Results 91 to 100 of about 9,966 (258)

Disproportionality analysis of interstitial lung disease associated with novel antineoplastic agents during breast cancer treatment: a pharmacovigilance studyResearch in context

open access: yesEClinicalMedicine
Summary: Background: Studies have shown that some antineoplastic agents may be associated with interstitial lung disease (ILD), but large-scale real-world data are lacking.
Zijun Zhu   +8 more
doaj   +1 more source

Aspirin in the Food and Drug Administration Adverse Event Reporting System: Missing Demographics and Underreporting

open access: yesTH Open, 2017
Background The U.S. Food and Drug Administration (FDA) Adverse Event (AE) Reporting System (FAERS) is a global passive surveillance repository requiring mandatory updates by pharmaceutical manufacturers. Oral antiplatelet agents (OAAs) including aspirin (
Victor L. Serebruany   +4 more
doaj   +1 more source

Drug Safety Monitoring in Children: Performance of Signal Detection Algorithms and Impact of Age Stratification [PDF]

open access: yes, 2016
Introduction: Spontaneous reports of suspected adverse drug reactions (ADRs) can be analyzed to yield additional drug safety evidence for the pediatric population.
Dodd, C.N. (Caitlin)   +5 more
core   +3 more sources

Comparative Safety Analysis of Avastin and Bevacizumab Biosimilars Based on Food and Drug Administration Adverse Event Reporting System

open access: yesBasic &Clinical Pharmacology &Toxicology, Volume 137, Issue 4, October 2025.
ABSTRACT Objective This study aimed to compare adverse event (AE) profiles between Avastin and bevacizumab biosimilars to support clinical decision‐making, given the limited availability of real‐world data. Methods A disproportionality analysis was conducted using the FDA Adverse Event Reporting System (FAERS) to identify and compare AE signals ...
Xiaoyu Zhang   +3 more
wiley   +1 more source

Broadening the capture of natural products mentioned in FAERS using fuzzy string-matching and a Siamese neural network

open access: yesScientific Reports
Increased sales of natural products (NPs) in the US and growing safety concerns highlight the need for NP pharmacovigilance. A challenge for NP pharmacovigilance is ambiguity when referring to NPs in spontaneous reporting systems.
Israel O. Dilán-Pantojas   +6 more
doaj   +1 more source

Phase diagram and aggregation dynamics of a monolayer of paramagnetic colloids

open access: yes, 2017
We have developed a tunable colloidal system and a corresponding simulation model for studying the phase behavior of particles assembling under the influence of long-range magnetic interactions.
Charbonneau, Patrick   +5 more
core   +1 more source

Expanding on Abraxane Safety: Temporal Insights and Future Directions for Adverse Event Analysis [Letter]

open access: yesInternational Journal of Nanomedicine
Fangcai Yang,1 Wukun Ge2 1Department of Clinical Nutrition, Ninghai First Hospital, Ningbo, Zhejiang, 315600, People’s Republic of China; 2Department of Clinical Pharmacy, Ninghai First Hospital, Ningbo, Zhejiang, 315600, People’s Republic of
Yang F, Ge W
doaj  

Drug-induced interstitial lung disease: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System from 2004 to 2021

open access: yesTherapeutic Advances in Drug Safety
Background: Drug-induced interstitial lung disease (DILD) is an increasingly common cause of morbidity and mortality. However, due to the lack of specificity, DILD detection remains an unsolved public health challenge.
Tingting Jiang   +11 more
doaj   +1 more source

Safety evaluation of irinotecan: a real-world disproportionality analysis using FAERS and JADER databases during the time period 2004-2024

open access: yesFrontiers in Pharmacology
IntroductionIrinotecan is a widely used chemotherapeutic agent for treating colorectal, pancreatic, and ovarian cancers. Despite its therapeutic efficacy, the safety profile of irinotecan necessitates continuous pharmacovigilance due to its association ...
Siyu Lou   +7 more
doaj   +1 more source

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