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Economic Study of Cefotaxime in the Treatment of Lower Respiratory Tract Infection

头孢噻肟治疗下呼吸道感染的经济学研究

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methods: 186 patients with bacterial pneumonia were selected and randomly divided into 3 groups. group a were treated with cefotaxime, group b with levofloxacin and group c with cloxacillin sodium. the curative effects and adverse drug reactions were observed and analyzed by pharmacoeconomics method.

方法:186例细菌性肺炎患者随机分为A、B、C组,分别给予头孢噻肟钠、左氧氟沙星、氯唑西林钠治疗,观察各组疗效、不良反应,并运用药物经济学方法进行分析。

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conclusion: cefotaxime was the optimal treatment for bacterial pneumonia.

结论:头孢噻肟钠治疗细菌性肺炎较佳。

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methods the current hplc methods in different pharmacopoeia and hplc-ms analysis were performed to study on the complete impurity profile of cefotaxime sodium.

方法采用现版的不同药典的相关HPLC法及HPLC-MS分析,研究头孢噻肟钠的完全杂质谱。

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determination of two components and related substances in cefotaxime sodium and tazobactam sodium for injection by hplc

HPLC测定注射用头孢噻肟钠他唑巴坦钠的含量及有关物质

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a comparison between the therapeutic efficacy of cefotaxime ( ctx) and ampicillin on neonatal purulent meningitis

头孢氨噻肟治疗新生儿化脓性脑膜炎疗效的对照分析

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stability after compatibility of cefotaxime sodium and cimetidine in different kinds of intravenous infusions

注射用头孢噻肟钠与西咪替丁注射液在4种输液中配伍后的稳定性

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objective study on the stability of cefotaxime sodium tazobactam sodium for injection.

目的:观察注射用头孢噻肟钠、他唑巴坦钠稳定性。

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determination of cefotaxime sodium/ sulbactam sodium for injection by hplc

HPLC法测定注射用头孢噻肟钠/舒巴坦钠的含量

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determination of sodium cefotaxime in renal dialysate from burn-injured patients by hplc

HPLC测定烧伤患者肾脏透析排出液中头孢噻肟钠的含量

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objective: to observe the stability of cefotaxime sodium for injection in pvc infusion bags, pp plastic infusion bottle, non-pvc multilayer polymer infusion bags and glass bottles.

目的考察注射用头孢噻肟钠在聚氯乙烯(PVC)输液袋、聚丙烯(PP)塑料输液瓶、非聚氯乙烯(NPVC)多层共挤膜输液袋及玻璃瓶包装输液中的稳定性差异。

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objective: to evaluate the stability of tinidazole and cefotaxime sodium mixed in infusion fluid at 4 ℃, 25 ℃ and 37 ℃ for 24 hours.

目的:考察4℃、25℃、37℃下24h内替硝唑葡萄糖注射液与注射用头孢噻肟钠的配伍稳定性。

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conclusion: the mixture of ornidazole injection and cefotaxime sodium for injection can be used after ( storing) at 4 ℃ for 8 h, 25 ℃ for 4 h and 37 ℃ for 1 h.

结论:奥硝唑注射液与注射用头孢噻肟钠的配伍液在配伍后4℃8h内、25℃4h内、37℃1h内可使用。

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the cumulative urinary excretion rates of cefotaxime sodium and tazobactam sodium were ( 49.6 ± 0.58)% and ( 80.0 ± 7.0)% after intravenous drip of a single 2.4 g dose, respectively.

单次给药中剂量组10h头孢噻肟钠和他唑巴坦钠累计尿排率为49.6±0.58%和80.0±7.0%。

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results: no significant change was noted in the detection results of all the items of cefotaxime sodium for injection in 4 kinds of infusion packages and under different temperatures;

结果注射用头孢噻肟钠在各温度条件下于4种包装输液中各检测项目均无明显变化,4组间比较无显著性差异(P0.1)。

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measurement and correlation of liquid-solid equilibrium of cefotaxime sodium in water-isopropanol

头孢噻肟钠在水-异丙醇中的液固平衡测量与关联

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clinical analysis of cefotaxime sodium treating 86 cases of neonatal septicemia

头孢噻肟钠治疗新生儿败血症86例临床分析

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Treatment of egg white lysozyme in combination with ampicillin or cefotaxime significantly inhibited bacteriolysis and reduced endotoxin release as well as TNF α and IL-6 production.

而鸡蛋清溶菌酶与β内酰胺类抗生素联合使用能阻止细菌溶解,降低细菌内毒素的释放,并减少巨噬细胞TNFα和IL6的产生。

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