In case of adverse drug reaction study, there is no control group and only the patients use the drug. After using the drug, some patients show some adverse drug reactions and others do not show these. We have now he genotyping data, patient subgroups depending on the different adverse drug reactions and odds ratio. Due to the division of the patients in different subgroups, the number of patients in each group is not very large. Now how can I prove that my sample size meets the 80% statistical power? Is there any special method of power calculation for the Pharmacogenomics adverse drug reaction?

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