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About 6% of participants taking Zepbound left the trial because of adverse events, compared with 8% of those taking semaglutide

Across the published literature, gastrointestinal models repeatedly demonstrated protective effects involving: gastric ulcers intestinal permeability disruption inflammatory bowel injury alcohol-induced gastric damage NSAID-related tissue injury ischemic injury environments compromised vascular supply within the digestive tissues Several research papers also indicate that BPC-157 appears unusually stable within gastric environments compared to many other peptide compounds

Reference List Clinical GI side effect background

Journal of Dermatological Treatment , 23(2), 97-102