: A 13-year-old, spayed, female Chihuahua dog was referred for evaluation of fever, lethargy, and dyspnea. Hematologic evaluation revealed severe neutropenia, thrombocytopenia, and mild anemia. The dog had been undergoing phenobarbital therapy for the past 7 weeks because of generalized seizures due to meningoencephalomyelitis of unknown etiology. After ruling out other possible causes of cytopenias, a tentative diagnosis was made of drug-induced blood cell dyscrasia. The neutropenia and thrombocytopenia resolved after discontinuation of phenobarbital (8 days and 15 days after discontinuation, respectively). This is the first case report in Korea to demonstrate blood dyscrasia associated with idiosyncratic adverse effects of phenobarbital.Keywords : leukopenia, neutropenia, phenobarbital, thrombocytopenia Phenobarbital (PB) is a long-acting barbiturate that enhances γ-aminobutyric acid-mediated increases in chloride conductance by opening chloride channels [11,12]. PB is a well-tolerated and effective anticonvulsant for various seizures and certain types of clinical epilepsy in dogs and cats [9,11,12].PB has infrequent complications including hyperactivity, restlessness, excessive sedation, ataxia, polyuria, polydipsia, and polyphagia; these typically occur during the initial phase of therapy [9,10]. In most dogs, these side effects usually are tolerated after 2 to 4 weeks of therapy [10]. No actual hepatocellular damage during PB treatment has been confirmed; however, PB administration can contribute to the induction of serum liver enzyme activities in dogs [2,8]. In addition, PB has infrequently been associated with hematologic adverse drug events (ADEs) in dogs, including reversible neutropenia, thrombocytopenia, and anemia [5,6]. Long term use of PB can also lead to bone marrow necrosis [13].This case report describes the clinical and laboratory features of PB-related cytopenia and treatment outcomes. To the best of authors' knowledge, this is the first case report demonstrating blood dyscrasia associated with idiosyncratic ADE of PB in our country (South Korea).A 13-year-old, spayed female Chihuahua dog, weighing 2.8 kg, was referred to Konkuk University Veterinary Teaching Hospital for evaluation of fever, lethargy, and anorexia. About 9 months previously, the dog had been admitted for evaluation of generalized seizure and diagnosed with meningoencephalomyelitis of unknown etiology (MUE), based on magnetic resonance imaging findings (Fig. 1), and cerebrospinal fluid (CSF) analysis showing mononuclear pleocytosis (208 cells/µL; reference range: 0-5 cells/µL). Further test results including a polymerase chain reaction test for canine distemper virus and CSF culture were negative. Despite the diagnosis of MUE in this dog, the owner was unable to administer any medication due to personal circumstances. Since that visit, the frequency of seizures had increased, so PB (2.5 mg/kg, per orally [po], quarter [q] 12 h, Hana Pharm, Korea) had been prescribed by the referring veterinarian approximately 7 weeks...