Pharmacovigilance is important for collecting, detecting, monitoring adverse events which the main objective. The reported should be assessed in order to know casual relationship and avoid unnecessary effects on recipient. Many people are vaccinating a short period, so it becoming much burden pharmacovigilance centers. international society of (ISOP), French national agency medicines health pro...

background: the annual statistics of drug and poison information centers (dpics) have critical role in public health planning. the objective of this study was to provide annual epidemiologic profile of drug inquiry and poisoning-related phone calls to iran's dpics during 2014-2015. methods: this was a descriptive retrospective study by reviewing reported phone calls of iranian dpics to central ...

background: the annual statistics of drug and poison information centers (dpics) have critical role in public health planning. the objective of this study was to provide annual epidemiologic profile of drug inquiry and poisoning-related phone calls to iran’s dpics during 2014-2015. methods: this was a descriptive retrospective study by reviewing reported phone calls of iranian dpics to central ...

While discussions continue about the precise role of data mining in drug safety, there can be little doubt that data mining algorithms have established themselves as a component of the pharmacovigilance “tool-kit”. The drug safety community should facilitate research into the development and testing of novel data mining and statistical algorithms that match the importance and complexity of the ...

The UK Drug Utilization Research Group's (DURG) Regional Meeting 'New Horizons: Pharmacovigilance' was hosted by the Drug Safety Research Unit (DSRU) at Southampton on 19 May 2000. Opening the meeting, Dr Keith Beard, UK DURG chairman, welcomed delegates and speakers and thanked the DSRU team for hosting the meeting. With reference to the theme of the meeting - new horizons in pharmacovigilance...

The introduction in clinical practice of pharmaceutical products known as biosimilars, as part of a more complex series of progress in the field of biological drugs, represents an excellent therapeutic resource. A biosimilar drug is a biological/biotechnological drug that is highly similar to an approved reference biologic product. Given their complexity, biosimilars require attention and a con...

The Therapeutic Goods Administration is strengthening pharmacovigilance, but strategies to encourage the conduct of pharmacoepidemiological research in Australia are needed.

detection of adverse drug reactions (adrs) in hospitals provides an important measure of the burden of drug related morbidity on the healthcare system. spontaneous reporting of adrs is scare and several obstacles to such reporting have been identified formerly. this study aimed to determine the role of clinical pharmacy residents in adr reporting within a hospital setting.clinical pharmacy resi...

background pharmacovigilance (pv) data are crucial for ensuring safety and effectiveness of medicines after drugs have been granted marketing approval. this paper describes the pv systems of india, uganda and south africa based on literature and key informant (ki) interviews and compares them with the world health organization’s (who’s) minimum pv requirements for a functional national pv syste...

d Q-T interval have been reported Lancer 1998;352:162-3. 5 Waller PC, Coulson RA, Wood SM. Regulatory pharmacovigilance in the United Kingdom: current principles and practice. Pharnracoepidemwl Drug Safety 1996;5:363-75. 6 Li Wan Po A, Zhang WY. What lessons can be rk reiterates our learnt from withdrawal of mibefradil from the market? Lancer 1998;351:1829-30. with 7 Lawson DH. Pharmacovigilanc...