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ADVERSE EFFECTS In the cagrilintide, single-agent study between 2% and 6% (26%) of participants in the cagrilintide groups discontinued treatment prematurely because of adverse events, compared with 7% (7%) of participants in the liraglutide 3.0 mg group and 3% (3%) in the pooled placebo group
The low-dose daily approach starts at 200 mcg per day and steps up to about 1 mg per day
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Research usually starts at the lower end for both, and doses are increased gradually as the models response and tolerance are observed
Fortified diets and low-dose oral supplements are frequently sufficient
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