Pharmacovigilance and Drug Safety Software

Clinical Research, Drug Safety and Pharmacovigilance

 Signals of adverse drug reactions (ADR) can be based on different study designs, including clinical trials, observational studies, meta-analyses, and case reports. Daniele Sartori sat down in the Research Corner to shine a light on the evidence base and features of ADR reports. Watch the film below Curious about the topic? Access the report for further reading  doi.org/10.1007/s40264-022-01258-0 #pharmacovigilance #PatientSafety | Uppsala Monitoring Centre | Facebook

📝 Adverse event reports typically contain structured data elements such as patient identifier, medicine name, and reaction. However, these elements may not capture the whole picture. Narrative fields allow reporters to disclose contextual information, such as the patient's full clinical course, bringing the medical story to light. When it comes to working with narratives, what challenges do #pharmacovigilance assessors face, and how may advances in artificial intelligence streamline analyses in