To review studies on the readability of package leaflets of medicinal products for human use. We conducted a systematic literature review between 2008 and 2013 using the keywords “Readability and Package Leaflet” and “Readability and Package Insert” in the academic search engine Biblioteca do Conhecimento Online, comprising different bibliographic resources/databases. The preferred reporting items for systematic reviews and meta-analyses criteria were applied to prepare the draft of the report. Quantitative and qualitative original studies were included. Opinion or review studies not written in English, Portuguese, Italian, French, or Spanish were excluded. We identified 202 studies, of which 180 were excluded and 22 were enrolled [two enro...
Background: Patient education is taken into account as one of the key components of comprehensive ca...
The non-adherence to and non-compliance with the prescribed course of medication are considered seri...
Package leaflet is regulated by the law with the neccessary information about a particular drug and ...
OBJECTIVE: To review studies on the readability of package leaflets of medicinal products for human ...
To review studies on the readability of package leaflets of medicinal products for human use. We con...
Tese de doutoramento, Farmácia (Sócio Farmácia), Universidade de Lisboa, Faculdade de Farmácia, 2016...
In Europe, package leaflets and the outside of medicine packaging provide information about medicine...
Purpose To explore and compare the opinions of physicians, pharmacists and potential users on the r...
ABSTRACT: Introduction: The written information on medicines has been acknowledged as an important...
Objectives: To assess the degree of readability and the length of the package leaflets of biosimilar...
Background: The package leaflet included in the packaging of all medicinal products plays an importa...
This article presents some findings which deal with text readability, obtained in a research project...
Introduction: All medicines for human use are marketed with a package leaflet. Every package leaflet...
An Analysis of the Factors influencing the Reading Package Leaflets of the Medical Products. The goa...
The graphical content of the Medicines Package Inserts (MPIs), such as illustrations and typographic...
Background: Patient education is taken into account as one of the key components of comprehensive ca...
The non-adherence to and non-compliance with the prescribed course of medication are considered seri...
Package leaflet is regulated by the law with the neccessary information about a particular drug and ...
OBJECTIVE: To review studies on the readability of package leaflets of medicinal products for human ...
To review studies on the readability of package leaflets of medicinal products for human use. We con...
Tese de doutoramento, Farmácia (Sócio Farmácia), Universidade de Lisboa, Faculdade de Farmácia, 2016...
In Europe, package leaflets and the outside of medicine packaging provide information about medicine...
Purpose To explore and compare the opinions of physicians, pharmacists and potential users on the r...
ABSTRACT: Introduction: The written information on medicines has been acknowledged as an important...
Objectives: To assess the degree of readability and the length of the package leaflets of biosimilar...
Background: The package leaflet included in the packaging of all medicinal products plays an importa...
This article presents some findings which deal with text readability, obtained in a research project...
Introduction: All medicines for human use are marketed with a package leaflet. Every package leaflet...
An Analysis of the Factors influencing the Reading Package Leaflets of the Medical Products. The goa...
The graphical content of the Medicines Package Inserts (MPIs), such as illustrations and typographic...
Background: Patient education is taken into account as one of the key components of comprehensive ca...
The non-adherence to and non-compliance with the prescribed course of medication are considered seri...
Package leaflet is regulated by the law with the neccessary information about a particular drug and ...