Prazitel Plus for dogs of small and medium breeds weighing up to 20 kg 2 tablets
DESCRIPTION
Prazitel plus tabulellae - tablets for deworming dogs 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
Prazitel plus in one tablet (0.55 g) contains as active ingredients praziquantel - 50 mg, pyrantel pamoat - 140 mg, fenbendazole - 100 mg, and as auxiliary substances milk sugar - 224.7 mg, potato starch - 17, 0 mg, calcium stearic acid - 5.8 mg, gelatin - 1.5 mg, sodium croscarmellose - 11.0 mg.
PHARMACOLOGICAL PROPERTIES
Prazitel plusВ® tablets are combined anthelmintic drugs. The combination of praziquantel and pyrantel pamoate, which are part of the drug, provides a wide spectrum of anthelmintic action for all phases of development of round and tapeworms parasitizing in dogs 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 mainly in the urine within 24 to 48 hours. Prazitel plusВ® tablets, according to the degree of their effect on the body, are classified as moderately hazardous substances (hazard class 3 according to GOST 12.1.007-76); in recommended doses, they do not have immunotoxic, sensitizing, embryotoxic and teratogenic effects.
INDICATIONS
Prazitel plusВ® tablets are prescribed for dogs and puppies with therapeutic and prophylactic purposes for nematodes (toxocariasis, toxascariasis, uncinariosis, ankylostomiasis) and cestodosis (echinococcosis, alveococcosis, mesocestoidosis, dipyldiosis, diphyllobothyroidism) and mixed cestodiasis.
DOSES AND METHOD OF APPLICATION
Prazitel plus В® tablets are used for therapeutic and prophylactic 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.
For therapeutic and prophylactic purposes, dogs are prescribed Prazitel plus В® tablets at a dose of 1 tablet per 10 kg of animal weight.
Pregnant bitches Prazitel Plus В® tablets are prescribed 3 weeks before delivery; lactating - 2-3 weeks after childbirth with caution under the supervision of a veterinarian.
Prophylactic deworming of dogs is recommended to be carried out 1 time in 3 months, as well as 10 days before vaccination, using the drug in a therapeutic dose.
No prior fasting diet or laxatives are required. 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 were no side effects when using Prazitel plusВ® 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 plusВ® tablets should not be used simultaneously with anthelmintics containing piperazine. Prazitel plusВ® tablets are not intended for use in productive animals.
The drug should not be used in emaciated and sick animals with infectious diseases, bitches in the first half of pregnancy, and puppies under 2 weeks of age.
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 plusВ® tablets, you should follow the general rules of personal hygiene and safety measures provided for when working with medicines. 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 plusВ®. 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 the manufacturer's sealed packaging, in a dry place protected from direct sunlight, separately from food and feed, at a temperature from minus 10 В° C to 25 В° C. Prazitel tablets should be kept out of the 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 of animals