What happens when an adverse event is reported?
报告出现不良事件后，将采取什么行动？
The most frequently reported adverse event was orthostatic hypotension.
报道中最常见的不良反应是直立性低血压。
Adverse event rates during the off-treatment phase were similar between groups.
在非治疗期间不良事件发生率两组相似。
OHSS in ART cycles is an adverse event that follows ovarian stimulation for IVF.
卵巢过度刺激综合征是在IVF过程中伴随着卵巢刺激的不良事件。
Understand that rhabdomyolysis is a rare adverse event reported with all stating.
知道横纹肌溶解是所有他汀类药物都有报道的罕见的不良事件。
Application site reactions were the most commonly reported adverse event (16.1%).
用药部位反应是最常见的不良事件(16.1%)。
If I am a manufacturer, what information must I submit in my individual adverse event reports?
如果我是制造商，在我的个人不良事件报告中我必须提交什么信息？
There were no remarkable adverse event and side effect in the rehabilitative observation group.
康复观察组没有明显的不良事件和副反应。
Medical adverse event is one of injuries caused not by diseases but by diagnosis and treatment process.
医疗不良事件是指因诊疗活动而非疾病本身造成的损害。
The FDA has conducted a new analysis of the available literature and post-marketing adverse event reports.
FDA已进行了一项新的分析研究现有的文献和上市后不良事件的报告。
The only serious adverse event was seen in a patient in the quinine group who developed fatal black water fever.
唯一的严重不利事件是奎宁组中有一名患者罹患了致命的黑尿热。
What makes hospitalized patients more vulnerable and increases their risk of experiencing an adverse event?
什么因素让住院病人更脆弱，增加他们发生负性事件的危险？
These days, the consequences of an adverse event in one part of the world are highly contagious and profoundly unfair.
如今，发生在世界一角的不良事件的后果具有高度的传染性和极度的不公平性。
OBJECTIVE: To discuss the concepts and methods of medical device adverse event monitoring and risk man-agernent .
目的：初步探讨医疗器械不良事件监测和风险管理的概念和方法。
FDA's review of adverse event reports found cases of significant weight gain and edema-warning signs of heart failure.
FDA不良反应调查报告发现明显体重增加和水肿病例提示心衰的体征。
AIM: to establish a statistical model to appropriately evaluate the relationship between clinical adverse event and treatment.
目的：建立一种统计学模型来评价临床不良事件与治疗间的关系。
Medical device adverse event monitoring is one of the most important methods to guarantee the safety of post-marketing products.
医疗器械不良事件监测是确保上市医疗器械安全有效的重要手段之一。
Adverse event rate in two groups were low, and most adverse events were local reaction such as dry pharynx and excessive phlegm.
两组不良反应发生率均低，以咽干、声嘶等局部反应为主。
Drug discontinuation due to an adverse event was also more frequent in the sirolimus cohort compared to those patients continued on CNI.
在西罗莫司组中因不良事件而导致停药的也多于继续使用CNI治疗的患者。
The current financial crisis has taught us how quickly an adverse event can spread throughout the systems that link us all so closely together.
当前的金融危机已告诉我们，不良事件可在把我们所有人密切联系在一起的系统中迅速传播。
There was no significant difference in the frequency of adverse event and serious laboratory abnormalities between entacapone and placebo groups.
不良事件的发生率与安慰剂组相比差异无显著意义。
Over the past 20 years, according to Runner, the FDA has received 141 adverse event reports regarding dental amalgams, with none resulting in death.
过去二十年，FDA接到了141个牙科使用汞合金后的不良反应报告，但没有导致死亡病例。
The CDC's vaccine adverse event Reporting System (VAERS) finds no link between Gardasil and adverse events reported by doctors and vaccine recipients.
CDC的疫苗不良反应事件监测中心(VAERS)没有发现加德西与医生和疫苗接种者报告的不良反应事件之间存在联系。
As of September 2006, a total of 17 cases had been reported to the US Vaccine Adverse Event Reporting System as occurring within 6 weeks after vaccination.
截止到2006年9月，美国疫苗不良事件报告系统总共收到17份病例报告(在接种后6周发生GBS)。
Although HCAI is the most frequent adverse event in health care, its true global burden has been unknown because of the difficulty in gathering reliable data.
尽管卫生保健相关感染是卫生保健方面碰到的最常见不良事件，但是其全球负担的真实情况尚不为人知，这是由于在收集可靠数据方面存有难度。
The bigger issue is that the FDA's problem-ridden Adverse Event Reporting System isn't a systematic measure of how often drugs really cause side effects.
更大的问题是，受问题支配的FDA的不良反应事件报告系统不能系统的衡量药品引起的真实副作用的多少。
The CDC said the vaccine Adverse Event Reporting System (VAERS) had also not detected any problems in connection with the vaccines affected by this recall.
疾病防治中心表示，疫苗不良事件报告系统(VAERS)也没有发现受到该召回影响的疫苗相关的任何问题。
Nausea was the most commonly reported adverse event with both agents, with slightly less persistent nausea in the liraglutide group than in the exenatide group.
两种药使用中报告频率最多的不良反应是呕吐，依拉鲁肽组相比依克那肽组持续呕吐的发生要稍轻些。
Nausea was the most commonly reported adverse event with both agents, with slightly less persistent nausea in the liraglutide group than in the exenatide group.
两种药使用中报告频率最多的不良反应是呕吐，依拉鲁肽组相比依克那肽组持续呕吐的发生要稍轻些。
应用推荐