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According to FDA-approved labeling, injection site reactions vary by product but are generally mild and transient

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Treatment response should be assessed through improvements in OSA-related outcomes, including symptom burden, sleep quality, and overall clinical status, while also monitoring for adverse effects associated with therapy

Los participantes que tomaron Foundayo, independientemente de la finalizacin del ensayo, perdieron un promedio de 25 libras (11.1%), en comparacin con 5.3 libras (2.1%) con placebo