Right off from the get go, this is wrong!
This makes no statement as to dosing, which is critical for PCT. In fact, it is by far the most important factor in avoiding ASIH.
MESO-Rx
Anabolic Steroids
PCT Simplified
- Thread starter Bansh
- Start date
Right off from the get go, this is wrong!
This makes no statement as to dosing, which is critical for PCT. In fact, it is by far the most important factor in avoiding ASIH.
Doc, what are your thoughts on the graphing tool? is 6mg per day a good target level for beginning a PCT?
Here's a link to the formulas used in the graph. http://steroidplot.com/about/
The formula used for calculating the rate of compound release at a given day t is:
λ * N(t)
Where λ is the decay constant equal to ln(2)/h, h being the half life of the compound given in days; and N(t) is the half-life equation given by:
N(t) = n * e^(-t/λ)
Where n is the original dose of the compound in mg and t is given in days.
Terminal Half-lives
The formula used for calculating the rate of compound release at a given day t is:
λ * N(t)
Where λ is the decay constant equal to ln(2)/h, h being the half life of the compound given in days; and N(t) is the half-life equation given by:
N(t) = n * e^(-t/λ)
Where n is the original dose of the compound in mg and t is given in days.
Terminal Half-lives
here's the reference for the half lives used in the graph. http://www.mediafire.com/view/d948i...e+pharmacokinetics+of+testosterone+esters.pdf.
For "PCT," make use of the Mean Residence Time [MRT]. In fact, due to the wide variation observed from individual to individual, I leaned towards 10 days [TC/TE]. The key is to ensure HPTA Functionality/Restoration. This is not done by trying to make the PCT as short as possible.
In recent years, more and more noncompartmental methods have been used for pharmacokinetic analysis. Twenty years ago statistical moment theory was introduced to pharmacokinetic analysis. The times for the individual molecules to be eliminated can be described in terms of a statistical distribution function, i.e. the individual molecules can be eliminated just by chance within the first minutes or might still reside in the body weeks later.
The mean residence time is a characteristic of this collective behaviour and is the mean of the residence times of individual molecules. The mean residence time can be regarded as the statistical moment analogy to half-life (t1/2). Assuming linear pharmacokinetics, the mean residence time (MRT) is characteristic for a special drug, independent of the administered dose.
In recent years, more and more noncompartmental methods have been used for pharmacokinetic analysis. Twenty years ago statistical moment theory was introduced to pharmacokinetic analysis. The times for the individual molecules to be eliminated can be described in terms of a statistical distribution function, i.e. the individual molecules can be eliminated just by chance within the first minutes or might still reside in the body weeks later.
The mean residence time is a characteristic of this collective behaviour and is the mean of the residence times of individual molecules. The mean residence time can be regarded as the statistical moment analogy to half-life (t1/2). Assuming linear pharmacokinetics, the mean residence time (MRT) is characteristic for a special drug, independent of the administered dose.
More ...
Even more ...
interesting stuff. Just when I thought I had figured out the whole concept of half lives, I get introduced to MRT.
Here's a reference tool for comparing nmol's to ng/dl ...... 15 nmol is roughly = to 425 ng/dl
http://www.nebido.com/tools/index.php/en/default/index/conversion-tool
Here's a reference tool for comparing nmol's to ng/dl ...... 15 nmol is roughly = to 425 ng/dl
http://www.nebido.com/tools/index.php/en/default/index/conversion-tool
0.0347 X ng/dL = nM/L
ATodd
Member
Weeks 1-12(12weeks): Arimidex @ .5mg/day (Everyday)
???
Funny, I thought it was important to have E2 levels >0. I guess you could do 0.5 of Arimidex ED and still have some E2, Bansh are you a preovulatory woman?
atodd
???
Funny, I thought it was important to have E2 levels >0. I guess you could do 0.5 of Arimidex ED and still have some E2, Bansh are you a preovulatory woman?
atodd
^lololll bro ur nips wont get longer unless you let someone breastfeed on those nipples nonstop loll
Word I was getting paranoid I got a little gynocamstia on the past and I'm starting to think its is getting worst but it might just b in my head thanks
Colt44
Well-known Member
I would avoid gear that gives you udders. [emoji230]
Sinister HellFire
Banned
How many Corageon's are there around here lately...I wonder...
T-Bagger
Elite
@Michael Scally MD - I know this is an older thread, but was wondering about your take on HCG, 1000 iu/week run with Arimidex, 1 mg/EOD, starting 2 weeks prior to cycle end and continuing same dosage for 1-2 weeks after cycle ends for PCT.
Many new things I'm reading lately are saying Nolva is next to worthless for PCT.
Many new things I'm reading lately are saying Nolva is next to worthless for PCT.
T-Bagger
Elite
Call it bro science I guess, since there isn't many reputable medical sources that will break down PCT (unless I'm completely off base). Most newer posts I'm reading on other boards are saying Clomid is the way to go and maybe another anti estrogen like Aromasin. I'll see if I can find anything reputable.
I read the dangerous, carcinogenic effects of Nolva here: http://www.cancer.gov/cancertopics/f...rapy/tamoxifen
I still would love to hear the doctor's thoughts on HCG & Adex only as PCT.
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