Comparison of thrombotic adverse events in patients treated with factor VIII products and emicizumab using the 2018-2022 US Food and Drug Administration Adverse Event Reporting System data: comment from Berkowitz et al.
Author:
Funder
Novo Nordisk Haemophilia Foundation
Novo Nordisk
Publisher
Elsevier BV
Reference9 articles.
1. Comparison of thrombotic adverse events in patients treated with factor VIII products and emicizumab using the 2018-2022 US Food and Drug Administration Adverse Event Reporting System data;Cho;J Thromb Haemost,2024
2. Conducting and interpreting disproportionality analyses derived from spontaneous reporting systems;Cutroneo;Front Drug Saf Regul,2024
3. Adverse drug reaction risk measures: a comparison of estimates from drug surveillance and randomised trials;Beau-Lejdstrom;Pharm Med,2019
4. Existence of notoriety bias in FDA adverse event reporting system database and its impact on signal strength;Neha;Hosp Pharm,2021
5. Benefits and strengths of the disproportionality analysis for identification of adverse drug reactions in a pharmacovigilance database;Montastruc;Br J Clin Pharmacol,2011
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