500mg Oxytetracycline Bolus
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Gaioiga Fa'afoma'i
Pharmacodynamics:Oxytetracyclinee masani ona faʻalavelave ma faʻalavelaveina le faʻapipiʻiina o le polotini, ma maua ai le aʻafiaga o le fasiotia o meaola ninii, e faasaga i siama kalama-lelei, siama kalama-leaga, mycoplasma, chlamydia, rickettsiae, spirochetes , Porcine eperythrocytes, ma isi mea faʻalavelave faʻalavelave.
E masani lava mo le niumonia manu, Staphylococcus, Bacillus anthracis, Tetanus, Pasteurella multocida, Haemophilus, Mycoplasma, Chlamydia, Rickettsia (eperythrocytic tino) ma isi siama ei ai se aafiaga lelei inhibitory.I le isi itu, fa'ama'i anufe manu, leptospirosis, niumonia puaa, malala kesi, sela, fa'ama'i pua'a, endometritis ma mastitis i pua'a, povi ma mamoe.Pullorum, Escherichia coli, faʻamaʻi Vibrio, faʻamaʻi umbilical, enteritis o manulele laiti;Vibriosis vai, fa'ama'i fua, fa'ama'i tuna, ma isi e iai fo'i se fa'atonuga lelei.
500mg Oxytetracycline bolusose tu'u gutu o lo'o i ai le oxytetracycline, o se vaila'au fa'ama'i lautele o lo'o i ai se fa'atonuga maualuga o le mautu ma le malosi o le antimicrobial.
Itu Aafiaga
Oxytetracyclinee iai i le vasega o le tetracycline ma ose vaila'au fa'ama'i fa'ama'i lautele.E mafai ona faʻateleina le fuaina o le alkaline phosphatase, toto urea nitrogen, serum amylase, serum bilirubin, ma serum aminotransferase (AST, ALT).O vaila'au umi e tatau ona siaki e le aunoa le toto ma le ate ma fatuga'o, aua o le oxytetracycline e faigofie ona afaina ai le ate.
Oxytetracycline e mafai ona ulufale i le fetus e ala i le placental pa puipui ma teuina i le vaega o le calcium o nifo ma ponaivi, e mafua ai le faʻaleagaina o nifo o le fetal, le toe faʻafouina o enamel ma faʻalavelaveina le tuputupu aʻe o ponaivi fetal.O le ai ai le mea e taʻua o "tetracycline nifo".Ae ui i lea, e leai se placenta o manulele, ae e mafai foi ona mafua ai le maaa o le atigi fuamoa i le taimi o le ovulation.O le mea lea, ina ia aloese mai fuamoa vaivai, e le fautuaina le fafagaina o le oxytetracycline i manulele fafine i le estrus.
Tulaga
(1) Fa'asa mo lulu ma'itaga.
(2) Aloese mai le fa'afefiloi ma vai paipa e maualuga le chlorine ma vaifofo alkaline.Aua le fa'aogaina pusa u'amea mo vaila'au.
(3) Aloese mai le fetaui ma meaʻai susu, vailaʻau o loʻo i ai le calcium, magnesium, alumini, ma le uʻamea, ma meaʻai e maualuga le calcium.E tatau ona ave ile manava gaogao a o lei fafagaina.
(4) O manu matutua, manu equine ma lapiti e le talafeagai mo le tu'u gutu.O le fa'aoga umi e mafai ona fa'atupu fa'ama'i fa'alua ole siama ma sigi e tete'e i vaila'au, ma fa'alavelave matuia e mafai ona mafua ai le sepsis ma le oti.
Hebei Veyong pharmaceutical Co., Ltd, na faavaeina i le 2002, o loʻo i Shijiazhuang City, Hebei Province, Saina, i tafatafa o le Laumua Beijing.O ia o se GMP-certified veterinary drug enterprise, faʻatasi ai ma le R&D, gaosiga ma le faʻatau atu o veterinary APIs, sauniuniga, meaʻai muamua ma meaʻai faaopoopo.I le avea ai o le Nofoaga Tutotonu Faʻatekonolosi Faʻatekonolosi, ua faʻatūina e Veyong se faiga fou R & D mo vailaʻau faʻasoifua fou, ma o le atunuʻu lauiloa faʻatekonolosi faʻavae atinaʻe vailaʻau, e 65 tagata tomai faʻapitoa.Veyong e lua faavae gaosiga: Shijiazhuang ma Ordos, lea o le Shijiazhuang faavae e aofia ai se vaega o le 78,706 m2, ma 13 oloa API e aofia ai Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, ma 11 saunia laina gaosiga e aofia ai tui, fofo tautala, paʻu. , premix, bolus, vailaau e tineia ai manu faalafua ma vailaau fa'ama'i, ma isi.Veyong e tu'uina atu API, sili atu i le 100 lava-igoa sauniuniga, ma OEM & ODM auaunaga.
Veyong faʻapipiʻi taua tele i le pulega o le EHS (Siosiomaga, Soifua Maloloina & Saogalemu), ma maua le ISO14001 ma OHSAS18001 tusi pasi.Veyong ua lisiina i totonu o atinaʻe faʻapisinisi faʻapitoa faʻapitoa i le Itumalo o Hebei ma e mafai ona faʻamautinoa le faʻaauau pea o oloa.
Veyong faʻatūina le faʻatonuga lelei atoatoa, maua le ISO9001 tusi pasi, Saina GMP tusi faamaonia, Ausetalia APVMA GMP tusi faamaonia, Etiopia GMP tusi faamaonia, Ivermectin CEP tusi faamaonia, ma pasia US FDA asiasiga.Veyong ei ai le 'au faʻapolofesa o le resitalaina, faʻatau ma auaunaga faʻapitoa, ua maua e le matou kamupani le faʻalagolago ma le lagolago mai le tele o tagata faʻatau e ala i le tulaga lelei o oloa, maualuga le faʻatau atu ma le maeʻa o le faʻatau atu, pulega ogaoga ma faasaienisi.Veyong ua faia le galulue faatasi mo se taimi umi ma le tele o pisinisi faava o malo pharmaceutical manu ma oloa auina atu i fafo i Europa, Amerika i Saute, Sasaʻe Tutotonu, Aferika, Asia, ma isi e sili atu i le 60 atunuu ma itulagi.
