Results 31 to 40 of about 149,065 (306)
Statistical Analysis System of Spontaneous Adverse Drug Reaction Reports
Journal of Korean Society for Clinical Pharmacology and Therapeutics, 2012 Background: Spontaneous adverse drug reaction (ADR) reporting data has been used for safety of post-market drug surveillance. A system has been required that is able to detect signals associated with drugs by analyzing the collected ADR data. Methods: We developed the web-based automated analysis system (ADR-detector).
Sira Kim +6 more
openaire +1 more source
An annotated corpus with nanomedicine and pharmacokinetic parameters [PDF]
, 2017 A vast amount of data on nanomedicines is being generated and published, and natural language processing (NLP) approaches can automate the extraction of unstructured text-based data. Annotated corpora are a key resource for NLP and information extraction
Jimenez, Ivan +2 more
core +2 more sources
Cadernos de Saúde Pública, 2021 : The U.S. Food and Drug Administration (FDA) has stated that the prescription of remdesivir should be cautious for patients with estimated glomerular filtration rate (eGFR) < 30 and some studies reported risk of adverse renal events.
Nayara Aparecida de Oliveira Silva +3 more
doaj +1 more source
Linked health data for pharmacovigilance in children : Perceived legal and ethical issues for stakeholders and data guardians [PDF]
, 2014 Peer reviewedPublisher ...
Bond, Christine M +4 more
core +2 more sources
South African Journal of Industrial Engineering, 2018 Since 2010, pharmaceutical organisations have begun to provide drug patents in sub-Saharan Africa through the UN Medicine Patent Pool. This initiative allows any pharmaceutical manufacturer to access these patents and manufacture the drugs, thereby ...
Huysamen, Biance +2 more
doaj +1 more source
Antibiotics, 2023 Antimicrobial resistance is considered one of the major threats to public health and is an important factor that influences the patient’s outcome in the intensive care unit.
Bogdan Ioan Vintila +8 more
doaj +1 more source
Complementing the US Food and Drug Administration Adverse Event Reporting System With Adverse Drug Reaction Reporting From Social Media: Comparative Analysis [PDF]
JMIR Public Health and Surveillance, 2020 Background Adverse drug reactions (ADRs) can occur any time someone uses a medication. ADRs are systematically tracked and cataloged, with varying degrees of success, in order to better understand their etiology and develop methods of prevention.
Zeyun Zhou, Kyle Emerson Hultgren
openaire +5 more sources
Drug Hepatotoxicity: Environmental Factors [PDF]
, 2017 Drug-induced liver injury presents as various forms of acute and chronic liver disease. There is wide geographic variation in the most commonly implicated agents.
Chalasani, Naga P., Stine, Jonathan G.
core +1 more source
Nurses' reporting of suspect adverse drug reactions: a mixed-methods study
Annali dell'Istituto Superiore di Sanità, 2015 OBJECTIVE: To assess nurses' knowledge, attitudes and practices (KAP) towards spontaneous adverse drug reactions (ADRs) reporting. METHODS: The mixed-method study was conducted following a quanti-qualitative sequential approach: a survey (using a KAP ...
Alessia De Angelis +4 more
doaj +1 more source
Journal of Korean Medical Science, 2022 Adverse drug reactions (ADRs) to first-line anti-tuberculosis (TB) drugs are common; however, there have been few reports of nationwide epidemiologic studies on ADRs to anti-TB drugs in Korea. This study aimed to investigate the clinical characteristics of various ADRs to first-line anti-TB drugs using a nationwide database of ADRs.We used the Korea ...
Soo Jie Chung +2 more
openaire +2 more sources