新药物在临床试验期间接受有限的安全性评估后，即正式注册并投放市场；在大规模普遍使用过程中，只能出现极为罕见的意外的副作用个案。
New medicines are registered and enter the market with limited safety evaluation during clinical trials; rare unexpected side effects can only be detected during large-scale use.
抑郁患儿治疗时，年龄、神经和身体发育的程度都是考虑的关键点，”迈克雅克（一位前临床心理医生和《抑郁症可传染》一书的作者）认为，“考虑到这些因素，经食品药品监督部门评估有7%的抗抑郁症药物可供患儿使用。”
Despite those concerns, the Food and Drug Administration estimates that 7% of antidepressants are still being prescribed to children.
在药品的整个生命周期(自批准前阶段到病人使用)，都保持警惕，对药物存有的风险和带来的益处进行评估。
Vigilant assessment of the risks and benefits of medicines applies throughout the life cycle of a medicine - from the pre-approval stage to use by patients.
研究者正评估这些及其他精神类药物在儿童和青少年中使用的安全性与有效性的问题。
Researchers are evaluating the safety and efficacy of these and other psychotropic medications in children and adolescents.
如果你计划使用此类药物，在操作前必须对插管的难点进行评估。
If you plan to use such agents, you must assess the difficulty of intubation before proceeding.
目前，委员会还要评估法国人研究得出的结果和这些药物在整个欧盟使用后的潜在影响。
The Committee will now also assess the results of the French study and its potential impact on the use of these medicines across the whole EU.
常规使用抗癫痫药物治疗新生儿癫痫是需要进行评估的。
The routine use of anticonvulsants to treat seizures in neonates needs to be evaluated.
评估日常例行使用来预防抗蛇毒血清副作用药物的效果。
To assess the effects of drugs given routinely with snake antivenom to prevent adverse effects.
研究人员对不同的药物进行分类，并使用标准危险评估模型对不同药物和心脏病发作及中风的危险性进行分析。
Researchers then categorized the different drugs and analyzed their relationship to heart attack and stroke using standard risk regression models.
结果进行了评估使用ITT公司，LOCF，分析方法所要求美国食品和药物管理局。
Results were evaluated using ITT-LOCF, the method of analysis required by the U. S. Food and Drug Administration.
结论：药物利用评估程序可以给医疗、护理、药局以及医院的管理者和社会提供有用的药物使用信息。
Conclusion: The DUE program can provide useful information to pharmacy, medical and nursing departments, hospital administration, and society in general.
使用鼻内镜和冠状位鼻窦ct评估一组人数为305人的经最大剂量药物治疗无效的慢性鼻-鼻窦炎患者。
A cohort of 305 consecutive patients with chronic rhinosinusitis refractory to maximal medical therapy was assessed clinically by nasal endoscopy and coronal sinus ct.
目的体外培养人无色素睫状上皮（NPE）细胞，比较抗青光眼药物贝他根与阿法根对NPE细胞增殖的影响，评估两种药物使用的安全性。
ObjectiveTo compare the effects of two antiglaucoma drugs( levobunlol and brimonidine) on cultured human non-pigment ciliary epithelial (NPE) cells and evaluate the safety of the two drugs.
目的体外培养人无色素睫状上皮（NPE）细胞，比较抗青光眼药物贝他根与阿法根对NPE细胞增殖的影响，评估两种药物使用的安全性。
ObjectiveTo compare the effects of two antiglaucoma drugs( levobunlol and brimonidine) on cultured human non-pigment ciliary epithelial (NPE) cells and evaluate the safety of the two drugs.
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