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Drug Safety|August 19, 2007
A modified prescription-event monitoring study to assess the introduction of Seretide Evohaler in England: an example of studying risk monitoring in pharmacovigilanceMichael J Perrio, Lynda V Wilton, Saad A W ShakirDrug Safety|April 7, 2012
Impact of safety-related regulatory action on clinical practice: a systematic reviewSigrid Piening, Flora M Haaijer-Ruskamp, Jonie T N de Vries, et al.Drug Safety|December 14, 2011
Cardiovascular events in patients taking varenicline: a case series from intensive postmarketing surveillance in New ZealandMira Harrison-Woolrych, Simran Maggo, Ming Tan, et al.Drug Safety|December 14, 2011
Experiences with adverse drug reaction reporting by patients: an 11-country surveyFlorence van Hunsel, Linda Härmark, Shanthi Pal, et al.Drug Safety|November 15, 2011
Pharmacogenetic risk for adverse reactions to irinotecan in the major ethnic populations of Singapore: regulatory evaluation by the health sciences authorityCynthia Sung, Pui Ling Lee, Liesbet L Tan, et al.Drug Safety|November 15, 2011
Comparing adverse event rates of oral blood glucose-lowering drugs reported by patients and healthcare providers: a post-hoc analysis of observational studies published between 1999 and 2011Liana Hakobyan, Flora M Haaijer-Ruskamp, Dick de Zeeuw, et al.Drug Safety|February 21, 2012
Risk minimization activities of centrally authorized products in the EU: a descriptive studyInge M Zomerdijk, Fakhredin A Sayed-Tabatabaei, Gianluca Trifirò, et al.Drug Safety|February 21, 2012
Embedding 'speaking up' into systems for safe healthcare product development and marketing surveillanceBrian Edwards, Bruce Hugman, Mary Tobin, et al.Drug Safety|December 17, 2011
Risk evaluation and mitigation strategies (REMS): educating the prescriberSusan C Nicholson, Janet Peterson, Behin YektashenasDrug Safety|June 14, 2011
Association between leukotriene-modifying agents and suicide: what is the evidence?Glen T Schumock, Todd A Lee, Min J Joo, et al.Pageof 309