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Still, the FDA stood its ground, giving 503A facilities until February 18 to stop production, and 503Bs until March 19but it wasnt going to enforce any of this while the lawsuit was pending

Generalizations such as one patient out of 10 had developed aspiration should not have been assumed as a 10% risk of aspiration for patients on GLP-1 RAs exists due to the sample size, for example

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In addition, longer-term studies beyond 12 days would be valuable to assess the durability of TMA suppression and microbiota stability