ObjectiveEating‐induced seizures (EIS) are a rare form of reflex seizures. The objective of this study was to report a series of cases of EIS involving patients admitted to our epilepsy unit, and to analyze the clinical characteristics, etiology, and treatment response of this type of infrequent seizure.MethodsWe performed a single‐center retrospective analysis of all consecutive patients diagnosed with epilepsy with eating‐induced seizures between 2008 and 2020.ResultsWe included eight patients (six women) with mean age 54.75 years (range: 40–79), and mean age at epilepsy onset 30.75 years (range: 9–58 years). EIS were triggered during a meal in 5/8 (at dinner 1/8, at breakfast in 1/8, and without time preference in 3/8), by a certain flavor in 1/8, by eating different textures or drinking soft drinks in 1/8, and by slicing food in 1/8. All patients suffered nonreflex seizures and 3/8 other types of reflex seizures. In 6/8 of patients, EIS originated in the right hemisphere. In 5/8, the EIS progressed to impaired awareness with oromandibular automatisms. In 6/8, the epilepsy was drug‐resistant. Temporopolar encephalocele was the most frequent etiology, in 4/8. Three of the eight underwent surgical treatment, with Engel IA 1 year in 3/3. Three of the eight were treated with vagal stimulation therapy, with McHugh A 1 year in 2/3.SignificanceIn our series, eating‐induced seizures were observed in patients with focal epilepsy. It was frequently drug‐resistant and started predominantly in the right hemisphere, due to temporal pole involvement in half of the patients.