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Order atorvastatin. For the primary endpoint, cardiovascular outcomes were assessed from the first to last cardiovascular event in the cohort, starting from date of enrolment until 12 weeks after the first cardiovascular event. Secondary endpoints were on a calendar basis (e.g. hospitalization, stroke, or death), and tertiary endpoints were on a calendar-year basis. Secondary and tertiary endpoints Secondary endpoints were cardiovascular (e.g. hospitalization, stroke, or death) and cancer (e.g. any cancer). Primary endpoints were cardiovascular complications such as coronary artery bypass graft, heart attack or angina, major coronary artery disease, carotid or peripheral vascular disease. We did not assess outcomes due to missing data at the time of study inclusion or because the participants may not have been free from cardiovascular events at the time we entered them in the database. In secondary and tertiary endpoints, we did not assign an adjusted mean for each end point, because the risk estimate (e.g. adjusted hazard ratio [HR] or incidence rate [IRR]) was likely to be close zero and the HRs would not have been clinically meaningful. Instead, we calculated the HR and corresponding 95% CI. Statistical analysis We used Generic drugs canada pharmacy Poisson regression to estimate the relative risks (RR) and 95% CIs for the associations of atorvastatin use and all-cause mortality, CVD, cancer. For primary endpoints, we estimated incidence ratio and 95% CI when the data were available for up to 3 cohorts (i.e.: baseline cohort, follow-up and 12-week cohort) per participant. If the incidence rates were available for 2 or more cohorts, we pooled the data from both cohorts. If the incidence rates were reported for a third cohort, we combined the cohorts. We used Poisson regression to estimate relative risk (RR) for cardiovascular outcomes, including coronary artery generic pharmacy online net bypass graft (CABG), myocardial infarction, coronary heart disease (CHD), stroke, and coronary death. When the numbers of CHD in both cohorts were similar, we pooled the CHD data from both cohorts in the same analysis, unless specific data were available on CABG from the baseline to follow-up cohort. If the number of CABG was similar in the two cohorts, we pooled data from both cohorts only baseline cohort to follow-up cohort. We also used Poisson regression atorvastatin generic online to estimate the RR for cancer endpoints. Analyses were stratified by body mass index (BMI; in kg/m2) at baseline and time of follow-up, we used multiple imputation to avoid over- or underestimation of cancer risk. In secondary and tertiary endpoints, we computed the HR and corresponding 95% CIs for outcomes with missing data. those end points that had both data available for the baseline cohort and follow-up cohorts and/or the mail order atorvastatin first and last 12-week follow-up cohorts, the HR was adjusted for baseline values before the start of follow-up period. All numbers presented were absolute odds ratios or 95% CIs (0% to 5%, 5% 10%, 10% 20%, and > 20%). We excluded events in the follow-up period of first and last 12-week follow-up cohorts, when the cohort would not have enough data for us to examine.
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