Composition:
A 600 mg tablet contains:
Active substances:
Praziquantel 50.00 mg
Pyrantel pamoate 150.00 mg
INDICATION(S)
The product is indicated for the treatment of nematodoses and cestodes in dogs and cats caused by adult and juvenile forms of Echinococcus spp., Taenia spp., Dipylidium caninum, Diphylobotrium erinacei, Mesocestoides corti, Toxocara caniÈ™, Toxascaris leonina, Ancylostoma caninum, Ancylostoma tubaeforme, Uncinaria stenocephala.
CONTRAINDICATIONS
Do not use in case of hypersensitivity to the active substances or to any of the excipients.
The product is not administered to puppies under 4 weeks of age and cats under 6 weeks of age.
ADVERSE REACTIONS
Very rarely, vomiting, anorexia, diarrhea can be observed when administering praziquantel, but without serious consequences. Dogs tolerate pyrantel pamoate very well, even in the case of multiple doses and therefore no adverse reactions occur.
TARGET SPECIES
Dogs and cats.
DOSAGE FOR EACH SPECIES, ROUTE(S) OF ADMINISTRATION AND METHOD OF ADMINISTRATION
The product is administered orally as follows:
– Dogs: 1 tablet/10 kg body weight
– Young cats: ¼ tablet/animal
– Adult cats: ½ tablet/animal
The treatment is administered 3 – 4 times a year.
RECOMMENDATIONS ON CORRECT ADMINISTRATION
To ensure the correct dose, body weight will be established as accurately as possible.
WITHDRAWAL TIME
Not applicable.
SPECIAL STORAGE PRECAUTIONS
Keep out of reach of children.
Store in the original packaging, at a temperature below 25 °C. Protect from light. Store in a dry place.
SPECIAL WARNING(S)
The following practices should be avoided, as they increase the risk of developing resistance and ultimately lead to ineffective treatment:
– frequent and repeated use of antiparasitics from the same class, over a long period of time, – underdosing which may result from underestimating the body weight of the animals.
People with known hypersensitivity to one of the components of the product should avoid contact with it. In case of accidental ingestion of the product or allergies caused by its contact with the skin, seek medical advice immediately and show the product package leaflet or the label.
There are no contraindications for the use of the product during pregnancy and/or lactation.
Do not administer concomitantly with products containing piperazine, as the anthelmintic effects of pyrantel and piperazine may be antagonistic. Concomitant administration with other cholinergics may cause toxicity. No toxic reactions have been reported in case of overdose.


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