20% sulfadiazine + 4% trimethopr acsi
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Sashi mai aiki
Sulfadiazine 20.00% w / v.
Ashimethoppim 4.00% w / v
Mataki na magunguna
Sulfadiazine itace matsakaici ingantaccen magani don amfani da tsari kuma wakili ne mai yawa. Hanyar aikinta saboda ta cika da P-Aminobenzenzo acid (PABA) kuma ta hana yin amfani da synthase na ƙwayoyin cuta yana takaitaccen tasirin antibacteria.
Ba a ciki
Ana nuna wannan siginar rashin hanyar a cikin lura da cututtukan cututtukan da aka haifar ta ko alaƙa da ƙwayoyin cuta mai hankali ga trimethopprim: sulfadiazine. Abubuwan da suka shafi aiki sun hada da dukkan kwayoyin-mara kyau da kuma marasa kyau da suka hada da: Actlinobacillilila, Actetae, Braceichia Coryneebacteria, Braceichia Colybacteria, Bracekipia Coly. Klobsella SPP, Pasteurella SPP, pneumoccici. Proteus, Salmoneli SPP. Staphylocci, streptococci, vibrio.
Sashi da Gudanarwa
Ta hanyar allurar subcutaneous kawai.
Dabbobi: Kudin da aka ba da shawarar shine 15 MG na kayan aiki na kilogram (1 ml per 16kg nauyin allurar rigakafi ko jinkirin yin allurar ciki.
Dawakai: Kudin da aka ba da shawarar shine 15 MG na kayan aiki na kilogiram na kilogiram na kilogiram (1 ml a kan allurar rigakafi 16), ta hanyar allurar ciki.
Karnuka da kuliyoyi: Kudin da aka ba da shawarar shine 30mg na aiki mai aiki a kowace jikin mutum na kilogiram (1 ml a kan nauyin kilo 8).
Karatun
Bai kamata a ba da allura ta hanyar hanyoyi baicin waɗanda aka ba da shawarar.
Ba za a gudanar da shi ba a cikin Intraperitoneally, Intra - Arterially ko da ta rikice.
Kada ku yi aikin dabbobin da sanannen sanannun masaniyar zamantakunku, lalata ƙwayar launin fata ko dyscrasias jini.
Gargadi na Musamman
1 Don gudanarwa na cikin dabara samfurin ya kamata a yi wa ɗan adam zuwa jiki zazzabi kuma a hankali a hankali a hankali tsawon lokaci kamar yadda yake da amfani.
2 A farkon alamar a hankali ya kamata a katse da allurar rigakafi kuma girgiza magani.
Ya kamata a sami isasshen ruwan sha yayin tasirin warkewa na samfurin.
Lokacin karuwa
Shanu: nama - kwana 12
Milk - kwanaki 4.
Ajiya
Kare daga hasken rana kai tsaye da kantin sayar da ƙasa 30 ℃.
An kafa Hebei Veyong Pharceuticical Co., Ltd, ya kafa a cikin 2002, wanda ya kasance a Shijiazhuang City, Lardin Hebeizhuang City, Lardin Hebeizhuzhuang City, lardin Hebei, China, a kusa da birnin birnin birnin. Tana da babban kasuwancin gungun dabbobi na Grm-Man, tare da R & D, samarwa da kuma tallace-tallace na dabbobi Apis, shirye-shiryen ciyawar da ƙari. A matsayinta na cibiyar fasaha na lardin, Veyong ya kafa tsarin R & D wanda ya kirkira don sabon magani na dabbobi, kuma shine asalin kirkirar fasaha bisa ga kwararrun dabbobi, akwai ƙwararrun fasaha guda 65. Veyong yana da tushe guda biyu mai maganin maye, ECTs. Veyong yana samar da APIs, fiye da 100 na lafazuka, da kuma aikin OEEM & ODM.
Veyong yana da mahimmanci ga Gudanar da EHS (Muhalli & Tsaro), kuma an sami takaddun shaida na ISO14001 da kuma takaddun shaida An jera Veyong a cikin masana'antar da ke fitowa daga masana'antu masu tasowa a lardin Hebei kuma na iya tabbatar da ci gaba da wadatar samfuran.
Veyong ya kafa cikakken tsarin sarrafa sarrafawa, ya sami takardar shaidar ISO9001, China Apvma GPP Takadiya, da kuma takardar shaidar CETETERT, kuma ta ba da sanarwar Takaddar FDA. Veyong yana da ƙwararrun ƙwararrun rijista, sabis na tallace-tallace, kamfaninmu ya sami dogaro da abokan ciniki da yawa, masu inganci Pre-tallace-tallace da sabis na tallace-tallace. Veyong ya yi hadin gwiwa da daddicces na dabbobi da yawa a duniya da aka fitar da kayayyaki da aka fitar dasu zuwa Turai, Afirka, Asiya, da sauransu sama da kasashe 60 da kuma yankuna da sauransu.
