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Clinical particulars
Target species
Pigs
Indications for use, specifying the target species
In pigs:
Symptomatic treatment of fever in the context of respiratory diseases in combination with an appropriate anti infective therapy, if necessary.
Contraindications
Do not use in cases of hypersensitivity to the active substance or to any of the excipients.
Do not use in animals with severe hepatic impairment,
Do not use in animals with severe renal impairment. See also Interaction with other medicinal products.
Do not use in animals suffering from dehydration or hypovolaemia
Special warnings for each target species
Animals with reduced water intake and/or disturbed general condition have to be treated parenterally.
In case of combined viral and bacterial aetiology of the disease, an appropriate anti infective therapy should be given concomitantly.
The anti-pyretic effect of the product is expected at 12 - 24 hours after the onset of treatment.
Special precautions for use
Special precautions for use in animals
None
Special precautions to be taken by the person administering the veterinary medicinal product to animals
The product can cause hypersensitive reactions (allergy). People with known hypersensitivity to paracetamol or any of the excipients should avoid contact with the product. The product may cause skin and eye irritation. Wear appropriate protective clothing, gloves, goggles and mask when handling the product.
In cases of accidental contact with the skin or eyes, rinse immediately with a large amount of water. If symptoms persist, seek medical advice and show the leaflet to the physician.
The product may be harmful if ingested. In the case of accidental ingestion, seek medical advice. Do not eat, drink or smoke while handling this product. Wash hands after use.
Adverse reactions (frequency and seriousness)
In rare cases, transient soft faeces can occur and can persist for up to 8 days after the withdrawal of treatment. This does not have any effect on the general condition of animals, and resolves without any specific treatment.
Use during pregnancy, lactation or lay
Laboratory studies in rats have not produced any evidence of teratogenic or foetotoxic effects at therapeutic doses. The administration of the product up to three times the recommended dose, during pregnancy or lactation, did not result in adverse effects. The product can be used during pregnancy and lactation.
Interaction with other medicinal products and other forms of interaction
Concurrent administration of nephrotoxic drugs should be avoided.
Amounts to be administered and administration route
In drinking water use
30 mg of paracetamol per kg body weight per day, for 5 days, orally, administered in the drinking water, equivalent to 0.75 ml of oral solution per 10 kg body weight per day for 5 days.
The intake of medicated drinking water depends on the clinical condition of the animals. In order to obtain a correct dosage, the concentration in the drinking water must be adjusted accordingly. To avoid under-dosing and to ensure a correct dosage, bodyweight should be determined as accurately as possible.
Recommendation for dissolution:
First add the necessary quantity of water for the preparation of the final solution in the container. Then add the product while stirring the solution. Preferably prepare the solution in water at ambient temperature (20°C – 25°C). For water at 25°C, there is an upper concentration limit of 40 ml of product per litre of drinking solution.
When using the product with a water proportioner, adjust the setting to 3% - 5%. Do not set proportioners below 3%.
The solution should be prepared freshly every 24 hours. No other source of drinking water should be available during the medication period.
Overdose (symptoms, emergency procedures, antidotes), if necessary
After administration of 5 times the recommended dose of paracetamol, liquid faeces with solid particles may occasionally occur. It does not have any effect on general body condition of animals.
N-acetylcysteine can be used in case of accidental overdose.
Excessive overdoses can cause hepatotoxicity.
Withdrawal period(s)
Meat and offal: zero days.