500 MG Oxytetracycline Bolus
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Ayyukan Pharmacological
Pharmacodynamics:Oxytetracyclineyafi tsoma baki tare da hana haɓakar furotin, ta haka ne ke haifar da tasirin kashe ƙwayoyin cuta, da ƙwayoyin gram-tabbatacce, ƙwayoyin gram-korau, mycoplasma, chlamydia, rickettsiae, spirochetes, Porcine eperytrocytes, da sauransu suna da tasirin hanawa.
Musamman ga ciwon huhu na dabba, Staphylococcus, Bacillus anthracis, Tetanus, Pasteurella multocida, Haemophilus, Mycoplasma, Chlamydia, Rickettsia (eperythrocytic jiki) da sauran kwayoyin cuta suna da tasiri mai kyau na hanawa.A gefe guda kuma, cututtukan tsutsa na dabba, leptospirosis, ciwon huhu, ciwon huhu, gas, asma, dysentery na alade, endometritis da mastitis a cikin alade, shanu da tumaki.Pullorum, Escherichia coli, Vibrio kamuwa da cuta, umbilical kumburi, enteritis na matasa tsuntsaye;Ruwan ruwa vibriosis, cutar sikelin, cutar sankara, da dai sauransu suma suna da tasirin sarrafawa mai kyau.
500 MG Oxytetracycline boluswani nau'i ne na baka wanda ke dauke da oxytetracycline, wani nau'in kwayoyin cuta mai fadi wanda ke da tsari mai girma na kwanciyar hankali da kuma aikin maganin rigakafi.
Side Effects
Oxytetracyclinena cikin ajin tetracycline kuma wakili ne mai faffadan ƙwayoyin cuta.Yana iya ƙara ma'auni na alkaline phosphatase, nitrogen urea nitrogen, serum amylase, serum bilirubin, da aminotransferase (AST, ALT).Magani na dogon lokaci ya kamata a kai a kai duba ayyukan jini da ayyukan hanta da koda, saboda oxytetracycline na iya haifar da hanta cikin sauƙi.
Oxytetracycline na iya shiga cikin tayin ta hanyar shingen placental kuma ya ajiye shi a cikin yankin calcium na hakora da kasusuwa, yana haifar da canza launin hakoran tayi, rashin lafiyar enamel da kuma hana ci gaban ƙasusuwan tayin.Za a sami abin da ake kira "tetracycline hakora".Duk da haka, tsuntsaye ba su da mahaifa, amma kuma yana iya haifar da taurin kwandon kwai a lokacin ovulation.Sabili da haka, don kauce wa ƙwai masu laushi, ba a ba da shawarar ciyar da oxytetracycline ga tsuntsayen mata a cikin estrus ba.
Gabatarwa
(1) An haramta shuka mai ciki.
(2) A guji hadawa da ruwan famfo mai yawan sinadarin chlorine da maganin alkaline.Kada ku yi amfani da kwantena na ƙarfe don magunguna.
(3) Guji dacewa da kayan kiwo, magungunan da ke ɗauke da alli, magnesium, aluminum, da baƙin ƙarfe, da ciyarwa tare da babban abun ciki na calcium.Ya kamata a sha a cikin komai a ciki kafin a ci abinci.
(4) Manya-manyan dawa, dabbobin doki da zomaye ba su dace da gudanar da baki ba.Aikace-aikace na dogon lokaci na iya haifar da kamuwa da cuta sau biyu na ƙwayoyin cuta da fungi masu jure wa miyagun ƙwayoyi, kuma lokuta masu tsanani na iya haifar da sepsis da mutuwa.
Hebei Veyong Pharmaceutical Co., Ltd, an kafa shi a shekara ta 2002, wanda yake a birnin Shijiazhuang na lardin Hebei na kasar Sin, kusa da babban birnin Beijing.Ita babbar sana'ar sayar da magungunan dabbobi ce ta GMP, tare da R&D, samarwa da tallace-tallace na APIs na dabbobi, shirye-shirye, ciyarwar da aka riga aka haɗa da ƙari.A matsayin Cibiyar Fasaha ta Lardi, Veyong ya kafa sabon tsarin R&D don sabbin magungunan dabbobi, kuma shine sanannen masana'antar fasahar kere kere ta ƙasa, akwai kwararrun fasaha 65.Veyong yana da biyu samar sansanonin: Shijiazhuang da Ordos, wanda Shijiazhuang tushe maida hankali ne akan wani yanki na 78,706 m2, tare da 13 API kayayyakin ciki har da Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, da kuma 11 shiri samar Lines ciki har da allura, ko foda bayani. , premix, bolus, magungunan kashe qwari da magungunan kashe qwari, da sauransu.Veyong yana ba da APIs, fiye da shirye-shiryen alamar mallaka 100, da sabis na OEM & ODM.
Veyong yana ba da mahimmanci ga gudanar da tsarin EHS (Muhalli, Lafiya & Tsaro), kuma ya sami takaddun shaida na ISO14001 da OHSAS18001.An jera Veyong a cikin dabarun masana'antu masu tasowa a lardin Hebei kuma yana iya tabbatar da ci gaba da samar da kayayyaki.
Veyong ya kafa cikakken tsarin gudanarwa mai inganci, ya sami takardar shedar ISO9001, takardar shaidar GMP ta kasar Sin, takardar shedar APVMA GMP ta Australia, takardar shaidar GMP ta Habasha, takardar shaidar Ivermectin CEP, kuma ta wuce binciken FDA na Amurka.Veyong yana da ƙwararrun ƙungiyar rajista, tallace-tallace da sabis na fasaha, kamfaninmu ya sami dogaro da goyan baya daga abokan ciniki da yawa ta kyakkyawan ingancin samfur, ingantaccen pre-tallace-tallace da sabis na tallace-tallace, mai tsanani da sarrafa kimiyya.Veyong ya yi dogon lokaci hadin gwiwa tare da da yawa duniya sanannun dabbobi Pharmaceutical Enterprises tare da kayayyakin da ake fitarwa zuwa Turai, Kudancin Amirka, Gabas ta Tsakiya, Afirka, Asiya, da dai sauransu fiye da 60 kasashe da yankuna.
