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Staying informed, maintaining open communication with your healthcare and trial team, and understanding the difference between established evidence and theoretical risk are the most important steps any patient can take

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Patients are getting what purport to be these substances, or are using drugs that are made with research-grade active ingredients, and I almost expect any day now theres going to be some serious patient adverse event or a series of patients who are made ill or worse by taking batches of these drugs that were not made to FDA standards or with active ingredients that are not made to FDA standards, Brunner said

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This is why many people who take traditional tablets feel like they aren't seeing the results they expected