The safety information on drug labels of a company marketing the same drugs in different countries is sometimes different. The aim of the present study is to understand the differences in the volume and content of safety information on the drug labels from the same manufacturers in three developed countries: the United States of America (USA), the United Kingdom (UK) and Canada. This study involved the calculation of the proportion of total safety information (PSI) and of contraindications (PCI) in comparison to all information on the label and the percentage of boxed warnings (PBW) among the 100 labels studied from each country. The PSI on the labels of different countries is different with USA labels bearing lesser value PSI and UK labels...
Cornelius VR, Liu K, Peacock J, Sharma M, Sauzet O. Useablity of Harm Profile Data in Product Descri...
This study was aimed at assessing the extent of safety learning from data pertaining to other drugs ...
This paper presents a review of the literature, including government legislations, policies, guideli...
Drug package inserts from ten nonsteroidal antiinflammatory drugs marketed in Saudi Arabia were comp...
Cornelius VR, Liu K, Peacock J, Sauzet O. Variation in adverse drug reactions listed in product info...
Purpose: Type 2 diabetes mellitus has reached epidemic proportions worldwide. Many patients with typ...
Objective: The aim of this study was to compare the provision of medicines information in medical ...
The primary focus of the pharmacovigilance (PV) practice has been on the collection, assessment, and...
OBJECTIVE: To compare consistency of adverse drug reaction (ADR) data in publicly available product ...
By going beyond individual case studies and solely quantitative surveys, this paper systematically e...
AIMS: To examine how countries differ in attitudes to adverse drug reactions by examining published ...
Good information on the harm of a drug is vital to inform risk-benefit decisions and undertake robus...
Objectives To assess consistency in the format and content, and overlap of subject and timing, of me...
By going beyond individual case studies and solely quantitative surveys, this paper systematically e...
This study was aimed at assessing the extent of safety learning from data pertaining to other drugs ...
Cornelius VR, Liu K, Peacock J, Sharma M, Sauzet O. Useablity of Harm Profile Data in Product Descri...
This study was aimed at assessing the extent of safety learning from data pertaining to other drugs ...
This paper presents a review of the literature, including government legislations, policies, guideli...
Drug package inserts from ten nonsteroidal antiinflammatory drugs marketed in Saudi Arabia were comp...
Cornelius VR, Liu K, Peacock J, Sauzet O. Variation in adverse drug reactions listed in product info...
Purpose: Type 2 diabetes mellitus has reached epidemic proportions worldwide. Many patients with typ...
Objective: The aim of this study was to compare the provision of medicines information in medical ...
The primary focus of the pharmacovigilance (PV) practice has been on the collection, assessment, and...
OBJECTIVE: To compare consistency of adverse drug reaction (ADR) data in publicly available product ...
By going beyond individual case studies and solely quantitative surveys, this paper systematically e...
AIMS: To examine how countries differ in attitudes to adverse drug reactions by examining published ...
Good information on the harm of a drug is vital to inform risk-benefit decisions and undertake robus...
Objectives To assess consistency in the format and content, and overlap of subject and timing, of me...
By going beyond individual case studies and solely quantitative surveys, this paper systematically e...
This study was aimed at assessing the extent of safety learning from data pertaining to other drugs ...
Cornelius VR, Liu K, Peacock J, Sharma M, Sauzet O. Useablity of Harm Profile Data in Product Descri...
This study was aimed at assessing the extent of safety learning from data pertaining to other drugs ...
This paper presents a review of the literature, including government legislations, policies, guideli...