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Description
Activating both at full dose simultaneously, with no titration runway, is what community sources describe as the failure mode that drives discontinuation
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These potential risks include contamination of the vials, inadequate sterility protocols, pain or irritation at the injection site, allergic reactions, or even possible drug interactions
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Optimising treatment should be a more acceptable means of rationing
Data from treatment-adherent participants was collected and included in the analyses for the trial product product estimand [1]
