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Expanded Regulatory Approvals for CVD Risk Reduction The FDA cleared Wegovys cardiovascular label in March 2024, following the publication of the SELECT trial results, which showed a 20% relative risk reduction in major adverse cardiovascular events
Negative reviewers describe persistent inconsistency or complete lack of effect
Injection site reactions , such as redness, itching, or bruising, can occur but are usually mild and resolve spontaneously
Cite: Coleman, Y
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