给药

The rats in control group were given distilled water, and the rats in experimental groups were given different doses of capsule（4.0、2.0、1.0g/kg）, then enhance the capillary permeability of abdominal skin of rats by using xylic acid,and the OD numerical value was detected.

(1)抗炎实验：将40只小鼠随机分为补肾利浊胶囊高、中、低剂量组及对照组各10只，补肾利浊胶囊高、中、低剂量组分别给予相应剂量的补肾利浊胶囊(分别为4.0、2.0、1.0 g/kg)，对照组给予蒸馏水，采用二甲苯酸致小鼠腹部皮肤毛细血管通透性增高，测定光密度值；(2)镇痛实验：40只小鼠分组及给药同抗炎实验，采用腹腔注射醋酸致小鼠出现扭体反应，纪录扭体次数并计算镇痛百分率；(3)抗前列腺炎实验：将雄性大鼠50只随机分为补肾利浊胶囊高、中、低剂量组及模型对照组及正常对照组，各10只。

Methods ①anti-inflammatory trial: 40 rats were randomly divided into control group, high-dose bushenlizhuo capsule group, middle-dose bushenlizhuo capsule group and low-dose bushenlizhuo capsule group(10 rats in each group).the rats in control group were given distilled water, and the rats in experimental groups were given different doses of capsule（4.0、2.0、1.0g/kg）, then enhance the capillary permeability of abdominal skin of rats by using xylic acid,and the od numerical value was detected.

(1)抗炎实验：将40只小鼠随机分为补肾利浊胶囊高、中、低剂量组及对照组各10只，补肾利浊胶囊高、中、低剂量组分别给予相应剂量的补肾利浊胶囊(分别为4.0、2.0、1.0 g/kg)，对照组给予蒸馏水，采用二甲苯酸致小鼠腹部皮肤毛细血管通透性增高，测定光密度值；(2)镇痛实验：40只小鼠分组及给药同抗炎实验，采用腹腔注射醋酸致小鼠出现扭体反应，纪录扭体次数并计算镇痛百分率；(3)抗前列腺炎实验：将雄性大鼠50只随机分为补肾利浊胶囊高、中、低剂量组及模型对照组及正常对照组，各10只。

Methods: Integrated and disrepaired skins in the rats were smeared with Salicylic AcidPhenol Liniment by the maximum tolerated dose only. The toxic reaction of the animals were observed and recorded continuously from the beginning of using the drug to 7 days, and evaluated by using the general standard of the reaction of skin stimulation in pharmacology. Animals were executed by taking off acanthi and blood was collected to check up the periphery blood routine and serum biochemistry at the end of the observation of the rats. And after the dissection, the pathological change of main visceras, such as heart, brain, liver and kidney were observed with naked eye and pathological slices. The data of this experiment was used to calculate the value of LD50 by using Bliss rule.

观察大鼠完整皮肤及破损皮肤一次性涂抹最大耐受量的小儿水杨酸苯酚搽剂所产生的毒性反应情况，从给药0时起至7 d连续观察记录动物的急性毒性和45 d连续的长期毒性反应，以皮肤刺激反应标准进行评分作毒理等级评价；对存活动物在观察结束时进行高位脱椎处死采血检测外周血常规和血清生化，解剖后裸眼和病理切片观察心、脑、肝、肾等主要脏器的病理变化。

The indices of APIC treated groups with the medium and high doses were higher than those of the model group significantly.

当归多糖铁低剂量给药组的各项检测指标与模型组相比，虽无显著性差异，但各项指标的恢复情况要略优于模型组。

The mice in the above groups were fed for 7 days. The drug groups were pretreated intragastrically with 3, 15g · kg-1 celery root; bifendate pills groups were pretreated intragastrically with 200mg · kg-1 bifendate. Control animals were given the same volumn physiological saline.

高、低剂量给药组按30、15g · kg-1灌胃芹菜根提取物，阳性对照组按200mg · kg-1灌胃联苯双酯滴丸，阴性对照组及模型对照组以等体积生理盐水灌胃，共7d 。

The patients were administered for 5 weeks.

给药时间均为5周。

Objective To investigate the method of applying risk management in the prevention of administering medicine error.

目的探讨护理风险管理在预防给药差错中的运用。

We have built a sound sales network and a set of standard administrated rules and regulations.

我们已建立了一个完善的销售网络和一套标准给药的规则。

In most states, testing is administrated by the state in a separate facility.

在大多数州，测试是由国家给药在一个单独的设施。

The respiratory function in 61 patients (71.8%) was improved at different extent by electronic bronchoscope treatment,such as aspirating sputum,washing,medicine treatment,and hemostasis,etc.

对61例(71.8%)患者经支气管镜吸痰、灌洗、给药、止血等治疗后不张肺叶均有不同程度复张，呼吸功能明显改善。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。