结果：得到合格的头孢噻肟钠。
Results. Qualified cefotaxime sodium was obtained satisfactorily.
目的：考察头孢噻肟钠皮试液稳定性。
Objective: To study the stability of cefotaxime sodium intracutaneous injection.
目的：采用分光光度法测定头孢噻肟钠含量。
The aim is to determine the Content of Cefotaxime sodium by spectrophotometry.
目的：建立头孢噻肟钠的细菌内毒素检查方法。
Objective: to set up a method of bacterial endotoxin test for cefotaxime sodium.
结论：头孢噻肟钠的热原检查可用细菌内毒素检测法。
Conclusions: Bacterial endotoxin test could be used for pyrogen test of cefotaxime sodium.
目的观察注射用头孢噻肟钠与奥硝唑氯化钠注射液配伍后的稳定性。
Objective To investigate the stability of the mixture of cefotaxime sodium injection and ornidazole sodium chloride injection.
试验中未发现应用注射用头孢噻肟钠配舒巴坦钠的严重药物不良反应。
There was no serious adverse drug reactions to cefotaxime sodium and sulbactam sodium in the clinical trial.
通过小试验提出了从头孢噻肟钠生产废渣中回收2硫醇基苯并噻唑(M)的方法。
A method for recovering 2 mercaptobenzothiazole (m) from dregs generated in the production of cefotaxime sodium has been developed in a small scale test.
结果表明，磷霉素钙与头孢噻肟钠联合应用对6株临床分离株具有协同抗菌作用。
It proved that there was synergia antibacterial activity in drug combination of FOM-Ca and Cefotaxime against 6 strains above.
目的：探讨头孢噻肟钠致过敏性休克的特点，预防休克的发生，促进临床合理用药。
Objective: to investigate the characteristics of allergic shock induced by cefotaxime sodium so as to prevent its occurrence and to promote the rational use of cefotaxime.
目的通过对7例头孢噻肟钠迟发型变态反应报告的分析，为临床合理用药提供参考。
Objective To provide information for rational drug usage in clinical practice, through analyzing 7 delayed-type hypersensitivity reports caused by Cefotaxime Sodium recently.
方法：利用分光光度法测定头孢噻肟钠含量比照hplc法，验视测定含量的准确性。
Method: determine the Content of Cefotaxime sodium by spectrophotometry. Methods than HPLC this method shows a good precision accuracy.
结果表明，头孢噻肟钠与磷霉素钙联合应用对治疗鸡大肠杆菌病具有较好的协同作用。
It proved better synergistic action of drug combination of FOM-Ca and Cefotaxime curing chicken colibacillosis.
结论：本法操作简便，结果准确，为有效控制头孢噻肟钠的残留溶媒建立了可靠的方法。
Conclusion: this method is easy to operate with precise results, which establishes a reliable method for the control of residue solvent of cefotaxime sodium.
目的评价注射用头孢噻肟钠配舒巴坦钠预防和治疗妇产科感染的安全性、有效性及不良反应。
AIM: To evaluate the clinical efficacy, safety and adverse drug reaction of cefotaxime sodium and sulbactam sodium in the prevention and treatment of bacterial infections in obstetrics and gynecology.
方法：采用一阶导数分光光度法和双波长光谱法测定各配伍液中头孢噻肟钠和西咪替丁的含量。
METHODS: to test the contents of cefotaxime sodium and cimetidine in all kinds of infusions using first order derivative and double wavelength spectrophotometry.
方法对注射用头孢噻肟钠他唑巴坦钠的伍用复方处方筛选、药学研究、毒理学等研究，评价其疗效和不良反应。
Methods Studies on screening of prescription, pharmaceutical and toxicological researches, therapeutic efficacy and adverse reactions were carried out.
方法：采用超滤法结合高效液相色谱法测出游离药物浓度，比较未加和加入甲硝唑后头孢噻肟钠的蛋白结合率。
Method: Ultrafiltration and HPLC were employed to measure the conc. of free drug. The difference in protein-binding between cefotaxime alone and together with metronidazole was examined.
利用荧光光谱法研究了不同温度下，头孢噻肟钠(CTX)、氯霉素(CHL)与牛血清白蛋白(BSA)的反应机理。
Interaction mechanism of cefotaxime sodium (CTX) and chloramphenicol (CHL) with bovine serum albumin (BSA) at different temperatures by fluorescence spectrometry method was studied.
方法：收集头孢噻肟钠上市以来国内38种主要药学期刊报道的头孢噻肟钠致过敏性休克的个案，采用描述性研究方法进行分析。
Method: the cases reports of cefotaxime sodium - induced allergic shock were collected from 38 main periodicals on pharmaceutics, and a descriptive analysis of the data was conducted.
方法：收集头孢噻肟钠上市以来国内38种主要药学期刊报道的头孢噻肟钠致过敏性休克的个案，采用描述性研究方法进行分析。
Method: the cases reports of cefotaxime sodium - induced allergic shock were collected from 38 main periodicals on pharmaceutics, and a descriptive analysis of the data was conducted.
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