Adverse drug reaction reporting systems

Results 81 to 90 of about 38,036 (299)

Spontaneous adverse drug reactions reported in a thirteen-year pharmacovigilance program in a tertiary university hospital

Frontiers in Pharmacology
ObjectivesWe aimed to assess the characteristics of adverse drug reactions (ADRs) collected in a university hospital.MethodsA retrospective analysis of ADRs spontaneously reported in the Hospital Pharmacovigilance Program database (RutiRAM) over a 13 ...
E. Montané +11 more
doaj +1 more source

Artificial Intelligence–Based Online Symptom Assessment Tools for Systemic Lupus Erythematosus Diagnosis: Patient Perspectives

Arthritis Care &Research, EarlyView.
Objective The objective of this article is to identify perceptions of patients with systemic lupus erythematosus (SLE) regarding artificial intelligence (AI)–based online symptom assessment tools, and the potential of these tools to address diagnostic barriers.
Olivia A. Stein +7 more
wiley +1 more source

An Overview of Clinical Pharmacology of Ibuprofen

Oman Medical Journal, 2010
Ibuprofen was the first member of Propionic acid derivatives introduced in 1969. It is a popular domestic and over the counter analgesic and antipyretic for adults and children.
Nousheen Aslam, Rabia Bushra
doaj

BICEPP: an example-based statistical text mining method for predicting the binary characteristics of drugs

BMC Bioinformatics, 2011
Background The identification of drug characteristics is a clinically important task, but it requires much expert knowledge and consumes substantial resources.
Tsafnat Guy +4 more
doaj +1 more source

Do your part for vaccine safety -- report to VAERS : Vaccine Adverse Event Reporting System, a national program for monitoring vaccine safety [PDF]

The Vaccine Adverse Event Reporting System (VAERS) is a national program that monitors the safety of vaccines after they are licensed. VAERS is managed by the U.S. Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration

core

Linking Activity Theory Within User-Centered Design: Novel Framework to Inform Design and Evaluation of Adverse Drug Reaction Reporting Systems in Pharmacy. [PDF]

JMIR Hum Factors, 2023
Fossouo Tagne J +3 more
europepmc +1 more source

Incorporation of Selenium into Sol–Gel‐Derived Bioactive Glass: Influence on Glass Structure, Bioactivity, and its Selective Cytotoxicity

Advanced Engineering Materials, EarlyView.
Selenium was incorporated into a sol–gel‐derived bioactive glass to enable sustained therapeutic ion release. The selenium‐containing glass preserved bioactivity while selectively inducing cytotoxicity in osteosarcoma cells and maintaining osteoblastic viability.
Breno Rocha Barrioni +7 more
wiley +1 more source

VAERS : Vaccine Adverse Event Reporting System : a national program for monitoring vaccine safety

The Vaccine Adverse Event Reporting System (VAERS), is a national program managed by the U.S. Centers for Disease Control and Prevention (CDC) and the U.S.

core +1 more source

Geriatrics, Gerontology and Aging
Objective: To describe suspected adverse drug events in older adults reported in VigiMed, the Brazilian National Health Surveillance Agency’s reporting system.
Gabriela Oliveira Buzelin Doria +7 more
doaj +1 more source

Pharmacovigilance: pharmacists’ perspective on spontaneous adverse drug reaction reporting

, 2017
Muhammad Abdul Hadi,1 Chin Fen Neoh,2 Rosdi M Zin,3 Mahmoud E Elrggal,4 Ejaz Cheema4 1School of Healthcare, Faculty of Medicine and Health, University of Leeds, Leeds, UK; 2Collaborative Drug Discovery Research Group, Faculty of Pharmacy, Universiti ...
Zin RM +4 more
core

pharmacovigilance
3. good health
humans

adverse drug reaction
drug monitoring
middle aged