What are most common side effects when starting HU (Hydroxyurea)?
What are the side effects most experienced when starting the HU? I'm still trying to decide if I'm going to start it on 1/26/24. My hematologist said we would go over the side effects then but I want to know what most have experienced since they would only report what "could" happen & not what DOES happen. Ex. It's a chemo pill- they usually cause hair loss. Does this apply with the dosages that we would need? After reading other posts, it's sounds like maybe 500 mg is the magic number for the HU dosage.
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
My reading seems to indicate that this mutation takes a long time to develop into enough stem cells to generate enough blood cells to cause problems. We've likely had our mutations for decades before we ever see an adverse effects.
In my case, my RBC was trending up for years before it crossed the threshold to go see a specialist.
I have been taking HU 500 mg daily for a month, and platelets went down from 800,000's to 5oo,oo's, which is good. My problem is extreme fatigue. I have always been very active, and now I get to half way through the day and I'm exhausted. I don't know if that's from the ET or the HU.
Congratulations on your success!
We are all different, but for many of us, once HU tamps down ET's manic overproduction of platelets, we gradually get our energy back.
Hope you will experience that too!
That was my pattern, too. Extreme fatigue, then improvement after I started HU. I think age can also slow us down. So can stress over having ET. If ET comes on in late middle age, there may be hormonal changes. It takes time to try different things and adjust to all these changes. I remember those menstruation and reproduction films they showed us in girls phys ed back in the 60s with the bunny rabbits and butterflies. Sometimes I feel I could use a film to about being an old lady!
There may be some truth in your comments that humans have anomalies lurking in our bodies that take decades to emerge. That being said, these anomalies create havoc due to some event that triggers them. Medical science is very good at fixing the “now”, but miss the mark on the “how”. All so called random occurrences have a trigger. We just don’t know all the answers.
My hematologist told me it takes about 10 yrs. before any thing starts showing. This means that mine started when I was in my mid 30s. I started noticing symptoms about 45 but chaulked them up to menopause starting. I got my official diagnosis when I was 47 but I hadn't had any labs drawn for several years so who knows when my levels actually started rising. I'm 48 now & they seem steady in the 600 -700 range without any medication help besides baby Aspirin.
Hi midterp76,
You summed up Everything so well. I have all of the same symptoms and have done all of the things you mentioned above except for the restasis (but I will ask my eye specialist if that is right for me). Interesting that we have both found the same solutions to our problems. And, no others do not realize all of our challenges. I see that as a good thing, mostly. I feel lucky that my friends and family do not worry about me. But I also wish I was better at making them understand that I have to take a lot of precautions and need a lot of rest. I am 70 yo with ET (triple negative for the past 22 years. I feel lucky that I am doing well. Thank you for posting, I am glad you are here.
Yes! Research tends toward profit (medicines for the "now") and not on restricting the "how."
I think all of us have suspicions about how we developed ET. The problem is that ET develops long after exposure to suspected carcinogens, and trying to find commonalities among patients is really hard. And if it turns out that fossil fuels, household chemicals, pesticides, chemical fertilizers, food additives or whatever causes cancer, that means potential regulation of business and industry, which many people oppose.
You are absolutely correct. I worked for a Fortune 500 company for all of my working career (38 years), and one of the carcinogens used in some of our manufacturing processes was a chemical used to clean electronic circuit boards (Trichloroethylene or TCE). That same chemical is used in the dry cleaning industry and was recently banned from use. Due to nature of my job I was constantly exposed to this chemical. My diagnosis of ET was discovered 30 years after I retired, and only after triple bypass surgery in 2024. I’m approaching my 88th birthday and the HU dosage I’m taking is doing it’s job without any significant side effects so, I’m grateful for that.
Thanks for the information been taking 500mg daily platelets dropping from 1036 to 796 took another test today 20 days later and only dropped to 732 they now want me to take 1000mg and be tested in another month. I really don't want to take that high dosage. How tired will I be ? I normally wait until 8pm to take my bill to not feel tired
I work daily just frustrated I thought they would at least decrease more by now. Also frustrated working with NP as I only met Dr first and she been on leave for her baby being born
Thinking about going to another dr.