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For the participant that actually experienced the adverse event, it depends on several things: is the treatment blinded? If so, the study doctor can unblind if that information is necessary to the patient care. If an adverse event happens in a 1:1 study medication: placebo trial, the study doctor will usually assume the participant is on study medication rather than unblinding. Feel free to ask more questions. It's just not the easiest thing to eloquently answer in full detail on the phone!
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