Carla Carnovale

Italy

RESEARCH PROJECT DIRECTOR for the Project: Systematic review of studies reporting adverse events following immunization (AEFI) in children from pharmacovigilance databases, in the context of the European training Programme in Pharmacovigilance and pharmacoepidemiology (Eu2P)MASTER.

Italy

Research fellow Project: multidisciplinary approach to strengthen post-marketing drug safety in frail patients: from clinical to basic pharmacology Aim: to design a multidisciplinary approach in order to identify a patient safety issues emerging from spontaneous reporting activity in fragile patients and integrate them with pharmacological research. Activities: • Monitoring of ADRs/AEFI reports from basic post-marketing activities to detect a signal. • Analysis of ADRs/AEFI reports from the international pharmacovigilance databases to explore the signal trough a disproportional analysis and the clinical-pharmacological assessment of unexpected ADR/AEFI drug/vaccine-induced and DDIs. • Data mining of administrative databases to strengthen post-marketing drug safety and to address the pressing health care problems. • Performing of systematic review/meta-analysis to explore the issue. • Performing of retrospective/prospective studies for signal exploration in clinical practice. :: Pharmacovigilance Service, Unit Clinical Pharmacology, Department of Biomedical and Clinical Sciences, University Hospital "Luigi Sacco"- University of Milan ASST Fatebenefratelli-Sacco Via G. B. Grassi, 74 - 20157 Milano, Italy

Italy

Reviewer for the following international journals:Current clinical pharmacology, Vaccine, Drug Safety, Pharmacological Research, Journal of Clinical Pharmacy and Therapeutics, Plos One, British Medical Journal, Journal of pharmacovigilance, Expert Opinion on Drug Safety, Current bionanotechnology, European Journal of Internal Medicine

Italy

Research fellowship. Activities: • Collaboration with Pharmacovigilance Regional Center to coordinate Pharmacovigilance Projects • Perform medical review of Adverse Event • Answering medical queries related to Adverse Events • Conduct review and clarification of Adverse Event in special population (pediatrics and geriatrics) • Holding Pharmacovigilance training course for health care professional • Strong knowledge of Public Health Administration policies and procedures • Writing Grant Proposal • Medical writing • Reviewer for major scientific journals in the fields of pharmacovigilance