Analysis and reporting of adverse events in randomised controlled trials: a review

por Phillips, Rachel, Hazell, Lorna, Sauzet, Odile, Cornelius, Victoria
Publicado 2019

The UK BIO-TRAC Study: A Cross-Sectional Study of Product and Batch Traceability for Biologics in Clinical Practice and Electronic Adverse Drug Reaction Reporting in the UK

por Klein, Kevin, Hazell, Lorna, Stolk, Pieter, Shakir, Saad
Publicado 2019

The risk of heart failure associated with the use of noninsulin blood glucose-lowering drugs: systematic review and meta-analysis of published observational studies

por Varas-Lorenzo, Cristina, Margulis, Andrea V, Pladevall, Manel, Riera-Guardia, Nuria, Calingaert, Brian, Hazell, Lorna, Romio, Silvana, Perez-Gutthann, Susana
Publicado 2014

Quality assessment of observational studies in a drug-safety systematic review, comparison of two tools: the Newcastle–Ottawa Scale and the RTI item bank

por Margulis, Andrea V, Pladevall, Manel, Riera-Guardia, Nuria, Varas-Lorenzo, Cristina, Hazell, Lorna, Berkman, Nancy D, Viswanathan, Meera, Perez-Gutthann, Susana
Publicado 2014

The Contribution of National Spontaneous Reporting Systems to Detect Signals of Torsadogenicity: Issues Emerging from the ARITMO Project

por Raschi, Emanuel, Poluzzi, Elisabetta, Salvo, Francesco, Koci, Ariola, Suling, Marc, Antoniazzi, Stefania, Perina, Luisella, Hazell, Lorna, Moretti, Ugo, Sturkenboom, Miriam, Garbe, Edeltraut, Pariente, Antoine, De Ponti, Fabrizio
Publicado 2015