Baytril 10% Oral Solution should not be used for prophylaxis. Official and local antimicrobal policies should be taken into account when the product is used. Fluoroquinolones should be reserved for the treatment of clinical conditions which have responded poorly, or are expected to respond poorly, to other classes of antimicrobials. Wherever possible, fluoroquinolones should only be used based on susceptibility testing. Use of the product deviating from the instructions given on the SPC may increase the prevalence of bacteria resistant to the fluoroquinolones and may decrease the effectiveness of treatment with other quinolones due to the potential for cross resistance. During the period of rapid growth, enrofloxacin may affect articular cartilage. Do not exceed the recommended dose. In accidental overdose there is no antidote and treatment should be symptomatic. For animal treatment only. This product should not be used for the treatment of poultry (chickens and turkeys). Baytril 10% Oral Solution is indicated for these animals. Not for use in exotic animals or birds intended for human consumption. User safety Wear impervious gloves when handling the product. Wash any splashes from skin or eyes immediately with water. Wash hands and exposed skin after use. Do not eat, drink or smoke whilst using the product. Withdrawal Periods Calves must not be slaughtered for human consumption during treatment. Calves may be slaughtered for human consumption only after 8 days from the last treatment.
Baytril 2.5% Oral Solution should not be used for prophylaxis.
Consult the Technical Services Department of Bayer prior to use in exotic animals.
Official and local antimicrobal policies should be taken into account when the product is used.
Fluoroquinolones should be reserved for the treatment of clinical conditions which have responded poorly, or are expected to respond poorly, to other classes of antimicrobials.
Wherever possible, fluoroquinolones should only be used based on susceptibility testing.
Use of the product deviating from the instructions given on the SPC may increase the prevalence of bacteria resistant to the fluoroquinolones and may decrease the effectiveness of treatment with other quinolones due to the potential for cross resistance.
During the period of rapid growth, enrofloxacin may affect articular cartilage. In the absence of data on its use in some exotic species, caution should be used when prescribing during these periods and a careful risk/benefit assessment made.
Do not exceed the recommended dose. In accidental overdose there is no antidote and treatment should be symptomatic.
For animal treatment only.
This product should not be used for the treatment of poultry (chickens and turkeys). Baytril 10% Oral Solution is indicated for these animals.
Not for use in exotic animals or birds intended for human consumption.
User safety
Wear impervious gloves when handling the product.
Wash any splashes from skin or eyes immediately with water.
Wash hands and exposed skin after use.
Do not eat, drink or smoke whilst using the product.
Withdrawal Periods
Calves must not be slaughtered for human consumption during treatment. Calves may be slaughtered for human consumption only after 8 days from the last treatment.
Not for use in exotic animals or birds intended for human consumption.
3. Baytril 2.5% Solution for Injection
ot for use in dogs less than one year of age or in exceptionally large breeds of dog with a longer growth period under 18 months of age.
Not for use in cats less than 8 weeks of age.
Baytril 2.5% Injection should not be used for prophylaxis.
Dogs:Not for use in dogs less than 1 year of age or in exceptionally large breeds of dog with a longer growth period under 18 months of age.
In dogs enrofloxacin may affect articular cartilage during the period of rapid growth.
Occasionally skin reactions have been seen after administration to kennelled greyhounds.
Cats:Retinotoxic effects including blindness can occur when the recommended dose is exceeded.
Exotic animals:Muscle bruising after injection in reptiles and birds has been reported occasionally.
Do not exceed the recommended dosage.
In dogs enrofloxacin may affect articular cartilage during the period of rapid growth.
Local tissue reactions may occasionally occur at the injection site. Normal sterile precautions should be taken.
Do not exceed the recommended dose. In accidental overdose there is no antidote and treatment should be symptomatic.
In target animal studies, cats have been shown to suffer ocular damage after receiving doses of more than 15mg/kg once daily for 21 consecutive days. Doses of 30mg/kg given once daily for 21 consecutive days have been shown to cause irreversible ocular damage. At 50mg/kg given once daily for 21 consecutive days, blindness can occur.
Not for use in exotic animals or birds intended for human consumption.
User safety:
Baytril 2.5% Solution for Injection is an alkaline solution. Wash any splashes from skin or eyes immediately with water
Do not eat, drink or smoke whilst using the product.
Care should be taken to avoid accidental self-injection. If accidental injection occurs, seek medical advice immediately.
4. Baytril 5% Solution for Injection
Dogs under 1 year of age should not be treated with Baytril as damage to the articular cartilage may occur during the period of rapid growth, specifically in large breeds of dog. As a precaution very large breeds of dog should not be treated with Baytril until they are 18 months of age because of their longer growth period. Not for use in cats less than 8 weeks of age.
Baytril 5% Injection should not be used for prophylaxis.
Cats: Retinotoxic effects including blindness can occur when the recommended dose is exceeded. In accidental overdose there is no antidote and treatment should be symptomatic.
In target animal studies, cats have been shown to suffer ocular damage after receiving doses of more than 15mg/kg once daily for 21 consecutive days. Doses of 30mg/kg given once daily for 21 consecutive days have been shown to cause irreversible ocular damage. At 50mg/kg given once daily for 21 consecutive days, blindness can occur.
Dogs: Occasionally skin reactions have been seen after administration to kennelled greyhounds.
Do not exceed the recommended dosage.
Repeat injections should be made at different sites.
Official and local antimicrobial policies should be taken into account when the product is used.
Fluoroquinolones should be reserved for the treatment of clinical conditions which have responded poorly, or are expected to respond poorly, to other classes of antimicrobials.
Whenever possible, fluoroquinolones should only be used based on susceptibility testing.
Use of the product deviating from the instructions given in the SPC may increase the prevalence of bacteria resistant to the fluoroquinolones and may decrease the effectiveness of treatment with other quinolones due to the potential for cross resistance.
During the period of rapid growth, enrofloxacin may affect articular cartilage.
Local tissue reactions may occur at the injection site. Normal sterile precautions should be taken.
Withdrawal Periods
MEAT
Cattle: Animals must not be slaughtered for human consumption during treatment. Animals may be slaughtered for human consumption only after 14 days from the last treatment.
Pigs: Animals must not be slaughtered for human consumption during treatment. Animals may be slaughtered for human consumption only after 10 days from the last treatment.
MILK
Not to be used in animals producing milk for human consumption.
User Safety: Baytril 5% Solution for Injection is an alkaline solution. Wash any splashes from skin and eyes immediately with water.
Do not eat, drink or smoke whilst using the product.
Care should be taken to avoid accidental self-injection. If accidental injection occurs, seek medical advice immediately.
5. Baytril Flavour Tabs
Not recommended for use in cats less than 8 weeks of age.
The product should not be used for prophylaxis.Do not exceed the recommended dose. In accidental overdosage vomiting, diarrhoea, and CNS/behavioural changes may occur. There is no antidote and treatment should be symptomatic.
In cats, retinotoxic effects including blindness can occur when the recommended dose is exceeded.
Not for use in dogs less than 1 year of age or in exceptionally large breeds of dog with a longer growth period under 18 months of age, as articular cartilage may be affected during the period of rapid growth.
6. Baytril Max Solution for Injection
Baytril Max 10% Solution for Injection should not be used for prophylaxis.
Official and local antimicrobial policies should be taken into account when the product is used.
Fluoroquinolones should be reserved for the treatment of clinical conditions which have responded poorly, or are expected to respond poorly, to other classes of antimicrobials.
Whenever possible, fluoroquinolones should only be used based on susceptibility testing.
Use of the product deviating from the instructions given in the SPC may increase the prevalence of bacteria resistant to the fluoroquinolones and may decrease the effectiveness of treatment with other quinolones due to the potential for cross resistance.
Do not exceed the recommended dose. In accidental overdose there is no antidote and treatment should be symptomatic
User safety
Baytril Max is an alkaline solution.
Wash any splashes from skin or eyes immediately with water.
Do not eat, drink or smoke whilst using the product.
Care should be taken to avoid self-injection. If accidental self-injection occurs, seek medical advice immediately.
Withdrawal Periods
Animals must not be slaughtered for human consumption during treatment. Cattle may be slaughtered for human consumption only after 14 days from the injection. Milk for human consumption must not be taken during treatment. Milk for human consumption may only be taken from cattle after 84 hours (i.e. 7 milkings) from the last treatment.
7. Baytril Piglet Doser
Baytril Piglet Doser
Contra-indications, warnings, etc
The product should not be used for prophylaxis.
Official and local antimicrobial policies should be taken into account when the product is used.
Fluoroquinolones should be reserved for the treatment of clinical conditions which have responded poorly, or are expected to respond poorly, to other classes of antimicrobials.
Whenever possible, fluoroquinolones should only be used based on susceptibility testing.
Use of the product deviating from the instructions given in the SPC may increase the prevalence of bacteria resistant to the fluoroquinolones and may decrease the effectiveness of treatment with other quinolones due to the potential for cross resistance.
Do not exceed the recommended dose. In accidental overdose there is no antidote and treatment should be symptomatic .
Consumer Safety
Withdrawal Period: Piglets: Meat: 10 days
User Safety
Wear impervious gloves when handling the product.
Wash any splashes from skin or eyes immediately with water.
Wash hands and exposed skin after use.
Do not eat, drink or smoke while using the product.
Environmental Safety
Any unused product or waste material should be disposed of in accordance with national requirements.