Esketamine (Spravato) has a centralized EU marketing authorisation (indication: adults with treatment‑resistant major depressive disorder in combination with an oral antidepressant) and is registered for supply in EU member states, including Estonia. The EMA granted the marketing authorisation on 18 December 2019. #
In practice in Estonia, Spravato is a prescription medicine that must be administered under clinical supervision (clinic setting) consistent with the EMA product information; availability in Estonia is documented in EU/market product listings that include Estonia as a supply country. Access is typically arranged through psychiatrists/approved treatment centres that can deliver the supervised dosing regimen; because Spravato is a specialist, controlled psychotropic product, treatment pathways emphasize clinic‑based administration and monitoring, consistent with EMA/SmPC risk‑mitigation measures. #
Reimbursement: there is no widely published, definitive national policy indicating universal public reimbursement of Spravato by the Estonian Health Insurance Fund for the TRD indication; in many EU countries the medicine is either funded via selective reimbursement decisions, hospital budgets, or private/out‑of‑pocket arrangements depending on national health‑technology assessment and negotiated pricing. In Estonia the common practical situation is that Spravato is accessible via prescription/clinic channels but access is constrained by specialist delivery requirements and by the absence of a broadly published, automatic public reimbursement entitlement (patients and clinics therefore typically rely on private payment, hospital/clinic special funding arrangements, or case‑by‑case reimbursement decisions). (Note: specific Haigekassa reimbursement decisions are administrative and can change; for the EMA authorisation see EMA documentation). #