Hello all, thanks again for your replies.

I definitely do not have PD. I was on tyrosine after the doctor told me about potential dopamine shortage and it worked. I believe I have isolated the cause. However, the tyrosine caused 1 side effect which was the pain in the liver/gallbladder area. So I am looking for a replacement.

Is it safe for a non PD patient to use Mucuna Pruriens? I know this will work along the same pathway as tyrosine but just need to know if it is safe.

Chemar, thanks for your guidance and defending me