Results 21 to 30 of about 1,331,435 (262)

Ocular Complications after COVID-19 Vaccination, Vaccine Adverse Event Reporting System

open access: yesVaccines, 2022
In December 2020, the U.S. Food and Drug Administration licensed COVID-19 vaccines for emergency use authorization. We investigated the ocular adverse event reports in patients reported to the Vaccine Adverse Event Reporting System (VAERS) following ...
Cyril N. A. Nyankerh   +2 more
doaj   +1 more source

Evaluating Ubrogepant-related adverse events using the FDA adverse event reporting system

open access: yesExpert Opinion on Drug Safety, 2023
Migraine has a high prevalence in the population and accounts for 12% of primary headaches. Ubrogepant is used for the treatment of acute migraine, and although some clinical trials have demonstrated the safety of Ubrogepant, its long-term safety in a large sample of the population remains to be investigated. We collected data from the US Food and Drug
Bing, Cao   +5 more
openaire   +2 more sources

Distributed Ledger Infrastructure to Verify Adverse Event Reporting (DeLIVER): Proposal for a Proof-of-Concept Study

open access: yesJMIR Research Protocols, 2021
BackgroundAdverse drug event reporting is critical for ensuring patient safety; however, numbers of reports have been declining. There is a need for a more user-friendly reporting system and for a means of verifying reports that have been filed.
Milne-Ives, Madison   +4 more
doaj   +1 more source

AE-GPT: Using Large Language Models to Extract Adverse Events from Surveillance Reports-A Use Case with Influenza Vaccine Adverse Events [PDF]

open access: yes, 2023
Though Vaccines are instrumental in global health, mitigating infectious diseases and pandemic outbreaks, they can occasionally lead to adverse events (AEs). Recently, Large Language Models (LLMs) have shown promise in effectively identifying and cataloging AEs within clinical reports.
arxiv   +1 more source

Simulating adverse event spontaneous reporting systems as preferential attachment networks [PDF]

open access: yesApplied Clinical Informatics, 2014
Summary Background: Spontaneous Reporting Systems [SRS] are critical tools in the post-licensure evaluation of medical product safety. Regulatory authorities use a variety of data mining techniques to detect potential safety signals in SRS databases.
Robert Ball   +2 more
openaire   +3 more sources

Educating Healthcare Professionals in Pharmacovigilance: Global Trends and Korea’s Status [PDF]

open access: yes, 2020
This narrative review introduces global trends in pharmacovigilance (PV) education for healthcare professionals and the status of PV education in Korea. Proactive participation of healthcare professionals, including physicians, pharmacists, and nurses in
Korean Medical Education Review (의학교육논단)
core   +1 more source

Serious Cardiovascular Adverse Events Reported with Intravenous Sedatives: A Retrospective Analysis of the MedWatch Adverse Event Reporting System [PDF]

open access: yesDrugs - Real World Outcomes, 2019
Serious cardiovascular adverse events (SCAEs) associated with intravenous sedatives remain poorly characterized.The objective of this study was to compare SCAE incidence, types, and mortality between intravenous benzodiazepines (i.e., diazepam, lorazepam, and midazolam), dexmedetomidine, and propofol in the USA over 8 years regardless of the clinical ...
Jonathan Weinstock   +8 more
openaire   +3 more sources

Assessment of Reye’s syndrome profile with data from the US Food and Drug Administration Adverse Event Reporting System and the Japanese Adverse Drug Event Report databases using the disproportionality analysis

open access: yesSAGE Open Medicine, 2020
Objectives: Reye’s syndrome is a rare and potentially fatal illness that is defined as encephalopathy accompanied by liver failure. The aim of this study was to assess Reye’s syndrome profiles by analyzing data from the spontaneous reporting system ...
Kiyoka Matsumoto   +13 more
doaj   +1 more source

Methods for Detecting and Measuring Adverse Hospital Events [PDF]

open access: yesIranian Journal of Public Health, 2005
Introduction: An adverse event is defined as an unexpected event such as a patient fall, a drug reaction or an infection, which leads to patient injury and is caused by healthcare management rather than patient own diseases.
A Baba-Akbari Sari   +1 more
doaj   +1 more source

Publicity and reports of behavioral addictions associated with dopamine agonists [PDF]

open access: yes, 2015
Background The development of behavioral addictions (BAs) in association with dopamine agonists (DAs, commonly used to treat Parkinson’s disease) has been reported.
Gendreau, Katherine E., Potenza, Marc N.
core   +1 more source

Home - About - Disclaimer - Privacy