Myelodysplastic syndromes (MDS): 1 mg/kg once every 3 weeks
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%)
We recommend implementing the following best practices in your laboratory: Aseptic Workspace: Always perform your liquid transfers inside a certified laminar flow hood or a thoroughly sanitized, draft-free workspace
This literature is not intended to diagnose, treat, prevent or cure any disease