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Description
Safety Profile and Side Effects Reported in the Trial The most common adverse effects were gastrointestinal particularly nausea, vomiting, and diarrhoea occurring most frequently during dose escalation and generally mild to moderate in severity
Most side effects are temporary, lasting 1 to 3 weeks at each new dose level
32 The primary outcome for the trial was the first occurrence of a major adverse cardiovascular event (death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke)
Each has slightly different absorption rates
But true success goes beyond the number on the scale
