The system should inform on medicines’ benefits and risks evaluation and on risks connected to misuse, the federation said, adding that the French need to have clear reference points on drugs.
Furthermore, Leem asked for initiatives to increase the awareness of French people, whilst offering to participate in these campaigns with tangible actions.
The federation pointed out that the side effects of third- and fourth-generation pills are well-known since long, they are indicated in the marketing authorisation and have been included in the patient information leaflet.
Drugs are developed by following a particularly demanding process, depending on a favourable benefit/risk ratio, which is regularly re-examined by healthcare authorities, Leem said.
Kexing Biopharm begins enrolment for Phase I trial of GB10 in China
Lupeng Pharmaceutical's rocbrutinib receives Chinese approval to treat R/R mantle cell lymphoma
Pharming secures FDA acceptance of Joenja filing for children with APDS
UCB and Biogen present Phase 3 data highlighting potential of dapirolizumab pegol in lupus treatment
Persist AI partners with Microsize and Micromacinazione to launch drug formulation platform
RedHill Biopharma advancing opaganib options for Ebola outbreak
Sun Pharma receives American Skin Association 2026 Corporate Leadership Award
Evogene completes Phase 1 study of BMC128 in combination with Nivolumab