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The most common adverse effects from the SURMOUNT trials include: Nausea: 24-33% of participants (dose-dependent) Diarrhea: 18-25% of participants Constipation: 13-17% of participants Vomiting: 8-12% of participants Decreased appetite: 10-15% of participants Most of these effects are mild to moderate and occur primarily during dose escalation periods

"Folic acid and vitamin B12 supplementation during pregnancy in a population subsisting on a suboptimal diet"

PMID: 25037177

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The current standard surveillance program includes multiple random biopsies obtained throughout the colon at regularly scheduled intervals

[28] Interactions [edit] See also [edit] References [edit] 1 2 3 GRCh38: Ensembl release 89: ENSG00000184481 Ensembl, May 2017 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000042903 Ensembl, May 2017 "Human PubMed Reference:"