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It estimates the population level treatment effect of semaglutide regardless of treatment adherence and/or other anti-obesity therapies and does not exclude data collected after discontinuation of treatment (e.g., due to tolerability issues) or after initiation of alternative treatment (e.g., due to lack of efficacy)

Starting with the lowest effective doses of both compounds and gradually titrating upward allows for better symptom monitoring and safety assessment

The safety margin between therapeutic and potentially harmful doses appears substantial

Your provider can advise you on next steps, refer you for appropriate prenatal care if needed, and document the exposure for monitoring purposes