FDA spustila nový systém hlásenia nežiaducich udalostí, ktorý zjednotí niekoľko existujúcich systémov na hlásenie rôznych typov nežiaducich udalostí. The agency announced this on Wednesday. The new system is called FDA Adverse. This system replaces previous separate databases, including FAERS. The aim is to simplify the process of reporting adverse events related to medicines and medical devices. The changes come in the context of the FDA's 2026 updates.