Drontal Multi Aroma Meat Xl 8 Tablets Dogs

NAME
DRONTAL PLUS FLAVOR XL, TABLETS FOR DOGS

PHARMACOTHERAPEUTIC CATEGORY
Paziquantel, combinations.

ACTIVE PRINCIPLES
Febantel 525 mg, pyrantel embonate (pyrantel pamoate) 504 mg, praziquantel 175 mg.

EXCIPIENTS
Corn starch, lactose, microcrystalline cellulose, polyvinylpyrrolidone (povidone), magnesium stearate, sodium lauryl sulfate, anhydrous colloidal silica, irradiated artificial meat flavor.

INDICATIONS
For the control of round worms (roundworms, hookworms, trichurids) ethenias (including Echinococcus spp.), In particular for infestations by: roundworms (Toxocara canis, Toxascaris leonina), hookworms (Ancylostoma caninum, Uncinaria stenocephala), trichuris vulpis (Trichuris ) and tapeworms (flat worms: Dipylidium caninum, Mesocestoides spp., Taenia ovis, T. pisiformis, T.hydatigena, T.multiceps, Echinococcus granulosus). swine and can also transmit to humans echinococcosis (hydatidosis, cystic form), a serious social disease of regions with sheep farming. Therapeutic and / or prophylactic intervention with this drug (possibly planned on a large scale) interrupts the biological cycle of the parasite and prevents transmission to humans. Destroy the stools released within 24 hours after treatment.

CONTRAINDICATIONS / SECONDARY EFFECT
Do not use in animals with known hypersensitivity to active ingredients to any of the excipients. Until sufficient trials are available in early pregnancy bitches, it should not be used in the first two thirds of gestation.

SAFETY IN REF. SPECIES
A dose of Drontal plus flavor XL equal to 10 times that recommended

USE / ROUTE OF ADMINISTRATION
Oral.

DOSAGE
The recommended dose is 15 mg of febantel, 14.4 mg of pyrantel embonate and 5 mg of praziquantel / kg body weight. This corresponds to 1 tablet for every 35 kg of body weight. To ensure correct administration, body weight should be determined as accurately as possible. The 3 components febantel, pirantel and praziquantel are optimally dosed in tablets, so the SINGLE administration of: 1 tablet every 35 kg of body weight (half tablet for 17.5 kg of live weight) frees the dog from all round worms and from all tapeworms at the same time. The tablet is given to the dog directly in the mouth or wrapped in meat, or crushed in food. It is not necessary to respect particular dietary measures: neither fasting nor purgatives. A single administration is sufficient for the complete deworming of dogs. To control Toxacara, lactating dogs should receive treatment after the second week of calving and every 2 weeks until weaning. For periodic control, the adult dog can be treated every 3 months. In case of massive infestation, the treatment must be repeated every 14 days.

STORAGE
The unused half of the tablets should not be stored. This veterinary medicinal product does not require any special storage conditions.

WARNINGS
Treatment should be based on the results of the parasitological examination on the stool. Pest resistance to any particular class of anthelmintics may develop after frequent and repeated use of an anthelmintic of that stage. Roundworm and hookworm infestation In some patients, the parasites Ancylostoma caninume Toxocara canis may not be completely eliminated by treatment resulting in a continuing risk of egg spreading into the environment. Stool control analyzes are recommended and, based on the results of these tests, if necessary, treatment with a nematicide product can be proceeded with. In debilitated or severely infested animals, the product should only be used after a risk / benefit assessment by the responsible veterinarian. Do not use in animals with known hypersensitivity to any ingredient of the product. Special precautions to be taken by the person administering the product to animals: people with known hypersensitivity to the active ingredients contained in this medicine should administer the product with caution. Wash hands after use. Avoid contact with eyes. Do not eat, drink or smoke while using the product. Overdose: a dose of product equal to 10 times that recommended has been tolerated by dogs and puppies without signs of harm.

WAITING TIME
Not relevant.

TARGET SPECIES
Dogs (weighing 35 kg or more).

INTERACTIONS
Do not use simultaneously with piperazine.

DIAGNOSIS AND PRESCRIPTION
Non-prescription veterinary medicinal product.

SIDE EFFECTS
Rare cases of gastrointestinal disturbances (vomiting, anorexia, diarrhea).

PREGNANCY AND BREASTFEEDING
In the absence of specific studies on the target species, use in the last period of pregnancy and during lactation only according to the assessment of the risk-benefit ratio. Do not use in pregnant bitches during the first two thirds (6 weeks) of pregnancy.