Print Page - any experience with PIRFENIDONE?

Title: any experience with PIRFENIDONE?
Post by: pey ron on April 08, 2018, 03:54:19 PM

Has anyone tried oral Pirfenidone?

Any experience? Any report of any improvement?

Title: Re: any experience with PIRFENIDONE?
Post by: james1947 on April 17, 2018, 06:47:52 AM

I don't think that some doctor will prescribe it for Peyronies.
Is for treatment of idiopathic pulmonary fibrosis (IPF).
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936814/

James

Title: Re: any experience with PIRFENIDONE?
Post by: pey ron on April 17, 2018, 03:06:35 PM

There are ways to procure it without a prescription. I am not advising anyone to self-medicate, but I'd like to hear the experiences from those who did.

Title: Re: any experience with PIRFENIDONE?
Post by: james1947 on April 20, 2018, 08:45:09 AM

Let's wait the answers Pey Ron :)

James

Title: Re: any experience with PIRFENIDONE?
Post by: pey ron on May 12, 2018, 03:28:27 AM

Anti-fibrotic action of pirfenidone in Dupuytren's disease-derived fibroblasts.

zhou2016.pdf - DocDroid (http://docdro.id/utoODgm)

Also relevant, this anecdotal evidence:

https://www.dupuytren-online.info/Forum_English/board/forum-archive-1/pirfenidone-3_2104.html

Peyronies Society Forums

Peyronies Disease TREATMENT Discussion Boards => Developmental Drugs & Treatments => Topic started by: pey ron on April 08, 2018, 03:54:19 PM