Workshops and meetings

Workshops:

  • Golder S.Adverse effects 2: Searching for adverse effects. Webinar Cochrane Learning Live. May 2017
  • Loke YK. Adverse effects 1: How to overcome the challenge of reviewing adverse effects. April 2017
  • Golder S, Köhler M. Adverse effects in systematic reviews: challenges for formulating the question and searching for different studies and sources of information. 24th Cochrane Colloquium, Seoul, South Korea, 23-27October 2016.
  • Golder S. Does searching social media for adverse event data improve patient outcomes? Elsevier Webinar. 27th April 2016.
  • “Serious Adverse Events: Challenges and new ideas” RSS HQ, Errol St, London 23 March 2015. For more information click here. 
  • Golder S. Where to find information on adverse drug effects. ISSG conference. Exeter;UK. July 2014
  • Golder S. Data sources and search strategies for identifying information on adverse drug effects. Health Libraries Group (HLG) conference. Oxford; UK July 2014.
  • Golder S. Where and how to search for adverse effects. MLA Chicago. May 2014
  • Golder S. Data Sources and Search Strategies for Identifying Adverse Effects for Systematic Reviews. Cochrane UK and Ireland Annual Symposium  Manchester; UK 2014.
  • Zorzela L. Golder S. Vohra S. Quality in reporting adverse events and the PRISMA Harms Extension. 21st Cochrane Colloquium, Quebec, Canada, September 2013.
  • Herxheimer A. Summarising evidence for harms in systematic reviews. 21st Cochrane Colloquium, Quebec, Canada, September 2013.
  • Golder S, Zorzela L. Search strategies and data sources for adverse effects reviews. 21st Cochrane Colloquium, Quebec, Canada, September 2013.
  • Loke YK. Webinar: If nothing happens, is everything alright? Assessing validity of adverse effects data. This webinar took place on 27 February 2013, but you can access it here. Systematic reviews of adverse effects are often hampered by findings of sparse data, or zero events. Results are frequently interpreted based on statements such as “no significant harm was found” or “the intervention was safe and well-tolerated.”
  • Reeves B, Shea B, Wells G, Loke Y. Methods for including non-randomised studies to answer questions about unintended harms of drugs Cochrane Colloquium, Auckland, New Zealand, October 2012.
  • Schmucker C, Loke Y. Incorporating data on adverse effects into systematic reviews Cochrane Colloquium, Auckland, New Zealand, October 2012.
  • Beyer F. Search strategies and data sources for adverse effects reviews.  17th Annual Meeting of UK and Ireland Contributors to The Cochrane Collaboration,  Loughborough, UK, 20th March 2012.  
  • Golder S, Schmucker C, Adams D, Herxheimer A. Selecting and interpreting data from relevant studies of adverse effects. 19th Cochrane Colloquium, Madrid, Spain, 21 October 2011
  • Golder S, Beyer F, Herxheimer A, Schmucker C. Search strategies and data sources for adverse effects reviews. 19th Cochrane Colloquium, Madrid, Spain, 21 October 2011
  • Derry S, Loke Y. Developing a protocol for evaluating adverse effects in systematic reviews. 17th Cochrane Colloquium, Singapore, Workshop 60, 14 October 2009
  • Gartlehner G, Herxheimer A. Systematic reviews, including a module on adverse effects (in German and English), Danube University, Krems, Austria. March - June 2009
  • Derry S, Loke Y. Adverse Effects Workshop. 14th Annual Meeting of UK & Ireland Contributors to the Cochrane Collaboration, Edinburgh Heriot Watt University, 19 March 2009
  • Herxheimer A, Golder S. Searching for, retrieving and incorporating adverse effects data. 16th Cochrane Colloquium, Freiburg, Germany, 7 October 2008
  • Herxheimer A, Golder S. Adverse effects workshop for Centre and Cochrane Review Group staff. Annual Continental European Cochrane Entities Meeting (CECEM). Milan, Italy, 8 May 2008
  • Loke Y, Golder S. Retrieving data for systematic reviews incorporating adverse effects. 13th Annual Meeting of UK and Irish Contributors to The Cochrane Collaboration. York, UK, 11 March 2008
  • Adverse events: what is important from a consumer perspective? 15th Cochrane Colloquium, Sao Paulo, Brazil, 26 October 2007
  • Identifying and incorporating adverse effects in systematic reviews, 14th Cochrane Colloquium, Dublin, 24 October 2006
  • Incorporating data on adverse effects in systematic reviews, 13th Cochrane Colloquium, Melbourne, October 2005
  • Incorporating data on adverse effects in systematic reviews, 12th Cochrane Colloquium, Ottawa, October 2004
  • Adverse Effects Workshop, UK Cochrane Contributors Meeting, Manchester, March 2004
  • Adverse Effects Workshop, 11th Cochrane Colloquium, Barcelona, October 2003
  • Adverse Effects Workshop, UK Cochrane Contributors Meeting, Warwick, March 2003
  • Adverse Effects Workshop, 9th Cochrane Colloquium, Lyon, October 2001

Meetings: