How long for Pentox to work?

Previous topic - Next topic

0 Members and 1 Guest are viewing this topic.

sonnyjim

I have been taking Pentox for 4 months now but haven't noticed any difference.

How long should I take it for before deciding that it isn't worth taking?

How long before I notice anything?
33yo, single
severe ed caused by injury to cs, soft glans, lack of sensation
penile implant: ams lgx 700

Gabriel

Sonny,

I've been taking pentox for one year, and never have seemed to notice any tiny difference from it.

BUT, there is SO much scientific evidence supporting its high probability to help us somehow, that I do plan on taking it as long as my Peyronie is there (at least, still active, or me still trying to regain length loss with traction).
- 35 yo, Peyronies Disease with chronic pain, general hourglassing with girth and length loss since 09/01/17.
- Pain almost cured with Hirudoid cream and diet/lifestyle changes (see my topics on this); deformity still here, but partly reduced with traction + VED.

sonnyjim

And how long have you had peyronies for ?

So why keep taking it if it does nothing? Because some study says it does ?
33yo, single
severe ed caused by injury to cs, soft glans, lack of sensation
penile implant: ams lgx 700

Vvv

What exactly do you expect Pentox to do? It does not cure, it only thins the blood when taking it

TonySa

Yes, in some cases reversed plaque-best to also include traction/VED
PxD 2 yrs 9/16.  Failed all treatment. 9/11/18: excision, grafting & implant Dr Karpman MtnView Ca, AMS CX 18cm + 3-1cm RTEs.
Pump failed.  2/11/20 Dr Karpman installed Titan 22cm +1cm RTE.

sonnyjim

After the acute stage though it's apparently useless right?

I must be past the acute stage so wondering if it is worth taking it still.
33yo, single
severe ed caused by injury to cs, soft glans, lack of sensation
penile implant: ams lgx 700

Gabriel

Sonny,

I've been in Peyronies Disease for 1 year and 1 month now; still acute (albeit finishing... well I hope so) ; and yes, still taking PTX only because studies and a LOT of anecdotical evidence and testimonies here support it.

I can't tell whether pentox played a role in my recent subsiding of pain, nor can I tell if the deformity would have been worse without me taking it for so long ; but I'm just doing a little math, relying on probabilities, and tell myself pentox is not a thing that I should stop taking right now (although I'm just taking 2*400mg and 1*400mg every other day, because it gives me annoying side effects, principally on heartbeats and fatigue).

About its utility in the chronic stage, things have already been discussed: if I'm not mistaken, there was kind of a consensus on pentox+cialis probably supporting traction/VED therapies... But we are here in the field of the experimental and anecdotical, so you'll have to test it on yourself (which I recommend you)!

- 35 yo, Peyronies Disease with chronic pain, general hourglassing with girth and length loss since 09/01/17.
- Pain almost cured with Hirudoid cream and diet/lifestyle changes (see my topics on this); deformity still here, but partly reduced with traction + VED.

sonnyjim

I have been for 4 months so far still noticed nothing. I am totally pissed off I wasn't told this in the early stages when I could of actually took it and probably avoided the ED and pain for a year.

Maybe I wouldn't be in this situation now with absolutely no feeling in my penis and no morning woods or spontaneous erections even with Viagra.

I will probably hang myself if I see no improvements soon because I can't live like this for one more year let alone for the rest of my life.

33yo, single
severe ed caused by injury to cs, soft glans, lack of sensation
penile implant: ams lgx 700