Thalidomide to treat multiple myeloma

 

Few drugs, if any, have achieved the sad notoriety of thalidomide. Introduced in the late 1950s, it caused congenital birth defects in thousands of children worldwide and has been one of the most cautionary tales in the history of medicine. The medicine was banned at the beginning of the 1960s. During the years that followed, some beneficial effects of thalidomide were recognised for various disorders, and in Europe, since the ban, thalidomide has been used off-license and prescribed on a compassionate basis, mainly in hospitals.
 
In 2002, the European Medicines Agency (EMEA) received four marketing authorisation applications for thalidomide, which brought issues back to the surface. For the thalidomide victim associations, it was simply unacceptable that the drug be licensed again, and for the patient associations, it represented a major medical progress against their ailment.
 
As of 2006, however, no marketing applications had been authorised. Eurordis continued to work with all stakeholders to encourage marketing authorisation for thalidomide under strong safety guidelines.
 
For more information: Eurordis’ newsletter article - November 2006

 

 
 
A voz das pessoas com doenças raras na EuropaEURORDIS A voz internacional das pessoas com doenças raras, Rare Diseases InternacionalRare Disease International Reúne doentes, famílias e especialistas para partilhar experiências num fórum multilinguístico. RareConnect O programa Rare Barometer é uma iniciativa da EURORDIS para a realização de inquéritos para transformar a experiência das pessoas com doenças raras em números e factos que podem ser partilhados com os responsáveis pela tomada de decisões.Rare Barometer An international awareness raising campaign taking place on the last day of February each year, Rare Disease Day is a EURORDIS initiativeRare Disease Day Adira ao maior encontro europeu das partes interessadas no âmbito das doenças raras na Conferência Bienal Europeia sobre Doenças Raras e Produtos Órfãos. A ECRD é uma iniciativa da EURORDISEuropean Conference on Rare Diseases