热评网论--安徽频道--人民网
 | |
| Clinical data | |
|---|---|
| Trade names | Draxxin, others |
| AHFS/Drugs.com | International Drug Names |
| Routes of administration | Intramuscular, subcutaneous |
| ATCvet code | |
| Legal status | |
| Legal status | |
| Identifiers | |
| |
| CAS Number | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.166.454 |
| Chemical and physical data | |
| Formula | C41H79N3O12 |
| Molar mass | 806.092 g·mol?1 |
| 3D model (JSmol) | |
| |
| |
| (verify) | |
Tulathromycin, sold under the brand name Draxxin among others, is a macrolide antibiotic used to treat bovine respiratory disease in cattle and swine respiratory disease in pigs.[2][7][8]
Medical uses
[edit]Tulathromycin is indicated for:
Cattle: Treatment and metaphylaxis of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis sensitive to tulathromycin.[3]
Treatment of infectious bovine keratoconjunctivitis (IBK) associated with Moraxella bovis sensitive to tulathromycin.[3]
Pigs: Treatment and metaphylaxis of swine respiratory disease (SRD) associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Mycoplasma hyopneumoniae, Haemophilus parasuis, and Bordetella bronchiseptica sensitive to tulathromycin.[3]
Sheep: Treatment of the early stages of infectious pododermatitis (foot rot) associated with virulent Dichelobacter nodosus requiring systemic treatment.[3]
Society and culture
[edit]Legal status
[edit]Tulathromycin (brand name Draxxin) was approved for medical use in the European Union in November 2003.[3]
Tulathromycin (brand names Tulissin and Tulaven) was approved for medical use in the European Union in April 2020.[9][10]
In July 2020, the Committee for Medicinal Products for Veterinary Use (CVMP) adopted positive opinions, recommending the granting of marketing authorizations for the veterinary medicinal products Increxxa and Tulinovet solutions for injection for cattle, pigs and sheep.[11][12] The applicant for Increxxa is Elanco GmbH.[11] The applicant for Tulinovet is VMD N.V.[12] Increxxa was approved for veterinary use in the European Union in September 2020.[5]
Brand names
[edit]It is marketed by Zoetis under the brand name Draxxin.[2]
It is marketed by Bimeda Inc. under the brand name Macrosyn, and by Merck & Co. under the brand name Arovyn.[13]
It is also sold under the brand name Increxxa.[2][5] by Elanco
References
[edit]- ^ "Health product highlights 2021: Annexes of products approved in 2021". Health Canada. 3 August 2022. Retrieved 25 March 2024.
- ^ a b c d "FDA Approves First Generic Tulathromycin Products for Cattle and Swine". U.S. Food and Drug Administration (FDA). 19 February 2021. Archived from the original on February 19, 2021. Retrieved 4 March 2023.
- ^ a b c d e f "Draxxin EPAR". European Medicines Agency (EMA). 17 September 2018. Retrieved 20 August 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- ^ "Tulinovet EPAR". European Medicines Agency. 17 July 2020. Retrieved 11 October 2021.
- ^ a b c "Increxxa EPAR". European Medicines Agency. 17 July 2020. Retrieved 5 March 2023.
- ^ "Draxxin PI". Union Register of medicinal products. 13 November 2003. Retrieved 26 December 2024.
- ^ Evans NA (2005). "Tulathromycin: an overview of a new triamilide antibiotic for livestock respiratory disease". Veterinary Therapeutics: Research in Applied Veterinary Medicine. 6 (2): 83–95. PMID 16094557.
- ^ Villarino N, Brown SA, Martín-Jiménez T (November 2013). "The role of the macrolide tulathromycin in veterinary medicine". Veterinary Journal. 198 (2). London, England: 352–7. doi:10.1016/j.tvjl.2013.07.032. PMID 24268476.
- ^ "Tulissin EPAR". European Medicines Agency (EMA). 21 February 2020. Retrieved 20 August 2020.
- ^ "Tulaven EPAR". European Medicines Agency (EMA). 21 February 2020. Retrieved 20 August 2020.
- ^ a b "Increxxa: Pending EC decision". European Medicines Agency. 17 July 2020. Archived from the original on July 18, 2020. Retrieved 17 July 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- ^ a b "Tulinovet: Pending EC decision". European Medicines Agency. 17 July 2020. Archived from the original on 11 November 2020. Retrieved 17 July 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- ^ "Arovyn". Merck. Retrieved 5 March 2023.
