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for example, P5 only took liraglutide for 1 month due to logistical issues, whilst P4 stopped just prior to the follow-up appointment due to perceived lack of efficacy

All subjects provided written informed consent prior to any trial-related activities

Third, the FDA has identified serious safety issues with some compounded products, including dosing errors that resulted in hospitalizations

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Administration Subcutaneous injection in the abdomen or upper thigh