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Drug-induced risk of depression: A 20-year real-world pharmacovigilance analysis based on the FAERS database. [PDF]

Medicine (Baltimore)
Xiang X, Yin L, Deng C, Feng Q.
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Adverse reactions to cosmetics reported to the Chongqing adverse drug reaction monitoring centre system in China

Contact Dermatitis, 2022
AbstractBackgroundCosmetic adverse reactions (CARs) are becoming widespread in China. However, a comprehensive analysis of data is lacking.ObjectiveTo analyse the clinical characteristics of patients with reported adverse reactions to cosmetics in Chongqing, China.MethodsCases with CARs reported to the Chongqing Adverse Drug Reaction Monitoring Centre ...
Sha Wang, Yang Jiang, Jing Lyu, Jiajia Li, Qingchun Diao   +4 more
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Evolution of Adverse drug reactions reporting systems: Paper-based to software-based

European Journal of Clinical Pharmacology, 2022
Abstract Adverse Drug Reactions (ADR) add a significant clinical and economic burden to the healthcare system of a country. Reporting ADRs is the cornerstone of detecting uncommon ADRs once the drugs are on the market. In many countries, ADR reporting is regulated by national regulatory bodies and various methods are employed to report ADRs.
M. T. Madhushika, T. P. Weerarathna, P. L. G. C. Liyanage, S. S. Jayasinghe   +3 more
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Systemic Barriers and Potential Concerns from Reporting Serious Adverse Drug Reactions

2022
About 1-10% of all serious adverse drug reactions (sADRs) are reported to the Food and Drug Administration (FDA) ( Moore T, Bennett C. Underreporting of Hemorrhagic and Thrombotic Complications of Pharmaceuticals to the U.S. Food and Drug Administration: Empirical Findings for Warfarin, Clopidogrel, Ticlopidine, and Thalidomide from the Southern ...
Matthew A, Taylor, Ashley C, Godwin, Shamia, Hoque, Charles L, Bennett   +3 more
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Assessing Adverse Drug Reactions Reported for New Respiratory Medications in the FDA Adverse Event Reporting System Database

Respiratory Care, 2021
Between 2012 and 2017, 25 new medications or combination products were approved by the Food and Drug Administration (FDA) for use in treatment of chronic lower respiratory diseases (CLRDs). With limited data on post-marketing patient exposure to these drugs, their safety profiles remain unknown. This study aims to provide post-marketing surveillance of
Hyunwoo, Kim, Colin M, Pfeiffer, Matthew P, Gray, Britney A, Stottlemyer, Richard D, Boyce, Sandra L, Kane-Gill   +5 more
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Patient satisfaction with a hospital adverse drug reaction reporting system

Journal of Pharmacy Practice and Research, 2020
AbstractAimTo evaluate patients' satisfaction with the adverse drug reactions (ADR) warning card model used within a metropolitan hospital network in Melbourne, Australia.Methods and ResultsA cross‐sectional survey, with interviewer‐administered questionnaire, of patients who experienced an ADR was conducted.
Matthew W. Scott, Michael McDonough, Grace O. Wong, Richard Summers, Marion Joy Spark   +4 more
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Identifying adverse reactions to drugs reporting systems

Clinics in Dermatology, 1986
Abstract The dermatologist's concern about adverse reactions to drugs can be viewed from two perspectives. Most often, dermatologists are confronted with skin reactions to drugs used in the treatment of a wide variety of noncutaneous diseases. Less frequently, but sometimes more dramatically, dermatologists care for a patient who may have developed a ...
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Developing an Adverse Drug Reaction Reporting System at a Teaching Hospital

Basic & Clinical Pharmacology & Toxicology, 2008
Abstract:  Adverse drug reactions (ADRs) are a frequent cause for hospitalization and occur often in hospitalized patients. The objective of this study was to establish an ADR reporting and monitoring system at a teaching hospital. The pharmacovigilance unit of Masih Daneshvari hospital was established by a clinical pharmacist and a clinical ...
Shadi, Baniasadi, Fanak, Fahimi, Gloria, Shalviri   +2 more
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