Results 51 to 60 of about 1,500,169 (183)

Pharmacovigilance: Empowering healthcare professionals [PDF]

Hospital Pharmacology, 2015
Introduction: Spontaneous reporting of adverse reactions is of greatest importance for obtaining information about adverse drug reactions (ADRs) after granting the marketing authorization.
Mugoša Snežana S., Stanković Maja V., Turković Nemanja M., Bešović Željka M., Šahman-Zaimović Majda M., Drljević Milorad D.   +5 more
doaj   +1 more source

Development and application of the vaccine reporting quality score to evaluate the vaccine adverse event reporting system

Frontiers in Immunology
Background and aimsEnsuring the documentation quality of spontaneous reports in the Vaccine Adverse Event Reporting System (VAERS) is important for signal detection, yet targeted tools for evaluating vaccine-specific reporting quality remain lacking ...
Zongkai Zhou, Zirong Mu, Nina Gu, Xu Sun, Zun Wu, Zuguo Tian, Wanhong Luo   +6 more
doaj   +1 more source

Spontaneous Adverse Drug Reaction Reporting Vs Event Monitoring: A Comparison

, 1991
Spontaneous adverse drug reaction (ADR) reporting is the mainstay of national and international drug safety evaluation in the post-approval phase. A major criticism of the method has been a high, but essentially unquantifiable, level of under-reporting ...
A P Fletcher
core   +1 more source

Contributing factors for the spontaneous reporting of adverse drug reactions.

, 2016
Contributing factors for the spontaneous reporting of adverse drug reactions.
Mo Se Lee (769575), Kwang Hoon Choi (769576), Yun Mi Yu (769569), Kyung Hee Choi (844715), Kyeong Hye Jeong (3168921), Jung Mi Oh (711439), Euni Lee (822530), Lee Kyung Kang (3168927), Wan Gyoon Shin (769570), Bon Sun Koo (3168924)   +9 more
core   +1 more source

An evaluation of knowledge, attitude and perception about adverse drug reactions and pharmacovigilance among intern doctors at a teaching hospital of Rajasthan

National Journal of Physiology, Pharmacy and Pharmacology, 2016
Background: Underreporting of adverse drug reactions (ADRs) by clinician is a common problem. As interns will be budding doctors to serve the community, this study was undertaken to evaluate knowledge, attitude and perception about ADR and ...
Manoj Kumar Saurabh, Rakesh Kumar Karnani   +1 more
doaj   +1 more source

Board diversity reporting [PDF]

, 2018
The majority of the UK’s largest companies have adopted policies on boardroom diversity but their reporting to stakeholders needs to improve. Research conducted for the Financial Reporting Council (FRC) by the University of Exeter Business School shows ...
Opara, V, Sealy, R, Tilbury, L, Page, A
core   +3 more sources

Disease-Modifying Therapies (DMTs) in Pregnant and Lactating Women with Multiple Sclerosis: Analysis of Real-World Data from EudraVigilance Database

Pharmaceuticals, 2023
(1) Background: The purpose of study was to compare the safety profile of glatiramer with natalizumab, alemtuzumab and ocrelizumab in pregnant and lactating women affected by multiple sclerosis (MS).
Liberata Sportiello, Raffaella Di Napoli, Nunzia Balzano, Annamaria Mascolo, Rosanna Ruggiero, Luigi Di Costanzo, Davida Monaco, Giorgia Teresa Maniscalco, Annalisa Capuano   +8 more
doaj   +1 more source

Antipsychotics and Torsadogenic Risk: Signals Emerging from the US FDA Adverse Event Reporting System Database [PDF]

, 2013
Background: Drug-induced torsades de pointes (TdP) and related clinical entities represent a current regulatory and clinical burden. Objective: As part of the FP7 ARITMO (Arrhythmogenic Potential of Drugs) project, we explored the publicly available US ...
MORETTI, Ugo, De Ponti F., Sturkenboom, M.C.J.M. (Miriam), De Ponti, F, Behr, E.R. (Elijah), Koci A, Spina, E, Sturkenboom M, Ariola Koci, Poluzzi E, Spina E, Raschi, E. (Emanuel), Ponti, F. (Fabrizio) de, Ugo Moretti, Spina, E. (Edoardo), Poluzzi, E, POLUZZI, ELISABETTA, Koci, A. (Ariola), Behr ER, Koci, A, Elijah R. Behr, Elisabetta Poluzzi, Poluzzi, E. (Elisabetta), Sturkenboom, MCJM, Moretti, U. (Ugo), Fabrizio De Ponti, KOCI, ARIOLA, Moretti, U, Emanuel Raschi, Raschi, E, Miriam Sturkenboom, DE PONTI, FABRIZIO, Moretti U, RASCHI, EMANUEL, Behr, ER, Raschi E, Edoardo Spina, SPINA, Edoardo, Sturkenboom, M   +38 more
core   +1 more source

Study on the Classification, Causality, Preventability and Severity of Adverse Drug Reaction Using Spontaneous Reporting System in Hospitalized Patients

Pharmacy, 2018
Hospital-based adverse drug reaction (ADR) monitoring and reporting programs intend to identify and quantify the risks associated with the use of medicines. To examine the causality, preventability and severity of ADR in a hospital setting; a prospective
Siraj Sundaran, Anjali Udayan, Keerthi Hareendranath, Basil Eliyas, Babu Ganesan, Ashik Hassan, Rajesh Subash, Vishnu Palakkal, Mohammed Saji Salahudeen   +8 more
doaj   +1 more source

Anaphylatic reactions to biological drugs:data from spontaneous reporting in Italy

, 2013
Anaphylatic reactions to biological drugs:data from spontaneous reporting in ...
Sottosanti L., Opri, Sibilla, Matarengolo E, CONFORTI, Anita, Sabaini A, Zocca, Margherita   +5 more
core   +1 more source