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An analysis of completeness and quality of adverse drug reaction reports at an adverse drug reaction monitoring centre in Western India

PURPOSE/AIM: The Adverse Drug Reaction [ADR] form is the source document for the Pharmacovigilance Programme of India [PvPI] and captures information first hand from the patient. The raw data from it then gets converted into an individual case safety report [ICSR] after entry into Vigiflow. The Nati...

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Dettagli Bibliografici
Pubblicato in:Perspect Clin Res
Autori principali: Mahajan, Manali Mangesh, Thatte, Urmila Mukund, Gogtay, Nithya Jaideep, Deshpande, Siddharth
Natura: Artigo
Lingua:Inglês
Pubblicazione: Medknow Publications & Media Pvt Ltd 2018
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6058509/
https://ncbi.nlm.nih.gov/pubmed/30090710
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/picr.PICR_105_17
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