Safety and efficacy are essential in the process of disease treatment. However, off-label medication use is inevitable because various medications do not contain regulatory labels for pediatric use. We aimed to examine off-label medication use and analyze the risk factors correlated with adverse drug reactions (ADRs). This study was performed retrospectively using electronic medical data from a pediatric intensive care unit (PICU) of a tertiary hospital in Korea from July 2019 to June 2020. A total 6,183 prescribed medications from 502 PICU patients were examined in the present study. A total of 80% were infants or children, and 96.0% of them were treated with off-label medications. It was discovered that 4,778 off-label cases (77.2%) of th...
Objective: To investigate the incidence and characteristics of hospital admissions related to advers...
The use of medicinal products (MP) with contraventions of officially approved instructions regulatio...
Background: Prescribing medications for an indication or age outside of the terms of U.S. Food and D...
Background: Given the growing use of off-label in pediatric practice, there is a growing interest on...
Background: A lack of drug safety and efficacy studies in pediatric patients is a major problem cont...
Objectives: The study objectives were to (1) determine the types and frequency of off-label (OL) or ...
Background. In the absence of standard pediatric prescribing information, clinicians often use medic...
Abstract Background Among factors influencing the higher risk of developing unknown or rare advers...
This review aims to give an updated overview of the worldwide situation of off-label and unlicensed ...
Introduction: There is a lack of pediatric documentation concerning efficacy and safety of many dru...
AIMS: The risk to develop adverse drug reactions (ADRs) is high for paediatric patients. This is, am...
Recently published studies examining the extent of off-label drug prescribing in various European pa...
Objectives: To characterise the prescription of non-formulary drugs to children and neonates at a Br...
Objective. To establish risk factors of unlicensed and off-label drug use by children outside the ho...
Despite the high prevalence of potential drug-drug interactions in pediatric intensive care units, t...
Objective: To investigate the incidence and characteristics of hospital admissions related to advers...
The use of medicinal products (MP) with contraventions of officially approved instructions regulatio...
Background: Prescribing medications for an indication or age outside of the terms of U.S. Food and D...
Background: Given the growing use of off-label in pediatric practice, there is a growing interest on...
Background: A lack of drug safety and efficacy studies in pediatric patients is a major problem cont...
Objectives: The study objectives were to (1) determine the types and frequency of off-label (OL) or ...
Background. In the absence of standard pediatric prescribing information, clinicians often use medic...
Abstract Background Among factors influencing the higher risk of developing unknown or rare advers...
This review aims to give an updated overview of the worldwide situation of off-label and unlicensed ...
Introduction: There is a lack of pediatric documentation concerning efficacy and safety of many dru...
AIMS: The risk to develop adverse drug reactions (ADRs) is high for paediatric patients. This is, am...
Recently published studies examining the extent of off-label drug prescribing in various European pa...
Objectives: To characterise the prescription of non-formulary drugs to children and neonates at a Br...
Objective. To establish risk factors of unlicensed and off-label drug use by children outside the ho...
Despite the high prevalence of potential drug-drug interactions in pediatric intensive care units, t...
Objective: To investigate the incidence and characteristics of hospital admissions related to advers...
The use of medicinal products (MP) with contraventions of officially approved instructions regulatio...
Background: Prescribing medications for an indication or age outside of the terms of U.S. Food and D...