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kafedif

Original price was: $60.00.Current price is: $55.00.

It is administered subcutaneously as a single dose.

SPECIAL CLINICAL AND SPECIAL WARNINGS FOR INFORMATION AND TARGET SPECIES

Because of the doping effect on race horses, the practice must be terminated 10 days before the race.

DRUG INTERACTIONS

There is no interaction with other drugs. Can be used together.

SYMPTOMS, PRECAUTIONS AND ANTIDOTE IN OVERDOSE

High doses can cause intermittent and constant fluttering with restlessness, insomnia, excitement. Respiratory acceleration, vomiting and shoots are observed. These effects can be prevented by barbiturates.

UNWANTED / SIDE EFFECTS

Peripheral dilates vessels, so it can cause a drop in blood pressure. It causes an increase in oxygen consumption in animals, an increase in body temperature, sweating, tremor and an increase in muscle tone.

WARNINGS ON DRUG RESIDUES IN FOOD

Drug residual purification time (ikas): The residual purification time for meat and milk in cattle, sheep and goats is “0” days. There is no harm in sending cattle, sheep and goats to the slaughter during the treatment and after the last drug application. Cow, dark and goat milk obtained during the drug use and after stopping can be made available for human consumption.

CONTRAINDICATIONS

Cafedif is a broad drug for the safety of treatment. However, high doses can cause restlessness, insomnia, excitement, intermittent and continuous fluttering. These effects can be prevented by barbiturates. High doses of parenteral administration to cats and dogs produce lethal effects.

USE IN PREGNANCY

There is no harm in using in pregnant animals.

GENERAL WARNINGS

Consult your veterinarian before use and if an unexpected effect is observed. Keep out of reach of children and away from food. Do not buy or use products with expired shelf life and damaged packaging.

STORAGE CONDITIONS AND SHELF LIFE

Store in a cool, dry place at room temperature (15-250 ° C) in its packaging. Shelf life is 5 years from the date of manufacture.

COMMERCIAL PRESENTATION

It is available in 10 ml and 20 ml clear glass vials, in a cardboard box.

APPROVAL DATE OF PROSPECTUS: 11.11.2005

REPUBLIC OF TURKEY MINISTRY OF FOOD, AGRICULTURE AND LIVESTOCK LICENSE DATE AND NO: 01.06.1977-4 / 394

PRODUCTION PLACE: Mefar İlaç San. Inc. Show in panorama view Ramazanoglu Mah. Ensar Cad. No: 20 34906 Kurtkoy – Pendik – Istanbul – Turkey

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Description

kafedif It is used in cases where the central nervous system and respiratory system need to be stimulated. At 1 ml; 250 mg of caffeine, 350 mg of sodium benzoate.

Cafedif
Injectable Solution
Veterinary Analeptic

COMPOSITION
It is a colorless, odorless, clear injection solution.
Caffeine: 250 mg
Sodium benzoate: contains 350 mg.

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PHARMACOLOGICAL PROPERTIES

The active ingredient of Kafedif is an alkaloid derived from caffeine xanthine. Cafedif is a highly effective CNS stimulus. Although the heart rate slows initially due to the stimulation of the central nervous system, it stimulates the heart muscle and accelerates the heartbeat regularly after a short time. Thus, the heart’s strength increases, pulse is accelerated, blood pressure rises and the coronary arteries are dilated, the heart feeds better. Stimulates striated muscles to increase contractile and effort strength (Doping). The cage exhibits its activity by inhibiting the activity of phosphodiesterase that breaks down sAMP and prolonging the half-life of this nucleotide in cells. The cafeteria is well absorbed from the application site and dispersed throughout the body. 80-85% is excreted in the urine within 48 hours.

Cafedif Indications

Cafedif is used as a stimulant in all situations in which the central nervous system and especially the respiratory center need to be stimulated.

DOSAGE AND ADMINISTRATION

By the advice of the veterinarian in another way: 5-15 mg / kg ca daily dose unless otherwise indicated

In horses and cattle (per 100 kg ca): 2-6 ml In
sheep and goats (per 50 kg ca): 1-3 ml In
dogs and cats (per 5 kg ca): 0.1-0.3 ml

 

CONTRAINDICATIONS

Cafedif is a broad drug for the safety of treatment. However, high doses can cause restlessness, insomnia, excitement, intermittent and continuous fluttering. These effects can be prevented by barbiturates. High doses of parenteral administration to cats and dogs produce lethal effects.

USE IN PREGNANCY

There is no harm in using in pregnant animals.

GENERAL WARNINGS

Consult your veterinarian before use and if an unexpected effect is observed. Keep out of reach of children and away from food. Do not buy or use products with expired shelf life and damaged packaging.

STORAGE CONDITIONS AND SHELF LIFE

Store in a cool, dry place at room temperature (15-250 ° C) in its packaging. Shelf life is 5 years from the date of manufacture.

COMMERCIAL PRESENTATION

It is available in 10 ml and 20 ml clear glass vials, in a cardboard box.

APPROVAL DATE OF PROSPECTUS: 11.11.2005

REPUBLIC OF TURKEY MINISTRY OF FOOD, AGRICULTURE AND LIVESTOCK LICENSE DATE AND NO: 01.06.1977-4 / 394

PRODUCTION PLACE: Mefar İlaç San. Inc. Show in panorama view Ramazanoglu Mah. Ensar Cad. No: 20 34906 Kurtkoy – Pendik – Istanbul – Turkey https://enongvetmedication.com/

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