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Adverse Reactions Associated with Discontinuation of Treatment in ADHD Clinical Trials In the controlled trial in pediatric patients ages 6 to 12 years (Study 1), 8% (18/218) of VYVANSE-treated patients discontinued due to adverse reactions compared to 0% (0/72) of placebo-treated patients

Personalized risk stratification would be made possible by the identification of clinical or genetic elements causing GLP-1RA-associated vestibular diseases

Additionally, preclinical animal models provide mechanistic insights but may not fully translate to human physiology, particularly in conditions such as osteoporosis, obesity-related bone changes, and joint infections

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(20) Baseline measurements of total, pelvic, and arm-leg BMC, CTX-1 and Procollagen Type I N-terminal propeptide (P1NP) were obtained before participants were assigned to the study or control group

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