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OK, so first things first: you definitely know more than you think

Peter Attia Physician & Longevity Specialist Three hundred million podcast downloads and a medical training path that ran through Johns Hopkins and the NIH

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2024;18:e12039

Adverse events (AEs) were recorded from the time of the participant signing informed consent through to the end of follow-up and were regarded as treatment-emergent adverse events (TEAEs) if beginning (or increasing in severity) after the first study dose and no later than the end of follow-up

Its not just about the medication or the numbers on the scale