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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Hlavní autoři:	Manali Mangesh Mahajan, Urmila Mukund Thatte, Nithya Jaideep Gogtay, Siddharth Deshpande
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wolters Kluwer Medknow Publications 2018-01-01
Edice:	Perspectives in Clinical Research
Témata:	ADR form completeness score India instrument pharmacovigilance quality assessment
On-line přístup:	http://www.picronline.org/article.asp?issn=2229-3485;year=2018;volume=9;issue=3;spage=123;epage=126;aulast=Mahajan
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