Piperazine Citrate Worm Tablets
Revised: February 2010
AN: 01728/2009
SUMMARY OF PRODUCT CHARACTERISTICS
NAME OF VETERINARY MEDICINAL PRODUCT
Piperazine Citrate Worm Tablets
QUALITATIVE AND QUANTITATIVE COMPOSITION
Active Ingredient: Piperazine Citrate, 500mg/tablet
PHARMACEUTICAL FORM
Tablet.
PHARMACOLOGICAL PROPERTIES
Summary Presentation of the Active Ingredient
Piperazine Citrate is an anthelmintic of low toxicity with a high efficiency against ascarids and some other nematodes.
Pharmacodynamic Properties
Piperazine acts to block neuromuscular transmission in the parasite by hyperpolarizing the nerve membrane, which leads to flaccid paralysis. It also blocks succinate production by the worm. The parasites, paralysed and depleted of energy, are expelled by peristalsis. It is active against the ascarids Toxocara canis, Toxocara cati/ roundworm, Toxascaris leonine and hookworms.
Pharmacokinetic Properties
Piperazine is rapidly absorbed from the GI tract, and piperazine base can be detected in the urine as early as 30 minutes after administration. The excretion rate is maximal at 1 – 8hr, and excretion is practically complete within 24hrs.
ATC Vet Code QP52AH01
CLINICAL PARTICULARS
Target species
Cat, Dog.
Indications for use, specifying the target species
Piperazine Citrate is indicated for the treatment and control of intestinal infections/ infestations of dogs and cats, and may be used from 2 weeks of age.
Contra-indications
Whilst piperazine salts have few side effects and are of low toxicity, care should be taken, especially with kittens and puppies, to ensure that the correct dosage is calculated by weighing the animal prior to administration of the drug. Animals weighing less than 1.25kg should be treated with a suitable anthelmintic licensed for this purpose.
Do not repeat treatment if vomiting occurs shortly after dosing.
Do not administer more than 6 tablets in a single dose. If no vomiting occurs the remaining dose may be given after 3 hours.
Undesirable effects, frequency and seriousness
Transient neurological effects and urticarial reactions have occasionally been noted.
Special precautions for use
Care should be exercised when giving piperazine to patients with a history of epilepsy and severe renal dysfunction.
Use during Pregnancy and Lactation
Consult a veterinary surgeon before treating pregnant animals.
Interaction with other medicaments and other forms of interaction
None known
Posology (dosage) and method of administration
Puppies and Kittens
200mg/kg as a single dose (1 tablet per 2.5kg bodyweight).
1stdose: 2 weeks of age
2nddose: 2 weeks later
Subsequent doses: every 2 weeks of age until 3 months of age and then at 3 monthly intervals.
Nursing Bitches and Queens
They should be treated at 2 weeks after giving birth and every 2 weeks until weaning. It is advisable to treat bitches and queens at the same time as the puppies or kittens.
Older dogs and cats
200mg/kg as a single dose (1 tablet per 2.5kg body weight) at 9 months of age. Repeat treatment at 3 monthly intervals.
Do notrepeat the treatment if vomiting occurs shortly after dosing.
Do not administer more than 6 tablets in a single dose. If no vomiting occurs the remaining dose may be given after 3 hours.
Overdose
Acute overdose
Piperazine has a wide safety margin, and acute overdose is unlikely. Where it does occur however, there may be symptoms of neurotoxicity. There is no known specific antidote.
Chronic overdose
Piperazine Citrate tablets are a single dose treatment. Chronic overdose is therefore not an issue.
Special warnings for each target species
None
Withdrawal periods
Not applicable.
Special precautions to be taken by the person administering the product to animals
Wash hands immediately after administering the tablets.
PHARMACEUTICAL PARTICULARS
Incompatibilities
None known
Shelf life
3 years
Special precautions for storage
Protect from light. DO NOT STORE ABOVE 25ºC. Store in a dry place.
Nature and contents of container
White cylindrical polypropylene containers (securitainer) with white tamper evident snap top polyethylene closure, containing 500 tablets, 75mm diameter x 130mm high.
Special precautions for disposal of unused product or waste materials, if any
None.
FINAL INFORMATION
Name and registered place of business of the holder of the marketing authorisation:
Ayrton Saunders Ltd
9 Arkwright Road
Astmoor Industrial Estate
Runcorn
Cheshire
WA7 1NU
Marketing authorisation number:
Vm16431/4003
Date of SPC:
February 2010
Date of issue of last renewal:
14 October 2009