Label: TULAVEN- tulathromycin solution

TULAVEN™ 25

(tulathromycin injection)

Injectable Solution

Antibiotic

25 mg of tulathromycin/mL

For use in suckling calves, dairy calves, veal calves, and swine. Not for use in ruminating cattle.

CAUTION: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.

TULAVEN™ 25 Injectable Solution is a ready-to-use sterile parenteral preparation containing tulathromycin, a semi-synthetic macrolide antibiotic of the subclass triamilide. Each mL of TULAVEN™ 25 contains 25 mg of tulathromycin as the free base in a 50% propylene glycol vehicle, monothioglycerol (5 mg/mL), citric acid (4.8 mg/mL) with hydrochloric acid and sodium hydroxide added to adjust pH. TULAVEN™ 25 consists of an equilibrated mixture of two isomeric forms of tulathromycin in a 9:1 ratio.

The chemical names of the isomers are (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[[2,6- dideoxy-3-C-methyl-3-O-methyl-4-C-[(propylamino) methyl]-α-L-ribo-hexopyrano-syl]oxy]-2-ethyl-3,4,10-trihydroxy-3,5,8,10,12,14-hexamethyl-11-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]-oxy]-1-oxa-6-azacyclopentadecan-15-one and (2R,3R,6R,8R,9R,10S,11S,12R)-11-[[2,6-dideoxy-3-C-methyl-3-O-methyl-4-C-[(propylamino)methyl]-α-L-ribo-hexopyrano-syl]oxy]-2-[(1R,2R)-1,2-dihydroxy-1-methylbutyl]-8-hydroxy-3,6,8,10,12-pentamethyl-9-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylohexopyranosyl]oxy]-1-oxa-4-azacyclotridecan-13-one, respectively.

Swine
TULAVEN™ 25 Injectable Solution is indicated for the treatment of swine respiratory disease (SRD) associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Bordetella bronchiseptica, Haemophilus parasuis, and Mycoplasma hyopneumoniae; and for the control of SRD associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, and Mycoplasma hyopneumoniae in groups of pigs where SRD has been diagnosed.

Suckling Calves, Dairy Calves, and Veal Calves
BRD – TULAVEN™ 25 Injectable Solution is indicated for the treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis.

Swine: Inject intramuscularly as a single dose in the neck at a dosage of 2.5 mg/kg (1 mL/22 lb) Body Weight (BW). Do not inject more than 4 mL per injection site.

Calves: Inject subcutaneously as a single dose in the neck at a dosage of 2.5 mg/kg (1 mL/22 lb) body weight (BW). Do not inject more than 11.5 mL per injection site.

The use of TULAVENTM 25 Injectable Solution is contraindicated in animals previously found to be hypersensitive to the drug.

FOR USE IN ANIMALS ONLY. NOT FOR HUMAN USE. KEEP OUT OF REACH OF CHILDREN. NOT FOR USE IN CHICKENS OR TURKEYS.

Swine: The effects of TULAVEN™ 25 Injectable Solution on porcine reproductive performance, pregnancy, and lactation have not been determined.
Intramuscular injection can cause a transient local tissue reaction that may result in trim loss of edible tissue at slaughter.
Cattle: The effects of TULAVEN™ 25 Injectable Solution on bovine reproductive performance, pregnancy, and lactation have not been determined.
Subcutaneous injection can cause a transient local tissue reaction that may result in trim loss of edible tissue at slaughter.

Swine: In one field study, one out of 40 pigs treated with tulathromycin injection 100 mg/mL at 2.5 mg/kg BW exhibited mild salivation that resolved in less than four hours.
Calves: In one BRD field study, two calves treated with tulathromycin injection 100 mg/mL at 2.5 mg/kg BW exhibited transient hypersalivation. One of these calves also exhibited transient dyspnea, which may have been related to pneumonia.
Post Approval Experience: The following adverse events are based on post approval adverse drug experience reporting for tulathromycin injection 100 mg/mL. Not all adverse events are reported to the FDA CVM. It is not always possible to reliably estimate the adverse event frequency or establish a causal relationship to product exposure using these data. The following adverse events are listed in decreasing order of reporting frequency in cattle: Injection site reactions and anaphylaxis/anaphylactoid reactions. For a complete listing of adverse reactions for tulathromycin injection 100 mg/mL or 25 mg/mL reported to the CVM see: http://www.fda.gov/reportanimalae.

At physiological pH, tulathromycin (a weak base) is approximately 50 times more soluble in hydrophilic than lipophilic media. This solubility profile is consistent with the extracellular pathogen activity typically associated with the macrolides1. Markedly higher tulathromycin concentrations are observed in the lung parenchyma as compared to the plasma, and these elevated concentrations can remain in lung tissue for several days beyond that which can be measured in the plasma. However the clinical relevance of these elevated lung concentrations is undetermined.
As a class, macrolides tend to be primarily bacteriostatic, but may be bactericidal against some pathogens2. When acting as a cidal compound, they tend to exhibit concentration independent killing; the rate of bacterial eradication does not change once serum drug concentrations reach 2 to 3 times the minimum inhibitory concentration (MIC) of the targeted pathogen. Under these conditions, the time that serum concentrations remain above the MIC becomes the major determinant of antimicrobial activity. Macrolides also exhibit a post-antibiotic effect (PAE), the duration of which tends to be both drug and pathogen dependent. In general, by increasing the macrolide concentration and the exposure time, the PAE will increase to some maximal duration3. Tulathromycin is eliminated from the body primarily unchanged via biliary excretion.
1 Carbon, C. 1998. Pharmacodynamics of Macrolides, Azalides, and Streptogramins: Effect on Extracellular Pathogens. Clin. Infect. Dis., 27:28-32.
2 Nightingale, C.J. 1997. Pharmacokinetics and Pharmacodynamics of Newer Macrolides. Pediatr. Infect. Dis. J., 16:438-443.
3 Andes D, Anon J, Jacobs MR, Craig WA. (2004). Application of pharmacokinetics and pharmacodynamics to antimicrobial therapy of respiratory tract infections. Clin Lab Med., 24:477-502.
Swine: Following intramuscular (IM) administration to feeder pigs at a dosage of 2.5 mg/kg BW, tulathromycin is nearly completely absorbed, with peak plasma concentrations achieved within ~0.25 hr. The volume of distribution exceeds 15 L/kg, which is consistent with extensive tissue binding. This large distribution volume results in a long terminal elimination half-life (60 to 90 hours) despite a rapid systemic free drug clearance (187 mL/kg/hr). There are no gender differences in swine tulathromycin pharmacokinetics.
Comparative Bioavailability Summary: Despite slightly lower peak concentrations with tulathromycin injection 25 mg/mL, a single IM dose of 2.5 mg tulathromycin/kg BW of either tulathromycin injection 100 mg/mL or 25 mg/mL resulted in comparable tulathromycin total systemic exposure. Therefore, tulathromycin injection 25 mg/mL is considered to be therapeutically equivalent to tulathromycin injection 100 mg/mL when administered to swine by IM injection at a dose of 2.5 mg tulathromycin/kg BW.
Calves: Following subcutaneous (SC) administration into the neck of feeder calves at a dosage of 2.5 mg/kg BW, tulathromycin is nearly completely absorbed, with peak plasma concentrations achieved within ~0.25 hr. The volume of distribution exceeds 11 L/kg4, which is consistent with extensive tissue binding. This large distribution volume results in a long terminal elimination half-life of more than 100 hours, despite a rapid systemic free drug clearance (170 mL/kg/hr). No pharmacokinetic differences are observed in castrated male versus female calves.
Comparative Bioavailability Summary: Despite lower peak concentrations with tulathromycin 25 mg/mL, a single SC dose of 2.5 mg tulathromycin/kg BW of either tulathromycin injection100 mg/mL or 25 mg/mL resulted in comparable total systemic tulathromycin exposure. Therefore, tulathromycin injection 25 mg/mL is considered to be therapeutically equivalent to tulathromycin injection 100 mg/mL when administered to calves by SC injection at a dose of 2.5 mg tulathromycin/kg BW.
4 Clearance and volume estimates are based on intersubject comparisons of 2.5 mg/kg BW administered by either subcutaneous or intravenous injection.

Swine: Tulathromycin has demonstrated in vitro activity against A. pleuropneumoniae, P. multocida, B. bronchiseptica, H. parasuis, and M. hyopneumoniae. The MICs of tulathromycin against indicated pathogens collected from field studies were determined using methods recommended by the Clinical and Laboratory Standards Institute (CLSI, M31-A and M31-A3). MICs for H. parasuis were determined using Veterinary Fastidious Medium and were incubated up to 48 hours at 35 to 37°C in a CO2-enriched atmosphere. These values are represented in Table 3.

*The correlation between in vitro susceptibility data and clinical effectiveness is unknown.
**The lowest MIC to encompass 50% and 90% of the most susceptible isolates, respectively

Calves: Tulathromycin has demonstrated in vitro activity against M. haemolytica, P. multocida, H. somni, and M. bovis, four pathogens associated with BRD. The MICs of tulathromycin against indicated pathogens collected from field studies using tulathromycin injection 100 mg/mL were determined using methods recommended by the CLSI (M31-A2). These values are represented in Table 4, below.

*The correlation between in vitro susceptibility data and clinical effectiveness is unknown.
**The lowest MIC to encompass 50% and 90% of the most susceptible isolates, respectively.

Swine: Plasma concentrations of tulathromycin administered as tulathromycin injection 100 mg/mL or 25 mg/mL were demonstrated to be therapeutically equivalent (see CLINICAL PHARMACOLOGY, Comparative Bioavailability Summary). Therefore effectiveness studies conducted with tulathromycin injection 100 mg/mL support the effectiveness for tulathromycin injection 25 mg/mL.
In a multi-location field study to evaluate the treatment of naturally occurring SRD, 266 pigs were treated with tulathromycin injection 100 mg/mL. Responses to treatment were compared to saline-treated controls. Success was defined as a pig with normal attitude, normal respiration, and rectal temperature of < 104°F on Day 7. The treatment success rate was significantly greater (P ≤ 0.05) in tulathromycin injection 100 mg/mL-treated pigs (70.5%) compared to saline-treated pigs (46.1%). M. hyopneumoniae was isolated from 106 saline-treated and non-treated sentinel pigs in this study.
Two induced infection model studies were conducted to confirm the effectiveness of tulathromycin injection 100 mg/mL against M. hyopneumoniae. Ten days after inoculation intranasally and intratracheally with a field strain of M. hyopneumoniae, 144 pigs were treated with either tulathromycin injection 100 mg/mL (2.5 mg/kg BW) intramuscularly or an equivalent volume of saline. Pigs were euthanized and necropsied 10 days post-treatment. The mean percentage of gross pneumonic lung lesions was statistically significantly lower (P < 0.0001) for tulathromycin injection 100 mg/mL-treated pigs than for saline-treated pigs in both studies (8.52% vs. 23.62% and 11.31% vs. 26.42%).
The effectiveness of tulathromycin injection 100 mg/mL for the control of SRD was evaluated in a multi-location natural infection field study. When at least 15% of the study candidates showed clinical signs of SRD, all pigs were enrolled and treated with tulathromycin injection 100 mg/mL (226 pigs) or saline (227 pigs). Responses to treatment were evaluated on Day 7. Success was defined as a pig with normal attitude, normal respiration, and rectal temperature of < 104°F. The treatment success rate was significantly greater (P < 0.05) in tulathromycin injection 100 mg/mL-treated pigs compared to saline-treated pigs (59.2% vs. 41.2%).

Calves: Plasma concentrations of tulathromycin administered as tulathromycin injection 100 mg/mL or 25 mg/mL were demonstrated to be therapeutically equivalent (see CLINICAL PHARMACOLOGY, Comparative Bioavailability Summary). Therefore effectiveness studies conducted with tulathromycin injection 100 mg/mL support the effectiveness for tulathromycin injection 25 mg/mL.

BRD - In a multi-location field study, 314 calves with naturally occurring BRD were treated with tulathromycin injection 100 mg/mL. Responses to treatment were compared to saline-treated controls. A cure was defined as a calf with normal attitude/activity, normal respiration, and a rectal temperature of ≤ 104°F on Day 14. The cure rate was significantly higher (P ≤ 0.05) in tulathromycin injection 100 mg/mL-treated calves (78%) compared to saline-treated calves (24%). There were two BRD-related deaths in the tulathromycin injection 100 mg/mL-treated calves compared to nine BRD-related deaths in the saline-treated calves.
Fifty-two tulathromycin injection 100 mg/mL-treated calves and 27 saline-treated calves from the multi-location field BRD treatment study had Mycoplasma bovis identified in cultures from pre-treatment nasopharyngeal swabs. Of the 52 tulathromycin injection 100 mg/mL-treated calves, 37 (71.2%) calves were categorized as cures and 15 (28.8%) calves were categorized as treatment failures. Of the 27 saline-treated calves, 4 (14.8%) calves were categorized as cures and 23 (85.2%) calves were treatment failures.
A Bayesian meta-analysis was conducted to compare the BRD treatment success rate in young calves (calves weighing 250 lbs or less and fed primarily a milk-based diet) treated with tulathromycin injection 100 mg/mL to the success rate in older calves (calves weighing more than 250 lbs and fed primarily a roughage and grain-based diet) treated with tulathromycin injection 100 mg/mL. The analysis included data from four BRD treatment effectiveness studies conducted for the approval of tulathromycin injection 100 mg/mL in the U.S. and nine contemporaneous studies conducted in Europe. The analysis showed that the BRD treatment success rate in young calves was at least as good as the BRD treatment success rate in older calves. As a result, tulathromycin injection 100 mg/mL was considered effective for the treatment of BRD associated with M. haemolytica, P. multocida, H. somni, and M. bovis in suckling calves, dairy calves and veal calves.
Two induced infection model studies were conducted to confirm the effectiveness of tulathromycin injection 100 mg/mL against Mycoplasma bovis. A total of 166 calves were inoculated intratracheally with field strains of Mycoplasma bovis. When calves became pyrexic and had abnormal respiration scores, they were treated with either tulathromycin injection 100 mg/mL (2.5 mg/kg BW) subcutaneously or an equivalent volume of saline. Calves were observed for signs of BRD for 14 days post-treatment, then were euthanized and necropsied. In both studies, mean lung lesion percentages were statistically significantly lower in the tulathromycin injection 100 mg/mL-treated calves compared with saline-treated calves (11.3% vs. 28.9%, P = 0.0001 and 15.0% vs. 30.7%, P < 0.0001).

Swine: Plasma concentrations of tulathromycin administered as 100 mg/mL or as 25 mg/mL injectable solution were demonstrated to be therapeutically equivalent (see CLINICAL PHARMACOLOGY, Comparative Bioavailability Summary). Therefore systemic target animal safety studies conducted with tulathromycin injection 100 mg/mL support the systemic safety for tulathromycin injection 25 mg/mL.
Safety studies were conducted in pigs receiving a single intramuscular dose of 25 mg/kg BW, or 3 weekly intramuscular doses of 2.5, 7.5, or 12.5 mg/kg BW (both studies utilized tulathromycin injection 100 mg/mL). In all groups, transient indications of pain after injection were seen, including restlessness and excessive vocalization. Tremors occurred briefly in one animal receiving 7.5 mg/ kg BW. Discoloration and edema of injection site tissues and corresponding histopathologic changes were seen in animals at all dosages and resolved over time. No other drug-related lesions were observed macroscopically or microscopically.
Sixteen growing pigs were injected with either saline or tulathromycin injection 25 mg/mL as a single injection of 4 mL. Injection site observations included two instances of erythema in the tulathromycin injection 25 mg/mL-treated group on Day 1 post-injection. No heat, sensitivity, firmness, necrosis, drainage, or swelling was observed at any injection sites in either treatment group. The gross and microscopic findings in the tulathromycin injection 25 mg/mL-treated group were consistent with inflammatory changes induced by injections and were considered to be mild or moderate with progression to macroscopic resolution by Day 28 post-injection and microscopic resolution by Day 42 post-injection.

Calves: Plasma concentrations of tulathromycin administered as 100 mg/mL or 25 mg/mL injectable solution were demonstrated to be therapeutically equivalent (see CLINICAL PHARMACOLOGY, Comparative Bioavailability Summary). Therefore systemic target animal safety studies conducted with tulathromycin injection 100 mg/mL support the systemic safety for tulathromycin injection 25 mg/mL.
A safety study was conducted in feeder calves receiving tulathromycin injection 100 mg/mL as a single subcutaneous dose of 25 mg/kg BW, or 3 weekly subcutaneous doses of 2.5, 7.5, or 12.5 mg/kg BW. In all groups, transient indications of pain after injection were seen, including head shaking and pawing at the ground. Injection site swelling, discoloration of the subcutaneous tissues at the injection site and corresponding histopathologic changes were seen in animals in all dosage groups. These lesions showed signs of resolving over time. No other drug-related lesions were observed macroscopically or microscopically.
An exploratory study was conducted in feeder calves receiving tulathromycin injection 100 mg/mL as a single subcutaneous dose of 10, 12.5, or 15 mg/kg BW. Macroscopically, no lesions were observed. Microscopically, minimal to mild myocardial degeneration was seen in one of six calves administered 12.5 mg/kg BW and two of six calves administered 15 mg/kg BW.
A safety study was conducted in preruminant calves 13 to 27 days of age receiving tulathromycin injection 100 mg/mL at 2.5 mg/kg BW or 7.5 mg/kg BW once subcutaneously. With the exception of minimal to mild injection site reactions, no drug-related clinical signs or other lesions were observed macroscopically or microscopically.
Sixteen growing cattle were injected with either saline (eight animals) as a single injection of 11.5 mL or tulathromycin injection 25 mg/mL (eight animals) as a single injection of either 2.5 mg/kg BW or a dose volume of 11.5 mL (whichever volume was higher). One calf in the tulathromycin injection 25 mg/mL-treated group was observed to have firmness at the injection site for a single day. Two tulathromycin injection 25 mg/mL-treated calves exhibited injection site swelling. In one calf, the swelling resolved within 48 hours. In the other calf, the swelling was observed over a three-day period, after which the calf underwent a scheduled necropsy, preventing further injection site observations. No injection site swelling was observed in saline-treated animals. At necropsy, three of the saline-treated calves and five of the tulathromycin injection 25 mg/mL-treated calves had altered tissue present at the injection site. The gross and microscopic findings in the tulathromycin injection 25 mg/mL-treated group were consistent with inflammatory changes induced by injections, were considered to be mild to marked, and progressed to macroscopic resolution and microscopic resolution by Day 42 post-injection.

Store at or below 25°C (77°F), with excursions up to 40°C (104°F). Use within 60 days of first puncture and puncture a maximum of 20 times. If more than 20 punctures are anticipated, the use of multi-dosing equipment is recommended. When using a draw-off spike or needle with a bore diameter larger than 16 gauge, discard any product remaining in the vial immediately after use.

TULAVEN™ 25 Injectable Solution is available in the following package sizes: 100 mL vial, 250 mL vial.
Approved by FDA under ANADA # 200-712

To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet, contact Ceva Animal Health at 1-800-999-0297 or www.ceva.com. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or http://fda.gov/reportanimalae.

Distributed by: Ceva Animal Health, LLC Lenexa, KS 66215

Made in France

Tulaven trademark is the property of Ceva Santé Animale S.A.

TULAVEN™ 25

(tulathromycin injection)

Injectable Solution

Antibiotic

25 mg of tulathromycin/mL

For use in suckling calves, dairy calves, veal calves, and swine.

Not for use in ruminating cattle.

CAUTION: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.

Approved by FDA under ANADA # 200-712

Net Contents:

100 mL

TULAVEN™ 25

(tulathromycin injection)

Injectable Solution

Antibiotic

25 mg of tulathromycin/mL

For use in suckling calves, dairy calves, veal calves, and swine.

Not for use in ruminating cattle.

CAUTION: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.

Approved by FDA under ANADA # 200-712

Net Contents:

100 mL

TULAVEN™ 25

(tulathromycin injection)

Injectable Solution

Antibiotic

25 mg of tulathromycin/mL

For use in suckling calves, dairy calves, veal calves, and swine.

Not for use in ruminating cattle.

CAUTION: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.

Approved by FDA under ANADA # 200-712

Net Contents:

250 mL

TULAVEN™ 25

(tulathromycin injection)

Injectable Solution

Antibiotic

25 mg of tulathromycin/mL

For use in suckling calves, dairy calves, veal calves, and swine.

Not for use in ruminating cattle.

CAUTION: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.

Approved by FDA under ANADA # 200-712

Net Contents:

250 mL