World experience in off-label medicines use is presented in the article. Data on the history of changes in tactics and approaches to solve the problem of medicines off-label use in the USA and some European countries, as well as in the European Union as a whole, are presented. The reasons, why doctors should use medicines off-label, are discussed. The expert opinion on the conditions ensuring the maximum safety in off-label medicines use is presented. In particular, the validity of obtaining patient informed consent is discussed. The article does not apply to the Russian regulation regarding “off-label” therapy but describes the foreign practice related to off-label medicines use. In addition, the results of some recently completed randomiz...
After a drug obtains marketing authorization, the usage depends on the regulation of off-label pre-s...
INTRODUCTION Concern about off-label prescriptions, that is to say prescriptions of a drug for thera...
Para haver o uso de um medicamento, o mesmo passa por um processo de aprovação que procura evidência...
World experience in off-label medicines use is presented in the article. Data on the history of chan...
European Union (EU) legislation on marketing authorisation of medicinal products aims to safeguard p...
Modern medicine faces many significant problems. This Article is about two of them. The first is tha...
Modern medicine faces many significant problems. This Article is about two of them. The first is tha...
96 p.ill.,SCIENTIFIC REPORT .8 -- 1 INTRODUCTION 8 -- 1.1 BACKGROUND AND SCOPE OF THE REPORT 8 -- 1....
The current state of the Russian and foreign regulatory framework for off-label prescription of medi...
For many years, the off-label use of drugs has been a debated issue for healthcare administrators, ...
Approval of a drug for clinical use requires production of data on efficacy and safety through submi...
Background: Medicine use is considered off-label when used for an indication, at a dose, via a route...
• Off-label prescribing is the prescription of a registered medicine for a use that is not included ...
Off-label use of drugs is widely known as unapproved use of approved drugs, and it can be perceived ...
Autor przedstawia europejskie regulacje prawne, które mają zwiększyć dostępność produktów leczniczyc...
After a drug obtains marketing authorization, the usage depends on the regulation of off-label pre-s...
INTRODUCTION Concern about off-label prescriptions, that is to say prescriptions of a drug for thera...
Para haver o uso de um medicamento, o mesmo passa por um processo de aprovação que procura evidência...
World experience in off-label medicines use is presented in the article. Data on the history of chan...
European Union (EU) legislation on marketing authorisation of medicinal products aims to safeguard p...
Modern medicine faces many significant problems. This Article is about two of them. The first is tha...
Modern medicine faces many significant problems. This Article is about two of them. The first is tha...
96 p.ill.,SCIENTIFIC REPORT .8 -- 1 INTRODUCTION 8 -- 1.1 BACKGROUND AND SCOPE OF THE REPORT 8 -- 1....
The current state of the Russian and foreign regulatory framework for off-label prescription of medi...
For many years, the off-label use of drugs has been a debated issue for healthcare administrators, ...
Approval of a drug for clinical use requires production of data on efficacy and safety through submi...
Background: Medicine use is considered off-label when used for an indication, at a dose, via a route...
• Off-label prescribing is the prescription of a registered medicine for a use that is not included ...
Off-label use of drugs is widely known as unapproved use of approved drugs, and it can be perceived ...
Autor przedstawia europejskie regulacje prawne, które mają zwiększyć dostępność produktów leczniczyc...
After a drug obtains marketing authorization, the usage depends on the regulation of off-label pre-s...
INTRODUCTION Concern about off-label prescriptions, that is to say prescriptions of a drug for thera...
Para haver o uso de um medicamento, o mesmo passa por um processo de aprovação que procura evidência...