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Targeted Oncology|March 31, 2019
Toxicities with Immune Checkpoint Inhibitors: Emerging Priorities From Disproportionality Analysis of the FDA Adverse Event Reporting SystemEmanuel Raschi, Alessandra Mazzarella, Ippazio Cosimo Antonazzo, et al.
Biodrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy|March 15, 2024
Safety of Biological Therapies for Severe Asthma: An Analysis of Suspected Adverse Reactions Reported in the WHO Pharmacovigilance DatabasePaola Maria Cutroneo, Elena Arzenton, Fabiana Furci, et al.
Aging Clinical and Experimental Research|April 7, 2025
Safety of direct oral anticoagulants reversal agents in older patients: an analysis of individual case safety reports of adverse drug reaction from VigiBase®Giada Crescioli, Niccolò Lombardi, Elena Arzenton, et al.
European Journal of Clinical Pharmacology|March 6, 2014
Pharmacological prioritisation of signals of disproportionate reporting: proposal of an algorithm and pilot evaluationFrancesco Salvo, Emanuel Raschi, Ugo Moretti, et al.
Frontiers in Drug Safety and Regulation|September 22, 2025
Conducting and interpreting disproportionality analyses derived from spontaneous reporting systemsPaola Maria Cutroneo, Daniele Sartori, Marco Tuccori, et al.
Plos One|November 27, 2013
Torsadogenic risk of antipsychotics: combining adverse event reports with drug utilization data across EuropeEmanuel Raschi, Elisabetta Poluzzi, Brian Godman, et al.
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