Because retatrutide remains an investigational medicinal product, any changes to dosing or treatment must be agreed with the trial investigator and undertaken in accordance with the clinical trial protocol
Canagliflozin should be discontinued if significant foot complications develop
How to Report Side Effects Healthcare professionals, patients and caregivers are encouraged to report any suspected adverse reactions to semaglutide, including NAION, via the MHRA Yellow Card scheme: Online at MHRA Yellow Card Reporting, if you are in the United Kingdom Online at FDA MedWatch if you are in the United States Via the Yellow Card app, available on the Apple App Store and Google Play Store Via the NowPatient app When reporting, provide as much information as possible, including medical history, any other medications being taken, when symptoms started and treatment dates
BNST, 160,161 which is associated with suppression of food intake and stress response
Therefore, people with a personal or family history of this type of cancer should not take it