Prazitel for cats 2 tablets

DESCRIPTION

Prazitel tablets (Prazitel tabulettae) - tablets for cats for deworming with nematodes and cestodes. In appearance, the drug is a flat-cylindrical tablet with a chamfer, a score and the PR logo, light yellow with a greenish tint.

COMPOSITION AND FORM OF ISSUE

As active ingredients, it contains praziquantel - 20.0 mg and pyrantel pamoate - 200.0 mg, and as auxiliary substances, potato starch - 10.0 mg, lactose - 80.0 mg, croscarmellose sodium - 6.0 mg, calcium stearic acid - 3.1 mg, gelatin - 0.9 mg;

PHARMACOLOGICAL PROPERTIES

Prazitel В® tablets are combined anthelmintic drugs. The combination of praziquantel and pyrantel pamoate, which are part of the preparation, provides a wide spectrum of anthelmintic action for all phases of development of round and tapeworms parasitizing in cats, kittens and puppies, incl. Toxocara canis, Toxocara mystax, Toxascaris leonina, Uncinaria stenocephala, Ancylostoma spp., Echinococcus granulosus, Alveococcus multilocularis, Mesocestoides lineatus, Dipylidium caninum, Diphyllobothrium latum. The mechanism of action of the active substances included in the drug is based on inhibition of fumarate reductase, persistent depolarization of muscle cells of the helminth, disruption of energy metabolism, which causes paralysis and death of the parasite and promotes its excretion from the gastrointestinal tract.

When administered orally, praziquantel is rapidly absorbed in the intestine and distributed in organs and tissues, excreted from the body mainly in the urine in a metabolized form; pyrantela pamoate is partially absorbed in the intestines and excreted from the body mainly in feces within 24 to 48 hours. Prazitel В® tablets, according to their impact on the body, are classified as moderately hazardous substances (hazard class 3 according to GOST 12.1.007-76); in recommended doses, they have no immunotoxic, sensitizing, embryotoxic and teratogenic effects.

INDICATIONS

Prazitel В® tablets are prescribed to cats, kittens and puppies with a therapeutic and prophylactic purpose for nematodes (toxocariasis, toxascariasis, uncinariosis, ankylostomiasis) and cestodoses (echinococcosis, alveococcosis, mesocestoidosis, dipylidiosis nematosis, diphylidiosis and diphylidiasis) and cestodiasis.

DOSES AND METHOD OF APPLICATION

Prazitel В® tablets are used for prophylactic and therapeutic purposes individually, once, in the morning feeding with a small amount of food (in a piece of sausage, meat, with minced meat, porridge). With a high degree of invasion, deworming is recommended to be repeated after 10 days.

Cats with a therapeutic purpose are prescribed Prazitel В® tablets for cats at a dose of 1 tablet per 4 kg of animal weight. Prophylactic deworming of cats is carried out 1 time in 3 months, as well as 10 days before vaccination.

No prior fasting diet or laxatives are required.

Symptoms arising from drug overdose have not been established. In case of non-observance of the established period of repeated treatments, the use of the drug should be resumed in the same dosage according to the same scheme.

SIDE EFFECTS

There are no side effects when using Prazitel В® tablets in accordance with this instruction. In animals, short-term salivation can be observed, which spontaneously passes and does not require the use of drugs.

CONTRAINDICATIONS

Possible individual intolerance to the components of the drug. Prazitel В® tablets should not be used simultaneously with anthelmintics containing piperazine. Prazitel В® tablets are not intended for use in productive animals.

SPECIAL INSTRUCTIONS

The peculiarities of the action of the drug during the first administration or upon its withdrawal were not revealed.

PERSONAL PREVENTION MEASURES

When working with Prazitel В® tablets, you should follow the general rules of personal hygiene and safety measures provided for working with medicinal products. At the end of work, you should thoroughly wash your hands with warm water and soap. In case of accidental contact of the drug with the skin or mucous membranes of the eyes, they must be rinsed with plenty of water. People with 3 hypersensitivity to the drug components should avoid direct contact with Prazitel В® tablets. In case of allergic reactions or accidental ingestion of the drug into the human body, you should immediately contact a medical institution (you should have instructions for use of the drug or a label with you). Empty packages from under the medicinal product must not be used for household purposes, they must be disposed of with household waste.

SHELF LIFE AND STORAGE

Store Prazitel tablets in a sealed manufacturer's packaging, in a dry place protected from direct sunlight, separately from food and feed, at temperatures from minus 10 C to 25 C. 5. Prazitel tablets should be stored out of reach of children.

The shelf life of the medicinal product, subject to storage conditions, is 3 years from the date of production. Prazitel tablets must not be used after the expiration date. Unused medicinal product is disposed of in accordance with legal requirements.

PACKAGING

Prazitel is produced packaged in 2 tablets in a blister strip made of polyvinyl chloride film and aluminum foil; in a contoured non-cell packaging made of paper with a polyethylene coating. Contour packages are placed individually in cardboard boxes (envelopes) with instructions for use.

Specifications

KolVUP

20

Manufacturer

Farmax

Temperature regime

from + 10 to +30

Teaser

the drug is active against round and tapeworms parasitizing in cats