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Hi Jon and all Could you get this from automating meta data on numbers needed to harm. Would it be available from regulatory data as safety would need to be established in all stages and also in after market research. There is the patient experience barometer which pharma also looks at which might be added as extra information. See how it is done within this sight http://treato.com/ Best Amy From: Jon Brassey <[log in to unmask]> Reply-To: Jon Brassey <[log in to unmask]> Date: Sunday, January 19, 2014 11:49 AM To: <[log in to unmask]> Subject: Adverse events Hi All, This is a real long-shot but does anyone know of a resource that quantifies the number and seriousness of a given drug's adverse event profile? In other words if you are choosing between two drugs with a similar efficacy and similar price you might want to compare adverse events. One intervention might have a few minor adverse events while the other intervention might have a few minor adverse events plus 1-2 major adverse events associated with it. So, one might be classed as low risk while the other moderate risk or even high risk. Any ideas? BW jon -- Jon Brassey Trip Database http://www.tripdatabase.com Find evidence fast