نتایج جستجو برای: pharmacovigilance pv
تعداد نتایج: 26071 فیلتر نتایج به سال:
This paper summarizes the first year of activity of the Ceará State Pharmacovigilance System (SIFACE) as a strategy to discuss practical and methodological problems related to developing pharmacovigilance in Brazil. Siface is being structured by the Group for the Prevention of Improper Use of Pharmaceuticals (GPUIM), based on hospital pharmacies. A total of 63 reports (119 suspected adverse dru...
UNLABELLED Analyzing the pattern and quality of scientific communications on pharmacovigilance can help the regional centers in Nepal and other developing countries to develop approaches for communicating effectively medicine safety issues. This kind of research is lacking in developing countries. OBJECTIVES To analyze the pattern and quality of scientific communications on drug safety produc...
Objective: To assess awareness of pharmacovigilance among the healthcare professionals and to evaluate the impact of an educational intervention for improving awareness of pharmacovigilance among physician, pharmacist and nurses in an Indian tertiary care teaching hospital. Material &Methods: A suitable self-administered Knowledge, attitude, practice (KAP) survey questionnaire was designed, val...
Pharmacovigilance aims to monitor drug safety using sources such as spontaneous reporting systems, biomedical literature or electronic health record data. Clinical trials represent a source of drug-event pairs data complementary to these sources for signal detection in pharmacovigilance platforms. The advantage of ClinicalTrials.gov (CTG) over other pharmacovigilance sources is the large number...
Nonallergic hypersensitivity and allergic reactions are part of the many different types of adverse drug reactions (ADRs). Databases exist for the collection of ADRs. Spontaneous reporting makes up the core data-generating system of pharmacovigilance, but there is a large under-estimation of allergy/hypersensitivity drug reactions. A specific database is therefore required for drug allergy and ...
Pharmacovigilance is a method of quick detection and reporting, of adverse drug reactions and adverse drug events after drug is in clinical use, thus preventing major drug events. Ignorance of physicians in developing world, about reporting adverse drug reaction is a big roadblock to pharmacovigilance. This cascades into many problems e.g.; increased lab to clinic interval, increased premarketi...
Fibrinogen concentrate use as a haemostatic agent has been increasingly explored. This study evaluates spontaneous reports of potential adverse drug reactions (ADRs) that occurred during postmarketing pharmacovigilance of Haemocomplettan P/RiaSTAP, and reviews published safety data. This descriptive study analysed postmarketing safety reports recorded in the CSL Behring pharmacovigilance databa...
Adverse drug reactions (ADRs) till date are still considered as one of the main problems therapy. Pharmacovigilance is monitoring safety by means spontaneous adverse-effect reporting systems, case control and cohort studies.
 This study evaluated levels awareness knowledge pharmacovigilance (i.e., ADR reporting) amongst final year students Rivers State College Health Science Technology, Po...
normal 0 false false false en-us x-none ar-sa microsoftinternetexplorer4 background: pharmacovigilance assesses the safety profile of drugs. its main aim is the increase of spontaneous reporting of adverse drug reactions (adrs).the italian drug agency (aifa; agenzia italianadel farmaco) is financing several projects to the aim of increasing reporting, and in calabria a pharmacovigilance informa...
The objective of this study is to conduct a literature review to assess the importance of pharmacoeconomics in developing pharmacovigilance activities as a working tool to guide the process of decision making in the health field. The authors have done a literature review in order to find information about pharmacovigilance and their relationship with the pharmacoeconomics field, as an important...
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