taxotere side effects

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  • websister
    websister Member Posts: 1,092
    edited January 2013

    Fight4two - have you had your hemoglobin checked? Chemo also affects the red blood cells and can cause anemia. When I am anemic my heart rate is faster and I feel short of breath with very little activity.



    PA eagles - enjoyed your post, good to hear, I am almost 6 weeks post and still having a lot of muscle pain in thighs

  • SherylB
    SherylB Member Posts: 450
    edited January 2013

    Thanks specialK,

    Yes I go get my Neulasta tomorrow, started the claritin today and my onc wants me to take ibuprofen 800 mg every am for the neulasta SE. I am drinking like a fish the cytoxan recommends a gallon of water a day. That is challenging I feel like I am floating. Have had 5 bottles (16.9) got 3 more to go. I really appreciate the feedback. Your posts are so informative and spot on.

    Take care, Sheryl

  • SpecialK
    SpecialK Member Posts: 16,486
    edited January 2013

    sherylb - glad you are drinking but don't forget that you should drink different kinds of fluids - too much water can skew your electrolytes.  Soup, juice, and Gatorade (I cut mine with water - you are in the right town for Gatorade, lol!) all count.  A number of the ladies took Aleve and got good pain relief from Neulasta and you take fewer pills, unless you have a script for 800mg Ibuprofen, and your MO is specific that it be that drug.

  • SherylB
    SherylB Member Posts: 450
    edited January 2013

    That is a wonderful suggestion I hadn't thought of just doing straight water diluting me. :)

  • jeanieb2
    jeanieb2 Member Posts: 319
    edited January 2013

    Well I saw the oncologist today and got results of my bone and CT scan.  The bone scan showed the same as it has been, nothing new, just same old cancer.  The CT showed a little thinning of the omentum, I thought it should be gone but he said it will probably never go completely away, our goal is to keep this from spreading.  My markers went to 64 from 74 so he wants me to take a chemo break.  I said for what 3 weeks, he said come and see me in 4 weeks and we will see what the markers say, he said if they go up ten points he would not start treatment again but if they went up 20 he would.  He also said my markers have always been a good indicator, whenever they have gone up we scan and there is something new and they have been that way all the time.  I am hesitant to take the break after 6 rounds of Tax and asked if I took the next 3 if the break would be longer, he said there is no guarantee if I took the next three that I would be able to be off for 6 months or longer, he said it is like a craps shoot, and he is right on that.  There are no guarantees in life.  So I am officially off Taxotere and Xeloda until markers go up.  We are scanning again in 3 months so that will also be a factor if things are showing any progression so we are not totally going by markers but both things together.  I figure it will be a couple of months or maybe 3 but whatever I can get will be good.  I know I will be on and off chemo for the rest of my life but that is OK, if I can get another 10 to 20 years that will be great and who knows by that time there may be something out there to help all of us to get rid of it forever.  I will be checking back on here to see how everyone is doing and I am sure with questions.  I asked the onco nurse today how long before I felt back to normal before chemo and she said it would probably be 2 months and maybe 6, I told her I would be back on it before that happened, she just laughed and so did I.  She said you would feel better but to get back to normal could be anywhere from 2 months and some people it is a year and I am thinking the first time it took me about a year or longer but then I had a bilateral mastectomy and lots of trouble with implants and blood clots so I think that is why it took me so long. 

    I hope all of you get that break soon and that the Taxotere works great for you all with minimal SE.  I know this last round was my worst I think, with my temp lasting for 2 full weeks, which it had not lasted that long before, but I made it through and when I go back on I will know what to expect, and I have just resigned myself to the fact of what will be will be and there is nothing I can do about it.  Although I have to admit I am excited about it I am also very nervous to not be covered so to speak by any chemo.

  • SpecialK
    SpecialK Member Posts: 16,486
    edited January 2013

    jeanieb - think of taking this break as a break from the negative SE and hope that your markers stay where they are.  I think that too many back-to-back Taxotere tx may start to do more harm than good also.  Sounds like a good plan.  I felt a difference after about 6 weeks so hopefully you will too!

  • SeattleMama
    SeattleMama Member Posts: 147
    edited January 2013

    fight4 - I found NUUN !!!  Its a tablet you dissolve in water that works like gatorade, without having to drink so much.

    It really worked for me.

  • Jennie93
    Jennie93 Member Posts: 1,018
    edited January 2013

    fight4two - my pulse rate has been high every time I'm at the doc - around 95.  They don't say anything about it.  I figure it's the stress.

    SherylB - I'm on the exact same regimen, except I get Zofran instead of Aloxi.  Most people say the SEs hit worst between day 3-5 but for me it has been more like day 4-8.  Nausea has not been much of a problem at all.  I wouldn't say so much that the SEs increase each time, but they are different each time.  And everyone reacts differently so you'll just have to wait and see.  Great thing about this place is, whenever a SE crops up, you can come on here any time day or night and ask "what worked for you?" and get some good advice.  :-)

  • MsW2012
    MsW2012 Member Posts: 226
    edited January 2013

    Hello, just weighing in on the pulse thing. Mine has been high since before I even started chemo and part of it is simply the stress of what we are going through. My pulse has been down to a reasonably healthy 70-75 from time to time but it has mostly been around 85-95. One day last week when I went in for chemo it was 104, and I was very concerned. I am gathering that this is just not particularly alarming for cancer patients. My doc said just yesterday that if it is accompanied by chest pain or breathlessness, then you must be seen. She also said she sometimes prescribes a beta blocker, if for any reason she is particularly concerned, for example if the heart rate is overly distressing for the patient. I know this isn't very comforting information but at least know that it is common.

  • jeanieb2
    jeanieb2 Member Posts: 319
    edited January 2013

    SpecialK - Thanks for letting me know how long it was before you felt a difference, I came home feeling so good yesterday and am very tired again today.  Of course I took Decadron on Wednesday because I was not sure if I would get a treatment or not so I think that was still in my system and I was doing the "Happy Dance" yesterday.  I also agree with you on it possibly doing more harm than good to do to many in a row plus I think the onc was thinking of not just the physical part but the mental part it can do to a person without even realizing it.  I am finally comfortable with the decision, kind of kept questioning myself yesterday and I know if I had said I wanted to continue he would have let me, but today I feel fine with the decision.  Knowing my markers are good indicators, they always have been, makes me feel OK with it also since we will do those on a monthly basis.  He also looked at my feet and said that was another good reason to take a break, I did not think they were that bad but he did not like the looks of them, so I am OK with what is going to happen.

  • fight4two
    fight4two Member Posts: 146
    edited January 2013

    Jennie and MsW - I just measured my resting heart rate and it was 118.  Seems extremely high.  Its good to know you both have high rates as well, but they don't seem quite as high.  Even though its high, I can't feel it racing - I would not have known.  My MO never measures my pulse.  I only learned of the fast rate because its standard procedure at the BS office.  Perhaps it has been like this all through chemo?  The thing that worries me is that the doctors have decided to move up my surgery (in 10 days!) and I'm not sure I want my pulse to still be high.  Does anyone know if they give you an echo before surgery?  I had an echo before chemo started, but never another one to see if my heart is STILL good.

    This added stress is probably terrible for my heart rate, ha!  Also, still haven't been able to shake my Taxotere fever.  Will go drink some more water now.

  • fight4two
    fight4two Member Posts: 146
    edited January 2013

    Websister - I haven't gotten the results of my blood test yet.  My hemoglobin has generally been around 10.2-10.4 the last month though.  I have been feeling a little shortness of breath lately as well.  Why do all medical ailments always crop up near the weekend?  Its always a struggle to decide "emergency room or try to make it through the weekend".

  • MsW2012
    MsW2012 Member Posts: 226
    edited January 2013

    Fight4two, I would definitely let your MO and your surgeon know about your high heart rate. It may still be ok but it needs to be addressed. I think they have a responsibility to either treat it or explain to you why it is ok, because it's terrible to go into surgery with a concern like that hanging over your head. I hope you find a solution. High heart rate can be so many things. Good luck.

  • websister
    websister Member Posts: 1,092
    edited January 2013

    Hi Fight4two - Your hemoglobin was a little low but fairly typical for chemo, it is possible that it has gone down since the last chemo.

    I am wondering if you might have an infection or be fighting a virus if you still have a fever. A fever can be a reason for your pulse to be higher. I would get the fever checked out if you haven't already - they could do a CBC and check on the hemoglobin and your WBC/neutrophils at the same time. They would not normally do an echo preop.

    Hope you get things worked out soon so your surgery doesn't have to be delayed.

  • jeanieb2
    jeanieb2 Member Posts: 319
    edited January 2013

    Has anyone had a break from Taxotere for a couple of months and then gone back on it?  I was wondering if you had any problems when you did go back on it.  I am on a break, don't now for how long, but I am wondering if or when I go back on will it be worse than before, the same or better?  I know we are all different but just wanted to know what others may have experienced with this.

  • blondiex46
    blondiex46 Member Posts: 5,712
    edited January 2013

    me was on for 2 rounds in August went off for 2 months then back on for 1 treatment off for a couple of weeks and back on now!!  I have no side effects at all cept for being tired for about 3 days after...

    Sandy

  • jeanieb2
    jeanieb2 Member Posts: 319
    edited January 2013

    Thanks Sandy, I was afraid the side effects might be worse.

  • blondiex46
    blondiex46 Member Posts: 5,712
    edited January 2013

    not for me...let me know tho!!

  • jeanieb2
    jeanieb2 Member Posts: 319
    edited January 2013

    Will do.  I am hoping to have 2 or 3 months or more off, but time will tell.

  • fight4two
    fight4two Member Posts: 146
    edited January 2013

    Finally got my blood test results back and everything looked good - in fact, even a little better than usual.  Ironically, I seem to have caught a cold this weekend. Or maybe, as you were hinting at, I was already fighting the cold (hence the elevated pulse and fever), and it finally took hold this weekend.  Darn.  Another stresser pre-surgery!

    I took a really hot shower the other day, and afterward, the tops of my feet felt like they were on fire.... for days....! I guess another SE of taxotere is temperature sensitivity of feet and hands.  I already knew my hands were sensitive, learned the hard way about my feet.  At least I think thats what it was.

    Was expecting to feel great this week, as it is the third week after my last tx, but instead I feel worse than usual cuz of this darn cold!  Hope the rest of you are feeling well.  Jeanie, i hope that you enjoy the break and that your SE are better when you go back on.

  • jeanieb2
    jeanieb2 Member Posts: 319
    edited January 2013

    fight4two - Thanks, I hope they are easier also.  I am still fighting with this low grade temp.  It was gone last Thursday-Saturday after 2+ weeks, had it a little yesterday and now this afternoon it is not going away.  It gets to 100 and I lay down and it goes down just a little.  I have not caught a cold or anything and can not figure out what in the world would be causing it.  It has been over 4 weeks since I got Tax last and finished up my Xeloda yesterday so thought I would be feeling much better by now.  I am sure it will pass soon, if not I may call the onc on Thursday and see what he has to say.  When I was there last week he had no idea but then I had quit running it when I saw him.  It is just a nuisance to not let you feel good but not bad enough to run to the doctor.  I know, I am whiningLaughing, so I will quit, it could be so much worse that is for sure. 

  • powermom
    powermom Member Posts: 195
    edited January 2013

    JeanieB - just a thought, could your low grade fever be a UTI or kidney infection? Seems like I remember that as a symptom years ago. Feel better.

  • blondiex46
    blondiex46 Member Posts: 5,712
    edited January 2013

    back on tomorrow of taxotere after my week off for 3 weeks on.....so far no side effects except being tired....

    Sandy

  • fight4two
    fight4two Member Posts: 146
    edited January 2013

    JeanieB, I am still struggling with the fever myself.  My dr is prescribing levaquin, which fights bacteria in the body.  I'm kind of afraid to take it because of all the possible horrible things that can happen as a result of taking the drug (per the four page printout that came with it when I picked it up).  They are doing urine cultures, chest xray, blood cultures and an echo on me, but since I am supposed to have surgery on Monday, they want me to take the levaquin just in case (before getting results). I feel chest pain (in my heart?) but that might be because my poor heart has been beating at 120-130 bpm.  Hopefully my fever will go down soon, so my heart can beat at a regular pace.  If you find out the cause of your fever or figure out how to fix it, please let me know!  I am constantly thirsty, but my urine is never dark, its practically clear!

    Sandy - hope you get no more SE's!

  • halfcan
    halfcan Member Posts: 253
    edited January 2013

    I am wearing HUGE pockets and I would love to take all of you with me for my LAST chemo tomorrow!  Smile   This is the first time that my blood work has so many flagged low numbers (WBC/3.1, RBC/2.9, HB/97, HCT/.28 and Neutrophils/1.6 but MO is pushing ahead so must not be too low I guess.   I was lucky on the last round and other than being completely exhausted (still am) the side effects were easier.  No fevers or blood clots or anything worse than the bone pain associated with the Nuepogen shots like before.   My fingers are crossed this last Taxotere will go smoothly too.  I was especially surprised to see my Neutrophil numbers down since I do the injections ... usually they are high!   Maybe it is a good thing that this is my last round ... the ol body must be getting tired of it all.

    I know some of you are having a hard time.  I sincerely hope things settle and things get easier for you!

    Hugs to all  xox 

  • blondiex46
    blondiex46 Member Posts: 5,712
    edited January 2013

    Fingers cross half....good luck!!

    Sandy

  • websister
    websister Member Posts: 1,092
    edited January 2013

    In your pockets tomorrow Halfcan - congratulations!

  • Traii
    Traii Member Posts: 1,138
    edited January 2013

    Congrats halfcan, great news last Taxotere!!   Will be there with you in your pocket next to Websister Smile

  • SeattleMama
    SeattleMama Member Posts: 147
    edited January 2013

    <<doin' a happy dance for Halfcan>> :)

  • blondiex46
    blondiex46 Member Posts: 5,712
    edited January 2013

    On my way to chemo for my 3 weeks on....this will be the 2nd round, I guess....who knows, lol

    Sandy

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