Esketamine (intranasal Spravato) is a centrally authorized product in Europe (European Medicines Agency) for treatment‑resistant depression and is subject to restricted distribution and supervised administration requirements; this EMA authorisation establishes that esketamine is a recognized medicinal product in the European regulatory framework, but the Faroe Islands operate their own national/local medicine importation, hospital formularies and reimbursement decisions which determine local availability and funding. The EMA summary for Spravato outlines the authorised indication (adults with treatment‑resistant depression, used with an oral antidepressant) and the requirement for supervised administration in a clinic setting. #.
Practical implication for the Faroe Islands: individual hospitals or the Faroese health authority would need to include esketamine on a local formulary or approve importation/prescribing pathways for it to be available and reimbursed; there is no publicly available Faroese national policy document (accessible in open sources) that establishes a universal, reimbursed esketamine program equivalent to larger EU health systems. Where esketamine is used, reimbursement and patient access are typically conditional (specialist psychiatrist prescribing, supervised administration, and local funding decisions). #