Aqupharm 18 Solution For Infusion

Summary

Revised: July 2015

AN: 01568/2014

	SUMMARY OF PRODUCT CHARATERISTICS
1.	NAME OF THE VETERINARY MEDICINAL PRODUCT
	Aqupharm 18 Solution for Infusion
2.	QUALITATIVE AND QUANTITATIVE COMPOSITION
	Active ingredients Sodium Chloride Glucose Anhydrous (or Glucose Monohydrate 4.4% w/v) Ions Sodium Chloride Also contains 150 calories per litre as glucose For full list of excipients, see section 6.1		0.18% w/v 4.0% w/v 30.0 mmol/l 30.0 mmol/l
3.	PHARMACEUTICAL FORM
	Solution for infusion A clear, colourless solution free from particulate matter.
4.	CLINICAL PARTICULARS

4.1	Target species
	Dogs and Cats
4.2	Indications for use, specifying the target species
	For maintenance therapy after the fluid balance has been restored. It can be used for the treatment of moderate/prolonged dehydration due to water loss, but in severe cases Aqupharm No. 1 (Sodium Chloride Injection BP) should be given before continuing with Aqupharm No. 18.
4.3	Contraindications
	Sodium overload may occur in cases with myocardial and renal damage. It should also be appreciated that in the period following surgical interference or severe trauma there may be an inability to excrete excessive sodium.
4.4	Special warnings for each target species
	In evaluating an animal for possible fluid therapy the state of hydration, electrolyte balance, acid-base balance, renal function and caloric balance should be considered. Evaluation will be based on history, physical examination and laboratory testing. In animals with potassium deficiency it may be necessary to give additional oral potassium supplements.
4.5	Special precautions for use

i.		Special precautions for use in animals
		Before use, the bag should be inspected and rejected if the solution is not clear or if the inner container is damaged. The solution should be prewarmed to 37ºC to prevent hypothermia. Thrombosis of a chosen vein is always a possibility with intravenous infusion. If infusion is protracted then another vein should be selected after 12-24 hours.
ii.		Special precautions for the person administering the veterinary medicinal product to animals
		Wash hands after use.
iii.		Other precautions
		None
4.6	Adverse reactions (frequency and seriousness)
	Hypernatraemia (sodium overload) or an inability to excrete excessive sodium – see Overdose.
4.7	Use during pregnancy, lactation or lay
	There are no contra-indications to use of this product during pregnancy and lactation.
4.8	Interaction with other medicinal products and other forms of interaction
	Drugs should not be mixed in infusion containers or through the giving sets unless the components are of known compatibility. The user should refer to the manufacturer’s literature for any drug substance which he or she proposes to co-administer, and also to the Appendix of Drug Incompatibilities in the current edition of The Veterinary Formulary.

4.9	Amount(s) to be administered and administration route
	Remove outer bag and protective giving set inlet tab. Push cannula fully into giving set. Prime giving set. Perform venepuncture and immediately attach giving set. Adjust infusion rate as required. Delivery is from a closed circuit, it does not need an air inlet. Giving sets should be changed every 24 hours. The quantity of fluid and electrolyte for administration will consider existing deficits, maintenance needs and continuing losses. The existing deficit is that which has been lost prior to examination. This must be estimated by evaluating the patient’s history, making a physical examination and using laboratory aids. Maintenance therapy is to replace normal losses occurring via urine, faeces, respiratory tract and skin. As a general rule, maintenance therapy requires 50 ml/kg bodyweight/day. Continuing losses during a disease period should be estimated whenever possible, i.e., quantity of vomit, diarrhoea or blood loss. The clinical response of the animal rather than formulae or equations should be used to guide fluid therapy. The intravenous route of administration is preferred. Indwelling intravenous catheters offer significant advantage in intravenous fluid therapy. Subcutaneous administration may be used for isotonic and non-irritating solutions. The rate of administration should be considered with each individual patient. The aim should be to correct about half of the calculated deficit in the first 1-2 hours. As a general rule the following formula is the maximum satisfactory rate (less where cardiovascular or pulmonary disease exists). Maximum rate = Body wt (kg) × 90 = ml fluid per hour This rate should be slowed after the first hour and considerably slowed if no urine flow is established. Signs of over rapid administration include restlessness, moist lung sounds, tachycardia, tachypnoea, nasal discharge, coughing, vomiting and diarrhoea.
4.10	Overdose (symptoms, emergency procedures, antidotes), if necessary
	Symptoms: Associated signs of hypernatraemia include pronounced thirst, dry mucous membranes, constipation, hyperpyrexia, CNS disturbances, and ultimately convulsions. A plasma Na+ concentration of > 150 mEq/l and a urine specific gravity of > 1.030 indicates a hypernatraemic state. Treatment of overdosage: Injection of a diuretic.
4.11	Withdrawal period(s)
	Not applicable
5.	PHARMACOLOGICAL PROPERTIES
	Pharmacotherapeutic group: Electrolytes with carbohydrates

	ATC Vet Code: QB 05 BB 02

5.1	Pharmacodynamic properties
	This product is an intravenous solution containing 30mmol/l of sodium, 30mmol/l of chloride and 150calories per litre of glucose. When administered intravenously it will provide maintenance fluid needs after fluid balance has been restored.
5.2	Pharmacokinetic properties
	Pharmacokinetics cannot readily be applied to fluid therapy since most of the infused solution is predominantly water, which on infusion will become incorporated into water rich plasma.

6.	PHARMACEUTICAL PARTICULARS

6.1	List of excipients
	Water for injections
6.2	Incompatibilities
	Ampicillin; Benzylpenicillin sodium; Cloxacillin sodium; Heparin sodium; Noradrenaline acid tartrate; Sulphadiazine sodium; Tetracyclines.
6.3	Shelf life
	Shelf-life of the veterinary medicinal product as packaged for sale: 2 years.
6.4	Special precautions for storage
	Do not store above 25^oC. For single use only; any remaining solution should be discarded. This product does not contain an antimicrobial preservative. Do not freeze.
6.5	Nature and composition of immediate packaging
	Packaging Format 1 A colourless, flexible polyvinyl chloride (PVC) bag with a blue PVC twist off giving set port and a re-sealable additives port, containing 500 ml or 1000 ml clear colourless solution. PVC bags are overwrapped with HDPE Packaging Format 2 A colourless, flexible polyvinyl chloride (PVC) bag with re-sealable polyisoprene/polycarbonate giving set and additive ports, containing 500ml or 1000ml clear colourless solution. PVC bags are overwrapped with polypropylene. Pack sizes Cardboard box containing 20 bags of 500 ml solution for infusion 10 bags of 1000 ml solution for infusion Not all pack sizes may be marketed.
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.

7.	MARKETING AUTHORISATION HOLDER
	Animalcare Ltd 10 Great North Way York Business Park Nether Poppleton York YO26 6RB
8.	MARKETING AUTHORISATION NUMBER
	Vm 10347/4010
9.	DATE OF FIRST AUTHORISATION
	Date: 7 June 1993
10.	DATE OF REVISION OF THE TEXT
	Date: July 2015

APPROVED 15/07/15

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