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Cardiovascular Event Rate Reduction in Statin Trials

Explore the impact of rosuvastatin on cardiovascular outcomes and lipid levels during a study period. Analyze baseline characteristics and adverse events. Examine cumulative incidence and trial outcomes based on study groups.

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Cardiovascular Event Rate Reduction in Statin Trials

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  1. Baseline Characteristics of the Trial Participants, According to Study Group* - Part I PM Ridker, et al. N Engl J Med 2008;359:2195-207

  2. Baseline Characteristics of the Trial Participants, According to Study Group* - Part II PM Ridker, et al. N Engl J Med 2008;359:2195-207

  3. Lipid and High-Sensitivity C-Reactive Protein Levels during the Follow-up Period, According to Study Group* PM Ridker, et al. N Engl J Med 2008;359:2195-207

  4. Outcomes According to Study Group PM Ridker, et al. N Engl J Med 2008;359:2195-207

  5. Cumulative Incidence of Cardiovascular Events According to Study Group PM Ridker, et al. N Engl J Med 2008;359:2195-207

  6. Effects of Rosuvastatin on the Primary End Point, According to Baseline Characteristics PM Ridker, et al. N Engl J Med 2008;359:2195-207

  7. Monitored Adverse Events, Measured Laboratory Values, and Other Reported Events of Interest during the Follow-up Period* PM Ridker, et al. N Engl J Med 2008;359:2195-207

  8. Trial schematic PM Ridker, et al. N Engl J Med 2008;359:2195-207 - Online Supplemental Appendix

  9. Relationship of the proportional reduction in cardiovascular event rate and mean LDL cholesterol difference between treatment groups in published statin trials PM Ridker, et al. N Engl J Med 2008;359:2195-207 - Online Supplemental Appendix

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