The following adverse effects were reported in patients receiving semaglutide injection or oral tablets across all clinical trials and at incidences higher than with placebo: nausea (11% to 44%), vomiting (5% to 24%), diarrhea (8.5% to 30%), abdominal pain (5.7% to 20%), abdominal distention (2% to 7%), constipation (3.1% to 24%), dyspepsia (0.6% to 9%), decreased appetite (6% to 9%), eructation (0.6% to 7%), flatulence (0.4% to 6%), gastroesophageal reflux disease (1.5% to 5%), gastroenteritis (4% to 6%), and gastritis (0.4% to 4%)
Use aseptic technique during preparation and reconstitution (if applicable)
Weeks 4-8 Full benefits typically manifest by week 4-6 of consistent use
Once absorbed, it binds to plasma proteins before it is transported around the body
While not FDA-approved for longevity enhancement, its used in supervised medical protocols for healthspan optimization and biological age management