beeldscherm schreef op 18 november 2018 10:43:
www.fda.gov/NewsEvents/Newsroom/Press...Statement by FDA Commissioner Scott Gottlieb, M.D., on the FDA’s efforts to hold industry accountable for fulfilling critical post-marketing studies of the benefits, safety of new drugs
The FDA remains committed to ensuring that FDA-approved drugs are safe and effective for Americans. As part of this commitment, we require evidence from premarket clinical trials that the medicine will be both effective and safe for use when prescribed according to its labeling. However, it’s not unusual for the FDA to identify issues that need additional evaluation either at the time of initial approval or later, once the drug has been marketed. These issues are evaluated through the conduct of additional post-marketing studies.
These post-approval studies are vital to enhancing patient safety and public health. They may be needed to further characterize the use of the product in the therapeutic armamentarium. Additionally, post-approval studies can allow for further evaluation of a potential safety issue or better characterize risk factors for a known safety issue. Once a drug is approved, invariably a larger population and wider range of patients will use the drug than were studied before approval. With this larger patient experience, new potential safety issues may emerge that were not seen in the studies conducted prior to approval. And such issues may require additional evaluation after the drug is marketed and used by patients for a period of time.
ik heb hier nogeens over nagedacht maar infeite kan dit niet want hiermee word bevestigd dat het Grote Geld regeert, VB Shire Lana in relatie met Ruconest Pharming,waar de ene word goedgekeurd met weinig Data, word de andere (nog) niet goed bevonden met (weinig ?) Data.....kk en een Shire (Takeda) kan in het geval van een claim dit makkelijker ophoesten dan een Pharming maw een kleiner bedrijf zal nogeens goed nadenken alvorens.....