The lack of FDA pre-market approval means potential risks may not be identified until after widespread consumer use
L.IulianoR.Le PeraI.Sama' I.MonacoC.CammarotaS.et al (2002)
Real-world data and patient feedback are collected to identify adverse effects or new indications, guiding future improvements or expanded use cases
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For them, Ozempic may actually make them more likely to conceive and the risk-benefit trade-off may be different from the general population, Shah said
Its effective and safe role is strictly governed by FDA guidelines and requires close medical supervision