DOXYVET

Description

COMPOSITION

DOXYVET soluble powder is a drug containing crystalline molecules and is a yellow powder.

Each 1 g contains Doxycycline hyclate 500 mg and special excipients.

INDICATIONS
DOXYVET soluble powder is indicated in the treatment of CRD caused by organisms susceptible to Doxycycline, ornithosis (caused by chlamydia psittaci), pasteurella multocida and
arthritis (caused by chlamydia psittaci) mycoplasma synoviae) in chickens and turkeys raised for meat. The drug is also used for gastrointestinal and respiratory diseases such as bacteremia, E. coli infections, coli infections and chlamydiosis in calves with new ruminant activity.

DOSAGE AND ADMINISTRATION

Unless recommended by your veterinarian.
DOXYVET soluble powder is administered orally
by mixing with water for oral administration.
Dosage of drugs
Calves: 10mg/kg TT
Chicken, turkey: 20mg/kg Bt
Actual dose:
Calves: 0.5g/25kg TT
Chicken, and turkey: 10g/250kg TT
Continuous use 3-5 days
Need to mix medicine for pets to drink with the corresponding amount of water.
Do not mix with milk when used for calves.
It is recommended that pets be allowed to quench their thirst for 2-3 hours before giving medication.

Medicated water must be freshly prepared every day.

SIDE EFFECTS

Doxycycline has no side effects if used at the recommended dose and schedule. In case of long-term use and frequent repeated use, gastrointestinal side effects may occur. Care should be taken to avoid overdose and the maximum course of treatment should not exceed 5 days.
Long-term use of doycillin in young animals can cause discoloration of bones and teeth.

DRUG INTERACTIONS

Do not use the drug with mineral supplements. The 2nd and 3rd chemotherapy minerals may reduce the absorption of tetracycline from the gastrointestinal tract. Therefore, it should not be used with milk for calves. Should give calves, calves medicine before or after drinking milk 2-3 hours.

Doxycycline is incompatible with ampicillin sodium, amikacin sulphate, penicillin, carbenycillin sodium, Chloramphenicol sodium succinate, cloxacillin sodium, mereridin HCL, methylcillin, sodium, novobiosin sodium, oxacillin sodium, cephalosporines, sodium barbiturates, phenitoin, sodium pentozbarbital sodium, calcium complex, hydrocortisone sodium succinate, methyl
prednizolon sodium succinate and B vitamins.

OVERDOSE AND MEASURES TO BE TAKEN

The drug is safe when used at the recommended dose and schedule. At high doses, the drug can cause autoinfection, nephrotoxicity, severe diarrhea, loss of appetite and vomiting.

DRUG STOP TIME

Duration of drug elimination: calves, chickens and turkeys should not be slaughtered during treatment and for 14 days, 4 days and 6 days, respectively, after the end of treatment. Eggs from medicinal chickens and turkeys should not be obtained for human consumption.

CONTRAINDICATIONS

Do not administer to animals with impaired renal function. Tetracyclines should not be given to dogs, cats, or horses. It can affect the horse's biota. It is also not recommended for rabbits, rats and hamsters because it can affect the gastrointestinal microflora. When administered to animals that already have good ruminant activity can be harmful, the drug is not recommended for use in adult ruminants. The drug should not be used concurrently with drugs with autotoxic effects. Do not administer to animals susceptible to tetracycline.

GENERAL WARNINGS

Please consult your veterinarian before use and in case of undesirable effects. Keep out of reach of CHILDREN. Do not exceed the recommendeddose during treatment.

NOTES TO MANAGERS

Avoid inhalation of dust. In case of contact with eyes and skin, rinse with plenty of water.

STORAGE CONDITIONS AND SHELF LIFE.

Shelf life 2 years from date of manufacture. Avoid direct light

END-OF-USE DIPOSAL AND WARNING FOR THE NON- TARGETED SPECIES
Expired packaging bags should be discarded

SPECIFICATIONS
The drug is packed in 1kg in polyethylene plastic boxes with carton boxes.