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Monster PLEXX PCT Dosing Questions


Ok, so after doing some research around the web, I realize I am probably going to get flamed for taking this compound... and unfortunately I can't go back and un-take it. So this is where I am... I finished my 3rd week and I began the cycle at 5'11" ~175-178lbs 12-14 bf% and am currently 5'11" ~192-195lbs.

I took additional milk thistle, omega 3,6,9, and men's vitamins along with 80-100+ ounces of water everyday... consumed 3,500-5,500 kcal/day... and of course, no alcohol. Strength and mass gains all around... and overall I'm extremely happy with the results... and surprisingly jumping from my starting weight to the weight I am now, I feel as though body fat % stayed relatively the same... I may even be slightly leaner.

So this is my question - it's Post-cycle time and I have access to these three compounds... Arimidex, Nolvadex, and Femara. My idea was looking to just take 2 of the 3, over possibly a 1 1/2-2 month long post-cycle to bring myself back to normal. How should I dose my PCT? Nolva then Arimidex? Just Arimidex?

I've tried to find out more information specifically on this compound and how I should dose as far as when to use an AI and when to use a SERM but am not finding much. I know there are some really knowledgable people on this site so I knew I would get better answers on here rather than another place... is there anyone who can help?

Info on Monster PLEXX

Serving Size 1 capsule - Serving Size 90

Dymethazine - (17b-hydroxy-2a,17b-dimethyl-5a-androstan-3-one-azine)...5mg

Halodrol 50 - (4-chloro-17a-methyl-androst-1,4-diene-3-17b-diol)...15mg

Superdrol - (2a,17a-dimethyl-5a-androst-3-one-17b-ol)...5mg

Max LMG (13-ethyl-3-methoxy-gona-2-5 diene-17-one)...20mg

ATD - (1-4-6 androstatriene-3-17-dione) Anti-Aromatase ...10mg
Milk Thistle 80% Silymarin ... 50mg N-Acetyl-L-Cysteine (NAC)...50mg


Read the SERM/AI sticky.

Youre lost.


Yes I'm lost :expressionless:


I have a co-worker who ran Monsterplexx, he just got a call from his doctor telling him that his bloodwork came back showing his liver values were toxic. Yes he made decent gains, but at the expense of his liver, not worth it. I would recommend not using this compound again. True AAS are far too easy to get a hold of(if you really do some research) and far safer.

As for your PCT, just go with 3-4 weeks of Nolvadex (tamoxifen) at 20 mg a day. None of the compounds listed in plexx aromatize, and even if they did, using an AI after the fact is not going to help. In addition, using an AI like Arimidex with Nolvadex is counterproductive as Nolvadex will actually lower the amount of Arimidex in your system.

Like I said above, 20mg a day will suffice, any more than that is not going to increase the PCT effectiveness. Good luck.


Prove it



A little lengthy but it it does a good job of explaining the competition between Nolva and Adex.

by Anthony Roberts -- Aromasin (Exemestane) is one of those weird compounds that nobody really knows what to do with. What we generally hear about it makes it very uninterestingâ?¦Itâ??s a third generation Aromatase Inhibitor (AI) just like Arimidex (Anastrozole) and Femera (Letrozole). Both of those two drugs are very efficient at stopping the conversion of androgens into estrogen, and since we have them, why bother with Aromasin? Itâ??s a little harder to get than the other two commonly used aromatase inhibitors, because itâ??s not in high demand, and thereâ??s never been a readily apparent advantage to using it. And I meanâ?¦lets face it: Itâ??s awkward-sounding. Aromasin doesnâ??t have much of a ring to it, and exemestane is even worse. Arimidex has a bunch of cool abbreviations ("A-dex" or just â??dex) and even Letrozole is just "Letro" to most people. Whereâ??s the cool nickname for Aromasin/exemestane? A-Sin? E-Stane? It just doesnâ??t work. Itâ??s the black sheep of AIs. And why do we even need it when we have Letrozole, which is by far the most efficient AI for stopping aromatization (the process by which your body converts testosterone into estrogen)? Letro can reduce estrogen levels by 98% or greater; clinically a dose as low as 100mcgs has been shown to provide maximum aromatase inhibition (2)! So why would we need any other AIs? Well, first of all, estrogen is necessary for healthy joints (3) as well as a healthy immune system (4). So getting rid of 98% of the estrogen in your body for an extended period of time may not be the best of ideas. This may be useful on an extreme cutting cycle, leading up to a bodybuilding contest, or if you are particularly prone to gyno, but certainly canâ??t be used safely for extended periods of time without compromising your joints and immune system.

So that leaves us with Arimidex, which isnâ??t as potent as Letrozole, but at .5mgs/day will still get rid of around half (50%) of the estrogen in your body. Problem solved, right? Use Arimidex on your typical cycles, and if you are very prone to gyno or are getting ready for a contest, use Letro.

But what about Post Cycle Therapy (PCT)?

I think at this point most people are sold on the use of Nolvadex (Tamoxifen Citrate) instead of Clomid for PCT, since both compete estrogen at the receptor site, both increase serum test levels, and both drugs may also alter blood lipid profiles favorably (6). But since 20mgs of Tamoxifen is equal to 150mgs of clomid for purposes of testosterone elevation, FSH and LH, but Tamoxifen doesnâ??t decrease the LH response to LHRH (6) I think most people agree to Nolvadexâ??s superiority for PCT.

Iâ??ve always been in favor of using Nolvadex during PCT, along with an AI, because reducing estrogen levels has been positively correlated with an increase in testosterone (7) so in my mind, itâ??s be beneficial to increase testosterone by as many mechanisms as possible while trying to recover your endogenous testosterone levels after a cycle. SO which AI do we use? Letro or A-dex? Well, why donâ??t we just keep using whichever one we used during the cycle, and add in some Nolvadex? Unfortunately, Nolvadex will significantly reduce the blood plasma levels of both Letrozole as well as Arimidex (8). So if we choose to use one of them with our Nolvadex on PCT, weâ??re throwing away a bit of money as the Nolvadex will be reducing their effectiveness.

This, of course, is where Aromasin comes in, at 20-25mgs/day.

Aromasin, at that dose, will raise your testosterone levels by about 60%, and also help out your free to bound testosterone ratio by lowering levels of Sex Hormone Binding Globulin (SHBG), by about 20% (12)â?¦SHBG is that nasty enzyme that binds to testosterone and renders it useless for building muscle. But what about using it along with Nolvadex for PCT?

To understand why Aromasin may be useful in conjunction with Nolvadex while both Letro and A-dex suffer reduced effectiveness, weâ??ll need to first understand the differences between a Type-I and Type-II Aromatase Inhibitor. Type I inhibitors (like Aromasin) are actually steroidal compounds, while type II inhibitors (like Letro and A-dex) are non-steroidal drugs. Hence, androgenic side effects are very possible with Type-I AIs, and they should probably be avoided by women. Of course, there are some similarities between the two types of AIsâ?¦both type I & type II AIs mimic normal substrates (essentially androgens), allowing them to compete with the substrate for access to the binding site on the aromatase enzyme. After this binding, the next step is where things differ greatly for the two different types of AIâ??s. In the case of a type-I AI, the noncompetitive inhibitor will bind, and the enzyme initiates a sequence of hydroxylation; this hydroxylation produces an unbreakable covalent bond between the inhibitor and the enzyme protein. Now, enzyme activity is permanently blocked; even if all unattached inhibitor is removed. Aromatase enzyme activity can only be restored by new enzyme synthesis. Now, on the other hand, competitive inhibitors, called type II AIâ??s, reversibly bind to the active enzyme site, and one of two things can happen: 1.) either no enzyme activity is triggered or 2.) the enzyme is somehow triggered without effect. The type II inhibitor can now actually disassociate from the binding site, eventually allowing renewed competition between the inhibitor and the substrate for binding to the site. This means that the effectiveness of competitive aromatase inhibitors depends on the relative concentrations and affinities of both the inhibitor and the substrate, while this is not so for noncompetitive inhibitors. Aromasin is a type-I inhibitor, meaning that once it has done its job, and deactivated the aromatase enzyme, we donâ??t need it anymore. Letrozole and Arimidex actually need to remain present to continue their effects. This is possibly why Nolvadex does not alter the pharmacokinetics of Aromasin (11).

Before we close the book on Aromasin, itâ??s worth noting that you can (and should) still use one of the non-steroidal AIs during your cycle to reduce estrogen, if necessary. When you are ready for PCT, you can then switch over to Aromasin and still experience the full effects of an AI, since there is no cross-over tolerance experienced between steroidal and non-steroidal AIs (9). Since Aromasin is about 65% efficient at suppressing estrogen (10), itâ??s certainly a very powerful agent, especially considering you wonâ??t experience reduced effectiveness because of your concurrent use of Nolvadex or from any sort of tolerance developed by using other AIs on your cycle(9). There is also a decent amount of preclinical data suggesting that Aromasin has a beneficial effect on bone mineral metabolism that is not seen with non-steroidal agents, and it may also have beneficial effects on lipid metabolism that are not found in the non-steroidal Letro and A-dex (9).

Finally, as weâ??re going to be using Nolvadex for PCT anyway, and we ought to be using an AI with it for maximum recoveryâ?¦I think Aromasin- considering itâ??s compatibility with Nolvadex and beneficial effects on bone mineral content and lipid profile, has finally stopped being the black sheep of AIs and found a home in our Cycles.


Anthony Roberts. lulz

I dont trust a word out of his mouth, sorry.


Has anyone come across a study that explains the mechanism by which nolva decreases the effectiveness of letro or explains how this decreased effectiveness was measured?