Results 21 to 30 of about 176,998 (309)
Drug therapeutic failures as a cause of admission to an intensive care unit at a university hospital
Journal of Research in Pharmacy Practice, 2019 Objective: Drug therapeutic failures (TFs) are included in pharmacovigilance reporting, as some authors consider them a type of adverse drug reaction.
Jair Antonio Ruiz-Garzon +2 more
doaj +1 more source
Siberian Journal of Life Sciences and Agriculture, 2023 Background. The study addresses an extremely important issue, namely quality and safety of meat and milk products that are consumed daily by majority of the population in the Russian Federation. Aim. To investigate safety of animal food products (meat
Irina V. May, Nadezhda V. Nikiforova
doaj +1 more source
npj Digital Medicine, 2021 The Sentinel System is a major component of the United States Food and Drug Administration’s (FDA) approach to active medical product safety surveillance.
Rishi J. Desai +15 more
doaj +1 more source
Microorganisms, 2021 Serotype-specific surveillance for invasive pneumococcal disease (IPD) is essential for assessing the impact of 10- and 13-valent pneumococcal conjugate vaccines (PCV10/13).
Maria Deloria Knoll +72 more
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Communications Medicine, 2022 Schouls et al. characterize antimicrobial resistance genes in MRSA isolates from humans and livestock in the Netherlands. The multidrug resistance gene cfr and the phenicol resistance gene fexA are identified in both types of samples, including in ...
Leo M. Schouls +13 more
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Preventive Medicine Reports, 2022 Monitoring tobacco use has become more complex with the proliferation of novel tobacco products, including heated tobacco products (HTPs). We assessed the latest prevalence and denial of tobacco product use in Japan, a major market for HTPs.
Satomi Odani, Takahiro Tabuchi
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Postmarketing Surveillance for "Modified-Risk" Tobacco Products [PDF]
Nicotine & Tobacco Research, 2011 The U.S. Food and Drug Administration (FDA) acquired authority to regulate tobacco products in 2009. This authority will provide a structured process for manufacturers to introduce products that may have "modified-risk" for morbidity or mortality relative to traditional tobacco products, with postmarketing surveillance and studies a condition of ...
openaire +2 more sources
Production Monitoring and Surveillance
Proceedings, 2014 An ongoing focus area for Saudi Aramco is the optimum field development and depletion of the mobile oil in the tar area, which is limited in extent and occurs mainly along of the periphery of the southeast flank of the field. Unlike many tar mats in other fields, the tar in this field is patchy and has a complex distribution in the reservoir.
openaire +2 more sources
Strengthening surveillance of consumer products in Canada: the vaping example [PDF]
Health Promotion and Chronic Disease Prevention in Canada, 2020 Introduction The overall objective of this study was to demonstrate how information collected by the Consumer Product Safety Program (“the Program”) can be used to identify emerging hazards. Specifically, this study characterized and quantified trends associated with vaping reports received by the Program over the past five years.
Minh T. Do +4 more
openaire +3 more sources
Neuropsychopharmacology ReportsAim This study aimed to verify the real‐world efficacy and safety of quetiapine fumarate extended‐release tablets (Bipresso® 50 mg and 150 mg; marketing authorization holder is KYOWA Pharmaceutical Industry Co., Ltd., Osaka, Japan) in patients with ...
Taro Kishi +3 more
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