20% Sulfadiazine+4% Trimethoprim Injection
Isithako Esisebenzayo
I-Sulfadiazine 20.00% w/v.
I-Trimethoprim 4.00% w/v
Isenzo se-Pharmacological
I-Sulfadiazine iwumuthi we-sulfa osebenza ngokusesilinganisweni ukuze usetshenziswe ngokwesistimu futhi iyi-bacteriostatic agent ebanzi.Indlela yayo yokusebenza ingenxa yokuthi ifana ngokwesakhiwo ne-p-aminobenzoic acid (PABA) futhi ingaqhudelana ne-PABA ukuze isebenze ku-dihydrofolate synthase kumabhaktheriya, ngaleyo ndlela ivimbele i-PABA ukuthi isetshenziswe njengento eluhlaza ukuze kuhlanganiswe i-tetrahydrofolate edingwa amagciwane, ngaleyo ndlela. ukuvimbela Ukuhlanganiswa kwamaprotheni ebhaktheriya kudlala umphumela we-antibacterial.
Indlcation
Lesi sixazululo Esijovayo siboniswa ekwelapheni izifo zesistimu ezibangelwa noma ezihambisana nezinto eziphilayo ezizwelayo kunhlanganisela ye-Trimethoprim: Sulfadiazine.I-spectrum yomsebenzi ihlanganisa kokubili i-Gram-positive kanye ne-Gram-negative organisms okuhlanganisa: Actinobacilli, Actinomycae, Bordetella spp, Brucella Corynebacteria, Escherichia coli, Haemophilus spp.I-Klebsiella spp, i-Pasteurella spp, i-Pneumococci.Proteus, Salmonella spp.Staphylococci, Streptococci, Vibrio.
Umthamo kanye nokuphatha
Ngomjovo we-subcutaneous kuphela.
Izinkomo: Izinga lethamo elinconywayo lingu-15 mg wezithako ezisebenzayo ngekhilogremu ngayinye yesisindo somzimba (1 ml ngesisindo somzimba esingu-16kg) ngomjovo we-intramuscular or slow intravenous.
Amahhashi: Izinga lethamo elinconyiwe lingu-15 mg wezithako ezisebenzayo ngekhilogremu ngayinye yesisindo somzimba (1 ml ngesisindo somzimba esiyi-16 kg), ngomjovo ohamba kancane ngomthambo.
Izinja namakati: Izinga lethamo elinconyiwe lingu-30mg wezithako ezisebenzayo ngekhilogremu ngayinye yesisindo somzimba (1 ml ngesisindo somzimba esingu-8 kg).
Contraindications
Umjovo akufanele unikezwe ngezinye izindlela ngaphandle kwalezo ezinconyiwe.
Akufanele inikezwe nge-intraperitoneally, intra-arterial noma intrathecally.
Unganikezi izilwane ezizwela i-sulfonamide eyaziwayo, ukulimala okukhulu kwesibindi se-parenchymal noma i-dyscrasias yegazi.
Izixwayiso Ezikhethekile
1 Ngokufakwa emthanjeni umkhiqizo kufanele ufudumale kuzinga lokushisa lomzimba futhi ujovwe kancane isikhathi eside njengoba kungenzeka.
2 Uma kunesibonakaliso sokuqala sokungabekezelelani umjovo kufanele uphazamiseke futhi kuqaliswe ukwelashwa kokushaqeka.
Amanzi okuphuza anele kufanele atholakale ngesikhathi somphumela wokwelapha womkhiqizo.
Isikhathi Sokuhoxiswa
Izinkomo : Inyama - izinsuku ezingu-12
Ubisi - izinsuku ezingu-4.
Isitoreji
Vikela elangeni eliqondile futhi ugcine ngaphansi kuka-30 ℃.
I-Hebei Veyong Pharmaceutical Co., Ltd, yasungulwa ngo-2002, etholakala eShijiazhuang City, eSifundazweni saseHebei, eChina, eduze kweNhloko-dolobha yaseBeijing.Uyibhizinisi elikhulu lemithi yezilwane eqinisekiswe yi-GMP, ene-R&D, ukukhiqizwa nokudayiswa kwama-API wezilwane, amalungiselelo, okuphakelayo okuxutshwe ngaphambili nezithasiselo zokudla.NjengeSikhungo Sezobuchwepheshe Sesifundazwe, i-Veyong isungule uhlelo olusha lwe-R&D lomuthi omusha wezilwane, futhi iyibhizinisi lezobuchwepheshe elaziwa kuzwelonke elisekelwe kudokotela wezilwane, kunochwepheshe abangama-65.I-Veyong inezisekelo ezimbili zokukhiqiza: i-Shijiazhuang ne-Ordos, lapho isisekelo se-Shijiazhuang sihlanganisa indawo engu-78,706 m2, nemikhiqizo ye-API engu-13 ehlanganisa i-Ivermectin, i-Eprinomectin, i-Tiamulin Fumarate, i-Oxytetracycline hydrochloride ects, kanye ne-11, imigqa yokukhiqiza ye-powder yokulungiselela , premix, bolus, izibulala-zinambuzane nesibulala-magciwane, njll.I-Veyong ihlinzeka ngama-API, amalungiselelo angaphezu kwe-100 elebula uqobo, kanye nesevisi ye-OEM & ODM.
I-Veyong ibheka ukubaluleka okukhulu ekuphathweni kohlelo lwe-EHS(Imvelo, Impilo Nokuphepha), futhi yathola izitifiketi ze-ISO14001 ne-OHSAS18001.I-Veyong isohlwini lwamasu amabhizinisi ezimboni asafufusa esifundazweni sase-Hebei futhi ingaqinisekisa ukuhlinzekwa okuqhubekayo kwemikhiqizo.
I-Veyong yasungula uhlelo oluphelele lokuphatha ikhwalithi, yathola isitifiketi se-ISO9001, isitifiketi se-China GMP, isitifiketi se-APVMA GMP yase-Australia, isitifiketi se-Ethiopia GMP, isitifiketi se-Ivermectin CEP, futhi yaphumelela ukuhlolwa kwe-US FDA.I-Veyong inethimba elichwepheshile lokubhalisa, ukuthengisa kanye nenkonzo yezobuchwepheshe, inkampani yethu ithole ukwethenjwa nokusekelwa kumakhasimende amaningi ngekhwalithi yomkhiqizo omuhle kakhulu, ikhwalithi ephezulu yokuthengisa kwangaphambili kanye nenkonzo yangemuva kokuthengisa, ukuphathwa okungathi sína nokwesayensi.I-Veyong yenze ukubambisana kwesikhathi eside namabhizinisi amaningi emithi yezilwane aziwa emhlabeni wonke ngemikhiqizo ethunyelwa eYurophu, eNingizimu Melika, eMpumalanga Ephakathi, e-Afrika, e-Asia, njll. emazweni nasezifundeni ezingaphezu kuka-60.