A 79-year-old woman developed hemichorea-hemiballismus following long-term overdose and misuse of caffeine/ chlorphenamine/methylephedrine hydrochloride/paracetamol.The woman, who had a history of hypertension, presented to the emergency department with an acute right-sided involuntary movements of 2 days. The involuntary movements continued throughout the day, but stopped while asleep. She could partially control them by her will, but could not be relieved by specific posture or touch. No limb numbness, fever, weakness, urinary and fecal incontinence or altered consciousness were observed. She had no preceding trauma or similar episode prior. Further, she was interviewed, during which she reported of chronic overdose (30mL) of over-the-counter cold syrup comprising of caffeine/ chlorphenamine/methylephedrine hydrochloride/paracetamol 1.8mg/0.124mg/0.486mg/14.94mg [acetaminophen, DLmethylephedrine hydrochloride, chlorpheniramine maleate and caffeine anhydrous] per mL of cough syrup due to long-term dizziness and that she had been taking an even higher dose during the previous week (recommended dose of the cold syrup: 12 mL/day). Neurological examination showed random, rapid, non-patterned, high-amplitude, flinging, flailing and violent involuntary movements of the right limbs, which was indicative of hemichorea-hemiballismus (HCHB). Rest of the physical and neurological examination was unremarkable. Laboratory tests (serum electrolyte level, urinalysis, complete blood count, liver function test, creatinine level, bilirubin level, blood glucose level, thyroid function and serum tests for heavy metal level), serum tests (for autoimmune disease, serum tumor marker levels) and cerebrospinal fluid examination were normal. MRI and CT scan of the brain were normal. Electroencephalography showed diffuse cortical dysfunction. Eleven days after the onset of involuntary movements, Tc-99methyl cysteinate dimer brain perfusion study (single-photon emission computed tomography [SPECT]) was performed showed relative hyperperfusion in the left basal ganglia. A diagnosis of cold syrup-induced HCHB was made based on the strong temporal relation and exclusion of any other cause of involuntary movements.The woman's cold syrup was discontinued, and she was treated with quetiapine. Her HCHB lasted for 2 weeks. Eight days after the initiation of quetiapine, her HCHB resolved. One month later, quetiapine was stopped. During 1 year follow-up, her HCHB did not reoccur [time to reaction onset not stated].