Lignol 2.0% W/V Solution For Injection
Revised: December 2012
AN: 01020/2012
SUMMARY OF PRODUCT CHARACTERICTICS
1. Name of Veterinary Medicinal Product
Lignol 2.0 % w/v Solution for Injection
2. Qualitative and Quantitative Composition
Active ingredients % w/v
Lidocaine hydrochloride / Lignocaine hydrochloride 2.0
Adrenaline acid tartrate*/ Epinephrine acid tartrate 0.00198
*Including a 10 % manufacturing overage
For a full list of excipients, see section 6.1.
3. Pharmaceutical Form
Solution for injection.
Sterile, aqueous solution.
4. Clinical Particulars
4.1 Target species
Cats, dogs and horses.
4.2 Indications for use, specifying the target species
A local anaesthetic agent for regional nerve block, paravertebral nerve block and infiltration anaesthesia, for use in cats, dogs and horses.
4.3 Contraindications
Do not use in cardiac or hepatic insufficiency.
Special warnings for each target species
None.
Special precautions for use
Special precautions for use in animals
Do not administer by intravenous injection.
Do not use for more than one induction of anaesthesia in any 24 hours.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
Following accidental self injection or ingestion seek medical advice taking the vial with you. Following eye contamination or excessive skin contact, irrigate/wash thoroughly with cold running water. Seek medical advice if irritation persists.
Other precautions
None.
4.6 Adverse reactions (frequency and seriousness)
None known.
4.7 Use during pregnancy, lactation or lay
Use with caution in pregnant animals.
4.8 Interaction with other medicinal products and other forms of interaction
None known.
4.9 Amounts to be administered and administration route
For local nerve block by subcutaneous injection.
Cat infiltration 1 ml
Dog infiltration 1-2 ml
Horse infiltration 50 ml max
For paravertebral block up to 10 ml each nerve.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
Local anaesthetics may have systemic adverse effects as a result of the raised plasma concentrations which occur when the rate of absorption exceeds the rate of breakdown. Toxicity causes excitation of the central nervous system, which may be followed by systemic depression leading to coma. Convulsions may be controlled with Diazepam.
4.11 Withdrawal periods
Horse meat: zero days.
5. Pharmacological Particulars
Pharmacotherapeutic group: Lidocaine, combinations
ATC Vet Code: QN01BB52
Pharmacodynamic properties
Lidocaine is a local anaesthetic of the amide type, used both by injection and for local application to mucous membranes.
5.2 Pharmacokinetic properties
Lidocaine has rapid onset of action when injected and spreads rapidly through surrounding tissues. The speed of onset and duration of action of Lidocaine may be increased by the addition of a vasoconstrictor.
Adrenaline is added to local anaesthetics, such as Lidocaine hydrochloride, to slow diffusion and limit absorption as it constricts arterioles and capillaries, so prolonging the duration of the effect and lessening the danger of toxicity.
6. Pharmaceutical Particulars
6.1 List of excipients
Sodium chloride
Sodium metabisulphite
Chlorocresol
Water for injections
6.2 Incompatibilities
None known.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 2 years.
Shelf life after first opening the immediate packaging: 28 days.
6.4 Special precautions for storage
Do not store above 25°C.
Discard unused material.
6.5 Nature and contents of immediate packaging
100 ml neutral amber glass vial fitted with a red rubber plug and an aluminium seal, containing a sterile, aqueous solution.
6.6 Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products, if appropriate
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.
MARKETING AUTHORISATION HOLDER
Dechra Limited
Dechra House
Jamage Industrial Estate
Talke Pits
Stoke-on-Trent
Staffordshire
ST7 1XW
UK
8. MARKETING AUTHORISATION NUMBER
Vm 10434/4028
DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
Date of first authorisation: 31 August 1993
Date of renewal of the authorisation: 31 August 2003
DATE OF ANY REVISION OF THE TEXT
Date: December 2012
Approved:
19/12/12
Page 4 of 4