Our aim was to investigate the ADR reports of drugs with a monitoring registry (MR drugs), in particular those related to abuse/misuse, medication error, overdose, which might indicate an unsafe use. We compared these reports with those of similar drugs without a registry (non-MR drugs), thus verifying whether the registries could be useful tools for a safer use of innovative drugs
A prospective pharmacovigilance signal detection study, comparing the real-world healthcare data (EU...
Background: In July 2012 a new European legislation (Directive 2010/84/EU and Regulation No. 1235/20...
<p>Rationale: The aim of this study is to investigate if following the implementation of the Regulat...
Introduction: Spontaneous reporting of adverse drug reactions (ADRs) is the basis of pharmacovigilan...
Objectives: The AIFA (Agenzia Italiana del Farmaco - Italian Medicines Agency) Monitoring Registries...
OBJECTIVES: The AIFA (Agenzia Italiana del Farmaco--Italian Medicines Agency) Monitoring Registrie...
Background: Spontaneous reporting of suspected adverse drug reactions (ADR) is considered the eorner...
<p><b>Background</b>: The number of suspected adverse drug reactions (ADRs) yearly submitted to the ...
Objective: To describe the evolution of adverse drug reactions (ADRs) spontaneously reporting in the...
Background: The reporting of adverse drug reactions (ADRs) is the mainstay of post-marketing surveil...
Enormous progress has been made globally in the use of evidence derived from patients’ clinical info...
Rationale: The aim of this study is to investigate if following the implementation of the Regulation...
Objective: To describe the characteristics of pediatric adverse drug reactions (ADRs) reported in It...
A prospective pharmacovigilance signal detection study, comparing the real-world healthcare data (EU...
Background: In July 2012 a new European legislation (Directive 2010/84/EU and Regulation No. 1235/20...
<p>Rationale: The aim of this study is to investigate if following the implementation of the Regulat...
Introduction: Spontaneous reporting of adverse drug reactions (ADRs) is the basis of pharmacovigilan...
Objectives: The AIFA (Agenzia Italiana del Farmaco - Italian Medicines Agency) Monitoring Registries...
OBJECTIVES: The AIFA (Agenzia Italiana del Farmaco--Italian Medicines Agency) Monitoring Registrie...
Background: Spontaneous reporting of suspected adverse drug reactions (ADR) is considered the eorner...
<p><b>Background</b>: The number of suspected adverse drug reactions (ADRs) yearly submitted to the ...
Objective: To describe the evolution of adverse drug reactions (ADRs) spontaneously reporting in the...
Background: The reporting of adverse drug reactions (ADRs) is the mainstay of post-marketing surveil...
Enormous progress has been made globally in the use of evidence derived from patients’ clinical info...
Rationale: The aim of this study is to investigate if following the implementation of the Regulation...
Objective: To describe the characteristics of pediatric adverse drug reactions (ADRs) reported in It...
A prospective pharmacovigilance signal detection study, comparing the real-world healthcare data (EU...
Background: In July 2012 a new European legislation (Directive 2010/84/EU and Regulation No. 1235/20...
<p>Rationale: The aim of this study is to investigate if following the implementation of the Regulat...