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Methods Study cohort (SURMOUNT-1 clinical trial) Ethical approval and study populations The study was conducted in accordance with the principles of the Declaration of Helsinki, Good Clinical Practice guidelines and all applicable regulatory requirements Study protocol and informed consent documents were approved by independent ethics committees and institutional review boards at all participating trial sites

This injection is for use in adults who have obesity (BMI of 30 kg/m2 or more) or who are overweight (BMI between 27 and 30 kg/m2) and have weight-related health problems like diabetes or high blood pressure

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Ongoing collaboration with healthcare providers ensures a proactive and supportive approach to managing potential side effects while working towards achieving the desired weight loss outcomes

In this video interview, Stephen J

Initial side effects like nausea or gastrointestinal symptoms may occur