Arimidex for hair loss
Common Questions and Answers about Arimidex for hair loss
arimidex
Hi:
You don't mention what cancer you had but being in the BC Forum I suppose you had just that. Do you remember what color was your chemo cocktail? Was it sort of pink or red?
If the color matches the chemo you got then your hair loss if from chemo though Arimidex also causes hair loss. While you are on Arimidex I don't believe you will see much hair growth. For further information on side effects from Arimidex the enclosed link is to an Arimidex Forum, check it:
http://www.
Hi Japdip,
Thanks for your reply. Yes, it was approved by my doc. The joint pain and hot flashes were much worse as well. I'm getting handfuls of hair every day in the bathtub drain. I am concerned that the hair loss is irreversible or may not grow back until I am finished with Arimidex. What I have read is the jury is still out if it's permanent or not, and I haven't read anything about going from one AI to another. I learned that Aromasin and Arimidex are quite different.
6 years after ending Chemo, I have less than half of hair regrowth, plus itchy scalp acne (or whatever anyone wants to call it). I wish everyone luck with getting their hair back. I never expected to not have regrowth. I wear a wig maybe once a week for a couple hours.
After the five years of taking it, will hair come back? This is distressing since I have lovely hair. Does the Famara or Remidex cause hair loss? If it doesn't, I am going to ask my doctor to switch me to one of the others.
I look forward to hearing from you since I just started this medication a few days ago.
Thank you,
Leeme
This discussion is related to <a href='/posts/show/258614'>Hair loss and Tamoxifen</a>.
Many thanks for your response and advice. I have been on both drugs together - Arimidex for 4 yrs, Fosamax for 3 yrs. I stopped the Arimidex 4 wks ago but have continued with weekly Fosamax. The bone pain in my hip and foot has diminished considerably, although I still have shooting pains in both thumbs and 1st 2 fingers. I am a little confused as to your advice......when you say "a possible brilliant solution is to take these drugs together WITH bone protective agents...
They say that the bad symptoms will eventually disappear and I sure hope that the belly problem will follow suit .My surgeon is thinking of prescribing Arimidex for an additional 2 years for better protection :( So after a total of seven years on this medicine, I hope that I'll have the strength to even exercise on my treadmill.. LOL...
Anyway,I am just thankful that I am cancer free now, hoping that the Arimidex is doing it's job .
My case is very similar to yours,my bone density is not very good either.I've been taking arimidex for almost a year now and so far, I've been tolerating it pretty well . For my bones I take Calcium+vitamin D, and once weekly Novo Alendronate which is the equivalent of what you are taking now.
Hi there - I have IDC breast cancer and Crohn's and have had monthly B12 shots for some 25 yrs. Luckily, I didn't lose my hair when on FEC chemo for breast cancer,as I had the cold cap treatment alongside, but it thinned enough that I could see my scalp on top of my head. 30+ yrs of steroids has thinned my bones significantly, so I was prescribed a bisphosphonate (Alendronate) alongside calcium (Calcichew) and Vitamin D3. My hair is a lot thicker now.
I have been on Arimidex for seven months and experienced an increase in libido, I am 72. The Oncologist checked for an increase in testosterone. Result: normal. The Doctor checked with an endocrinologist. The Arimidex is blocking the estrogen production and the body recognizes the testosterone more readily and reacts. Are there other women with this reaction?
After seeing an endocrinologist who ran all types of blood work which came back normal with the exception of his estrogen level a bit higher then normal and had an X-ray of his hand which showed bones of a 13 half to 14 half yr old (I was told was good ) want to give my son arimidex. My question is......is this safe for teen boys. I read its not FDA approved for children.
Anyone taking Arimidex or has taken it in the past. I am looking for feedback if it helped lower the ca 125???
My CA 125 is rising from 93 to 156 and now in the 230's... however nothing has changed on my pet scan and no
measurable disease... I am seeing my onc on Monday...and he had recommended to try if i want Arimidex.
I have other options like trying different chemo's... but then we are just treating the number... I wanted to give this
a try.... what do you think...
Hi - after I finished chemo and starting rads in 2003 I was prescribed tamoxifen, took it for 2 months and my Oncologist changed me to Arimidex (one of the aromatose inhibitors) which I think has a 50% better prognosis for non recurrence than the old "gold standard" tamoxifen. I was thrilled, as it had just come on to the market here in England.
However, 4 yrs down the line, I stopped it 4 weeks ago, due to severe bone pain (hips, hands and feet) and the pain has gone!
I have only had Arimidex. I only took it for about 2 months during my remission. I didn't really understand that it could have actually prevented my recurrence. It did cause a similiar bone pain to the carbo/taxol I had done. For that reason I quit taking it. There are doctors also using one now called Femara. Maybe one of those would work for you.
So very sorry to hear of your wife's spread but you sound a wonderful caring husband - she is very lucky to have you.
Regarding Arimidex, after a WLE,and total axillary removal 5 yrs ago, I had 6 FEC chemo and 25 rads. During rads I was prescribed tamoxifen, took it for 2 months and my then Onc (discharged me after chemo and rads and since retired so I have no one now) switched me to Arimidex.
30am, at 12:30p I went to bed for a few hours. Long story, short....I've been feeling horrible since last Tuesday. No energy, very tired and shaky, MENTAL FOG, very emotional, I've cried at least one time everyday since. Even when I was diagnosed with BC i believe I cried only once. I feel I can't do this for 5 years. I tried 1/2 pill yesterday to see if there is any difference, I think there is.
s my understanding from reading that Lupron is typically used in younger children than 12 and for those who did start Lupron at the younger ages, it is stopped around this age. Unfortunately, there are side effects that are undesirable with the use of pediatric Lupron. I will also tell you that both of my sons by 12 were full on puberty including facial hair!
But perhaps your son is younger than the original poster. Tell us more and we'll try to help!!
Hi,
I found this information for you.I am also taking Arimidex and of course I am very interested in knowing more about this medication.My breast surgeon told me also that by taking Arimidex reduces the development of new breast cancers by 50 per cent.
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Arimidex most effective in breast cancer study.
) I also now occasionally consult a holistic MD (referred by my oncologist) for nutritional advice. I am thinking of adding a supplement with the arimidex (broccoli seed extract - a natural aromatase inhibitor) and monitoring estradiol/estrone with blood tests after starting the supplement. If there were a negative interaction between the arimidex and the broccoli seed extract, how accurate would the blood test's estrogen results be?
I have been on Anastrozole for year, 4 more to go (5 ys.) I have the worse Joint pain, stiffness, hurts to walk, get up from chair, I get out of bed hurting, I ache everyday. My skin and stays so dry, my hair grew back after chemo, but is lifeless, thin, etc. I do not like this Pill and want to discontinue, but my Oncologist said it is doing me more good, to keep taking it. This pill is really aging me, dry wrinkly skin, no energy, cant walk and move like I want to.
Hi, I have been on Arimidex for about four months now and wondered if anyone else has had the following side effects:
1. Osteopenia
2. Polyps on Liver
I came off Tamoxifen after 2.5 years as it had no effect on me, my estrodial was about four times higher than it should have been and I had ovarian cysts and uterine fibroids, so had an abdominal hysterectomy, with oopherectomy.
Hi again,
First a caution/disclaimer: I am not a doctor, so please don't use any information or opinions I offer to try to convice your wife's oncologist to alter his plan! (They really hate it when someone over the Internet thinks s/he knows better than the treating physicians what is best for their patients, and I don't blame them a bit!
I would seem odd to have this type of reaction since you've been on Arimidex for over 2 years but I suppose anything is possible. Since the Oncologist thinks your symptoms may be caused by something other than the drug you might want to ck. with a Neurologist regarding this numbness OR perhaps an Internist, since this may even be a circulatory issue.Sounds like it's going to be a process of elimination in order to find the cause. Regards ....
I just completed 5 years on arimidex and have been asked to be part of a study and go on it for another 5 years. Has cancer reoccurred in patients while they have been on arimidex, not due to the drug, but due to the cancer. In other words, does taking arimidex prevent cancer from reoccurring while a patient is on it?
A related discussion, <a href="/posts/Pediatrics/Is-arimidex-safe-for-teen-boys/show/1816779">Is arimidex safe for teen boys</a> was started.
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