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Drug Safety|October 1, 2024
Investigation of the Role of Chemical Analysis in Causality Assessment of Herbal and Dietary Supplement-Induced Liver InjuryDina Halegoua-DeMarzio, Victor J Navarro, Ashley Davis, et al.
Drug Safety|September 19, 2024
Disproportionality Analysis and Characterisation of Medication Errors in EudraVigilance: Exploring Findings on Sexes and Age GroupsVictor Pera, Jan A Kors, Erik M van Mulligen, et al.
Drug Safety|February 24, 2024
A Comparison of Signals of Designated Medical Events and Non-designated Medical Events: Results from a Scoping ReviewDaniele Sartori, Jeffrey K Aronson, Nils Erlanson, et al.
Drug Safety|February 27, 2024
In Utero Exposure to Antibiotics and Risk of Serious Infections in the First Year of LifeMylène Tisseyre, Mathis Collier, Nathanaël Beeker, et al.
Drug Safety|February 14, 2024
Sociodemographic Characteristics of Adverse Event Reporting in the USA: An Ecologic StudyMonica A Muñoz, Gerald J Dal Pan, Yu-Jung Jenny Wei, et al.
Drug Safety|February 14, 2024
Consensus Guidelines: Best Practices for the Prevention, Detection and Management of Hepatitis B Virus Reactivation in Clinical Trials with Immunosuppressive/Immunomodulatory TherapyEric B Cohen, Arie Regev, Anju Garg, et al.
Drug Safety|November 21, 2023
Comparative Analysis of Information Provided in German Adverse Drug Reaction Reports Sent by Physicians, Pharmacists and ConsumersPatrick Christ, Diana Dubrall, Matthias Schmid, et al.
Drug Safety|November 16, 2023
Cognitive Safety is Largely Ignored in Clinical Drug Trials: A Study of Registered Study ProtocolsArne Reimers, Hanna Ljung
Drug Safety|October 30, 2023
Long-Term Real-World Post-approval Safety Data of Multiple Biosimilars from One Marketing-Authorization Holder After More than 18 Years Since Their First Biosimilar LaunchSreedhar Sagi, Pradeep Anjaneya, Sameer Kalsekar, et al.
Drug Safety|November 5, 2023
Impact of Covid-19 Vaccination on Spontaneous Pharmacovigilance Reporting in FranceSibylle de Germay, Allison Singier, Francesco Salvo, et al.
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