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*Pregnancy category: AU: B3
Pregnancy category: AU: B3
*Metabolism: Kidney and non-kidney
Metabolism: Kidney and non-kidney
*Excretion: Bile duct (70%); kidney (30%)
Excretion: Bile duct (70%); kidney (30%)
*AHFS/Drugs.com: International Drug Names
AHFS/Drugs.com: International Drug Names
*ATCvet code: QJ01MA90 (WHO) QD06BA51 (WHO)
ATCvet code: QJ01MA90 (WHO) QD06BA51 (WHO)
*Bioavailability: 80% in dogs, 65-75% in sheep
Bioavailability: 80% in dogs, 65-75% in sheep
*Elimination half-life: 4–5 hours in dogs, 6 hours in cats, 1.5 - 4.5 hours in sheep
Elimination half-life: 4–5 hours in dogs, 6 hours in cats, 1.5 - 4.5 hours in sheep
*Antimicrobial Agents Used in Rabbits
 




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Broome RL, Brooks DL. Efficacy of enrofloxacin in the treatment of respiratory pasteurellosis in rabbits. Lab Anim Sci 1991;41:572-576.
Broome RL, Brooks DL. Efficacy of enrofloxacin in the treatment of respiratory pasteurellosis in rabbits. Lab Anim Sci 1991;41:572-576.


Baytril has also been effective to treat  early onset cases in trials 2014.
https://bmcvetres.biomedcentral.com/articles/10.1186/s12917-014-0276-6
Alternative treatment of serious and mild Pasteurella multocida infection in New Zealand White rabbits
Orsolya Palócz, János Gál, Paul Clayton, Zoltán Dinya, Zoltán Somogyi, Csaba Juhász & György Csikó
BMC Veterinary Research volume 10, Article number: 276 (2014)
Pasteurella multocida causes numerous economically relevant diseases in livestock including rabbits. Immunization is only variably effective. Prophylactic
antibiotics are used in some species but are contra-indicated in rabbits, due to their adverse effects on the rabbit microbiota. There is therefore a substantial
need for alternative forms of infection control in rabbits; we investigated the effect of oral β-glucan on P. multocida infection in this species.


Results
Thirty-five New Zealand White rabbits were randomly divided into five groups of seven animals. Three groups were inoculated with Pasteurella multocida
intranasally (in.), a physiologically appropriate challenge which reproduces naturally acquired infection, and received either (1-3), (1-6) β-glucans or placebo.
Four other groups were inoculated both in. and intramuscularly (im.), representing a supra-physiological challenge, and received either (1-3), (1-6) β-glucans,
antibiotic or placebo. β-glucans given prophylactically were highly effective in protecting against physiological (in.) bacterial challenge. They were less
effective in protecting against supra-physiological bacterial challenge (in. and im.), although they extended survival times. This latter finding has practical
relevance to breeders as it extends the window in which heavily infected and symptomatic animals can be salvaged with antibiotics.


Conclusions
===GI stasis protocol===
In our study, (1-3), (1-6) β-glucans were highly effective in protecting against a model of naturally acquired P. multocida infection and extended survival times
• Use only when indicated; enrofloxacin or trimethoprim/sulfa are generally the drugs of choice; use parenterally until stools are passed; metronidazole may be indicated for anaerobe overgrowth
in the supra-physiological model. Enrofloxacin(baytril) was effective in protecting against supra-physiological infection. We are currently reviewing the use of combined
 
prophylaxis.
 
 
 






===GI stasis protocol===
• Use only when indicated; enrofloxacin or trimethoprim/sulfa are generally the drugs of choice; use parenterally until stools are passed; metronidazole may be indicated for anaerobe overgrowth


*Broome RL, Brooks DL, Babish JG, et al. Pharmacokinetic properties of enrofloxacin in rabbits. Am J Vet Res 1991;52:1835-1841.
*Broome RL, Brooks DL, Babish JG, et al. Pharmacokinetic properties of enrofloxacin in rabbits. Am J Vet Res 1991;52:1835-1841.
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==notes==
==notes==
May cause arthropathies in young dogs, but similar effects using standard dosages in rabbits have not been reported; SC and IM injections may cause muscle necrosis or sterile abscesses; dilute before giving parenterally
May cause arthropathies in young dogs, but similar effects using standard dosages in rabbits have not been reported; SC and IM injections may cause muscle necrosis or sterile abscesses; dilute before giving parenterally
==References==
Exotic animal formulary / editor, James W. Carpenter ; associate editor, Christopher J. Marion. -- 4th ed.  p. ; cm.
ISBN 978-1-4377-2264-2 (pbk.) I. Carpenter, James W. (James Wyman). II. Marion, Christopher J.
[DNLM: 1. Veterinary Drugs--Formularies. 2. Animals, Domestic--Formularies. 3. Animals,  Wild--Formularies. 4. Animals, Zoo--Formularies. 5. Drug Therapy--veterinary--Formularies. SF 917]

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