Veraflox 2.5%
Active substance
ATC code
Species
Cats
Indications
Treatment of:
• acute infections of the upper respiratory tract caused by susceptible strains of Pasteurella multocida, Escherichia coli and the Staphylococcus intermedius group (including S. pseudintermedius).
• wound infections and abscesses caused by susceptible strains of Pasteurella multocida and the Staphylococcus intermedius group (including S. pseudintermedius).
Dose to be administered and administration route
Oral use.
Doses
The recommended dose is 5 mg/kg bodyweight of pradofloxacin once daily. Due to the graduation of the syringe the resulting dose range is 5 to 7.5 mg/kg bodyweight according to the following table:
Bodyweight of Cat (kg) |
Dose of Oral suspension to be given (ml) |
Pradofloxacin dose (mg/kg bw) |
> 0.67 - 1 |
0.2 |
5 – 7.5 |
1 – 1.5 |
0.3 |
5 – 7.5 |
1.5 – 2 |
0.4 |
5 – 6.7 |
2 – 2.5 |
0.5 |
5 – 6.3 |
2.5 – 3 |
0.6 |
5 – 6 |
3 – 3.5 |
0.7 |
5 – 5.8 |
3.5 – 4 |
0.8 |
5 – 5.7 |
4 – 5 |
1 |
5 – 6.3 |
5 – 6 |
1.2 |
5 – 6 |
6 – 7 |
1.4 |
5 – 5.8 |
7 – 8 |
1.6 |
5 – 5.7 |
8 – 9 |
1.8 |
5 – 5.6 |
9 – 10 |
2 |
5 – 5.6 |
To ensure a correct dose, bodyweight should be determined as accurately as possible to avoid under dosing.
To facilitate accurate dosing, the 15 ml bottle of Veraflox oral suspension is supplied together with a 3 ml oral dosing syringe (graduation: 0.1 to 2 ml).
Duration of treatment
The duration of the treatment depends on the nature and severity of the infection and on the response to treatment. For most infections the following treatment courses will be sufficient:
Indication |
Duration of treatment (days) |
Wound infections and abscesses |
7 |
Acute infections of the upper respiratory tract |
5 |
The treatment should be reconsidered if no improvement of the clinical condition is observed within 3 days after starting the treatment.
Method of administration
Shake well before use. | Draw out the equivalent dosage into the syringe. | Administer directly into the mouth. |
In order to avoid cross-contamination, the same syringe should not be used for different animals. Thus, one syringe should only be used for one animal. After administration, the syringe should be cleaned with tap water and stored in the carton box together with the veterinary medicinal product.
Adverse reactions
Mild transient gastro-intestinal disturbances including vomiting have been observed in rare cases.
The frequency of adverse reactions is defined using the following convention:
- very common (more than 1 in 10 animals treated displaying adverse reaction(s)
- common (more than 1 but less than 10 animals in 100 animals treated)
- uncommon (more than 1 but less than 10 animals in 1,000 animals treated-)
- rare (more than 1 but less than 10 animals in 10,000 animals treated)
- very rare (less than 1 animal in 10,000 animals treated, including isolated reports).
References
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Art. Nr. | 04895/5010 |
EAN | 4007221032281 |