Pharmacology explains efficacy of Draxxin® for SRD

Reprinted from:

Pharmacologic research demonstrating how Draxxin® (tulathromycin) injection behaves in the pig explains why this antimicrobial remains a valuable treatment for swine respiratory disease (SRD).

Developed by Zoetis scientists exclusively for veterinary use, Draxxin was the first antimicrobial in a macrolide class known as triamilides. A derivative of erythromycin, it is active against Actinobacillus pleuropneumoniae (APP), Pasteurella multocida, Bordetella bronchiseptica, Haemophilus parasuis and Mycoplasma hyopneumoniae (M. hyo) — all pathogens that can cause or contribute to SRD.1

“Even before its clinical efficacy was established, our scientists found Draxxin is rapidly released from an intramuscular injection site, that it’s readily distributed throughout the body and that it persists in the lungs,” said Ashley Johnson, DVM, Zoetis.

Johnson cited two key pharmacokinetic studies. In the first, Zoetis investigators administered the recommended dose of 2.5 mg/kg bodyweight either by intravenous injection (IV) into the ear or by intramuscular (IM) injection into the neck, then periodically obtained blood samples.2

Rapid release, extensive distribution

Plasma concentrations in the IV and IM groups were similar, but notable was the speed at which Draxxin was released from the IM injection site, the veterinarian said. The Tmax value, which is the amount of time a drug is present in serum at the maximum concentration, was only 15 minutes, she said. That study also demonstrated that Draxxin is highly bioavailable.3

In a second pharmacokinetic study, Zoetis scientists evaluated drug concentrations in plasma and lungs after IM administration to healthy pigs. Lung concentrations were 61.4 times the plasma AUC (Figure 1, Table 1). AUC stands for “area under the curve” and reflects the concentration of a drug and the length of time it’s present in blood plasma, Johnson continued.

The elimination half-life of Draxxin in the lungs — the time it takes for the concentration of Draxxin to decline by 50% — was about 6 days. “That’s an extremely long half-life,” she commented.

At the time the studies were conducted, the investigators concluded that “The high distribution to lung and slow elimination following a single dose of [Draxxin] are desirable pharmacokinetic attributes for an antimicrobial drug indicated for the treatment of respiratory disease in swine.”

Immune cell accumulation

One of the antimicrobial’s most powerful attributes is its accumulation in immune cells, specifically alveolar macrophages and neutrophils, which are phagocytic white blood cells that fight off bacteria,4 Johnson said.

When the uptake of Draxxin by neutrophils and alveolar macrophages was monitored for 4 hours after administration, the accumulation of Draxxin was significantly higher compared to accumulation of erythromycin (p < 0.03),5,6 she said (Figure 2).

Established clinical relevance

The clinical relevance of the early pharmacokinetic research is well established, Johnson continued.

In one of the studies involving 240 healthy pigs about 6 weeks of age, animals were divided into one of six treatment groups.7 Pigs in five of the groups received an IM injection of Draxxin at 2.5 mg/kg bodyweight, but each group received the injection a different number of days — at 3, 5, 7, 9 or 11 days — before pigs were challenged intranasally with APP serotype 5. To provide a control, the sixth group was not treated but was challenged.

Compared to controls, mortality was significantly reduced in groups treated 5, 7 or 9 days before challenge (Figure 3). However, mortality was lowest in the group treated 3 days before challenge, and it was also significantly lower than mortality among those treated 11 days before challenge.

The mortality results indicate the duration of antimicrobial effectiveness for Draxxin against clinical disease caused by intranasal inoculation of the APP serotype 5 is up to 9 days, Johnson said.

Pigs treated with Draxxin 3 and 5 days before challenge also had significantly reduced weighted lung lesions compared to untreated controls. The weighted percentage of total lung lesions for pigs treated on 3, 5 or 7 days before challenge was significantly (p = 0.0214) less than those of pigs treated 9 days before challenge (Figure 4).

M. hyo efficacy

M. hyo, which remains a common and costly cause or contributor to SRD,8 is highly susceptible to Draxxin, Johnson said. The minimum concentration inhibiting growth of 90% of the isolates (MIC90) has been shown to be 0.05 μg/mL. Moreover, swine lung tissue concentrations of Draxxin well above the MIC90 level persist for at least 15 days after a single IM dose (Figure 5).9

Several studies have demonstrated the clinical efficacy of Draxxin against M. hyo.10,11,12 In one of the studies, investigators evaluated the long-term performance and health of pigs treated with one IM dose of Draxxin after the animals were challenged once daily for 3 consecutive days with an M. hyo field isolate. Draxxin was administered between 11 and 23 days after the challenge.

Compared to saline-treated controls, pigs treated with Draxxin had a significantly improved average daily gain (p ≤ 0.0121), they ate more and had a markedly improved overall feed-to-gain ratio. Mortality was also lower: 4.2% in treated pigs compared to 8.7% in controls.

Compilation of field trials

The efficacy of Draxxin was likewise demonstrated in large field trials with 3,600 weaned pigs infected with SRD pathogens.13,14,15 Pigs in the studies were from three sources: a commercial production system in the Midwest, a research facility with pigs obtained from sow farms and a second commercial Midwest production system with pigs that also had influenza A. Caregivers in the study did not know which of the pigs were or were not treated with Draxxin.

Compared to untreated controls, nursery mortality in pigs treated with Draxxin was from 33% to 54% lower. Numerically, fewer pigs had to be retreated, and in two of the studies where it was documented, fewer pigs had to be moved to hospital pens.

Draxxin was also credited with a weight advantage in the nursery ranging from 1.54 pounds to 2.91 pounds, and in two of the studies where pigs were weighed through finishing, treated pigs had a significant advantage ranging from 3.23 pounds to 4.2 pounds (Figure 6).

“The pharmacokinetic findings with Draxxin clearly explain its efficacy for SRD but even more important are the antimicrobial’s practical benefits,” Johnson said. “When only one dose is needed, compliance is likely to be better, there’s less stress on animals when fewer injections are needed as well as lower labor costs.”

Zoetis also has provided extra convenience by offering Draxxin 25 (tulathromycin injection), which has a lower concentration formulated for smaller pigs.


Important Safety Information for Swine:

Withdraw Draxxin/Draxxin 25 five (5) days prior to slaughter in swine. Do not use in animals known to be hypersensitive to the product. See the full Prescribing Information attached.  Click here to see prescribing information for Draxxin.  Click here to see prescribing information for Draxxin 25.


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1 Overview of respiratory diseases of pigs. Merck Veterinary Manual. pigs/overview-of-respiratory-diseases-of-pigs
2 Benchaoui HA, et al. Pharmacokinetics and lung tissue concentrations of tulathromycin in swine. J Vet Pharmacol Ther. 2004;27:203-210.
3 Ibid.
4 Fischer CD, et al. Direct and Indirect Anti-Inflammatory Effects of Tulathromycin in Bovine Macrophages: Inhibition of CXCL-8 Secretion, Induction of Apoptosis, and Promotion of Efferocytosis. Antimicrob Agents Chemother. 2013 March;57(3): 1385-1393.
5 Siegel TW, et al. Cellular uptake of the triamilide tulathromycin by bovine and porcine phagocytic cells in vitro. J Anim Sci 2004;82(1):186.
6 Fischer CD, et al. Direct and Indirect Anti-Inflammatory Effects of Tulathromycin in Bovine Macrophages
7 McKelvie J, et al. Comparative efficacy of tulathromycin injectable solution (Draxxin) for the treatment of experimentally induced respiratory infections in swine. 2005 Am Assoc Swine Vet annual meeting, Toronto.
8 Mycoplasmal pneumonia (enzootic pneumonia), Iowa State Unimversity. mycoplasmal-pneumonia
9 Benchaoui HA, et al. Pharmacokinetics and lung tissue concentrations
10 Data on file. Study Report No. 1121R-60-07-292, Zoetis LLC.
11 Data on file. Study Report No. 1121C-60-04-230, Zoetis LLC.
12 Data on file. Study Report No. 1121C-60-03-209, Zoetis LLC.
13 King D, et al. Effects of Draxxin at weaning in pigs on control of swine respiratory disease including “low” level of PRRS involvement and subsequent performance of pigs. 2013 Am Assoc Swine Vet annual meeting, San Diego.
14 King D, et al. Effects of Draxxin at weaning for control of swine respiratory disease in pigs experiencing a natural outbreak. 2014 Am Assoc Swine Vet annual meeting, Dallas.
15 Sievers C, et al. Effect of tulathromycin or ceftiofur free acid on post-weaning performance and economic return in porcine reproductive and respiratory syndrome virus infected pigs. 2014 Am Assoc Swine Vet annual meeting, Dallas.



Discoveries is a series of  research news reports written by the editors of Pig Health Today on behalf of the US Pork Business of Zoetis.


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