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FDA Launches Dashboard to Provide Access to Real-Time Adverse Event Data for Cosmetics Faegre Drinker Biddle & Reath LLP

Red Bull Turn It Up: Event Info Red Bull

Real-World Data: Anti-VEGF Agents Each Show Unique Adverse Event Signals Ophthalmology Advisor

FDA starts publishing daily adverse event data European Pharmaceutical Review

Intellia stock dips following safety event in Phase III gene therapy trial Clinical Trials Arena

Improve Safety Reporting in Patient Services with AI and Human Insight IQVIA

Improving entity recognition using ensembles of deep learning and fine-tuned large language models: A case study on adverse event extraction from VAERS and social media ScienceDirect.com

Comparative analysis of adverse event profiles of lanreotide and octreotide in somatostatin-responsive endocrine and neoplastic diseases Nature

Pharmacovigilance Assessment of Compounded GLP-1 Receptor Agonists: Insights From the FDA Adverse Event Reporting System Endocrinology Advisor

Waldo: AI tool can scan social media for hidden health risks Medical Xpress

Adverse event profile differences between maribavir and valganciclovir: findings from the FDA adverse event reporting system Frontiers

Discrepancies in safety reporting for chronic back pain clinical trials: an observational study from ClinicalTrials.gov and publications BMC Medical Research Methodology

AI's Promising Role In Adverse Event Management Of Small Molecule Drugs Pharmaceutical Online

(PDF) Innovation in Pharmacovigilance: Use of Artificial Intelligence in Adverse Event Case Processing researchgate.net

A realworld pharmacovigilance study of trazodone based on the FDA adverse event reporting system Nature

Safety reporting in neonatal clinical trials: reflections towards optimal, globally relevant approaches | Trials | Full Text BioMed Central

Analysis of nationwide adverse event reports on Isoniazid and Rifampin in tuberculosis prevention and treatment in South Korea Nature

A real-world disproportionality analysis of FDA adverse event reporting system (FAERS) events for avatrombopag Nature

Neurogene’s stock sinks after adverse event with Rett syndrome gene therapy Clinical Trials Arena

Adverse event assessment in a parenting programme: experiences from a multisite randomised controlled trial BioMed Central

Adverse event signal extraction from cancer patients’ narratives focusing on impact on their daily-life activities Nature

Reduce Reconciliation of Clinical Serious Adverse Events (SAE) Veeva

Triptorelin associated adverse events evaluated using FAERS pharmacovigilance data Nature

Olutasidenib Continues to Induce Durable Remissions in IDH1-Mutant R/R AML Targeted Oncology

Patient dies in Rocket’s Phase II Danon disease gene therapy trial Clinical Trials Arena

A real-world pharmacovigilance analysis of omadacycline in FDA adverse event reporting system (FAERS) database Frontiers

Utilizing group-based models to identify adverse event patterns after an intervention Frontiers

A Model to Estimate Cytokine Release Syndrome and Neurological Event Management Costs Associated With CAR T-Cell Therapy ScienceDirect.com

Second Malignancy Risk With CAR T-Cell Therapy on Par With Other Treatments MedPage Today

Safety comparisons among different subcutaneous anticoagulants for venous thromboembolism using FDA adverse event reporting system Nature

Pharmacovigilance analysis of neurological adverse events associated with GLP-1 receptor agonists based on the FDA Adverse Event Reporting System Nature

Data quality and timeliness analysis for post-vaccination adverse event cases reported through healthcare data exchange to FDA BEST pilot platform Frontiers

WATCH: Steelers Style 2024 Recap Steelers.com

The mega Sephoria beauty event returns to Dubai this November whatson.ae

Pharmacovigilance study of the association between peripheral neuropathy and antibody–drug conjugates using the FDA adverse event reporting system Nature

The design, implementation, and impact of an automated patient-reported outcome data collection and adverse event surveillance tool: a randomized trial BMC Health Services Research

Inappropriate clinical management decisions are possible secondary to use of Bazett formula for QTc in context of chemotherapy cancer treatment 2 Minute Medicine

Prospective assessment of inter-rater reliability of a neonatal adverse event severity scale Frontiers

Indication and adverse event profiles of denosumab and zoledronic acid: based on U.S. FDA adverse event reporting system (FAERS) Frontiers

A real-world safety signal detection study of ondansetron based on FAERS reports from 2014 to 2024 Nature

Disproportionate adverse event signals of selumetinib in neurofibromatosis type I: insights from FAERS Frontiers

Safety assessment of neurokinin-1 receptor antagonist: real-world adverse event analysis from the FAERS database Frontiers

Adverse events in single-arm clinical trials with non-fatal time-to-event efficacy endpoint: from clinical questions to methods for statistical analysis BMC Medical Research Methodology

Study Reports Safety Data in Children on JAK Inhibitors Medscape

Seven Percent of Outpatients Experience One or More Adverse Event HealthDay

Adverse events in different administration routes of semaglutide: a pharmacovigilance study based on the FDA adverse event reporting system Frontiers

American Eagle Highlights BTS Denim in NYC Sourcing Journal

Submissions Open for DHS Automotive Vehicle Cybersecurity Assessment Event Homeland Security Today

Impact of the COVID-19 pandemic on the spontaneous reporting and signal detection of adverse drug events Nature

Psychiatric adverse events associated with GLP-1 receptor agonists: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System database Frontiers

Gender differences in spontaneous adverse event reports associated with zolpidem in South Korea, 2015–2019 Frontiers

Clinical drug interactions between linezolid and other antibiotics: For adverse drug event monitoring British Pharmacological Society | Journals

Inter-rater reliability of the neonatal adverse event severity scale using real-world Neonatal clinical trial data Nature

FDA Launches Adverse Event Reporting System Public Dashboard Center for Biosimilars

Post-marketing safety surveillance of dalfampridine for multiple sclerosis using FDA adverse event reporting system Frontiers

Contrastive analysis on the safety of brand and generic nebivolol: a real-world pharmacovigilance study based on the FDA adverse event reporting system Frontiers

Build a system for catching adverse events in real-time using Amazon SageMaker and Amazon QuickSight Amazon Web Services

Supporting Pharma in AE Reporting Is Tricky Specialty Pharmacy Continuum

A real-world disproportionality analysis of apalutamide: data mining of the FDA adverse event reporting system Frontiers

Sex differences of fall-risk-increasing drugs in the middle-aged and elderly: a descriptive, cross-sectional study of FDA adverse event reporting system Nature

Drug-induced QT prolongation and torsade de pointes: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System database Frontiers

Dr. Dietrich on Optimal Adverse Event Management for Neratinib in Breast Cancer OncLive

Assessing the safety of bedaquiline: insight from adverse event reporting system analysis Frontiers

Statistical methods for the analysis of adverse event data in randomised controlled trials: a scoping review and taxonomy BMC Medical Research Methodology

BPS Publications British Pharmacological Society | Journals

Years-Old List of Alleged Pfizer COVID-19 Vaccine 'Side Effects' Is Misleading Snopes

Evaluation of antibiotic-induced taste and smell disorders using the FDA adverse event reporting system database Nature

Understanding current practice, identifying barriers and exploring priorities for adverse event analysis in randomised controlled trials: an online, cross-sectional survey of statisticians from academia and industry BMJ Open

City of Atlanta honors star NBA player with mural during event debuting first signature shoe WSB-TV

Analysis of chemotherapy-induced peripheral neuropathy using the Japanese Adverse Drug Event Report database Nature

Impacto del riesgo de múltiples interacciones farmacológicas en el perfil de eventos adversos de pacientes con hepatitis C tratados con antivirales de acción directa pangenotípicos en España SciELO España

Veterinary cooperative oncology group – common terminology criteria for adverse events (VCOG-CTCAE) following chemotherapy or biological antineoplastic therapy in dogs and cats v1.1 Wiley Online Library

Patient stratification and identification of adverse event correlations in the space of 1190 drug related adverse events Frontiers

Report a possible side effect GSK

Serious adverse event reporting in investigator-initiated clinical trials The Medical Journal of Australia