The control of the Clostridium perfringens type A associated diarrhea in suckling piglets by vaccination
D. Sperling, J. Vanhara, T. Jirasek, N. Guerra
The-control-of-the-C (1.44 MB)DownloadTulaven® is an effective solution for the metaphylaxis and treatment of bacterial pathogens involved in PRDC in all production phases (farrowing, nursery and finishing period).
Available in :
Easy to administrate (one shot): Its concentration dedicated exclusively to swine (25 mg/ml)
facilitate optimal administration in farrowing and weaning piglets with only one shot.
Safe and high effective: Tulathromycin has unique effect due to its rapid and extensive
distribution into the lung tissue (target tissue of respiratory pathogens). Very long duration and
potential effect can be estimated based on plasma/lung ratio of tulathromycin in lungs. At 408 h
(17 days) post-tulathromycin administration, the lung/plasma ratio was >300 for both lung lobes
during the Pk/Pd study.
Tulathromycin provides at least 9 days of complete protection against A. pleuropneumoniae
during the challenge trial. Duration of treatment effect for 15 days was observed based on clinical
symptoms and examination of bronchoalveolar lavage (BAL) for H. parasuis and P. multocida.
Tulathromycin provide 14 days clinical effect for SRD associated with B. bronchiseptica based on
Day 14 clinical cure rate. Treatment effect of tulathromycin for minimally 13 days was established
following experimental infection of swine with Mycoplasma hyopneumoniae. Due to the very
low and stable MIC90 for M. hyo strains and Tulathromycin relatively high concentration in lungs
we can assume even longer effect.
Easy to administrate (one shot)
Safe and high effective
D. Sperling, J. Vanhara, T. Jirasek, N. Guerra
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Evaluation-of-the-ef (1.21 MB)DownloadFrom one country to another, product lines are adapted to local demand and regulatory requirements. For further information, please take a look at the CEVA Santé Animale site for your country. Warning: the information provided on the products depends on national registrations. Access to technical information is restricted to authorised persons.