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Este contenido se tradujo de la edicin en ingls de Medscape .
The dosing protocol involves a gradual titration over several months, starting low to minimize gastrointestinal side effects and increasing to the target maintenance dose
Fatigue is listed as a common adverse effect in FDA prescribing information for several GLP-1 receptor agonists
including a prior authorization protocol that requires chart documentation of a type 2 diabetes diagnosis based on a recent A1C (measurement of average blood sugar levels) equal to or greater than 6.5%
Instead, analysts evaluate incremental cost-effectiveness ratios (ICERs), typically expressed as cost per quality-adjusted life year (QALY) gained
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