The data collected from the study will be used to predict adverse drug events and to provide physicians with information to compare the safety and effectiveness of various prescription medications. The patient consent form contains enough information for individuals to make an informed, voluntary decision when they decide to allow clinicians to access their information. All participants have the right to withdraw from the study at any time by contacting the research team. As soon as they withdraw from the project, all transfer of that person's information is stopped and there is no penalty for ending participation. The normal services and standard of care will continue to be available to both consenting and non-consenting patients.