Adverse events associated with use of immunoglobulin in pediatric patients reported to the US Food and Drug Administration Adverse Event Reporting System, 2001-2023. [PDF]
Wei S +4 more
europepmc +1 more source
Postmarketing safety surveillance for GSK's AS01<sub>E</sub>-adjuvanted respiratory syncytial virus prefusion F protein-based vaccine in the USA: protocol for a non-interventional postauthorisation safety study. [PDF]
Adimadhyam S +19 more
europepmc +1 more source
Controversial efficacy of antithrombin followed by recombinant thrombomodulin administration in patients with sepsis-induced disseminated intravascular coagulation: an analysis of postmarketing surveillance data. [PDF]
Eguchi Y, Nagafuchi H, Ikeda T.
europepmc +1 more source
After the green light: Evaluating drugs in Phase IV studies.
Meher BR, Mishra A.
europepmc +1 more source
GLP-1 receptor agonists and functional gastrointestinal obstruction: mechanistic rationale, emerging evidence, and clinical implications. [PDF]
Riaz L +4 more
europepmc +1 more source
The Value of A Postmarket Knowledge Exchange [PDF]
openaire +2 more sources
Postmarket Safety Actions for Novel Oncology Drugs Granted FDA's Accelerated Approval.
Mooghali M +4 more
europepmc +1 more source
Policy Without Penalty: A Review of Pediatric Research Equity Act Noncompliance Letters. [PDF]
Green DJ +3 more
europepmc +1 more source
Navigating hepatotoxicity of antibody-drug conjugates: from mechanistic insights to clinical and postmarketing evidence. [PDF]
Dong Y +9 more
europepmc +1 more source
Unanticipated Adverse Events With Tirzepatide: Three Cases Underscoring the Importance of Postmarketing Monitoring. [PDF]
Colorado M +2 more
europepmc +1 more source

