Results 291 to 300 of about 476,894 (337)

Drug-induced pancreatitis: a real-world analysis of the FDA Adverse Event Reporting System and network pharmacology. [PDF]

Front Pharmacol
Xie H, Jiang L, Peng J, Hu H, Han M, Zhao B.   +5 more
europepmc   +1 more source

Adverse events following 9-valent human papillomavirus vaccine (GARDASIL® 9) reported to the Vaccine Adverse Event Reporting System (VAERS), 2015-2024. [PDF]

Hum Vaccin Immunother
Liu Q, Liang G, Song Y.
europepmc   +1 more source

Melasma secondary to drugs: a real-world pharmacovigilance study of the FDA adverse event reporting system (FAERS). [PDF]

BMC Pharmacol Toxicol
Qu Y, Wang S, Xie H, Meng X, Cui B, Xiao Z.   +5 more
europepmc   +1 more source

Sodium-glucose cotransporter-2 inhibitors and ketoacidosis in heart failure: analysis of US Adverse Event Reporting System (FAERS). [PDF]

Eur Heart J Open
Yeung SL, Wang M, Lou M, Ng TMH.
europepmc   +1 more source

Real-World pharmacovigilance analysis of drug-related conjunctivitis using the FDA adverse event reporting system database. [PDF]

Sci Rep
Li X, Sun YQ, Liu MM, Tang JF.
europepmc   +1 more source

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Adverse events reported to the U.S. Food and Drug Administration Adverse Event Reporting System for tisagenlecleucel

American Journal of Hematology, 2021
AbstractThe U.S. Food and Drug Administration (FDA) approved the first chimeric antigen receptor T‐cell therapy, tisagenlecleucel, in August 2017. We sought to describe adverse events (AEs) reported to the FDA Adverse Event Reporting System (FAERS) for tisagenlecleucel in the post‐marketing period. We searched FAERS reports to identify U.S.
Graça M. Dores, Christopher Jason, Manette T. Niu, Silvia Perez‐Vilar   +3 more
openaire   +2 more sources

Causality assessment of adverse events reported to the Vaccine Adverse Event Reporting System (VAERS)

Vaccine, 2012
Adverse events following immunization (AEFI) reported to the national Vaccine Adverse Event Reporting System (VAERS) represent true causally related events, as well as events that are temporally, but not necessarily causally related to vaccine.We sought to determine if the causal relationships between the vaccine and the AEFI reported to VAERS could be
Nicola P. Klein, Elizabeth D. Barnett, Steve Black, Katherine M. Edwards, William G. Adams, Jerold Klein, Cornelia L. Dekker, Colin D. Marchant, Christine G. Casey, Roger Baxter, Philip LaRussa, Kathleen Jakob, Anita M. Loughlin, Robert Sparks   +13 more
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Introduction of a Mobile Adverse Event Reporting System Is Associated With Participation in Adverse Event Reporting

American Journal of Medical Quality, 2018
Physicians underutilize adverse event reporting systems. Web-based platforms have increased participation; thus, it was hypothesized that a mobile application would increase adverse event reporting. The authors developed a mobile reporting application for iOS and Android operating systems and performed a retrospective review on reporting rates by ...
Chuanhong Liao, Colin Pesyna, Daniel S. Rubin, Sharon Jakubczyk, Avery Tung   +4 more
openaire   +2 more sources