Gleevec cost
Common Questions and Answers about Gleevec cost
gleevec
Hi, I don't know the answer -- but since both CML and Gleevec toxicity produce anemia because of marrow suppression, maybe it's not possible to tell the difference. E.g., both would show a low reticulocyte count.
This full text paper on anemia from Gleevec https://onlinelibrary.wiley.com/doi/full/10.1002/ajh.23879 shows that other signs such as red blood cell size can vary, so that doesn't seem to help. Sorry.
Is it possible that after taking gleevec for only two weeks WBC droped from 36.7 to 7? All other blood counts are also came back to normal range. Could doctor make mistake in diagnosis of CML? Maybe I should get seg second opinion?
I was diagnosed with CML and given Gleevec 400 ml. After taking gleevec for 2 weeks doctor took additional blood test. My WBC dropped from 36.5 to 7.1 and all other blood counts came down to normal range. I'm wondering if gleevec could give such fast hematological response or I was possibly misdiagnosed originally. I don't and didn't have any symptoms, my spleen and liver weren't enlarged, no enlarged lymph. Should I get second opinion asap? Please, help me.
After two weeks on 400mlg gleevec my WBC droped from 36.5 to 7.1. My doctor told to come for additional test in two weeks. Now my WBC is 1.3 and absolute neutrophils count is 0.04. I was told to stay home on antibiotics. How long it may take for my counts to clime back to safe range. And of course, I'm off gleevec right now. Does it seem that dose of 400mlg is too high for me.
Am on Gleevec 400mg, now having problems with blisters on the palm. What can I do about it?
I was diagnosed last year and was immediatley put on gleevec 400mg/day.At my last consult my metabolic stats had risen,hence blood tests to determine if the gleevec is no longer working.I am still in firstphase and wonder what my options are if the gleevec is no longer an option.Amin pretty good form,just very tired and a lot of bone pain.
I have CML and was treated with Gleevec for 4 years and achieved remission. I have for the past several months been experiencing sudden onset of weakness which last for hours, to days. My blood pressure which has remained under control for several years with atenolol has been running 145/105 and higher for the past three to four months. I have a feeling of fullness in my stomach, and I have sporatic episodes of mild coughing, this occurs maybe once a week.
You might find he starts to be able to tolerate the pill. Gleevec is first choice for treating CML, and if he is doing good in every other way then encourage him that he is doing great.
I hope this helps you. I would be glad to help you with any other questions.
i get my heart checked every 2 weeks now and i am fine with the qt thing. i take the chemo pill called gleevec and have to force myself to eat so i dont get sick when i take it. how long will these withdrawel problems go on? i have xanax to take (1mg) but dont work to good. i should would appreciate any advice from any one on how to deal with these issues, family dr says its anxiety but i think its the withdrawels from the high dose of elavil.
I want to become a mother again. I have a 19 y/o. I am a newly wed. My husband has no children we are considering IVF but it is so costly. Not sure if I am able d/t high FSH. didn't get result for AMH as of yet. But if its not possible for me to have one biologically we are considering using DE. My question. Is it cheaper using a family or friend as a donor in comparison using an anonymous donor. Where I am living, it cost $16,500 for DE...IVF cost almost $20,000.
Oh my goodness! That is so expensive. Here in new zealand all medical care is absolutely free. It seems unethical to charge someone to give birth!
Can anyone give me a ballpark of the cost for the suppressant drugs after a transplant. Just want to get an idea, know no one can give me exacts but any info would help. Thanks.
umm in the usa without insurance, n im chronic.
hello again, thanks to all the people that responded. was wondering about the cost of meds. interferon and ribavirin, im checking with my ins. to see what they will cover. i may have misspoke about this thing on hepititusccure.net i dont think it is herbal? it deals with fatty liver tissue. but its only 50 bucks to read about it so i dont really have anything to lose. going back to doc in 3 mo. not sure why till i decide on tx. if tx takes care of virus, do people go back to normal lifestyle?
The difference between the full cost of a treatment (which the uninsured often are charged), and the amount the insurance company tells them they will pay is often quite a bit. If you have cash and offer to pay up front (for a discount) you may get charged less than what they can get out of the insurance company, because it's less hassle and instant money for them.
Just a thought, even if you had to borrow the money.
Will your Endo accept results from another facility?
In what country are you? In the USA, it is anywhere from $18,000 to $30,000.
Anyways, the rep told me that ribavarin only comes in 200mg and a 3 months supply would cost me $10.00 co-pay. The peg/interferon would be a 30.00 co-pay for a month. This was the pharmacy and member service that said that. Does this seem right? I always thought tx was expensive like in the thousand of dollars. I have Kaiser but I don't have the deluxe plan or anything just the basic.
I should mention that I have CML but it has been in remission for the last two years and I am no longer taking Gleevec.
I am scheduled to be looked at by a group that kills the nerve endings in the heart that causes AF but there is an 18 month waiting period.
My question is how many times can I be cardioverted and what is the downside of having it so often?
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