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The combined primary endpoint of death from cardiovascular disease, nonfatal myocardial infarction, or nonfatal stroke occurred in 569 (6.5%) of patients in the semaglutide group versus 701 (8.0%) of patients in the placebo group, yielding a significant hazard ratio of 0.8 for a 20% relative risk reduction

[1] When combined, the cumulative effect on heart rate and blood pressure may be clinically significant, particularly in patients with pre-existing cardiovascular disease, uncontrolled hypertension, or arrhythmias

Disease claims on the label or listing: Any supplement claiming to cure, treat, or prevent a disease is violating FSSAI and ASCI regulations

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Oral BPC 157 is studied almost exclusively for its effects directly on the gastrointestinal tract