The burden of schizophrenia remains high, with one in 100 people affected globally over a lifetime. 1 Symptoms are disabling, with auditory hallucinations, delusions, lack of motivation, cognitive impairment, and functional deficits. Despite advances in our understanding of the biological underpinnings of the illness, cure remains elusive. Antipsychotic medications are the mainstay of pharmacological treatment, but selecting the optimal medication for the individual patient is a delicate balance between efficacy and physical side-effects.People with schizophrenia die up to 18 years earlier than the general population, largely due to avertable cardiometabolic diseases, 2 with a standardised mortality ratio of more than 3. 3 The risks are multifactorial, and include a genetic predisposition for abnormal glucose, poor diet, sedentary behaviour, and, notably, metabolic adverse reactions to antipsychotic medications. 4 In The Lancet, Maximilian Huhn and colleagues 5 report a network meta-analysis of antipsychotic medications for the acute management of schizophrenia that includes 402 studies of 32 different antipsychotics with data for 53 463 participants (mean age 37·40 years [SD 5·96], 29 949 [56·02%] male and 23 514 [43·98%] female, mean illness duration 11·90 years [SD 5·19]). This is the largest and most comprehensive meta-analysis of antipsychotic medication for acute psychosis to date. The use of a network meta-analysis allows comparisons between agents that might not have been directly compared in clinical trials. Other strengths include consideration of the placebo response rate, study sample size, publication year, baseline severity, sponsorship, comparability of doses, and patient demographics, using both meta-regression and sensitivity analyses of excluding poorer-quality studies. None of these factors greatly altered outcomes.Many of the results are unsurprising. Clozapine remains the most effective antipsychotic for acute psychotic symptoms; however, it is now reserved for patients with treatment-refractory schizophrenia. 6 Several commonly used second-generation antipsychotics, including However, G6PD deficiency is also a contraindication for use of tafenoquine, and because of its prolonged action, it might require more stringent restriction in those with relatively low G6PD levels. Demonstration of safety with tafenoquine might allow it to eventually replace primaquine as a single-dose anti-relapse therapy. For now, the report by Taylor and colleagues 5 offers a potential strategy for halving the length of therapy for eliminating hypnozoites, which is an incremental yet important advance in the treatment of vivax malaria.