Medine.co.uk

Liquid Life-Aid Oral Solution

Revised: 03 February 2009

AN: 01067/2008


SUMMARY OF PRODUCT CHARACTERISTICS


1. Name of the veterinary medicinal product


Liquid Life-Aid Oral Solution

2. Qualitative and quantitative composition


Active Substance(s) % w/v

Glucose Monohydrate 30.6675

Sodium Chloride 5.3750

Sodium Propionate 0.2625

Potassium Dihydrogen Orthophosphate 2.5425

Glycine 3.8750

Excipient(s)


Quinolene Yellow (E104) 0.0200


For a full list of excipients, see section 6.1


3. Pharmaceutical form


Oral solution.

A yellow oral solution.


4. Clinical Particulars


4.1 Target species


Calves

Pigs

Sheep


Indications for use, specifying the target species


Liquid Life-Aid is indicated in the reversal of the process of dehydration and electrolyte loss associated with scours in calves and pigs whether due to nutritional bacterial or viral causes. It is also indicated as an aid in recovery from pregnancy toxaemia and reversal of hypoglycaemia in sheep.


4.3 Contraindications


None.

4.4 Special Warnings for each target species


Piglets must not be left without a supply of prepared solution, drinking water or sow's milk during the period of treatment.

Weaned pigs sometimes over-drink the prepared solution if given ad lib.

The concentration should be reduced to 50% of normal when this is encountered.

4.5 Special precautions for use


Special precautions for use in animals


Adequate colostrum should have been fed to calves. Normal feeding should be resumed after the course of treatment. Fresh solutions should be prepared for each administration and if unused within 24 hours should be discarded.


Special precautions to be taken by the person administering the veterinary medicinal product to animals


Wash hands after use.


4.6 Adverse reactions (frequency and seriousness)

No undesirable effects.

4.7 Use during pregnancy, lactation or lay


Liquid Life-Aid can be safely administered during pregnancy and lactation.


4.8 Interaction with other medicinal products and other forms of interaction


None known.

4.9 Amounts to be administered and administration route


Calves and Pigs:

Liquid-Life-Aid is intended for oral administration only after dilution with 11.5 times its own volume of water.


Bought in calves: For nutritional support, administer 2 litres of prepared solution replacing the first feed on arrival. For the next feed give 1 litre of solution and 1 litre of milk replacer after which normal diet may be resumed.


Scouring calves: All milk and milk replacer is withdrawn. 2 litres of freshly prepared solution to be given twice daily for 2 days. For the next 4 feeds (2 days) 1 litre of solution and 1 litre of milk replacer to be administered. Thereafter normal diet is resumed. If symptoms are severe, the solution may be fed 3 or 4 times daily. The solution may be given for a maximum of 4 days only, when administered on its own.


Pigs - Suckling pigs: When symptoms appear, fresh solution to be made available to the whole litter in a clean container, with access to water and sow's milk maintained throughout dosing period. Allow approximately 200-300 ml (7-10 fl oz) of solution per piglet daily, the amount being determined by the age of the piglets, the number in the litter and the severity of the symptoms. Occasionally restriction of the water supply for a few hours may be necessary to encourage pigs to start drinking the prepared solution. Treatment may be continued for up to 8 days in total if symptoms persist.


Weaned pigs: Fresh solution to be made available to pigs showing signs of scour, allowing up to 1 litre daily for each weaner depending on the age of the pigs and the severity of the symptoms. It is advisable to restrict solid feed intake for the initial 1-2 days of dosing but fresh water supply should be maintained. Treatment may be continued for up to 8 days in total if symptoms persist.


Periods of stress: Liquid Life-Aid may be administered to animals for 2-3 days following periods of stress i.e. transporting.


Sheep: In case of pregnancy toxaemia in sheep 160ml of undilutedproduct should be administered using a suitable drenching bottle. Treatment should be repeated 3- 6 times daily as required.


Overdose (symptoms, emergency procedures, antidotes), if necessary


Not applicable.


Withdrawal period


Meat/Milk – Zero days/hours.


5. pharmacological properties


Pharmacotherapeutic group: Metabolic & Fluid Preparation


ATC Vet Code: QA07CQ02


Pharmacodynamic properties


Liquid Life Aid on reconstitution contains the following available ions, Sodium, Potassium, Phosphate, Propionate, Chloride, plus Glycine and Dextrose. Following oral administration to calves and pigs the animals intestinal absorptive mechanisms remain functional. This maintains the absorption of sodium and water into the blood and a reversal of the dehydration process which is the major cause of death in scours.

The glucose, glycine and propionate provide rapid source of replacement energy where ketosis results from high glucose demands.


6. Pharmaceutical particulars


6.1 List of excipients

Quinolene Yellow (E104)

Sodium Formaldehyde Sulphoxylate

Disodium Edetate Dihydrate

Chlorocresol

Sodium Hydroxide/Hydrochloric Acid (for pH adjustment)

Water Purified


Incompatibilities


None known.


Shelf life


Shelf-life of the veterinary medicinal product as packaged for sale : 18 months.


Special precautions for storage


Store in a dry place. Care should be taken to replace the lid tightly once the bottle has been opened.


Nature and composition of immediate packaging


1 litre blue high density translucent polyethylene dispenser bottle with blue polypropylene wadded caps.


Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products


Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.


7. MARKETING AUTHORISATION HOLDER


Norbrook Laboratories Limited

Station Works

Newry

Co. Down, BT35 6JP

Northern Ireland


8. MARKETING AUTHORISATION NUMBER(S)


Vm 02000/4074


9. DATE OF FIRST AUTHORISATION

14thAugust 1991

10. DATE OF REVISION OF THE TEXT


February 2009