Canada14d
Submit an adverse event following immunization (AEFI) report to a province, territory or government department
A health care professional can submit an AEFI report. If you are a vaccine recipient who has recently been vaccinated and have experienced an adverse event following immunization, please ask your ...
Frontiers23d
Adverse event reporting of faricimab: a disproportionality analysis of FDA adverse event reporting system (FAERS) database
Given its increasingly widespread use in retinal vascular diseases, understanding its adverse events (AEs) in real-world settings is crucial. This study employed the FDA Adverse Event Reporting System ...
FierceBiotech1mon
Pliant discontinues late-stage lung disease trial for lead asset after safety review
Pliant Therapeutics has discontinued a phase 2b/3 trial after recording at least a 7% higher rate of adverse events tied to idiopathic pulmonary fibrosis (IPF) in the treatment arms compared to ...
Indiatimes1mon
Indian-made generic drugs linked to more severe adverse events than US equivalents, study finds
A new study reveals that generic drugs manufactured in India have a higher association with severe adverse events such as hospitalization, disability, and death compared to those made in the U.S ...