Assessment of the Post-Marketing “Drug Ineffective” Reports Received by the Saudi Vigilance System
Hana Jaffar Al Khabbaz, Talal A. Alsoaiby & Rayan I. Alolayet · Journal of Pharmaceutical Research International · 2023
Aim: Drug Ineffective (DI) reports are Adverse Drug Events (ADE) important for post-marketing surveillance (PMS). Currently drug safety information from the DI reports received by the Saudi Food and Drug Authority (SFDA) via the Saudi Vigilance System (SVS) is undetermined. The...