Medine.co.uk

Maxyl 500 Mg/G Powder For Use In Drinking Water For Chickens, Turkeys, Ducks And Pigs

Issued: October 2014

AN: 00388/2013

SUMMARY OF PRODUCT CHARACTERISTICS


NAME OF THE VETERINARY MEDICINAL PRODUCT


MAXYL 500 mg/g POWDER FOR USE IN DRINKING WATER FOR CHICKENS, TURKEYS, DUCKS AND PIGS[AT, BG, CY, DE, DK, HU, IE, IT, NL, PL, PT, UK]


Maxyl vet 500 mg/g powder for use in drinking water for chickens, turkeys, ducks and pigs[SE]


BETAMAXYL 500 mg/g POWDER FOR USE IN DRINKING WATER FOR CHICKENS, TURKEYS, DUCKS AND PIGS[ES]


QUALITATIVE AND QUANTITATIVE COMPOSITION


Each gram contains:


Active substance:

Amoxicillin (equivalent to 500 mg amoxicillin trihydrate) 436 mg


For a full list of excipients, see section 6.1.


PHARMACEUTICAL FORM


Powder for use in drinking water.

A white powder. Clear and colourless liquid when in solution.


CLINICAL PARTICULARS


Target species


Chickens, turkeys, ducks and pigs.


Indications for use, specifying the target species


Treatment of infections in chickens, turkeys and ducks caused by bacteria susceptible to amoxicillin.


Pigs: For the treatment of pasteurellosis.


Contraindications


This product should not be administered to rabbits, guinea pigs, hamsters, gerbils or any other small herbivore.


Do not use in animals with known hypersensitivity to penicillins or other ß-lactam antibiotics or to any of the excipients.


Do not administer to animals with renal disease including anuria or oliguria.


Special warnings for each target species


None


Special precautions for use


Special precautions for use in animals


Not effective against beta-lactamase producing organisms.

Pigs: The uptake of medication by animals may be altered as a consequence of illness. In case of insufficient water uptake, animals should be treated parenterally instead.

Official, national and regional antimicrobial policies should be taken into account when the product is used.

Use of the product should be based on susceptibility testing of the bacteria isolated from the animal. If this is not possible, therapy should be based on local (regional, farm level) epidemiological information about susceptibility of the target bacteria.

Use of the product deviating from the instructions given in the SPC may increase the prevalence of bacteria resistant to the amoxicillin and may decrease the effectiveness of the treatment.


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


Penicillins and cephalosporins may cause hypersensitivity (allergy) following injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross reactions to cephalosporins and vice versa. Allergic reactions to these substances may occasionally be serious.

People with known hypersensitivity the active substance or if you have been advised not to work with such preparations should avoid contact with the veterinary medicinal product.

Handle this product with great care to avoid exposure, taking all recommended precautions.

If you develop symptoms following exposure such as a skin rash, you should seek medical advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty with breathing are more serious symptoms and require urgent medical attention.

Avoid inhalation of dust. Wear either a disposable half-mask respirator conforming to European Standard EN149 or a non-disposable respirator to European Standard EN140 with a filter to ENl43.

Wear gloves during preparation and administration of medicated water or liquid feed.

Wash any exposed skin after handling the product or medicated water or feed. Wash hands after use.


Adverse reactions (frequency and seriousness)


Penicillins and cephalosporins may cause hypersensitivity reactions which may occasionally be serious.


Use during pregnancy, lactation or lay


Laboratory studies in rats have not produced any evidence of a teratogenic effect due to the administration of amoxicillin.

Use only according to the benefit/risk assessment of the responsible veterinarian.

Do not use in birds producing eggs for human consumption or within 3 weeks of onset of laying.


Interaction with other medicinal products and other forms of interaction


The product should not be administered with antibiotics that have a bacteriostatic mode of action, such as tetracyclines, macrolides, sulphonamides.


Amounts to be administered and administration route


In drinking water use.


Prepare the solution with fresh potable water immediately before use. Any medicated water which is not consumed within 12 hours should be discarded and the medicated drinking water replenished.


In order to ensure consumption of the medicated water, animals should not have access to other water supplies whilst being treated.


The following formula may be used to calculate the required concentration of product (in milligrams of product per litre of drinking water):


x mg product per kg bodyweight per day

X

mean bodyweight (kg) of animals to be treated

= x mg product per litre drinking water

mean daily water consumption (l) per animal


To ensure a correct dosage, bodyweight should be determined as accurately as possible to avoid underdosing. The uptake of medicated water depends on the clinical condition of the animal. In order to obtain the correct dosage the concentration of amoxicillin has to be adjusted taking into account water intake.


Chickens

The recommended dosage is 15 mg amoxicillin trihydrate per kg bodyweight per day (corresponding to 30 mg product/kg·bodyweight/day).

The total period of treatment should be for 3 days or in severe cases for 5 days.


Ducks

Recommended dosage is 20 mg amoxicillin trihydrate/kg bodyweight per day (corresponding to 40 mg product/kg bodyweight/day) for 3 consecutive days.


Turkeys

Recommended dosage is 15-20 mg amoxicillin trihydrate/kg bodyweight per day (corresponding to 30-40 mg product/kg·bodyweight/day) for 3 days or in severe cases for 5 days.


Pigs

Administer in the drinking water to give 20 mg amoxicillin trihydrate/kg bodyweight (corresponding to 40 mg product/kg·bodyweight) daily for up to 5 days.


After the end of the medication period the water supply system should be cleaned appropriately to avoid intake of sub-therapeutic amounts of the active substance.


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


No problems with overdosage have been reported. Treatment should be symptomatic and no specific antidote is available.


Withdrawal periods


Meat and offal:

Chickens 1 day

Ducks 9 days

Turkeys 5 days

Pigs 2 days


Not authorised for use in laying birds producing eggs for human consumption and within 3 weeks of onset of laying.


PHARMACOLOGICAL PROPERTIES


Pharmacotherapeutic group:Beta-lactam antibiotic, penicillins

ATCVet code:QJ01CA04


Pharmacodynamic properties


Amoxicillin is a bactericidal antibiotic belonging to the group of semisynthetic penicillinswith a broad spectrum of activity against Gram positive and Gram negative bacteria. It owes its activity to the inhibition of the development of the peptidoglycan network structure in the bacterial cell wall.



Pharmacokinetic particulars


Amoxicillin is well absorbed following oral administration and it is stable in the presence of gastric acids. Excretion of amoxicillin is mainly in the unchanged form via the kidneys to give high concentration in renal tissue and urine. Amoxicillin is well distributed in body fluids.


Studies in birds have indicated that amoxicillin is distributed and eliminated more rapidly than in mammals.

Biotransformation appeared a more important route of elimination in birds than in mammals.


PHARMACEUTICAL PARTICULARS


List of excipients


Anhydrous citric acid


Incompatibilities


In the absence of compatibility studies, this veterinary product must not be mixed with other veterinary medicinal products.


Shelf life


Shelf life of the veterinary medicinal product as packaged for sale: 21 months

Shelf life after first opening the immediate packaging: 3 months

Shelf life after dilution or reconstitution according to directions: 12 hours


Special precautions for storage


Do not store above 30ºC.

Keep the bags tightly closed.


Nature and composition of immediate packaging


Thermosealed bags made of polyester, aluminium and polyethylene complex.


Pack sizes:

400g bag

1kg bag

Box with 15 bags of 1kg.


Not all pack sizes may be marketed.



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.


MARKETING AUTHORISATION HOLDER


Vetpharma Animal Health, S.L.

Les Corts, 23

08028 Barcelona

Spain


MARKETING AUTHORISATION NUMBER


Vm32509/4019


DATE OF FIRST AUTHORISATION


Date:08 October 2014


DATE OF REVISION OF THE TEXT


Date:October 2014


PROHIBITION OF SALE, SUPPLY AND/OR USE


For animal treatment only.

To be supplied only on veterinary prescription


Approved: 08/10/2014

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