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The dose schedule outlines the standard four-week intervals used in clinical trials
A company spokesman for Hims confirmed that it believes (incorrectly) that it is exempt from including long read-outs of risks and side effects typically shown in pharma TV commercials and therefore made no effort to comply with FDA guidelines
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Limited data from unintentional exposures to GLP1-RAs in early pregnancy (at least 500 pregnancies) suggest no increased risk of birth defects compared to pregnancies in women with similar conditions
L.MalmgrenS.JingX.et al (2012)
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