[PDF] from populationmedicine.orgM Kulldorff, RL Davis, M Kolczak, E Lewis… - Sequential …, 2011 - Taylor & Francis Because of rare but serious adverse events, pharmaceutical drugs and vaccines are sometimes withdrawn from the market, either by a government agency such as the Food and Drug Administration (FDA) in the United States or by the manufacturing pharmaceutical company. In other ... Cited by 23 - Related articles - All 13 versions
MK Rommers, IM Teepe-Twiss… - Drug Safety, 2011 - ingentaconnect.com Background Adverse drug events (ADEs) are an important problem in hospital practice. Computerized physician order entry (CPOE) and clinical decision support systems (CDSS) are useful tools in the prevention of ADEs. In the Netherlands there are some basic CDSS within CPOE ... Related articles - All 3 versions
S Weiss-Smith, G Deshpande, S Chung… - Archives of internal …, 2011 - Am Med Assoc The Adverse Event Reporting System (AERS) of the US Food and Drug Association (FDA) is the largest repository of passively reported adverse drug events in the world. 1 Approximately one-half million reports are received by the FDA annually. Designed as a safety net, ... Related articles - All 3 versions
AJ Buckton, D Prabhu, C Motamed… - HIV …, 2011 - Wiley Online Library Objectives The aim of the study was to estimate the levels of transmitted drug resistance (TDR) in HIV-1 using very sensitive assays to detect minority drug-resistant populations. Methods We tested unlinked anonymous serum specimens from sexual health clinic attendees, ... Cited by 1 - Related articles - All 3 versions
[PDF] from accelr8.comIS Douglas, C Price, K Overdier… - American Journal of …, 2011 - accelr8.com ... of 2 mini-BAL per patient (~8 unique isolates) Rapid Microbiological Identification and Major Drug Resistance Phenotyping with Novel Multiplexed Automated Digital Microscopy (MADM) for Ventilator-associated Pneumonia (VAP) Surveillance... View as HTML - All 4 versions
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