Results 41 to 50 of about 47,791 (152)

A KAP study of pharmacovigilance among junior residents and interns of a tertiary care hospital [PDF]

, 2018
Background: Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other possible drug-related problems.
Korde, Rupa Arun, S., Radhika M.
core   +2 more sources

Neurologic toxicity associated with immune checkpoint inhibitors: a pharmacovigilance study

Journal of Immunotherapy for Cancer, 2019
BackgroundImmune checkpoint inhibitors (ICI) produce durable antitumor responses but provoke autoimmune toxicities, including uncommon but potentially devastating neurologic toxicities. The clinical features, including the spectrum, timing, and outcomes,
Douglas B. Johnson, A. Manouchehri, A. Haugh, Henry T. Quach, J. Balko, B. Lebrun-Vignes, A. Mammen, J. Moslehi, J. Salem   +8 more
semanticscholar   +1 more source

Fatal adverse drug reactions: A worldwide perspective in the World Health Organization pharmacovigilance database

British Journal of Clinical Pharmacology, 2021
Adverse drug reactions (ADRs) are important causes of death. However, the main involved drugs are relatively unknown. The present study was performed to characterise death‐related drugs recorded in a large pharmacovigilance database during the last 10 ...
J. Montastruc, Margaux Lafaurie, Claire de Canecaude, G. Durrieu, A. Sommet, F. Montastruc, H. Bagheri   +6 more
semanticscholar   +1 more source

Strengthening Pharmacovigilance System to Capture Safety Data from HIV Clients on ART in Tanzania: Identification of Gaps in Safety Reporting System [PDF]

, 2013
In Tanzania, pharmacovigilance system is implemented by Tanzania Food and Drugs Authority (TFDA) that monitors drug use countrywide. TFDA is the main national custodian for recording, analyzing and disseminating safety information that is generated ...
Baraka, Vito, Fakih, Bakar, Francis, Filbert, Kabanywanyi, Abdulnoor, Maiga, Deo, Makunde, Williams, Massaga, Julius, Mmbando, Bruno, Msovela, Judith, Mushi, Adiel   +9 more
core  

Cardiovascular Safety Profile of Romosozumab: A Pharmacovigilance Analysis of the US Food and Drug Administration Adverse Event Reporting System (FAERS)

Journal of Clinical Medicine, 2021
Background: Cardiovascular safety concerns for major cardiovascular events (MACE) were raised during the clinical trials of romosozumab. We aimed to evaluate the cardiovascular safety profile of romosozumab in a large pharmacovigilance database. Methods:
Annika Vestergaard Kvist, Junaid Faruque, E. Vallejo-Yagüe, S. Weiler, E. Winter, A. M. Burden   +5 more
semanticscholar   +1 more source

Pharmacokinetic Herb-Drug Interactions: Insight into Mechanisms and Consequences [PDF]

, 2015
Herbal medicines are currently in high demand, and their popularity is steadily increasing. Because of their perceived effectiveness, fewer side effects and relatively low cost, they are being used for the management of numerous medical conditions ...
Horie, Toshiharu, Oga, Enoche Florence, Sekine, Shuichi, Shitara, Yoshihisa   +3 more
core   +1 more source

Comparative study and assessment of the knowledge, attitude and practice of pharmacovigilance among first, second and third professional medical students of PMCH, Dhanbad [PDF]

, 2020
Background: Pharmacovigilance awareness among medical students is very important for preventing ADR underreporting. Present study was conducted to know extent of Pharmacovigilance awareness among students and impact of Pharmacovigilance teaching.Methods:
Choudhary, A. K., Kumari, Mona
core   +2 more sources

A National Adverse Drug Reaction Reporting System for Malta [PDF]

, 2004
The mission of the Medicines Authority (MA) in Malta is to contribute to protection of public health through regulation of the safety, quality and efficacy of medicines for human use on the local market and to ensure that healthcare professionals and ...
Arthur, Niamh, Bonett, Michael, Vella Bonanno, Patricia   +2 more
core  

Exploring healthcare professionals’ knowledge, attitude, and practices towards pharmacovigilance: a cross-sectional survey

Journal of Pharmaceutical Policy and Practice, 2021
Spontaneous reporting of adverse drug reactions (ADRs) is a method of monitoring the safety of drugs and is the basic strategy for the post-marketing surveillance of the suspected drugs.
R. Hussain, M. Hassali, F. Hashmi, Tayyaba Akram   +3 more
semanticscholar   +1 more source

Monitoring the manufacturing and quality of medicines: a fundamental task of pharmacovigilance

Therapeutic Advances in Drug Safety, 2021
The collection and assessment of individual case safety reports (ICSRs) is important to detect unknown adverse drug reactions particularly in the first decade after approval of new chemical entities. However, regulations require that these activities are
M. Sardella, G. Belcher, Calin Lungu, T. Ignoni, Manuela Camisa, D. Stenver, Paolo Porcelli, M. D'antuono, Nicola Gian Castiglione, Anna Adams, Giovanni Furlan, Ilaria Grisoni, Sarah Hall, Laura Boga, Valentina Mancini, Mircea Ciuca, David Chonzi, Brian D Edwards, A. Mangoni, M. Tuccori, E. Prokofyeva, F. De Gregorio, Mario Bertazzoli Grabinski Broglio, Bert van Leeuwen, Paola Kruger, Christian Rausch, H. Le Louet   +26 more
semanticscholar   +1 more source