官方服务：
资源简介：
Antimalarials adverse events during a cohort and randomized controlled trial
应用场景：
创建时间：
2018-11-10
相关数据集
AERSLD: Adverse Events as Linked Data (from AERS)
A linked data version of the AERS (currently FAERS) dataset of the US Food and Drug administration for the years 2005-2012. The dataset has been linked to Drugbank, DBPedia (v3.7), Diseaseome, Sid
Figshare2017-05-08 更新60
Comparing adverse events of tenecteplase and alteplase: a real-world analysis of the FDA adverse event reporting system (FAERS)
The aim of this study is to monitor, identify, and compare the adverse events (AEs) related to tenecteplase and alteplase, with the objective of exploring the potential safety of tenecteplase for acut
NIAID Data Ecosystem20
Adverse Events.
*One case occurred after sunitinib treatment and was likely related to reirradiation performed prior to protocol therapy.
Figshare2015-12-02 更新20
Interventions to improve spontaneous adverse drug reaction reporting by healthcare professionals and patients: systematic review and meta-analysis
The aim of this study was to evaluate the effectiveness of interventions used for improving ADR reporting by patients and healthcare professionals. A systematic review of literature was conducted by s
Taylor & Francis Group2021-05-07 更新60
Frequency of additional risk factors for rhabdomyolysis.
Frequency of additional risk factors for rhabdomyolysis.
Figshare2015-12-02 更新20
