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Panacur 10% Oral suspension 1 Litre
Panacur 10% Oral suspension 1 Litre is used in the treatment of nematodes in horses and cattle. Panacur 10% Oral suspension 1 Litre is effective against encysted mucosal small redworm larvae in horses at both adult and larvae stages. Panacur 10% Oral suspension 1 Litre has an ovicidal effect on roundworm eggs. In cattle it is also effective against Cestodes. This suspension eradicates large strongyles and adult and larval small strongyles. Also controls ascarids and oxyurids species as well as Tapeworm.
Active Ingredient: Fenbendazole
Target Species: Horses, Cattle, Sheep
Treats and Controls: Encysted mucosal small redworm larvae in horses at both adult and larvae stages. Roundworm eggs. In cattle it is also effective against Cestodes. Large strongyles and adult and larval small strongyles. Ascarids Oxyurids and Tapeworm.
Administration Method: For oral administration only. Should be shaken well before use as is, without further dilution. Any standard dosing gun or drenching equipment may be used to administer treatment. To ensure correct dosage, the animals body weight should be determined as accurately as possible. Routine dosage for cattle and horses: 7.5 ml per 100 kg bodyweight.
Withdrawal time: Cattle: Meat and offal: 14 days. Milk: 4 days. Horses: Meat and offal: 14 days. Do Not use on mares producing milk for human consumption.
Dosage: Routine dosage for cattle and horses: 7.5 ml per 100 kg bodyweight.
Body weight | Worm dose volume | Applications per 1 Litre pack |
---|---|---|
100 kg | 7.5 ml | 133 |
200 kg | 15 ml | 66 |
300 kg | 22.5 ml | 44 |
400 kg | 30 ml | 33 |
500 kg | 37.5 ml | 26 |
600 kg | 42.5 ml | 23 |
700 kg | 50 ml | 20 |
800 kg | 57.5 ml | 17 |
900 kg | 65 ml | 15 |
1000 kg | 72.5 ml | 13 |
Features of Panacur 10% 1LTR:
Click here to Download Data Sheet
Health Products Regulatory Authority
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Panacur 10 % w/v Oral Suspension
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains
Active Substance
Fenbendazole 100 mg
Excipients
Sodium Methyl Parahydroxybenzoate 2.000 mg
Sodium Propyl Parahydroxybenzoate 0.216 mg
Benzyl alcohol 4.835 mg
For a full list of excipients see section 6.1.
3 PHARMACEUTICAL FORM
Oral suspension
4 CLINICAL PARTICULARS
4.1 Target Species
Horses and cattle
4.2 Indications for use, specifying the target species
For the treatment of immature and mature stages of nematodes of the gastro-intestinal and respiratory tracts of cattle and horses including encysted mucosal small redworm larvae in horses.
Panacur has an ovicidal effect on roundworm eggs.
Also effective against cestodes in cattle.
For the treatment of horses infected with adult large strongyles and adult and larval small strongyles.
Also controls ascarids and oxyurids species.
For the treatment of cattle infected with adult and immature stages of:
Haemonchus spp.,
Ostertagia spp.,
Trichostrongylus spp.,
Cooperia spp.,
Nematodirus spp.,
Bunostomum spp.,
Trichuris spp.,
Strongyloides spp.,
Oesophagostomum spp.,
Capillaria spp.,
Dictyocaulus spp.
Used at the recommended dose and time, Panacur is effective against inhibited larvae of Ostertagia spp. and against Moniezia spp. of tapeworm.
4.3 Contraindications
Do not use in cases of hypersensitivity to the active substance or to any of the excipients.
4.4 Special warnings for each target species
Care should be taken to avoid the following practices because they increase the risk of development of resistance and could ultimately result in ineffective therapy:
• Too frequent and repeated use of anthelmintics from the same class, over an extended period of time.
• Underdosing, which may be due to underestimation of body weight, misadministration of the product, or lack of calibration of the dosing device.
Suspected clinical cases of resistance to anthelmintics should be further investigated using appropriate tests (e.g. Faecal Egg Count Reduction Test).
Where the results of the test(s) strongly suggest resistance to a particular anthelmintic, an anthelmintic belonging to another pharmacological class and having a different mode of action should be used.
Resistance to benzimidazoles has been reported in gastro-intestinal nematodes in horses.
Therefore, the use of this product should be based on local epidemiological information about susceptibility of the nematodes and recommendations on how to limit further selection for resistance to anthelmintics.
4.5 Special precautions for use
Special precaution(s) for use in animals
As with other anthelmintics, veterinary advice should be sought on appropriate dosing programmes and stock management to achieve adequate parasite control and reduce the likelihood of anthelmintic resistance developing. Special precautions to be taken by the person administering the veterinary medicinal product to animals
Direct contact with the skin should be kept to a minimum.
Wear suitable protective clothing including impermeable rubber gloves.
Wash hands after use.
4.6 Adverse reactions (frequency and seriousness)
None known.
4.7 Use during pregnancy, lactation or lay
Can be administered at any stage of pregnancy or lactation.
4.8 Interaction with other medicinal products and other forms of interaction
None known.
4.9 Amounts to be administered and administration route
For oral administration only.
The suspension should be shaken well before use and is ready for use without further dilution.
The product can be administered by any standard dosing gun or drenching equipment.
To ensure administration of a correct dose, body weight should be determined as accurately as possible; accuracy of the dosing device should be checked.
Routine dosage for cattle and horses:
7.5 mg fenbendazole/kg bodyweight as a single dose corresponding to 7.5 ml per 100 kg bodyweight.
Examples:
BODY WEIGHT | VOLUME |
---|---|
UP TO 100kg | 7.5 ml |
100-200kg | 15ml |
200-300kg | 22.5ml |
300-400kg | 30ml |
For bodyweight in excess of 400 kg use 30 ml plus an additional 3.75 ml per 50 kg.
Treatment should be repeated every 6-8 weeks during the grazing season.
Treatment of specific indications in horses:
For the treatment of mucosal stages of Trichonema spp. - 30 mg/kg.
For the treatment of migrating stages of Strongylus vulgaris and Strongylus edentatus - 60 mg/kg.
Alternatively for the control of migrating larval stages of large strongyles and encysted mucosal stages of small strongyles (cyathostomes) administer 7.5 mg/kg fenbendazole daily for five days.
Diarrhoea caused by Strongyloides westeri in sucking foals should be treated with a dose of 25 ml Panacur 10% per 50 kg bodyweight (50 mg fenbendazole/kg bodyweight).
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
None known.
4.11 Withdrawal period(s)
Cattle:
Meat and offal: 14 days
Milk: 4 days
Horses:
Meat and offal: 14 days
Not authorised for mares producing milk for human consumption.
5 PHARMACOLOGICAL or IMMUNOLOGICAL PROPERTIES
Pharmacotherapeutic group:
Anthelmintics;
Benzimidazoles and related substances
ATCvet code:
QP52AC13
5.1 Pharmacodynamic properties
Fenbendazole is an anthelmintic belonging to the benzimidazole-carbamate group.
It acts by interfering with the energy metabolism of the nematode.
The anthelmintic affects both adult and immature stages of gastro-intestinal and respiratory nematodes.
This anthelmintic efficacy is based on inhibition of the polymerisation of tubulin to microtubuli.
5.2 Pharmacokinetic properties
Fenbendazole is only partly absorbed after oral administration and is then metabolised in the liver.
The half-life of fenbendazole in serum after oral application of the recommended dose is
10-18 hours in cattle,
21-33 hours in sheep and
10 hours in pigs.
Fenbendazole and its metabolites are distributed throughout the body but highest concentrations are found in the liver.
The elimination of fenbendazole and its metabolites occurs primarily via the faeces (>90%) and to a smaller extent as well in the urine and milk.
Fenbendazole is metabolised to its sulfoxide, then to sulfone and amines.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Colloidal Silicon Dioxide
Sodium Carboxymethyl Cellulose
Povidone 25000
Sodium Citrate Dihydrate
Citric Acid Monohydrate
Sodium Methyl Parahydroxybenzoate
Sodium Propyl Parahydroxybenzoate
Benzyl Alcohol
Purified Water
6.2 Incompatibilities
None known.
6.3 Shelf-life
Shelf-life of the veterinary medicinal product as packaged for sale: 3 years
6.4 Special precautions for storage
Do not store above 25°C. Protect from freezing.
6.5 Nature and composition of immediate packaging
Multidose aluminium foil sealed polyethylene containers with polypropylene screw caps containing
250 ml, 1 litre and 2.5 litres of suspension.
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
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements.
The product should not enter water courses as this may be dangerous for fish and other aquatic organisms.
7 MARKETING AUTHORISATION HOLDER
Intervet Ireland Limited
Magna Drive
Magna Business Park,
Citywest Road
Dublin 24
Ireland
8 MARKETING AUTHORISATION NUMBER(S)
VPA10996/111/001
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
Date of first authorisation: 01/10/1999
Date of last renewal: 30/09/2009
10 DATE OF REVISION OF THE TEXT
September 2017
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