PFS Foundation

We facilitate clinical research on PFS, generate awareness of the condition, provide support to PFS patients and lobby for stricter regulations on finasteride.

[PFS Foundation @PFSFoundation]

https://t.co/yrtCJDWIee #PostFinasterideSyndrome

[PFS Foundation @PFSFoundation]

https://t.co/tJ8AFc7xyw

#PostFinasterideSyndrome

[PFS Foundation @PFSFoundation]

@SamaHoole Excellent summation of the problem!

[PFS Foundation @PFSFoundation]

@katug05 Such cases are not rare. This is a true epidemic.

[PFS Foundation @PFSFoundation]

https://t.co/TWZ5z1TY42

[PFS Foundation @PFSFoundation]

https://t.co/vjuDercjoc

[PFS Foundation @PFSFoundation]

Citing 19 Suicides and 170 Reports of Suicidal Ideation, British Regulator MHRA Announces Label Changes and Other Measures to Minimize Finasteride’s Risks #PostFinasterideSyndrome https://t.co/8641AScudP

[PFS Foundation @PFSFoundation]

"I Couldn't Find Any Doctor Willing to Help Me… I'm Desperate," Jalan Lotfolahpour Wrote to the PFS Foundation at Age 20. Six Years Later, He Was Found Dead After Mixed-Drug Intoxication #PostFinasterideSyndrome https://t.co/rB1P9accwN

[PFS Foundation @PFSFoundation]

Robb Dixon of SIDEfxHUB interviews Dr. Will Powers, fresh off his attendance at the First World Congress on PSSD, PFS and PAS #PostFinasterideSyndrome https://t.co/WFQSLJdSdX

[PFS Foundation @PFSFoundation]

David Healy, MD, Chief Scientific Officer at Data Based Medicine, weighs in on last week's First World Congress on PSSD, PFS and PAS #PostFinasterideSyndrome https://t.co/WBlngCpP2U

[PFS Foundation @PFSFoundation]

https://t.co/b8n18SNEfq

[PFS Foundation @PFSFoundation]

Robb Dixon of SIDEfxHUB sits down with Dr. Ken Peters of William Beaumont School of Medicine, who organized the First World Congress on PSSD, PFS and PAS, to discuss the event—and next steps #PostFinasterideSyndrome https://t.co/XoopiqTuRH

[PFS Foundation @PFSFoundation]

@Lex0cpq Good question. But for the moment, suffice it to say that the team will soon start plotting out the resultant paper that will appear in JSM. And that paper, ideally, will include next steps re new research and funding efforts. The moment I have anything to report, I will do so.

[PFS Foundation @PFSFoundation]

#PostFinasterideSyndrome

[PFS Foundation @PFSFoundation]

#PostFinasterideSyndrome

[PFS Foundation @PFSFoundation]

#PostFinasterideSyndrome

[PFS Foundation @PFSFoundation]

Beginning tomorrow, getting finasteride in France will require informed consent, as the French press is reminding everyone #PostFinasterideSyndrome https://t.co/jSQd9mkZxr

[PFS Foundation @PFSFoundation]

“I...would never take the medication,” said urologist Jonathan Clavell. “Because if I were one of the unlucky few who turns out to get [PFS], I know I’d regret it.” #PostFinasterideSyndrome https://t.co/wk6nqfUUfV

[PFS Foundation @PFSFoundation]

Just realized that Kevin Ali, the CEO of Organon, which currently owns Propecia, was booted in October due to improper sales practices. Reuters: "Ali has agreed he will not be entitled to [his] severance." #PostFinasterideSyndrome https://t.co/vqvITol64D

[PFS Foundation @PFSFoundation]

"The Post-Finasteride Syndrome Foundation...has recorded nearly 27,000 adverse reactions to the drug worldwide and 126 known suicides," reports Men's Health UK in We Need to Talk About Finasteride #PostFinasterideSyndrome https://t.co/c88UsRKpLO