Esketamine nasal spray (SPRAVATO®) is a registered, prescription-only therapeutic product in Singapore and may be used in specialist psychiatric settings for the registered indications. The Health Sciences Authority (HSA) approved SPRAVATO® (registration SIN16033P) on 27 Oct 2020 for Treatment‑Resistant Depression (in combination with an oral antidepressant) and subsequently approved an additional indication for acute short‑term treatment of certain severe depressive episodes (indication approval entry dated 08 Dec 2021). SPRAVATO® is to be administered under clinical supervision with post‑dose monitoring and is subject to product labelling and usage safeguards in its product information. # #.
Regulatory/administration context: SPRAVATO® is prescription‑only and intended for administration under supervision in hospital/clinic environments; HSA product information specifies blood‑pressure monitoring and post‑administration observation requirements and that the product should be supplied only to specialist psychiatric services. The Ministry of Health (MOH) and HSA require controlled‑drug handling and record‑keeping for such products. #.
Reimbursement/access nuance: SPRAVATO® is an HSA‑registered medicine, but routine public reimbursement/subsidy for SPRAVATO® is not universally published as an entitlement; access typically requires treatment at specialist centres and payment terms are set by the treating hospital/clinic and the patient's insurer. Where patients seek SPRAVATO®, funding may be via private insurance (case‑by‑case) or out‑of‑pocket unless a particular hospital/clinic has a specific subsidy arrangement. Explicit nationwide public reimbursement for SPRAVATO® (e.g., standard MediShield or national subsidy policy) is not documented on HSA approval pages; providers or payors should be contacted for specific coverage policies.