QUALITATIVE AND QUANTITATIVE COMPOSITION

Gentamicin Sulphate Ph. Eur. IDENTICAL TO (8801) 0.3% w/v gentamicin base.


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3. PHARMACEUTICAL FORM

Sterile, isotonic solution in dropper bottles.


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4. CLINICAL PARTICULARS

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4.1 Therapeutic indications

Genticin eye/ear drops are indicated:

1. For the treatment of superficial eye and ear infections caused by organisms sensitive to gentamicin.

2. For prophylaxis against infection in trauma of the eye or ear.


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4.2 Posology and method of administration

Adults, including the elderly and children

Eyes: 1 or 2 drops should be instilled in the affected eye up to six times a day, or more frequently if required. (Severe infections may require 1 or 2 drops every fifteen to twenty minutes initially, reducing the frequency of instillation gradually as the infection is controlled).

Ears: The area should be cleaned and 2 - 3 drops instilled in the affected ear three to four times a day and at night, or more frequently if required.


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4.3 Contraindications

Hypersensitivity to gentamicin or to any of the ingredients. Known or suspected perforation of the ear drum is a contra-indication to use in otitis externa only.


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4.4 Special warnings and precautions for use

Long-term continuous topical therapy should be avoided. Prolonged use may lead to skin sensitisation and the emergence of resistant organisms. Cross sensitivity with other aminoglycoside antibiotics may occur.

In severe infections, topical use of gentamicin should be supplemented with appropriate systemic antibiotic treatment.

Gentamicin may cause irreversible partial or total deafness when given systemically or when applied topically to open wounds or damaged skin. This effect is dose-related and is enhanced by renal and/or hepatic impairment and is more likely in the elderly.

The condition of the ear drum must always be checked before this medicinal product is prescribed. The medicinal product must not be used if the integrity of the ear drum cannot be guaranteed.

Irreversible toxic effects may result from direct contact of gentamicin with the middle and inner ear. The benefits of gentamicin therapy should be considered against the risk of infection itself causing hearing loss.

Contact lenses should be removed during the period of treatment of ocular infections.

Serious adverse reactions including neurotoxicity, ototoxicity and nephrotoxicity have occurred in patients receiving systemic gentamicin therapy. Although these effects have not been reported following topical otic use of gentamicin, caution is advised when used concomitantly with systemic aminoglycosides.


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4.5 Interaction with other medicinal products and other forms of interaction

Concurrent use with other potentially nephrotoxic or ototoxic drugs should be avoided unless considered essential by the physician.


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4.6 Pregnancy and lactation

Safety for use in pregnancy and lactation has not been established. Gentamicin should only be used in pregnancy or lactation when considered essential by the physician, after careful assessment of the potential risks and benefits.


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4.7 Effects on ability to drive and use machines

Patients should be advised that the use of Genticin in the eye may cause transient blurring of vision. If affected, patients should not drive or operate machinery until vision has cleared.


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4.8 Undesirable effects

Irritation, burning, stinging, itching and dermatitis may occur. In the event of irritation, sensitisation or super-infection, treatment should be discontinued and appropriate therapy instituted.

Gentamicin may cause nephrotoxicity when given systemically. However, it is likely that systemic absorption following topical administration does not constitute a comparable risk.


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4.9 Overdose

The oral ingestion of the contents of one bottle is unlikely to cause any significant adverse effect.


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5. PHARMACOLOGICAL PROPERTIES

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5.1 Pharmacodynamic properties

Gentamicin is a bactericidal antibiotic which acts by inhibiting protein synthesis.


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5.2 Pharmacokinetic properties

Topical application of gentamicin can result in some systemic absorption. Treatment of large areas can result in plasma concentrations of up to 1µg/ml.

> 90% Gentamicin is excreted in the urine by glomerular filtration.

< 10% is bound to plasma protein.

T½ = 2 - 3 hours in individuals with normal kidney function, but can be increased in cases of renal insufficiency.


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5.3 Preclinical safety data

Not relevant.


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6. PHARMACEUTICAL PARTICULARS

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6.1 List of excipients

Benzalkonium chloride BP, Borax Ph. Eur., Sodium chloride Ph. Eur., Water, purified Ph. Eur.


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6.2 Incompatibilities

None known.


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6.3 Shelf life

3 years. Discard contents 4 weeks after opening.


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6.4 Special precautions for storage

Store below 25°C. Do not freeze.


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6.5 Nature and contents of container

Genticin eye/ear drops are available in 10ml dropper bottles.


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6.6 Special precautions for disposal and other handling

Not applicable.


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7. MARKETING AUTHORISATION HOLDER

Amdipharm PLC

Regency House

Miles Gray Road

Basildon

Essex

SS14 3AF

United Kingdom


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8. MARKETING AUTHORISATION NUMBER(S)

PL 20072/0057


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9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

20 December 1994


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10. DATE OF REVISION OF THE TEXT

December 2010


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LEGAL STATUS

POM

Genticin is a registered trade mark

Item Code



More information about this product

Link to this document from your website: http://www.medicines.org.uk/emc/medicine/21757/SPC/


Active Ingredients/Generics

 
   gentamicin sulphate