Anyone suffering from persistent finasteride side effects is encouraged to report them to the appropriate agency.
- If you are living in the United States, please use the FDA's MedWatch Online Voluntary Reporting Form 3500
- For all other countries, download the World Health Organization's Collaborating Centre for International Drug Monitoring list of pharmacovigilance agencies (be sure to scroll down to the world map at the bottom of the page).
FDA Citizen Petition
In September 2017, the PFS Foundation filed a Citizen Petition with the FDA, asking that the agency "require the immediate removal of Propecia (and generic formulations of finasteride, 1 mg, for androgenic alopecia) from the market." To date, the FDA has not responded to the petition, but it can be accessed here at Regulations.gov.
In addition to agencies like the U.S. Food and Drug Administration and World Health Organization, PFS patients are encouraged to report their persistent side effects to RxISK.org, a global, independent pharmacovigilance organization whose database is used by patients, doctors and pharmacists to research prescription drugs and their side effects, ideally to identify problems early on in the life of a drug.