Direct patient reporting of adverse drug reactions (ADRs) is available in many countries, as patients are often knowledgeable about their health conditions and medicines. This study aimed to assess whether patients can recognize ADRs and whether they know how to proceed with ADR reporting. The study also assesses ADR information sources and the main barriers to reporting. Through the purposive and snowball sampling techniques, 42 consumers participated in focus group discussions. All discussions were audio recorded, transcribed verbatim, and analyzed for thematic content analysis. The thematic content analysis yielded four major themes: knowledge about medication safety, ADRs, and pharmacovigilance; information sources about medicines and A...
Background: Health-care professionals across the globe are obligated to report adverse drug reaction...
Objective: To evaluate the perception of drug use among elderly people, about adverse drug reactions...
Continuous monitoring of the safety profile of medicinal products is essential also after marketing ...
Lithuania is the leader in pharmacovigilance among the three Baltic countries. However, comparisons ...
Patient reporting of adverse drug reactions (ADRs) has become an important element of pharmacovigila...
OBJECTIVE: To give an overview of the views of different types of reporters (patients and healthcare...
OBJECTIVE: To give an overview of the views of different types of reporters (patients and healthcare...
Objective: To analyze the attitude of pharmaceutical professionals working in Lithuanian community p...
Introduction: Adverse drug reactions (ADRs) are threat to the patient’s safety and the quality of li...
Introduction: Pharmacovigilance is an arm of patient care. No one wants to harm patients, but unfort...
Background: Patients are important stakeholders in pharmacovigilance; however, little formal evaluat...
Adverse drug reactions (ADRs) are anxious unintended responses to drugs that occur at a dose usually...
Background: Pharmacovigilance systems are crucial for monitoring, ensuring the safe use of medicatio...
Aim: To assess the attitudes and perceptions of medical practitioners towards adverse drug reaction ...
Objectives: Spontaneous reporting is an important tool in pharmacovigilance. However, its success de...
Background: Health-care professionals across the globe are obligated to report adverse drug reaction...
Objective: To evaluate the perception of drug use among elderly people, about adverse drug reactions...
Continuous monitoring of the safety profile of medicinal products is essential also after marketing ...
Lithuania is the leader in pharmacovigilance among the three Baltic countries. However, comparisons ...
Patient reporting of adverse drug reactions (ADRs) has become an important element of pharmacovigila...
OBJECTIVE: To give an overview of the views of different types of reporters (patients and healthcare...
OBJECTIVE: To give an overview of the views of different types of reporters (patients and healthcare...
Objective: To analyze the attitude of pharmaceutical professionals working in Lithuanian community p...
Introduction: Adverse drug reactions (ADRs) are threat to the patient’s safety and the quality of li...
Introduction: Pharmacovigilance is an arm of patient care. No one wants to harm patients, but unfort...
Background: Patients are important stakeholders in pharmacovigilance; however, little formal evaluat...
Adverse drug reactions (ADRs) are anxious unintended responses to drugs that occur at a dose usually...
Background: Pharmacovigilance systems are crucial for monitoring, ensuring the safe use of medicatio...
Aim: To assess the attitudes and perceptions of medical practitioners towards adverse drug reaction ...
Objectives: Spontaneous reporting is an important tool in pharmacovigilance. However, its success de...
Background: Health-care professionals across the globe are obligated to report adverse drug reaction...
Objective: To evaluate the perception of drug use among elderly people, about adverse drug reactions...
Continuous monitoring of the safety profile of medicinal products is essential also after marketing ...