Arimidex for hypogonadism
Common Questions and Answers about Arimidex for hypogonadism
arimidex
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...
It would be really important to rule out any underlying reasons for issues of low testosterone and if they diagnosed you with secondary hypogonadism. They would look for issues such as diabetes ,issues with your pituitary gland, what medications you are taking. In general, being obese can cause it as well. We are happy you work on your weight maintenance program and think that is terrific! Keep that up. But it must be said that primary and secondary hypogonadism can both be congenital.
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.
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.
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.askapatient.com/viewrating.asp?drug=20541&name=arimidex
Don't forget Arimidex is an Estrogen Inhibitor, that should give you a clue on what to expect.
Take your time and read all you can from the enclosed forum link.
Best regards.
So I went to my Endo recently and I was explaining a few symptoms to him (fatigue, high blood pressure, general weakness and feeling crappy), and he decided to test a few hormones. My Testosterone Serum was 251 ng/dL, and the range listed is 348-1197. There's nothing wrong with my testicles so he's saying it's Hypogonadotrophic Hypogonadism, which is just a fancy way of saying something besides your testes is causing the low testosterone.
) 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?
Yes, you can cave secodary hypogonadism without a pituitary tumor. It is called idiopathic hypogonadism. there seem to be some changes in the cells that make gonadotrophins (that drive the testes).
If a tumor or any other lesión was not found, what is left to be done is what you are already receiving, that is replacement therapy. This means Levothyroxin and androgens.
Neither of These abnormalities carry a bad prognosis or threat to life. You should be OK.
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.
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?
I wish it was hypogonadism but i was injecting sostenon 250 every week for 2 months and didnt aleiviate the symptoms it was the same even though my total teatosterone went fromow normal to high normal i started at 299 and went up to 849. But still didnt improve any of the symptoms. My tsh and t4 are normal im wiating on the free t3. Iwanted to do a rt3 but they dont have those down here in mexico.
A related discussion, <a href="/posts/Pediatrics/Is-arimidex-safe-for-teen-boys/show/1816779">Is arimidex safe for teen boys</a> was started.
I started taking Arimidex about five months ago. Since then I have had many of the typical side effects such as hand/joint pain, neuropathy in my hands, hot flashes, wakefulness at night etc. However, my sight in one eye has also begun to noticeably deteriorate. I know, because I had my eyes checked and a new eye prescription just before I started taking Arimidex. I saw my eye doctor again last week and my vision has deteriorated from 20/40 to 20/70 (with correction) in just a few months.
In general, it is individuals who have cancers that are estrogen and/or progesterone receptor positive that benefit from endocrine treatments such as Arimidex. It is possible for a recurrence to differ from the original cancer in terms of hormone receptor status. It is also possible to have false negatives when testing. For these reasons, there may be times when endocrine treatments can be tried for recurrent disease, even if the original cancer was hormone receptor negative.
Does Arimidex have to actually kill you vs. maiming you for life, in order to be pulled off the market? At 58, I may need a hip replacement because I took Arimidex for two years! DeeDee
This discussion is related to <a href='http://www.medhelp.org/posts/show/260593'>Arimidex Long Term Side Effects</a>.
I don't know of anything unless you would reduce the caloric intake although it might not be totally due to food. It might also depend on what those calories are coming from. Good Luck....
Though there is a good theoretical basis for the use of arimidex on endometriosis, I believe that this is still an off-label indication for the drug and the clinical basis for its use is still from phase II clinical trials (studies with still low number of patients). Until such time that the indication of endometriosis can be demonstrated in large phase III clinical trials, the use of arimidex for endometriosis is still controversial.
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...
Well, for me Arimidex was so very horrible, I barely lasted three days on it. I was in an almost catatonic state of depression two hours after I took the first dose, and then got just about every other bad side effect soon after.
Femara, in comparison, relative to the other, was not so bad at all and I lasted almost thirty days.
But not every woman has the same problems, or any at all. Many though do have some problems.
I was diagnosed in 08 and am her2 positive. I went through chemo,radiation and 1 year of hercepton. Since then I"ve beem on arimidex. My main complaint other then hot flashes (terrible lol) is fatigue. It seems that I"ve lost alot of energy. The fatigue comes shortly after I start a project. Because of the hot flashes I get little sleep some nights but does the arimidex also cause fatigue? Is a side effect of hercepton fatigue (taken in 09,,,,?
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?
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 .
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