In 2022, the FDA approved dupilumab for treatment of eosinophilic esophagitis (EoE). The aims of this study were to report physician and patient perspectives on initiating dupilumab. A 2-pronged approach was used: 1) data on physician prescribing practices was gathered via a retrospective chart review of EoE patients prescribed dupilumab, and 2) pediatric patients on dupilumab were also approached regarding completion of questionnaires regarding reasons for initiation. During this time, 42 patients were prescribed dupilumab. From the physician’s perspective, the primary reasons for dupilumab included non-response to topical corticosteroids (TCS) (52%), non-adherence (28%), adverse effects (10%), or to treat multiple atopic diseases (5%). The median dupilumab initiation time, from day prescribed to first injection, was 37 days (IQR 37). Almost all required prior authorization (98%), while 17% required letter of appeal and 2% required peer-to-peer. Fifteen patients (36%) completed the questionnaire portion of the survey. From the patient’s perspective, the primary reasons for dupilumab initiation included non-response to TCS (27%), non-adherence to TCS (27%), concern about adverse effects of TCS (7%), and treatment of multiple atopic diseases (33%). In conclusion, physicians are prescribing dupilumab primarily for non-response to TCS and almost all required prior authorization with a long delay to starting dupilumab.