Results 311 to 320 of about 143,193 (344)
Some of the next articles are maybe not open access.
Under-reporting of adverse drug reactions
European Journal of Clinical Pharmacology, 1998Spontaneous reporting is the most common method used in pharmacovigilance and the best one to generate signals on new or rare adverse drug reactions (ADRs). Under-reporting is a major drawback of this system. The objective of this study was to quantify the extent of under-reporting in general practice and to assess the factors which influence it ...
Y. Moride +5 more
openaire +2 more sources
Multiple sclerosis as an adverse drug reaction: clues from the FDA Adverse Event Reporting System
Expert Opinion on Drug Safety, 2018Possible relationship between drug exposure and multiple sclerosis (MS) development is insufficiently investigated, and further challenged by the incomplete understanding of MS etiopathogenesis. The study aims to investigate whether drug exposure could contribute to MS, by analyzing worldwide spontaneous reporting archives of adverse drug reaction ...
Antonazzo, Ippazio Cosimo +7 more
openaire +5 more sources
Annals of Pharmacotherapy, 2008
Background: Adverse drug reaction (ADR) spontaneous reporting is the primary method of postmarketing drug surveillance: although it is an important part of postmarketing drug surveillance, it is underused. Before 2004, almost no ADRs were reported in our 400-bed hospital.
Aránzazu Aguinagalde +5 more
openaire +3 more sources
Background: Adverse drug reaction (ADR) spontaneous reporting is the primary method of postmarketing drug surveillance: although it is an important part of postmarketing drug surveillance, it is underused. Before 2004, almost no ADRs were reported in our 400-bed hospital.
Aránzazu Aguinagalde +5 more
openaire +3 more sources
Discovery of New Adverse Drug Reactions
JAMA, 1984Recently, several studies of spontaneous reporting systems (SRSs) have reported on the published literature's role in producing first reports of new adverse drug reactions. In order to provide further information on other components of SRS, the Food and Drug Administration's SRS was examined with regard to its effectiveness and efficiency in ...
Deanne E. Knapp, Allen C. Rossi
openaire +3 more sources
Journal of Clinical Epidemiology, 2002
The spontaneous reporting system (srs) is the most important early warning system of adverse drug reactions. As there is serious under-reporting we studied the respective knowledge and attitudes of two samples of physicians in Germany. Five hundred randomly sampled physicians and 815 physicians who had actually reported an ADR were included; the ...
K.-H Munter +3 more
openaire +2 more sources
The spontaneous reporting system (srs) is the most important early warning system of adverse drug reactions. As there is serious under-reporting we studied the respective knowledge and attitudes of two samples of physicians in Germany. Five hundred randomly sampled physicians and 815 physicians who had actually reported an ADR were included; the ...
K.-H Munter +3 more
openaire +2 more sources
Adverse drug reactions: Analysis of spontaneous reporting system in Europe in 2007–2009
European Journal of Clinical Pharmacology, 2012Spontaneous reporting systems in European countries are crucial for collecting adverse drug reaction (ADR) reports. The aim of this study was to evaluate reporting activity among countries and their strategy to increase the number of reports. We also established the best measure for assessment quantity of reports.This was a retrospective observational ...
Jiri Vlcek +2 more
openaire +3 more sources
Seminars in Thrombosis and Hemostasis, 2005
According to their code of professional conduct, German physicians are obliged to report suspected cases of adverse drug reactions (ADRs) to the Drug Commission of the German Medical Association (AkdA). On the basis of an agreement between the German Medical Association and the Federal Institute for Drugs and Medical Devices (BfArM) a common ...
Bruno Müller-Oerlinghausen +3 more
openaire +2 more sources
According to their code of professional conduct, German physicians are obliged to report suspected cases of adverse drug reactions (ADRs) to the Drug Commission of the German Medical Association (AkdA). On the basis of an agreement between the German Medical Association and the Federal Institute for Drugs and Medical Devices (BfArM) a common ...
Bruno Müller-Oerlinghausen +3 more
openaire +2 more sources
Systemic Barriers and Potential Concerns from Reporting Serious Adverse Drug Reactions
2022About 1-10% of all serious adverse drug reactions (sADRs) are reported to the Food and Drug Administration (FDA) ( Moore T, Bennett C. Underreporting of Hemorrhagic and Thrombotic Complications of Pharmaceuticals to the U.S. Food and Drug Administration: Empirical Findings for Warfarin, Clopidogrel, Ticlopidine, and Thalidomide from the Southern ...
Matthew A, Taylor +3 more
openaire +2 more sources
2019
Antibiotics are associated with adverse drug reactions (ADR), such as Clostridium difficile infection (CDI), Torsade de pointes/QT prolongation (TdP/QTP), acute kidney injury (AKI), hypoglycemia, and rhabdomyolysis. ADRs lead to significant morbidity and mortality, as well as high health care costs.
Teng, Chengwen, 0000-0001-9239-2125
openaire +3 more sources
Antibiotics are associated with adverse drug reactions (ADR), such as Clostridium difficile infection (CDI), Torsade de pointes/QT prolongation (TdP/QTP), acute kidney injury (AKI), hypoglycemia, and rhabdomyolysis. ADRs lead to significant morbidity and mortality, as well as high health care costs.
Teng, Chengwen, 0000-0001-9239-2125
openaire +3 more sources
An adverse-drug-reaction-reporting system at a teaching hospital in India
American Journal of Health-System Pharmacy, 2003Nidhin Mohan +2 more
openaire +3 more sources