Being still in the acute phase of Peyronies Disease, I'm still figuring out the best course of action. Trying to do anything I can to at least minimize the worsening of the condition.
I was recently prescribed colchicine, vitamin E, and CoQ10 as oral treatments/supplements.
Does anyone know how colchicine compares to pentox as an oral treatment? I'm not finding much conclusive research. My urologist says I can add pentox if I choose, but I was hoping somebody might have additional thoughts. Thanks in advance.