Compounded T cream or gel, Cabergoline, and Danazol dose

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txmx

Member
Quick question as I head to my endo. If I wanted to use a compounded T cream or gel (total T at baseline would be around 300), what prescription would I ask for (not sure my endo knows about T compounding). My insurance may not cover Testim gel. Also, what dosages/days of Cabergoline (for managing dopamine) and Danazol (to try and lower 79 SHBG) would be good to try? Thanks.
 
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Nelson Vergel

Founder, ExcelMale.com
You can try a 2 percent testosterone cream from empowerrxpharmacy.com

The script should read: Transdermal testosterone cream, 200 mg/ml, 30 ml. Apply 1 ml per day after showering

You should not take Cabergoline without knowing your prolactin level. Low prolactin can be bad for the immune system.

Danazol use in men is off label most doctors would not prescribe it. It is a mild androgen with no anabolic effects but with negative effects on good cholesterol (HDL) and coagulation markers. It decreases sex hormone binding globulin like anabolic steroids do. Danazol has been extensively used in women for managing a wide range of conditions such as endometriosis, menorrhagia and benign breast conditions such as mastalgia and cystic disorders. Its use in men has been limited to treatment of enlargement of the male breast (gynecomastia) and limited research into its use as a male contraceptive. The previous uses of danazol in women and men have all been at relatively high concentrations, for example doses of 200 to 600 mg. Used alone it can decrease testosterone blood levels since it shuts down the HPT axis. When used with testosterone replacement, it may increase free testosterone. Doses used in men on TRT are 50-100 mg daily.
 

txmx

Member
Thank you, Nelson. As it turned out, my endo denied the cabergoline due to my prolactin being at 4 before I ever started on clomiphene 16 months ago. We have no idea what it is at today since he did not test it again. He denied the danazol and wants to refer me to a urologist for that avenue. He denied me trying Testim since my TT is at 675 on clomiphene, even though Free T is at 8 because of SHBG at 79. I reminded him of all my low T tests before going on clomiphene (259, 337). His response was to extend my clomiphene prescription and wish me a happy new year :) He did say I could come off the clomiphene and go back to whatever my baseline would be now (which he thought might be higher than before), and then if T was still low then be able to try exogenous T. I may just need to go to someone else. He seems to think if your numbers are within Labcorp range, then you are doing ok, regardless of lack of subjective response, low libido, lack of muscle development, osteoporosis (I did get a Fosamax script).
 

tmckenzie

Member
Real bright dr. Gave you you fosamax but not testosterone. Guess he got a nice gift from the folks who makes fosamax. Give you T, might not need fosamax.
 

txmx

Member
Real bright dr. Gave you you fosamax but not testosterone. Guess he got a nice gift from the folks who makes fosamax. Give you T, might not need fosamax.

Exactly. Actually, he prescribed Actonel (328.00 for 3 months), which is way expensive compared to generic of Fosamax (12.50 for 3 months). I had to get him to change it. So much for his nice gifts from Actonel :eek: And I did mention that T would assist with bone building but he did not seem to grasp that fact. Ah, well.
 

Kelly

Member
The quickest way to suppress shbg is to elevate testosterone. Your doc seems to be missing this point.
Having a good D level will also help with shbg as can nettle root.
 

txmx

Member
Kelly, I tried Nettle Root and Avena Sativa. Neither one seemed to help. On the D, I'm taking 6000iu daily and D levels seem pretty well optimized at 60.
 

DHM

New Member
Id like to dig this thread back up for an update.

Im also interested in lower SHBG and ultimately getting to the root cause of the increase, some docs say its environmental toxicity. If estrogen is driving protein signaling and Ive got optimal E2 levels, what other areas do we need to look at?
 

Gene Devine

Super Moderator
Id like to dig this thread back up for an update.

Im also interested in lower SHBG and ultimately getting to the root cause of the increase, some docs say its environmental toxicity. If estrogen is driving protein signaling and Ive got optimal E2 levels, what other areas do we need to look at?


SHBG is one of those hormones that finds it's own level.

As long as your Total and Free Testosterone levels are in good levels there's really not much you can do.

If you inject twice a week you may want to consider once weekly injections as bigger testosterone injections can and will push down SHBG levels.

You may want to try adding Stinging Nettle Root to your supplements as it has been known to lower SHBG to some extent.
 

DHM

New Member
Thanks Gene!


My free T ranges from 8.9-6.7 on the labcorp scale (5 labs, batting 1000).


Total ranges from high 300s to High 500s.


SHBG has always been on the upper quartile (37 and up).


Need to get an E2 sensitive ordered next round.


I would try Nettle but hear too many null results.


Been on Clomid stim test, levels doubled but so did SHBG so whatever was made got automatically taken away!


Im targeting a Danazol treatment and if E2s come back high, low dose Arimidex or Nolvadex.
 

OMI100

Member
I am getting my compounded "T" from empowerrxpharmacy.com
I was getting it through CareMark and BC/BS insurance.
They were going crazy asking for all kinds of documentation from my DR.
Turned into a real goat rope....
I get filled from Empwer now.
Cost is less than my co-pay was with CareMark....
All they needed was a script from my DR.
CK them out whenever you get a script.
 

Nelson Vergel

Founder, ExcelMale.com
USE OF DANAZOL IN THE TREATMENT OF HYYPOGONADISM IN MEN

Androgen Deficiency in the Ageing Male, also referred to as 'The Male Climateric', 'The male menopause' and the 'Andropause' causes a highly characteristic pattern of symptoms which was first recognised nearly sixty years ago (Werner,A. JAMA 112,15,1441-3,1939). As described at that time, the syndrome includes loss of energy, drive and libido, depression, irritability, joint pains and stiffness, and even such typical symptoms of the female menopause as night sweats and hot flushes.
It has been found (Carruthers, M. 'The Male Menopause, Harpercollins', London, 1996) that the symptoms associated with this condition arise due to an absolute or relative insufficiency of testosterone, particularly the latter, caused by a reduction in the Free Active Testosterone (FAT); that is a lack of testosterone present in an unbound state in blood plasma. Testosterone in vivo can be bound to sex hormone binding globulin (SHBG) and to a lesser extent, albumin. When bound the testosterone is not freely available to the body or bioavailable. One of the best measures of this is the 'Free Androgen Index'(FAI). This is calculated by dividing the Total Testosterone (TT) by the 'Sex Hormone Binding Globulin' (SHBG) and multiplying by a hundred to express it as a percentage. In the healthy, asymptomatic male this is normally in the range 70-100%. Symptoms of the andropause regularly appear when this drops below 50%, except in a few cases where the TT is low and the body appears to compensate by reducing SHBG levels to maintain the FAI.
It has been found that hypogonadism and also the male menopause can be prevented or treated by freeing bound testosterone so that it becomes bioavailable again. Testosterone may be freed, for example,by:
· 1. decreasing the number of potential binding sites available for testosterone in vivo, for example by reducing the level of SHBG using compounds which antagonise the action of androgens in stimulating SHBG synthesis,and/or
· 2. introducing an agent which competes for the binding sites, thereby displacing bound testosterone which is returned to systemic circulation.
Pharmaceutical, pharmacological and biological compounds that may act effectively include ethisterone and ethisterone derivatives and/or precursors.
One such compound, danazol, is a well-established therapeutic agent which has been extensively used in the female for managing a wide range of conditions such as endometriosis, menorrhagia and benign breast conditions such as mastalgia and cystic disorders. Its use in the male is not widely known and has been limited to treatment of enlargement of the male breast (gynaecomastia) and limited research into its use as a male contraceptive. The previous uses of danazol in women and men have all been at relatively high concentrations, for example doses of 200 to 600 mg, and at these concentrations it has been shown that total plasma testosterone is reduced.
It has now been found that using danazol in the male at dose level reduced from that at which it would be conventionally used, for example at a daily dose of not more than 100 mg, reintroduction of testosterone to the systemic circulation in the form of Free Active Testosterone is remarkably effective; that is the FAT is increased leading to a highly effective treatment of the symptoms associated with hypogonadism and with the male menopause.
Danazol is effective, non-hepatotoxic, and does not have intrinsic androgenic, oestrogenic or progestogenic actions. It is an ideal agent for displacing and hence activating testosterone as it has a high affinity for androgen receptors, low affinity for progesterone receptors, and does not interact with oestrogen receptors to any significant extent.
The importance of only giving low doses of danazol, for example not more than 50 -100mg daily, to men being treated for hypogonadism is because at this low dose, as shown by the clinical studies described later in this application, there is direct suppression of SHBG synthesis by the liver, with a corresponding increase in FAI, apparently without reduction of endogenous total testosterone production.
Danazol may be for treatment of hypogonadism resulting from any biological or physical cause. In particular, Danazol may be for treatment of any condition where systemic free active testosterone is reduced due to raised levels of SHBG, for example, conditions caused by concurrent/prior treatment with estrogens, anti-convulsants and/or exposure to xeno-estrogens.
Preferably not more than 100 mg of danazol, preferably the daily dose between 25-100 mg. The dose is varied according to body weight, TT and SHBG concentrations.
Danazol may be administered on its own or as an adjunct to other methods of relieving sexual dysfunction problems in men such as libido disorders and impotence, such as applications of alprostadil (Caverject and Medicated Urethral Systems for Erection - MUSE), and drugs which enhance relaxation of the corpora cavernosae in the penis, for example those which increase nitric oxide production such as the oral preparation sildenafil (Viagra).
Danazol together with testosterone is used in the treatment of the male menopause.
The dosage level required for the activity is much lower than that used in known dose regimes where danazol is used in the female to treat, for example endometrosis. The preferred dosage is between 25 - 100 mg per day as opposed to 200 to 800 mg per day used previously in different treatments. The dose may be administered orally, nasally, as a solid implant, or intravenously, intramuscularly or transdermally.
In a preferred embodiment a dose of 25 mg of danazol is administered to the patient daily in the form of a capsule.
The usage of danazol, optionally in combination with low dosage testosterone treatment, appears to give for the first time a unique opportunity to adjust the level of TT, SHBG and hence FAI to mimic a normal youthful endocrine pattern even in middle-aged and elderly men. This should give clinical benefits in both treating hypogonadal men, and in the field of preventive medicine, where maintaining an adequate level of testosterone activity is being shown to be a key factor.


APS Pharmacy suggested dosing for Danazol
25mg (capsule or troche), once a day.
**Danazol can also be compounded together with Anastrozole in one capsule.
*** Danazol is a non-scheduled (non-controlled) medication
 

Tom Larabee

Member
USE OF DANAZOL IN THE TREATMENT OF HYYPOGONADISM IN MEN

The usage of danazol, optionally in combination with low dosage testosterone treatment, appears to give for the first time a unique opportunity to adjust the level of TT, SHBG and hence FAI to mimic a normal youthful endocrine pattern even in middle-aged and elderly men. This should give clinical benefits in both treating hypogonadal men, and in the field of preventive medicine, where maintaining an adequate level of testosterone activity is being shown to be a key factor.


APS Pharmacy suggested dosing for Danazol
25mg (capsule or troche), once a day.
**Danazol can also be compounded together with Anastrozole in one capsule.
*** Danazol is a non-scheduled (non-controlled) medication

Very interesting read especially the results paragraph at the end.

Do we know anyone who has used this in these lower doses to free up bound T?
 

tmckenzie

Member
Been searching and cannot get a good answer. My last tests had me at 826 total, 36 free. Sgbh is always low. Feel great, sex drive sucks. Am I right in thinking my free t should be much higher? E2 and all libido killers at last check were good.
 

marston_john

New Member
USE OF DANAZOL IN THE TREATMENT OF HYYPOGONADISM IN MEN

Androgen Deficiency in the Ageing Male, also referred to as 'The Male Climateric', 'The male menopause' and the 'Andropause' causes a highly characteristic pattern of symptoms which was first recognised nearly sixty years ago (Werner,A. JAMA 112,15,1441-3,1939). As described at that time, the syndrome includes loss of energy, drive and libido, depression, irritability, joint pains and stiffness, and even such typical symptoms of the female menopause as night sweats and hot flushes.
It has been found (Carruthers, M. 'The Male Menopause, Harpercollins', London, 1996) that the symptoms associated with this condition arise due to an absolute or relative insufficiency of testosterone, particularly the latter, caused by a reduction in the Free Active Testosterone (FAT); that is a lack of testosterone present in an unbound state in blood plasma. Testosterone in vivo can be bound to sex hormone binding globulin (SHBG) and to a lesser extent, albumin. When bound the testosterone is not freely available to the body or bioavailable. One of the best measures of this is the 'Free Androgen Index'(FAI). This is calculated by dividing the Total Testosterone (TT) by the 'Sex Hormone Binding Globulin' (SHBG) and multiplying by a hundred to express it as a percentage. In the healthy, asymptomatic male this is normally in the range 70-100%. Symptoms of the andropause regularly appear when this drops below 50%, except in a few cases where the TT is low and the body appears to compensate by reducing SHBG levels to maintain the FAI.
It has been found that hypogonadism and also the male menopause can be prevented or treated by freeing bound testosterone so that it becomes bioavailable again. Testosterone may be freed, for example,by:
· 1. decreasing the number of potential binding sites available for testosterone in vivo, for example by reducing the level of SHBG using compounds which antagonise the action of androgens in stimulating SHBG synthesis,and/or
· 2. introducing an agent which competes for the binding sites, thereby displacing bound testosterone which is returned to systemic circulation.
Pharmaceutical, pharmacological and biological compounds that may act effectively include ethisterone and ethisterone derivatives and/or precursors.
One such compound, danazol, is a well-established therapeutic agent which has been extensively used in the female for managing a wide range of conditions such as endometriosis, menorrhagia and benign breast conditions such as mastalgia and cystic disorders. Its use in the male is not widely known and has been limited to treatment of enlargement of the male breast (gynaecomastia) and limited research into its use as a male contraceptive. The previous uses of danazol in women and men have all been at relatively high concentrations, for example doses of 200 to 600 mg, and at these concentrations it has been shown that total plasma testosterone is reduced.
It has now been found that using danazol in the male at dose level reduced from that at which it would be conventionally used, for example at a daily dose of not more than 100 mg, reintroduction of testosterone to the systemic circulation in the form of Free Active Testosterone is remarkably effective; that is the FAT is increased leading to a highly effective treatment of the symptoms associated with hypogonadism and with the male menopause.
Danazol is effective, non-hepatotoxic, and does not have intrinsic androgenic, oestrogenic or progestogenic actions. It is an ideal agent for displacing and hence activating testosterone as it has a high affinity for androgen receptors, low affinity for progesterone receptors, and does not interact with oestrogen receptors to any significant extent.
The importance of only giving low doses of danazol, for example not more than 50 -100mg daily, to men being treated for hypogonadism is because at this low dose, as shown by the clinical studies described later in this application, there is direct suppression of SHBG synthesis by the liver, with a corresponding increase in FAI, apparently without reduction of endogenous total testosterone production.
Danazol may be for treatment of hypogonadism resulting from any biological or physical cause. In particular, Danazol may be for treatment of any condition where systemic free active testosterone is reduced due to raised levels of SHBG, for example, conditions caused by concurrent/prior treatment with estrogens, anti-convulsants and/or exposure to xeno-estrogens.
Preferably not more than 100 mg of danazol, preferably the daily dose between 25-100 mg. The dose is varied according to body weight, TT and SHBG concentrations.
Danazol may be administered on its own or as an adjunct to other methods of relieving sexual dysfunction problems in men such as libido disorders and impotence, such as applications of alprostadil (Caverject and Medicated Urethral Systems for Erection - MUSE), and drugs which enhance relaxation of the corpora cavernosae in the penis, for example those which increase nitric oxide production such as the oral preparation sildenafil (Viagra).
Danazol together with testosterone is used in the treatment of the male menopause.
The dosage level required for the activity is much lower than that used in known dose regimes where danazol is used in the female to treat, for example endometrosis. The preferred dosage is between 25 - 100 mg per day as opposed to 200 to 800 mg per day used previously in different treatments. The dose may be administered orally, nasally, as a solid implant, or intravenously, intramuscularly or transdermally.
In a preferred embodiment a dose of 25 mg of danazol is administered to the patient daily in the form of a capsule.
The usage of danazol, optionally in combination with low dosage testosterone treatment, appears to give for the first time a unique opportunity to adjust the level of TT, SHBG and hence FAI to mimic a normal youthful endocrine pattern even in middle-aged and elderly men. This should give clinical benefits in both treating hypogonadal men, and in the field of preventive medicine, where maintaining an adequate level of testosterone activity is being shown to be a key factor.


APS Pharmacy suggested dosing for Danazol
25mg (capsule or troche), once a day.
**Danazol can also be compounded together with Anastrozole in one capsule.
*** Danazol is a non-scheduled (non-controlled) medication

Definitely a good read.

It's difficult to find much data on Danazol online as it relates to HRT.
TT 600+
Free T barely registered.

Getting started, it was recommended I take Danazol @ 25mg 1x per day.
Nothing else except some vitamins.

Until I found this, I was worried I was being 'mistreated', for lack of a better word. The claim is, that by freeing up some of the free test, I should notice a change whereas none of mine is being used anyway. There is a chance that MAYBE the total will even rise.

I think at the low dose, it won't lower my total t. From what I am understanding now anyway. After a few weeks considering adding HCG injections.

The idea is, to not add a treatment of testosterone unless it is necessary. Once started, it becomes a necessity.

Anyway, thanks for the post. I realize it is a little dated. If anything new has been discovered, please share.
 
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