The Pharmacovigilance Risk Assessment Committee (PRAC) has initiated a review of Deanxit, a fixed-dose combination medicine used for treating depression and anxiety. This review is part of the committee’s ongoing efforts to assess the safety and efficacy of medicinal products. The agenda for the PRAC meeting held from 26 to 29 October 2026 includes discussions on various ongoing referrals, including those for flupentixol/melitracen-containing products and parenteral iron-containing products.
This review could have implications for manufacturers and suppliers of Deanxit and similar medications, as any findings may influence regulatory decisions and market access. Stakeholders should monitor the outcomes of this review closely, as it may affect prescribing practices and patient access to these therapies.
Source: ema.europa.eu · Image: Visit of a delegation from the European Federation of Pharmaceutical Industries and Associations (EFPIA) , to the European Commission (P-066111-00-10) by Europäische Kommission – Audiovisueller Dienst, Christophe Licoppe, Yügen, CE – , CC BY 4.0, via Wikimedia Commons
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