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But clinical trials use standardized dosing for statistical analysis
Plaintiffs point to pre-approval clinical trials and post-marketing adverse event reports that accumulated evidence of severe gastrointestinal complications years before manufacturers updated warning labels to reflect these serious risks
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Such pharmacies are legally allowed to make versions of GLP-1 RA drugs so long as they remain on the FDAs shortage list a mechanism of pharmaceutical law designed to ensure that patients can get the drugs they need when original manufacturers are overwhelmed by demand
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