PRAC December 2023: recommendation of measures to minimise the risk of serious side effects with medicines containing pseudoephedrine

During its December 2023 meeting, the Pharmacovigilance Risk Assessment Committee of the European Medicines Agency recommended new measures for medicines containing pseudoephedrine to minimise the risk of serious side effects and requested further clarifications in the framework of the GLP-1 receptor agonists’ review. 

Annual report on the donation of human body material: increase in the declarations of explicit content and reduction in opposition

In Belgium, each individual, after their death, is presumed to be a potential donor. Since 2020, as well as organ donation, any Belgian citizen has had the option to express their will, explicit consent or opposition to the post-mortem donation of human body material like skin, cartilage, tendons or heart values for transplantation, the manufacture of medicines (advanced therapies) and for scientific research.

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