Results 21 to 30 of about 4,636,278 (309)

Safety and efficacy of tocilizumab for rheumatoid arthritis: a systematic review and metaanalysis of clinical trial studies

Rheumatology, 2021
The present systematic review and meta-analysis was conducted to assess the effect of tocilizumab (TCZ) in patients with rheumatoid arthritis (RA). We systematically searched all potential articles in the main databases, including PubMed, Scopus, EMBASE,
Amal Saki, Elham Rajaei, Fakher Rahim
doaj   +1 more source

Global Assessment of Pediatric Patient Safety Tool for identifying safety incidents in pediatric patients [PDF]

Revista Paulista de Pediatria, 2023
Objective: The aim of this study was to evaluate the accuracy of the Global Assessment of Pediatric Patient Safety (GAPPS) in order to identify patient safety incidents with patient harm or adverse events (AEs).
Marilise Borges Brandão, Ana Paula Hermann, Mônica Nunes Lima   +2 more
doaj   +1 more source

Vaccine Adverse Events [PDF]

Workplace Health & Safety, 2012
Millions of adults are vaccinated annually against the seasonal influenza virus. An undetermined number of individuals will develop adverse events to the influenza vaccination. Those who suffer substantiated vaccine injuries, disabilities, and aggravated conditions may file a timely, no-fault and no-cost petition for financial compensation under the ...
openaire   +2 more sources

Serious adverse events and fatal adverse events associated with nivolumab treatment in cancer patients

Journal for ImmunoTherapy of Cancer, 2018
Background Nivolumab, an immune checkpoint inhibitor, has revolutionized the treatment of many cancers. Due to its novel mechanisms of action, nivolumab induces a distinct profile of adverse events. Currently, the incidence and risk of developing serious
Bin Zhao, Hong Zhao, Jiaxin Zhao
doaj   +1 more source

Rheumatological Adverse Events Following Immunotherapy for Cancer

Medicina, 2022
Background and Objectives: The occurrence of rheumatological side effects in a patient after receiving immunotherapy for cancer is becoming increasingly common. Oncologists often fail to diagnose and refer affected patients to rheumatologists. This paper
Ioana Cretu, Bogdan Cretu, Catalin Cirstoiu, Adrian Cursaru, Mihaela Milicescu, Mihai Bojinca, Ruxandra Ionescu   +6 more
doaj   +1 more source

Adverse events of auricular therapy: A systematic review [PDF]

, 2014
The aim of this study was to systematically evaluate the literature on adverse events associated with auricular therapy (AT). Case reports, case series, surveys, and all types of clinical trials reporting adverse events of AT were included.
Suen, L. K. P., Suen, Lorna K. P., Molassiotis, A., Molasiotis, A., Wang, T., Tan, J.-Y., Molassiotis, Alexander, Wang, Tao, Tan, Jing-Yu   +8 more
core   +1 more source

Research and Discussion on the Whole Lifecycle Supervision of Typical Class Ⅱ Wound Dressing Products

Zhongguo yiliao qixie zazhi
In this study, the pre-market regulatory requirements for typical Class Ⅱ wound dressings, as well as the status of testing and post-market adverse events monitoring, were reviewed from the perspective of the whole lifecycle of medical devices ...
Lan ZHANG, Ye ZENG, Xin XIE, Jiaohui BAO, Xiaohe YANG, Weiming QI   +5 more
doaj   +1 more source

Adverse Events Following Immunization

Zdorovʹe Rebenka, 2014
Lecture "Adverse eventsfollowing immunization"recommendedfor postgraduate education ofGeneral practitionersandpediatricians.
L.I. Chernyshova
doaj   +1 more source

META-INSTI: metabolic adverse events following integrase strand transfer inhibitor administration in spontaneous adverse event reports

, 2023
Background: Metabolic effects of integrase strand transfer inhibitors (INSTIs) have been reported. The FDA Adverse Event Reporting System (FAERS) is a publicly available database that captures spontaneously reported adverse events.
Lara Fakhouri, Spencer E Harpe, Milena M Murray   +2 more
core   +1 more source

Research and Discussion on the Supervision of Registration and Sales Units for In Vitro Diagnostic Reagents

Zhongguo yiliao qixie zazhi
This study reviewed the pre-market regulatory requirements for the division of registration units, registration and filing status, as well as the actual sales and usage status of in vitro diagnostic reagent registration units from the perspective of full
Qinfang DONG, Jun YANG, Lingang JIN, Ling LI, Qiying AIXINJUELUO, Xiaohe YANG   +5 more
doaj   +1 more source