The new "Trebinase"... Worth the try or is it another snake oil ?

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Gabriel

Hello guys,

While browsing Amazon for new oral solutions that I know have very few chances to work, I stumbled into this: https://www.amazon.com/Trebinase-Serrapeptase-Nattokinase-Lumbrokinase-Available/dp/B06Y2HPZNR, with the official "Please-buy-my-miracle-product" website: https://www.pivotalhealth.info/trebinase/

So, basically it contains stuff that some of us already experienced without any success (nattokinase), stuff on which we seem to have mixed feelings (bromelain, serrapeptase), and stuff I absolutely don't know but seem to be relevant for Peyronies Disease (lumbrokinase, seaprose, protease, lipase, amla). About seaprose, there seem to be very few solid information about it; I just found one Wikipedia article in italian, which explains it is supposed to be a good multi-purpose and fibrinolytic enzyme, as for lumbrokinase.

In my opinion, all of this reminds of the unfortunately well-known "Super-cool-new-miracle-enzyme" drill; but does someone have another feeling (and maybe enough useless money to try these caps for a few months  :D) ?  
- 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.

TonySa

I'm thinking of spending a extra $240 a month on H-100 since there is one study supporting it.  My reluctance is it's overpriced for a compounded medication and Dr Levine on the original study is not mentioned on the website—maybe he doesn't believe in it?  At least some support vs this supplement website...who knows what's actually in the pills unless it carries the regulated USP label, but interested to hear anyone's experience.
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.

pey ron

I would try it but I don't think I can. I am already taking north of 6000mg of pentox a day, if I add fibrinolytic enzymes I might get a brain aneurysm or intestinal bleeding. And since I'm too young for Peyronies, I am also too young to die...
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james1947

Pey Ron

6000 mg Pentox per day is 5 time the regular dose of 1200 mg per day!
A doctor prescribed you this quantity?
How long you are taking this daily quantity?

James
Age 71, Peyronies from Jan 2009 following penis fracture during sex. Severe ED.
Lost 2" length and a lot of girth. Late start, still VED, Cialis & Pentox helped. Prostate surgery 2014.
Got amazing support on the forum

Gabriel

Yep, agree with James on this one : be very careful Pey Ron, personnally I'm taking 800mg/day, and begun to experience bad side effects (dizziness, nausea...) when I tried to go up to 1200mg (which made me go back to 800mg) !
- 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.

james1947

After 18 months on 3*400 mg Pentox a day, I started to have heavy flue every 6 weeks or so.
As one of the side effects is stated that Pentox weakening the immune system. Stopped Pentox, the flue gone.

James
Age 71, Peyronies from Jan 2009 following penis fracture during sex. Severe ED.
Lost 2" length and a lot of girth. Late start, still VED, Cialis & Pentox helped. Prostate surgery 2014.
Got amazing support on the forum