Results 71 to 80 of about 1,500,169 (183)

A Standardized Dataset of a Spontaneous Adverse Event Reporting System

open access: yes, 2022
One of the largest spontaneous adverse events reporting databases in the world is the Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS). Unfortunately, researchers face many obstacles in analyzing data from the FAERS database. One
Azreen Syazril Adnan   +4 more
core   +1 more source

Pharmacovigilance knowledge in Brazil: perception of participants of oncology patient advocacy group on adverse events reporting

open access: yesBrazilian Journal of Oncology, 2018
Objective: Pharmacovigilance revolves around the maintenance and understanding of drug safety through detection and evaluation of spontaneous adverse events (AE) reporting.
Guilherme Silva Julian   +4 more
doaj   +1 more source

Identifying in-market application of Pelargonium root extract EPs 7630 for the treatment of COVID-19: analysis of pharmacovigilance data

open access: yesFrontiers in Pharmacology
Introduction: Phytopharmaceutical products are successfully used for acute respiratory infections and may therefore be promising candidates for adjuvant symptomatic treatment of COVID-19.
Fathi Abdul Malek, Petra Funk
doaj   +1 more source

A real-world data analysis of ocular adverse events linked to anti-VEGF drugs: a WHO-VigiAccess study

open access: yesFrontiers in Pharmacology
IntroductionVascular endothelial growth factor (VEGF) is key to wet age-related macular degeneration (wAMD). Anti-VEGF drugs are the main treatment in clinics.
Chen Li   +3 more
doaj   +1 more source

Spontaneous Cholecystocolic Fistula: Case Report

open access: yesJOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2014
Cholecystocolic fistula is a rare billiary-enteric fistula with variable clinical presentation. Despite modern diagnostic tool a high degree of suspicion is required to diagnose it preoperatively. These fistulae are treated by open as well as laparoscopic surgery, with no difference in intraoperative and postoperative complications. We are describing a
Nandkishore Gora   +4 more
openaire   +3 more sources

Spontaneous pneumothorax in pregnancy: a case report

open access: yesTuberkuloz ve Toraks, 2011
Spontaneous pneumothorax is an extremely rare condition during pregnancy. Rupture of a subpleural apical bulla or blebs are the most common cause of spontaneous pneumothorax in young pregnant women. It is believed to be due to increase respiratory activity associated peripartum period.
Afshin, Mohammadi   +2 more
openaire   +2 more sources

Enhanced knowledge of spontaneous reporting with structured educational programs in Korean community pharmacists: a cross-sectional study

open access: yesBMC Medical Education, 2017
Background While spontaneous reporting (SR) is one of the important public health activities for community pharmacists to guard patients’ safety, very few studies examined educational activities and its effects on knowledge about the SR system in Korea ...
Yun Mi Yu, Euni Lee
doaj   +1 more source

Spontaneous pneumothorax in pregnancy – Case report

open access: yesJournal of Obstetrics and Gynaecology, 2005
(2005). Spontaneous pneumothorax in pregnancy – Case report. Journal of Obstetrics and Gynaecology: Vol. 25, No. 2, pp. 202-203.
S, China, C K, Roseblade
openaire   +2 more sources

Evaluation of patient reporting of adverse drug reactions to the UK ‘Yellow Card Scheme’: literature review, descriptive and qualitative analyses, and questionnaire surveys [PDF]

open access: yes, 2011
Background: The monitoring of adverse drug reactions (ADRs) through pharmacovigilance is vital to patient safety. Spontaneous reporting of ADRs is one method of pharmacovigilance, and in the UK this is undertaken through the Yellow Card Scheme (YCS ...
DJ McLernon   +54 more
core   +1 more source

A Comparison of Active Surveillance Programs Including a Spontaneous Reporting Model for Phamacovigilance of Adverse Drug Events in a Hospital [PDF]

open access: yes, 2012
Background/Aims: Spontaneous reporting systems have several weak points, such as low reporting rates and insufficient clinical information. Active surveillance programs, such as ward rounds and a clinical data repository (CDR), may supplement the weak ...
이재현, 윤일선, 박중원
core  

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