Worried by pentox

[TEHX]

I had pentox for 6 months. I saw that my plaques are better and more small. I never had pain and my erections always was good and now too. I am reading now that some members have a regresion of the hard plaque when they stop pentox. Is this usual? I dont understand the sciencist cause of this regresion. Is casual or normally when the pentox stop the disease worst. Thx a lot.

[Sta]

Theoretically like any other medicine administered for a long time it may carouse relapse should you stop taking it at once. Go off smoothly reducing the dosage slowly.

In my opinion PTX is at the best useless for Peyronies Disease as it all subjective impression when it "helps" or when it "makes the things worse" upon giving up. If it worked Peyronies Disease would not be that big problem by far....

[james1947]

TEHX

Stopped Pentox after 18 months (3*400 mg daily) because of immune system problems.
Had no any regression, stopped more than two years ago!!!

James

[skunkworks]

In my opinion PTX is at the best useless for Peyronies Disease as it all subjective impression when it "helps" or when it "makes the things worse" upon giving up. If it worked Peyronies Disease would not be that big problem by far....

Studies carry more weight than your opinion, which is why Pentox is one of the recommended treatments on this forum.

[Sta]

[Full quote deleted by admin, please check the forum rules for posting]

Exactly. That is why I pointed it was "my opininon"...I wish it helped everyone!