How long before side effects from Hydrea start?

Hello, my doctor said up to 600 is safe and acceptable for my platelet count. I’m not sure if you Have other health issues that may contribute to the max number acceptable but my oncologist is board certified and I trust him. Age may be a factor as well. I’m 58. I’m sure there is a reason your doctor said this. Yes the range is 150-450 but that’s for healthy people not us 🙃

Questions about acceptable platelet counts come up often: Might be helpful to remember that clot risk factors for any count that typically runs >450 depends on age, previous embolism, and mutation type. Any count >1,000 may trigger vonWillebrand Syndrome, which can result in bleeding episodes and must be treated with platelet reduction meds or, in an emergency, plateletpheresis. Do ask yr doc about your specific risks because they vary from patient to patient.

I have been on hydroxyurea for 7 years no probs. Now noticing increased erythema--hands, feet, face w/ rash--and more severe itching. GP ordered tests and ruled out autoimmune diseases like lupus. ET? HU side effects? Something unrelated? I see the hemo next week, so hope to know more and will report back.

Well, I guess I'm healthier than I thought, according to your analysis!

I hope so! Please ask your doctor as everyone has different circumstances. Hang in there!

Over two years I had no hair loss or other noticeable symptoms. Clearly I was fortunate.
I took the med MWF only as it was driving platelets below acceptable levels. U have to find sweet spots.
Good luck on your journey.

I’m 72, on 500mh/day for 1.5 years. I’ve had some intermittent inside elbow itching for which I use cream and my shins “feeling” like sunburned—goes away in 15 mins. I’ve noticed both are gone now that it’s cooler out and I’m not in the pool or sun as much. Those are the only side effects I’ve noticed. My hair is very thick—no changes. Good luck on your journey.