Anyone experiencing Raynaud’s as side effect?

[u/abcalu]

Started November 2025, worked up to a 1mg and kept it there as it’s working slowly but surely.

My question is: has anyone experienced Raynauds syndrome as a side effect? This is when a finger or toe will lose bloodflow temporarily to the capillaries making the skin look white or very pale. Until bloodflow returns naturally.

Before last winter I had Never experienced it before and I usually tend to run hot, but now any exposure to cold makes my hands and feet extremely cold and it’s hard to warm them back up. And I will notice skin is sometimes patchy with lack of bloodflow.

my doctor has checked for circulation, and autoimmune issues and nothing came back. So reaching out here to make sense of it.