Purpose: Biologic agent-induced cardiotoxicity is markedly concerning. Rheumatoid arthritis (RA) treated with biologic agents is known to have the potential for cardiotoxicity; however, existing clinical evidence is not adequate to explain real-world patterns of cardiotoxicity. In this study, we quantify the risk of cardiotoxicity in patients with rheumatoid arthritis treated with biological agents.Methods: Cardiotoxicity reports induced by four types of biologic agents, abatacept, adalimumab, tocilizumab, and etanercept were used to mine data from the FDA's adverse event reporting system (FAERS) database from January 1, 2004 through September 30, 2020. Reports of cardiotoxic events were analyzed using a reporting odds ratio (ROR) algorithm...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Romosozumab is a novel drug for the treatment of osteoporosis. The adverse reactions of romosozumab ...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Introduction: The molecular and pharmacological complexity of biologic disease-modifying antirheum...
BACKGROUND: Baricitinib is approved for the treatment of rheumatoid arthritis (RA). The authors retr...
Objectives: To describe the cumulative incidences of adverse drug reactions (ADRs) associated with d...
OBJECTIVE: Adverse event reports (AERs) submitted to the US Food and Drug Administration (FDA) were ...
Adverse event reports (AERs) submitted to the US Food and Drug Administration (FDA) were reviewed to...
Objective To explore the potential adverse reactions of acalabrutinib by mining and analyzing the ph...
ObjectiveOver the years when biologic psoriasis therapies (TNF inhibitors, IL-12/23 inhibitors, IL-2...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
AbstractObjectiveTargeted drugs dramatically improve the treatment outcomes in cancer patients; howe...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Background: Despite their efficacy, immune checkpoint inhibitors (ICIs) can cause significant immune...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Romosozumab is a novel drug for the treatment of osteoporosis. The adverse reactions of romosozumab ...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Introduction: The molecular and pharmacological complexity of biologic disease-modifying antirheum...
BACKGROUND: Baricitinib is approved for the treatment of rheumatoid arthritis (RA). The authors retr...
Objectives: To describe the cumulative incidences of adverse drug reactions (ADRs) associated with d...
OBJECTIVE: Adverse event reports (AERs) submitted to the US Food and Drug Administration (FDA) were ...
Adverse event reports (AERs) submitted to the US Food and Drug Administration (FDA) were reviewed to...
Objective To explore the potential adverse reactions of acalabrutinib by mining and analyzing the ph...
ObjectiveOver the years when biologic psoriasis therapies (TNF inhibitors, IL-12/23 inhibitors, IL-2...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
AbstractObjectiveTargeted drugs dramatically improve the treatment outcomes in cancer patients; howe...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Background: Despite their efficacy, immune checkpoint inhibitors (ICIs) can cause significant immune...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Romosozumab is a novel drug for the treatment of osteoporosis. The adverse reactions of romosozumab ...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...