Patient information leaflets (PILs) are required with all licensed medicines throughout the European Union (EU) and they must include information about all side effects and their likelihood. This has led to criticism of a lack of balance, with little information included about potential benefits. Recent European Medicines Agency guidance proposed the inclusion of benefit information, and this study examined the current prevalence and type of such information in PILs in the EU.A survey and content analysis of the English translation of PILs in the EUwas carried out. Random quota sampling was used on the most frequently dispensed (n = 50) and newly licensed medicines (n = 50) in 2011/2. Leaflets were searched for benefit information meeting p...
Objective: Product Information Leaflets (PILs) are an important source of information for patients o...
<p><strong>Abstract</strong> – This paper analyses how Patient Information Leaflets (PILs) of over-t...
Package leaflet is regulated by the law with the neccessary information about a particular drug and ...
INTRODUCTION: Patient information leaflets (PILs) are required with all licensed medicines throughou...
Introduction: Patients’ perceptions of side effect risks are important influences on their medicine-...
Objectives: To explore consumers’ beliefs and preferences for benefit information in medicine leafle...
Information about medicines in Europe does not really fulfil its potential. For patients, it is ofte...
Introduction: Criticisms of the mandated patient information leaflets (PILs) supplied with all medic...
This paper analyses how Patient Information Leaflets (PILs) of over-the-counter medical products co...
IntroductionThai patients do not routinely receive patient information leaflets (PILs) with medicine...
IntroductionThai patients do not routinely receive patient information leaflets (PILs) with medicine...
Objective To evaluate the frequency with which relevant and accurate information about the benefits ...
Objective -- to compare the acceptability and the degree of understandability of two drug informatio...
Background: In the European Union (EU), all medicines are mandated to be provided with a patient inf...
Objective: Product Information Leaflets (PILs) are an important source of information for patients o...
Objective: Product Information Leaflets (PILs) are an important source of information for patients o...
<p><strong>Abstract</strong> – This paper analyses how Patient Information Leaflets (PILs) of over-t...
Package leaflet is regulated by the law with the neccessary information about a particular drug and ...
INTRODUCTION: Patient information leaflets (PILs) are required with all licensed medicines throughou...
Introduction: Patients’ perceptions of side effect risks are important influences on their medicine-...
Objectives: To explore consumers’ beliefs and preferences for benefit information in medicine leafle...
Information about medicines in Europe does not really fulfil its potential. For patients, it is ofte...
Introduction: Criticisms of the mandated patient information leaflets (PILs) supplied with all medic...
This paper analyses how Patient Information Leaflets (PILs) of over-the-counter medical products co...
IntroductionThai patients do not routinely receive patient information leaflets (PILs) with medicine...
IntroductionThai patients do not routinely receive patient information leaflets (PILs) with medicine...
Objective To evaluate the frequency with which relevant and accurate information about the benefits ...
Objective -- to compare the acceptability and the degree of understandability of two drug informatio...
Background: In the European Union (EU), all medicines are mandated to be provided with a patient inf...
Objective: Product Information Leaflets (PILs) are an important source of information for patients o...
Objective: Product Information Leaflets (PILs) are an important source of information for patients o...
<p><strong>Abstract</strong> – This paper analyses how Patient Information Leaflets (PILs) of over-t...
Package leaflet is regulated by the law with the neccessary information about a particular drug and ...