MDDC: An R and Python Package for Adverse Event Identification in Pharmacovigilance Data [PDF]
arXivThe safety of medical products continues to be a significant health concern worldwide. Spontaneous reporting systems (SRS) and pharmacovigilance databases are essential tools for postmarketing surveillance of medical products. Various SRS are employed globally, such as the Food and Drug Administration Adverse Event Reporting System (FAERS ...
arxiv
VA releases adverse event data: Clinicians must report to nationwide system [PDF]
, 2000 Nancy Tarleton Landis
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Analysis of CFSAN Adverse Event Reporting System and Twitter
, 2019 For the public health monitoring, FDA is releasing the public data for consumer complaint data. This CARES database contains information on product complaint reports submitted to FDA. It includes dietary supplements and food adversary incidents. Also, the FDA is trying to utilize SNS data like Twitter as real-time monitoring tools. In this analysis, we
openaire +1 more source
Journal of Applied Clinical Medical Physics, EarlyView.Abstract Purpose Breast cancer is a neoplastic disease with high prevalence among women. Radiotherapy is one of the principal treatment modalities for this disease, but it poses significant challenges. This study aimed to compare and evaluate the technical and dosimetric performance of conventional C‐arm linac systems and a new design, Halcyon, in the ...
Mustafa Çağlar +8 more
wiley +1 more source
Assessing the safety of bedaquiline: insight from adverse event reporting system analysis
Frontiers in PharmacologyBackgroundThe development and marketing of Bedaquiline (BDQ) represent significant advancements in treating tuberculosis, particularly multidrug-resistant forms.
Jiaqiang Wu +3 more
doaj +1 more source
Concomitant Risk Factors in Reports of Torsades de Pointes Associated with Macrolide Use: Review of the United States Food and Drug Administration Adverse Event Reporting System [PDF]
, 2002 Douglas Shaffer +3 more
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Using deep learning generated CBCT contours for online dose assessment of prostate SABR treatments
Journal of Applied Clinical Medical Physics, EarlyView.Abstract Prostate Stereotactic Ablative Body Radiotherapy (SABR) is an ultra‐hypofractionated treatment where small setup errors can lead to higher doses to organs at risk (OARs). Although bowel and bladder preparation protocols reduce inter‐fraction variability, inconsistent patient adherence still results in OAR variability.
Conor Sinclair Smith +8 more
wiley +1 more source
Postmarketing Safety Surveillance for Typhoid Fever Vaccines from the Vaccine Adverse Event Reporting System, July 1990 through June 2002 [PDF]
, 2004 Elizabeth Begier +3 more
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Detecting adverse high-order drug interactions from individual case safety reports using computational statistics on disproportionality measures [PDF]
arXivAdverse drug interactions are a critical concern in pharmacovigilance, as both clinical trials and spontaneous reporting systems often lack the breadth to detect complex drug interactions. This study introduces a computational framework for adverse drug interaction detection, leveraging disproportionality analysis on individual case safety reports.
arxiv
Co-training for Extraction of Adverse Drug Reaction Mentions from Tweets [PDF]
arXiv, 2018 Adverse drug reactions (ADRs) are one of the leading causes of mortality in health care. Current ADR surveillance systems are often associated with a substantial time lag before such events are officially published. On the other hand, online social media such as Twitter contain information about ADR events in real-time, much before any official ...
arxiv