20% Sulfadiazine + 4% Trimethoprim Injection
Isithako esisebenzayo
Sulfadiazine 20.00% w/v.
I-Trimethoprim 4.00% w/v
Isenzo se-Pharmacological
I-Sulfadiazine lichiza lesulfa elisebenzayo ngokuphakathi kusetyenziso lwenkqubo kwaye liyi-bacteriostatic agent ebanzi.Indlela yokusebenza kwayo kukuba i-structural ifana ne-p-aminobenzoic acid (PABA) kwaye inokukhuphisana ne-PABA ukuba isebenze kwi-dihydrofolate synthase kwiibhaktheriya, ngaloo ndlela ikhusela i-PABA ukuba isetyenziswe njengento eluhlaza ukwenza i-tetrahydrofolate efunwa yibhaktheriya, ngaloo ndlela. inhibiting I-synthesis yeprotheni yebhaktheriya idlala umphumo we-antibacterial.
Indlcation
Esi Sicombululo se-Injectable siboniswa kunyango lwezifo zenkqubo ezibangelwa okanye ezinxulumene nezilwanyana ezithintekayo kwi-Trimethoprim: inhlanganisela ye-Sulfadiazine.I-spectrum yomsebenzi ibandakanya zombini i-Gram-positive kunye ne-Gram-negative eziphilayo eziquka: i-Actinobacilli, i-Actinomycae, i-Bordetella spp, i-Brucella Corynebacteria, i-Escherichia coli, i-Haemophilus spp.Klebsiella spp, Pasteurella spp, Pneumococci.Proteus, Salmonella spp.Staphylococci, Streptococci, Vibrio.
Umthamo kunye nolawulo
Ngenaliti engaphantsi kwesikhumba kuphela.
Iinkomo: Umlinganiselo wedosi ekhuthazwayo yi-15 mg yezithako ezisebenzayo ngekhilogram nganye yobunzima bomzimba (1 ml nge-16kg yobunzima bomzimba) ngenaliti ye-intramuscular okanye ecothayo.
Amahashe: Umlinganiselo wethamo elicetyiswayo yi-15 mg yezithako ezisebenzayo ngekhilogram yobunzima bomzimba (1 ml nge-16 kg ubunzima bomzimba), ngokucotha ngokucotha ngenaliti emithanjeni.
Izinja neekati: Umlinganiselo wethamo elicetyiswayo yi-30mg yezithako ezisebenzayo ngekhilogram yobunzima bomzimba (1 ml nge-8 kg ubunzima bomzimba).
Contraindications
Isitofu akufuneki sinikwe ngezinye iindlela ngaphandle kwezo zicetyiswayo.
Akufunekanga ilawulwe nge-intraperitoneally, intra-arterial or intrathecally.
Musa ukunikezela kwizilwanyana ezinobuntununtunu be-sulfonamide eyaziwayo, umonakalo omkhulu wesibindi we-parenchymal okanye i-dyscrasias yegazi.
Izilumkiso Ezikhethekileyo
1 Kulawulo lwemithambo imveliso kufuneka ifudunyezwe kubushushu bomzimba kwaye itofwe ngokucothayo ixesha elide njengoko kunokwenzeka.
2 Kuphawu lokuqala lokunganyamezeli inaliti kufuneka iphazamiseke kwaye unyango lomothuko luqaliswe.
Amanzi aneleyo okusela kufuneka afumaneke ngexesha lesiphumo sonyango lwemveliso.
Ixesha lokurhoxisa
Iinkomo : Inyama - iintsuku ezili-12
Ubisi - iintsuku ezi-4.
Ugcino
Khusela elangeni kwaye ugcine ngaphantsi kwe 30℃.
I-Hebei Veyong Pharmaceutical Co., Ltd, yasekwa kwi-2002, ehlala kwisiXeko saseShijiazhuang, kwiPhondo laseHebei, eChina, ecaleni kwe-Capital Beijing.Ulishishini elikhulu leyeza lezilwanyana eliqinisekisiweyo le-GMP, eline-R&D, imveliso kunye nokuthengiswa kwee-APIs zonyango lwezilwanyana, amalungiselelo, ukutya okuxutywe kwangaphambili kunye nezongezo zokutya.NjengeZiko lobuGcisa lePhondo, iVeyong iye yaseka inkqubo yeR&D ehlaziyiweyo yeyeza elitsha lezilwanyana, kwaye lishishini elaziwa kuzwelonke leteknoloji esekelwe kunyango lwezilwanyana, kukho iingcali zobugcisa ezingama-65.I-Veyong ineziseko ezimbini zokuvelisa: i-Shijiazhuang kunye ne-Ordos, apho isiseko se-Shijiazhuang sihlanganisa indawo ye-78,706 m2, kunye neemveliso ze-API ze-13 ezibandakanya i-Ivermectin, i-Eprinomectin, i-Tiamulin Fumarate, i-Oxytetracycline hydrochloride ects, kunye ne-11, i-injection oral solutions, i-injection oral solutions. , i-premix, i-bolus, i-pesticides kunye ne-disinfectant, njl.IVeyong ibonelela ngee-APIs, ngaphezulu kwe-100 yamalungiselelo eleyibhile, kunye nenkonzo ye-OEM & ODM.
I-Veyong ibona ukubaluleka okukhulu kulawulo lwenkqubo ye-EHS(Environment, Health & Safety), kwaye ifumene i-ISO14001 kunye nezatifikethi ze-OHSAS18001.I-Veyong idweliswe kumashishini amashishini asakhasayo anobuchule kwiPhondo laseHebei kwaye inokuqinisekisa ukubonelela ngokuqhubekayo kweemveliso.
I-Veyong yaseka inkqubo epheleleyo yolawulo lomgangatho, yafumana isatifikethi se-ISO9001, isatifikethi se-GMP sase-China, isiqinisekiso se-APVMA se-GMP sase-Australia, isatifikethi se-GMP sase-Ethiopia, isatifikethi se-Ivermectin CEP, kwaye siphumelele ukuhlolwa kwe-US FDA.I-Veyong ineqela lobuchwephesha lobhaliso, intengiso kunye nenkonzo yobugcisa, inkampani yethu ifumene ukuthembela kunye nenkxaso kubathengi abaninzi ngomgangatho wemveliso ogqwesileyo, umgangatho ophezulu wokuthengisa kwangaphambili kunye nenkonzo yasemva kokuthengisa, ulawulo olunzulu kunye nolwenzululwazi.I-Veyong yenze intsebenziswano yexesha elide kunye namashishini amaninzi amachiza ezilwanyana awaziwayo ngamazwe ngamazwe kunye neemveliso ezithunyelwa eYurophu, eMzantsi Melika, kuMbindi Mpuma, e-Afrika, e-Asia, njl. ngaphezu kwamazwe angama-60 kunye nemimandla.