Esketamine (Spravato) is an authorised medicinal product at the European/EMA level for treatment-resistant depression: the EMA product page documents its authorisation and the restrictive conditions of use. #.
In Norway the national rollout, public financing and reimbursement have been subject to national health technology and procurement reviews. Norwegian health bodies (including the Directorate for Medical Products / Direktoratet for medisinske produkter and Norway’s decision-making forums for new treatments) have repeatedly reviewed Spravato and public reimbursement/implementation decisions have been limited; authorities have raised concerns about long‑term effectiveness, cost‑effectiveness and budget impact, and Norwegian bodies have declined broad public funding in several evaluations. This means that while the drug holds EU/EMA authorisation, its routine availability and public reimbursement in Norway (and therefore on Bouvet Island under Norwegian law) is constrained and dependent on national decisions. # # #.
Practical consequence for Bouvet Island: because the island has no resident population or local healthcare infrastructure and Norwegian law applies, there is no on‑island reimbursement program; any access would depend on Norwegian national health policy and hospital/clinic provisions on the Norwegian mainland. #.