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V.Med - Bulk Mix Hybrid One 600mg (Super Bulk)

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V.MED BULK MIX 

HYBRID ONE 600MG

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V.Med Bulk Mix Hybrid One 600 mg

Deca-Durabolin is the brand and trade name for the anabolic steroid Nandrolone. Specifically, Deca-Durabolin is the trade name for Nandrolone Decanoate – the decanoate ester variant of Nandrolone. “Deca”, as it is informally known as among bodybuilders, ranks among the top three anabolic steroids where it is the second most popular and widely utilized anabolic steroid in existence.

CATEGORY: Hybrid Injectables

CONTENT: Trenbolone Enanthate Testosterone Cypionate Nandrolone Decanoate

PRESENTATION SIZE: 10ml bottle

STRENGTH: 600mg per ml

TOTAL STRENGTH: 6000mg per 10ml bottle

DESCRIPTION:

**This product is a combination of the following three ingredients – **

  • Nandrolone Decanoate 200mg/ml
  • Testosterone Cypionate 200mg/ml
  • Trenbolone Enanthate 200mg/ml

When profiling this compound, we must look at the profile of every individual compound and then look at the synergistic effect of the three compounds together. 

**Overview and History of Deca 300mg Long Acting (nandrolone decanoate) **

Deca-Durabolin is the brand and trade name for the anabolic steroid Nandrolone. Specifically, Deca-Durabolin is the trade name for Nandrolone Decanoate – the decanoate ester variant of Nandrolone. “Deca”, as it is informally known as among bodybuilders, ranks among the top three anabolic steroids where it is the second most popular and widely utilized anabolic steroid in existence. First place is held by none other than Dianabol (Methandrostenolone), and third by Winstrol (Stanozolol). There is good reason for why Deca-Durabolin is so well liked by bodybuilders and athletes, and is even held in high regard by the medical establishment as well.

Nandrolone Decanoate was first introduced within the scientific community in 1960[1], making it among the first handful of pioneer anabolic steroids developed. It was developed by Organon, and not long afterwards in 1962 it was released onto the prescription drug market as Deca-Durabolin. Not many are aware, however, that Nandrolone did exist a few years prior in 1957, as the fast-acting Nandrolone Phenylpropionate ester variant. Nandrolone Phenylpropionate did gain significant popularity, but unfortunately its very short half-life imposed limitations on its use, requiring every-other-day injections at a minimum, and so Nandrolone was reinvented as Deca-Durabolin with the decanoate ester affixed to it. The decanoate ester grants Nanadrolone a much longer half-life of approximately 15 days as opposed to the phenylpropionate variant’s 4 days (approximate).

It enjoyed extensive application as a medicinal drug among the medical establishment over time and gained popularity among bodybuilders and athletes for its purportedly ‘mild’ nature. There is some truth to this, but much misunderstanding and myth as well, which will be explained shortly. Deca is only slightly stronger than Testosterone where anabolism is concerned, with a strength rating of 125. By comparison, Testosterone’s anabolic strength rating is 100. However, it possesses a very low androgenic rating of 37, making it favorable for those who are either sensitive to or with to avoid androgenic side effects. Additionally, Nandrolone possesses very low Estrogenic activity and binds very poorly with the aromatase enzyme, which is the enzyme responsible for the conversion of androgens into Estrogen.Only about 20% of Nandrolone is converted into Estrogen in comparison to Testosterone’s conversion rates[2]. The fact that Deca is a Progestin (as all 19-nor compounds are) is what contributes to this low estrogenic activity[3]. Looking further into this, we can also see that Nandrolone experiences aromatization into Estrogen in the liver, but in areas of the body where there is normally a high degree of Estrogen conversion (in fat tissue, for instance), Deca is considerably resistant here[4].

Deca is classified as a 19-no compound because it lacks the 19th carbon that Testosterone possesses, making it a Progestin and therefore express an affinity for the Progesterone receptor[5]. This can present some potential side effects and issues that are unique to 19-nor compounds, and are unseen in most other anabolic steroids.

One particular point to address here is the common claim that Deca-Durabolin is good for the joints and bone tissue, which is indeed true. However, the proposed explanations that circulate among athletes and bodybuilders as to why this is the case are often incorrect myths and misconceptions. Deca does not “lube the joints”, “store water in connective tissue and joints”, or any other such preposterous nonsense. In actuality, Nandrolone promotes very significant increases in collagen synthesis[6], more so than most other anabolic steroids. Other studies have also demonstrated an ability for Deca to also promote vast increases in bone mineral content[7]. What does all of this mean for the athlete? It means that bodybuilders and athletes can experience positive effects on connective and joint tissue, strengthening them during bulking, strength gaining, and mass gaining cycles. It grants them the ability to lift heaver weight with an enhanced recovery of bone and connective tissue, as well as a greater tolerance to the stressors on joints and bone that are produced by intense exercise and resistance training.

Deca-Durabolin Side Effects

As previously noted, Deca is often cited as an anabolic steroid that is very ‘mild’ by comparison to other compounds where side effects are concerned. Unfortunately, this is a mix of fact and fiction that needs to be addressed, and most of these ‘Deca is a mild steroid’ claims are from a bygone era where not much was yet known about these drugs, and today we know much more. Deca-Durabolin is by all accounts both a mild and harsh anabolic steroid, possessing both such properties.

The good news is that Deca-Durabolin experiences a very low aromatization rate into Estrogen, making estrogenic side effects less of an issue compared to other anabolic steroids. Although Estrogen related side effects are not totally and utterly eliminated with Deca, it is more manageable and users should therefore still be conscious of this fact. Estrogenic side effects can include bloating, water retention, blood pressure increases as a result of water retention, and gynecomastia.

As a Progestin, Deca can also increase Prolactin levels in the body. All of the Progesterone and Prolactin related issues can manifest in the form of side effects that are very similar to Estrogen – puffy nipples, gynecomastia, bloating, etc. Anti-estrogens and aromatase inhibitors are known for combating these side effects effectively even if they are attenuated through the Progesterone receptor. However, for Prolactin issues, the use of vitamin B6 in order to control Prolactin levels has been demonstrated in studies using 600mg daily[8]. Anti-prolactin drugs such as Cabergoline and Bromocriptine are also very effective at reducing elevated Prolactin levels effectively, and are often the first line of treatment in Prolactin issues[9][10][11].

Nandrolone is not a C17-AA oral anabolic steroid, and therefore no effects on the liver exist with this compound. Deca does express a small degree of androgenic effects, and therefore much like its estrogenic properties, is less of a concern but should still be monitored and kept in mind. Androgenic side effects can include increased oily skin and acne, increased bodily and facial hair growth, increased risk of male pattern baldness (MPB), and an increased risk of benign prostatic hyperplasia (BPH).

Nandrolone does also express side effects that are common among all anabolic steroids: disruption and/or shutdown of the HPTA (Hypothalamic Pituitary Testicular Axis), and negative cardiovascular implications. For a long time, Deca was cited as an anabolic steroid that was mild on its impact on the HPTA and natural endogenous Testosterone levels. This is simply untrue as studies have demonstrated that at even as low as 100mg per week of Deca-Durabolin, suppression of endogenous Testosterone production rapidly reached close to 60%, and even higher (and faster) when larger dosages of Deca are used[12]. This is common of any 19-nor compound, and the severe and rapid suppression is due to Deca Durabolin and other 19-nors being Progestins by nature[13].

Deca is quite concerning where impacts on the cardiovascular system are concerned, especially with recent discoveries that were not known several decades ago. First and foremost, Deca has shown to decrease HDL (“good” cholesterol) levels by 26% over 10 weeks of administration[14]. And, when compared with Testosterone, Nandrolone tends to exhibit far worse negative cholesterol alterations on average[15]. If these potential cardiovascular issues were not concerning enough, fairly recent data has demonstrated that Deca is 11 times more damaging to blood vessels than Testosterone[16].

Deca-Durabolin Cycles and Uses

Deca-Durabolin is naturally reserved by most athletes and bodybuilders for bulking, mass-adding, and strength-gaining cycles. This is due in part to its positive and beneficial effects on connective and bone tissue, allowing a greater rate of healing in these areas and an added injury preventative when heavier weights are used and more intense physical activity is engaged in.

Being that Deca Durabolin is a long-acting long estered variant of Nandrolone (possessing a half-life of 15 days), Deca-Durabolin cycles are and should be at least 12 weeks in length. Here it is often combined with similar long-estered compounds, such as Testosterone Cypionate. Because of its long acting nature, most users will not experience the ‘kick-in’ of the compound until at least several weeks into the cycle, and this is where many individuals will insert a kickstarting compound into the Deca-Durabolin cycle for the first few weeks. This is typically any oral anabolic steroid, such as DianabolWinstrolAnadrolAnavar, etc. However, for the purposes of bulking and strength gaining, most individuals tend to lean towards compounds generally suitable for these goals, such as Anadrol (Oxymetholone) or Dianabol (Methandrostenolone) for the first 4 – 6 weeks. These compounds are used because of their mass-adding properties that lend themselves to Deca and Testosterone quite well.

This is where the typical age-old cycle stack of Testosterone / Deca / Dianabol is often discussed. Quite simply put, this is the most popular cycle stack in all history. The Testosterone/Nandrolone/Dianabol stack was originally devised, pioneered, and popularized by the golden era bodybuilders of the 1960s and 1970s. This particular stack is often recommended for all tiers of users (beginners, intermediates, and advanced) as it is a timeless stack that will provide quality gains to any user no matter the experience.

Deca-Durabolin Dosages and Administration

As a prescription drug and medication, Nandrolone Decanoate was originally recommended to be prescribed at a dosage of 50 – 100mg every 3 – 4 weeks, for no longer than 12 weeks. Because every medical condition, disability or disease can be different, the prescription recommendations for Deca have changed to suit the individual patient’s needs. For instance, anemic patients were prescriped 100 – 200mg per week, a Deca Durabolin dosage that is considerably larger than the common prescription doses.

For the purpose of performance and physique enhancement, Deca is usually used by beginners in the range of 300 – 500mg per week. Intermediate users normally do not have to venture above the 500mg mark within that beginner range, especially when Deca Durabolin is stacked with other compounds such as Testosterone and/or another oral compound as a kickstarter. Advanced users should likewise have no major requirement to veer outside this dose range, but should an advanced user require a higher dose to elicit gains, a range of approximately 600 – 800mg or greater should suffice, especially if Nandrolone is the primary anabolic compound of a cycle and Testosterone is simply run as a supportive compound at TRT (Testosterone Replacement Therapy) doses.

How to Buy Deca-Durabolin

With Deca holding its place as the second most widely utilized and second most popular anabolic steroid ever used, it tends to be an extremely common and considerably cheap product on the anabolic steroid black market. Both pharmaceutical and underground lab (UGL) versions of this drug exist.

Anywhere from a decent source to pricy sources can be known to sell pharmaceutical grade Deca-Durabolin pricing in the range of $11 – $23 for a single 2ml vial containing 100mg/ml (typically an example of Norma Hellas Greece or Organon Greece products). If you buy Deca Durabolin and seek an underground product from the same type of source ranges from $90 – $145 for a single 10ml vial containing 200mg/ml.

Deca-Durabolin Information: Nandrolone (AKA Deca, Deca Durabolin, Nandrolone Decanoate, Nandrolone Phenylpropionate) **Chemical Name: **19-norandrost-4-en-3-one-17beta-ol, 17β-Hydroxyestra-4-en-3-one Molecular Weight: 274.40 g/mol **Formula: **C18H26O2 Original Manufacturer: Organon **Half Life: ** 15 days **Detection Time: **17 – 18 months **Anabolic Rating: **125 **Androgenic Rating: **37

Deca-Durabolin References:

  1. De Visser, J. et al. Acta Endocrin. (Kbh.) 35 (1960):405.
  2. Biosynthesis of Estrogens, Gual C, Morato T, Hayano M, Gut M and Dorfman R. Endocrinology 71 (1962):920-25.
  3. Competitive progesterone antagonists: receptor binding and biologic activity of testosterone and 19-nortestosterone derivatives. Reel JR, Humphrey RR, Shih YH, Windsor BL, Sakowski R, Creger PL, Edgren RA. Fertil Steril 1979 May;31(5):552-61.
  4. Aromatization of androstenedione and 19-nortestosterone in human placental, liver, and adipose tissues (abstract). Nippon Naibunpi Gakkai Zasshi. 1986 Jan 20;62(1):18-25.
  5. Studies of biological activity of certain 19-nor steroids in female animals. Pincus G, Chang M, Zarrow M, Hafez E, Merril A. December 1956.
  6. 1990 Nov;39(11):1167-9.
  7. Effects of nandrolone Deca Durabolin on bone mineral content. R, Righi GA, Turchetti V, Vattimo A.
  8. Influence of administration of pyridoxine on circadian rhythm of plasma ACTH, cortisol prolactin and somatotropin in normal subjects. Barletta C, Sellini M, Bartoli A, Bigi C, Buzzetti R, Giovannini C. Boll Soc Ital Biol Sper. 1984 Feb 28;60(2):273-8.
  9. Verhelst J, Abs R, Maiter D, et al. (July 1999). “Cabergoline in the treatment of hyperprolactinemia: a study in 455 patients”. J. Clin. Endocrinol. Metab. 84 (7): 2518–22. doi:10.1210/jc.84.7.2518. PMID 10404830.
  10. Webster J, Piscitelli G, Polli A, Ferrari CI, Ismail I, Scanlon MF (October 1994). “A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea. Cabergoline Comparative Study Group”. N. Engl. J. Med. 331 (14): 904–9. doi:10.1056/NEJM199410063311403. PMID 7915824.
  11. Colao A, Di Sarno A, Guerra E, De Leo M, Mentone A, Lombardi G (April 2006). “Drug insight: Cabergoline and bromocriptine in the treatment of hyperprolactinemia in men and women”. Nat Clin Pract Endocrinol Metab 2 (4): 200–10. doi:10.1038/ncpendmet0160. PMID 16932285.
  12. The administration of pharmacological doses of testosterone or 19-nortestosterone to normal men is not associated with increased insulin secretion or impaired glucose tolerance. Karl E. Friedl et al. J Clin Endocrinol Metab 68:971, 1989.
  13. Influence of nandrolone decanoate on the pituitary-gonadal axis in males. Bijlisma J, Duursma S, Thijssen J, Huber O. Acta Endocrinol 101 (1982):108-12.
  14. Metabolic effects of nandrolone decanoate and resistance training in men with HIV. Sattler FR, Schroeder ET, Dube MP, Jaque SV, Martinez C, Blanche PJ,Azen S,Krauss RM. Am J Physiol Endocrinol Metab. 2002.
  15. Lipemic and lipoproteinemic effects of natural and synthetic androgens in humans. Crist DM, Peake GT, Stackpole PF, Clin Exp Pharmacol Physiol 1986 Jul;13(7):513-8.
  16. Toxicol Lett. 2007 Mar 8; 169(2):129-36.
  17. Instagram - @international_muscle_page
  18. Instagram - @joseph_davidson_jaco

**Overview and History of testosterone cypionate **

Testosterone Cypionate is one of the many esterified variants of Testosterone available, and is most likely the second most popular esterified variant (the first being Testosterone Enanthate). It is an injectable form of Testosterone with a slow rate of release and a longer half-life. However, the release rates and half-life of both Testosterone Cypionate and Testosterone Enanthate are very much identical and the two compounds are easily interchangeable (for example, an individual can easily run a 10 week cycle of Testosterone and switch between Testosterone Enanthate and Testosterone Cypionate seamlessly). Testosterone Cypionate possesses a half-life of approximately 12 days while Testosterone Enanthate possesses a half-life of approximately 10 days – hardly much difference. The interesting fact about Testosterone Cypionate, however, is that it seems to have a distinct favor of popularity among American bodybuilders and athletes over the Enanthate variant. These distinctions are not extreme, however, and the commonality of use and availability of both variants is almost equal with Testosterone Enanthate ever so slightly more popular. Neither variant possesses any advantages over the other.

Testosterone Cypionate was first created in the mid-1950s, and was released on the prescription drug market under the brand name Depo-Testosterone and manufactured by UpJohn (however, its brand name at first was labeled as Depo-Testosterone cyclopentylpropionate but was shortened for obvious reasons). Unlike Testosterone Enanthate, which is primarily known as an international item, Testosterone Cypionate is known to be the US answer to the Enanthate variant (although Testosterone Enanthate is utilized almost just as equally in the US). Testosterone Cypionate has held such a positive track record that it is in fact still in production by Upjohn (who merged with Pfizer in 2009) today. As Testosterone Cypionate was the American response to the international product Testosterone Enanthate, many American bodybuilders and athletes throughout the 1960s, 70s, and 80s preferred the use of Testosterone Cypionate over the Enanthate variant for no reason other than the support of an American product, very much akin to an issue of pride (once again, the Cypionate and Enanthate variants of Testosterone are both almost 100% identical and there is no practical reason to prefer one compound over the other).

However, there have been very minimal reports of various pateints that prefer Testosterone Cypionate to Testosterone Enanthate if only because of the fact that some individuals tend to respond better at the injection site. A very small percentage of individuals have reported irritated injection sites in response to the Enanthate variant, and find the Cypionate variant to be much easier in terms of the injection site comfort and reaction. Medically, Testosterone Cypionate, like Enanthate, is used primarily for the treatment of androgen-deficient male patients (hypogonadism and andropause). Other although minor uses of Testosterone Cypionate in the medical field included: the treatment of individuals deficient in bone density and strength, treating uncontrollable menstrual bleeding (menorrhagia), osteoporosis treatment, treatment for frail elderly patients and individuals recovering from periods of extensive muscular atrophy. In recent years, just like Testosterone Enanthate, Testosterone Cypionate has been investigated in its use as a male birth control drug at a dose of 200mg weekly.

Testosterone Cypionate in the 1970s, like all anabolic steroids at the time, had undergone a narrowing of approved medical application in its use. The FDA had narrowed its approved medical uses down to the treatment of male androgen deficiency (hypogonadism and andropause). Testosterone Cypionate held an even stronger case for its narrowing of approved applications due to the fact that Testosterone itself is quite the strong androgen unsuitable for use in females and children where other more suitable anabolic steroids (such as Anavar and Primobolan) could be used instead.

Chemical Characteristics of Testosterone Cypionate

As previously mentioned, Testosterone Cypionate is simply Testosterone with the Cypionate ester bound to the Testosterone chemical structure. Specifically ‘Cypionate’ is Cypionic acid, but once bound to Testosterone it is properly referred to in chemistry as an ester bond (or ester linkage). Cypionic acid is chemically bound to the 17-beta hydroxyl group on the Testosterone structure. Esterified anabolic hold a greater degree of solubility in fats, and therefore release slower from the injection site in comparison to un-esterified Testosterone – however, this is not the main reason as to why esters extend the release rate and half-life of the given anabolic steroid it is attached to. The primary reason for the augmentation of its half-life and release rate is due to the fact that when Testosterone Cypionate enters the bloodstream, enzymes will bind to the Testosterone Cypionate molecule and break the bond between the ester and the hormone, which takes a varying amount of time depending on the size of the ester in question. This is why larger esters such as Cypionate, Enanthate, Decanoate, and so forth all possess longer half-lives than the smaller shorter esters such as Propionate, Phenylpropionate, Acetate, etc. Therefore, the end result is that the ester is removed from the hormone via enzymes, and what is left over following this chemical interaction is pure Testosterone that is free to do its work in the body. This process of enzymes cleaving off the ester from the Testosterone molecule is what is ultimately responsible for the slower release rates. Pure Testosterone alone with no ester bonded to it possesses a half-life of approximately 2 – 4 hours. When the Cypionate ester is attached to it, creating Testosterone Cypionate, the half-life of Testosterone is now extended to 12 days, which results in a slower release and activity of the hormone.

Properties of Testosterone Cypionate

Testosterone Cypionate’s attributes and expressive properties follows what any individual would expect from Testosterone preparation, with the exception of the differing release rates and half-lives. It must be made clear right now to the reader that Testosterone is very much literally the original anabolic steroid, which is manufactured endogenously naturally in all humans and in the vast majority of animal species. Two important facts result from this: 1. Testosterone is utilized as the base measurement by which all other anabolic steroids are measured against, and, 2. Because Testosterone is the most natural anabolic steroid already manufactured by the human body, Testosterone is considered the safest anabolic steroid for use, as every individual’s body is already accustomed to the effects of Testosterone only to a lesser degree. Essentially, the use of Testosterone for the purpose of physique and performance enhancement is simply the supplementation of additional Testosterone – this could easily be defined as the practice of administering (either through injection or ingestion) more of a hormone into the body that it already manufactures and utilizes.

Testosterone Cypionate Side Effects

Where side effects are concerned, Testosterone Cypionate could be described as being moderate. It is often compared to its almost identical brother, Testosterone Enanthate. The truth of the matter is that Testosterone Cypionate has a longer half-life due to its longer fatty acid ester chain, which does modulate its side effect profile ever so slightly, but this is really a matter of splitting hairs and never noticeable. At its core, it is a Testosterone variant and therefore will carry with it all of the side effects known to Testosterone. Testosterone is the primary male hormone manufactured in humans and in all vertebrates, and is the father of all anabolic steroids. Of course, when it comes to any discussion of side effects, one must take into account that there will be varying differences between individuals due to factors such as individual body reaction, age, sensitivity, and genetics. These are all factors that determine whether someone may experience certain side effects at a greater or lesser degree, or whether they may not experience these side effects at all.

Estrogenic side effects are the first and primary concern that almost all anabolic steroid users consider and research surrounding Testosterone Cypionate. Testosterone itself is known for being an aromatizable anabolic steroid (meaning, it converts – aromatizes – into Estrogen in the body). The aromatization rate of Testosterone Cypionate in relation to other anabolic steroids is moderate at best. The rate of aromatization is also heavily dependent on the dosage, and thus the total blood plasma levels of Testosterone at any one given time. The general rule is that more Testosterone equals more aromatization into Estrogen. Potential estrogenic side effects include the following: water retention and bloating, increases in blood pressure (resultant from water retention), increased fat gain/retention, and potential development of gynecomastia.

Being that Testosterone Cypionate is an androgen, users are also susceptible to androgenic side effects as well. Testosterone is also known for its reduction to a much more powerful androgen, Dihydrotestosterone (DHT), in the body – particularly in higher degrees in various tissues, such as the scalp, prostate, and skin. This is where the real bulk of the androgenic side effects come from, as opposed to Testosterone’s direct interaction with androgen receptors itself. Potential androgenic side effects include the following: increased oily skin (sebum secretion), increased acne formation (linked to sebum secretion), bodily and facial hair growth, and the increased risk of experiencing male pattern baldness (MPB) if the individual possesses the genetic predisposition for it.

Much like Testosterone Enanthate, Testosterone Cypionate has been found in studies to exert absolutely no hepatotoxic (liver toxic) activity in the body, even when administered orally at what would be considered extreme doses.

Because Testosterone is, of course, an androgenic anabolic steroid, it does impose suppression and shutdown of the hypothalamic testicular pituitary axis (HPTA) during use. In other words, it will cause the body to stop manufacturing its own natural endogenous Testosterone. Other known potential side effects that follow Testosterone Cypionate use include negative cardiovascular impacts, most notably the reduction of ‘good’ (HDL) cholesterol in the bloodstream during use.

Testosterone Cypionate Cycles and Uses

As with almost any Testosterone variant or derivative, Testosterone Cypionate cycles tend to almost always be utilized for the purpose of bulking, mass gaining, and strength gaining periods of training. Though its ideal use is for this purpose, this is not to say that it cannot be used effectively (albeit at a lower dosage) for cutting cycles where fat loss is the primary goal. For the purpose of bulking and/or gaining mass and strength, Testosterone Cypionate is usually employed at a higher dosage (approximately 500mg/week). It is usually utilized at this dosage for a period of 12 – 14 weeks due to its longer ester, and therefore longer half-life. Testosterone Cypionate possesses a half-life of around 10 – 12 days. By comparison, its close counterpart Testosterone Enanthate is almost the same, with a half-life of around 7 – 10 days.

No matter the cycle goal, whether it is cutting or bulking, Testosterone Cypionate is usually utilized with and stacked with other anabolic steroids that possess very similar characteristics for obvious reasons. It is a common companion to compounds such as Deca-Durabolin (Nandrolone Decanoate), which is usually run for the same 10 – 12 week length as Testosterone Cypionate, and a ‘kickstarting’ compound such as Dianabol 

(Methandrostenolone) is usually included from the start of the cycle until it is discontinued at around week 4 or 6.

In the event that one wishes to try to use Testosterone Cypionate in a cutting or fat loss cycle, it can be employed in the manner of a supportive compound only to maintain natural and normal levels of Testosterone in the body while a stronger compound better suited to the fat loss role does the job. This is known as using Testosterone Cypionate at a TRT (Testosterone Replacement Therapy) dosage of around 100mg/week.

Testosterone Cypionate Dosing and Administration

Medically, Testosterone Cypionate is prescribed at 250mg once every 2 – 4 weeks, which is also dependent on the physician’s protocol, and the patient’s progress in his TRT therapy.

In the realm of bodybuilding and performance enhancement, Testosterone Cypionate is normally run at around 300 – 500mg weekly as a beginner dosage range. Intermediate Testosterone Cypionate dosages are often in the range of 500 – 750mg per week, and advanced users are known for running as high as 1,000mg or more per week of Testosterone Cypionate.

As Testosterone Cypionate possesses a half-life of around 10 – 12 days, it is recommended that Testosterone Cypionate is administered once per week at an absolute minimum. However, if one wishes to experience the best results possible, ideally Testosterone Cypionate would be administered two times per week where the dosage is split evenly between injections. For example, a Testosterone Cypionate dosing of 500mg/week should be administered as 250mg on Monday and 250mg on Thursday every week. This minimizes peaks and valleys in blood plasma levels, and thus also reduces certain unwanted side effects due to spiking blood plasma levels of the hormone.

Testosterone Cypionate Legality

Anabolic steroid laws vary quite a bit across the globe, with the vast majority of countries and regions imposing very little to no laws or restrictions on their possession or use. Therefore, it is important that the legality of Testosterone Cypionate in the three most common Western nations be covered here (USA, Canada, and the UK)

In the United States, Testosterone Cypionate is classified as a Schedule III drug in the Controlled Substances Act, and thus the possession and use of any Testosterone product without a valid physician’s prescription would be considered a felony. Needless to say, trafficking, importation, and the purchase of EQ or any anabolic steroid is a criminal act.

In the United Kingdom, Testosterone Cypionate falls under Schedule IV, whereby possession and use of Testosterone without a physician’s prescription is legal for personal use. Importation of Testosterone Cypionate for personal use without a prescription is also not a felony.

Canadian law is similar to the UK, where it is a Schedule IV drug, and as such, possession and use of Testosterone Cypionate for personal use without a valid physician’s prescription is not a felony and is legal. However, trafficking of the substance is a felony.

Research of the laws in your country or region beforehand is paramount in order to make the appropriate decisions, and what to expect in regards to what you could be getting into. Ignorance of the law is no excuse.

How to Buy Testosterone Cypionate

Testosterone Cypionate is a moderately popular compound within the anabolic steroid world, and often competes with Testosterone Enanthate for popularity. There should be no problems locating this product on the market, as it is quite common and also easily manufactured. This also guarantees that Testosterone Cypionate is one of the cheaper products out there. There are both human-grade pharmaceutical grade Testosterone Cypionate products out there, as well as underground lab (UGL) grade products on the market. The differences are obvious here, with quality control being the main issue, and that pharmaceutical grade Testosterone Cypionate is usually more expensive for obvious reasons.

Testosterone Cypionate can be purchased from online sources and vendors, as well as the traditional in-person transactions (i.e. ‘gym-dealers’). Prices may vary. Pharmaceutical Testosterone Cypionate can be found for around $13 – $15 for a single 1ml vial containing 250mg/ml (which is usually the standard for pharmaceutical grade glass ampoules). Underground Testosterone Cypionate normally sells for $60 – $90 for a single 10ml vial containing 250mg/ml.

Testosterone Cypionate Information:

17b-hydroxy-4-androsten-3-one

Testosterone base + cypionate ester

**Formula: **C27 H40 O3

**Molecular Weight: **412.6112

**Molecular Weight (base): **288.429

Molecular Weight (ester): 132.1184

Formula (base): C19 H28 O2

Formula (ester): C8 H14 O2

**Melting Point (base): **155

Melting Point (ester): 98 – 104 C

Effective Dose (Men): 300-2000mg+ week

Effective Dose (Women): Not recommended (androgenic)

Active life: 12-14 days

Detection Time: 3-4 months

Anabolic/Androgenic ratio: 100/100.

Testosterone Cypionate References:

  1. Instagram - @international_muscle_page
  2. Instagram - @joseph_davidson_jaco

**Overview and History of Tren 200mg Long Acting (trenbolone enanthate) **

It is difficult to determine where Trenbolone Enanthate places itself in terms of popularity among the three main variants of Trenbolone (Trenbolone Acetate, Trenbolone Enanthate, and Trenbolone Hexahydrobenzylcarbonate). Some might agree that Trenbolone Enanthate is a close tie with Trenbolone Hexahydrobenzylcarbonate (Parabolan) in terms of second most popularity next to Trenbolone Acetate, which has reserved first place among athletes and bodybuilders for preference. Trenbolone is a very potent and powerful anabolic steroid that, in this case, is a long-estered variant. That is to say that Trenbolone Enanthate is affixed with the Enanthate ester, a long ester that extends the half-life of Trenbolone upwards of 7 – 10 days. This is quite different from Trenbolone Acetate, which expresses a half-life of approximately 3 days. Ultimately, there are both advantages and disadvantages to both, which will be addressed shortly. Trenbolone Enanthate in terms of release rate and pharmacokinetics is literally identical to Testosterone Enanthate (or any anabolic steroid affixed with the Enanthate ester). Anabolic steroids such as Trenbolone Enanthate are designed to provide a fairly quick release of the hormone into the body in the initial 2 days or so after initial administration, and blood plasma levels remain high, slowly tapering off over a two week period. This could be considered a sustained release. Because the half-life of Trenbolone Enanthate is quite close to Parabolan (Trenbolone Hex), the two are easily interchangeable with one another.

It should be made perfectly clear, however, that the esters affixed to the hormone (Acetate, Enanthate, or Hex) merely serve to alter the release rate and half-life of the drug – they do not alter the strength, potency, or pharmacodynamics of the hormone that the ester is affixed to. Trenbolone Acetate expresses a 3 day half-life, Trenbolone Enanthate expresses a 7 – 10 day half-life, and Trenbolone Hexahydrobenzylcarbonate (Parabolan) expresses a 14 day half-life.

Trenbolone as the base hormone is an extremely powerful hormone, approximately 5 times the strength of Testosterone in both anabolic and androgenic strength, making Trenbolone an extremely potent anabolic steroid. Roussel-UCLAF was the firm during the late 1960s to initially synthesize and investigate Trenbolone, first with Trenbolone Acetate, and then with other long-acting Trenbolone esterified variants[1]. The interesting aspect of Trenbolone’s history is that Enanthate was not specifically researched by Roussel-UCLAF, though was metaphorically ‘on the backburner’. It was never officially manufactured as an FDA-approved (or any equivalent) pharmaceutical drug meant for human use or sale on the prescription market. The other two variants of Trenbolone (Acetate under the brand name Finajet/Finaject and Hex under the brand name Parabolan) both experienced brief periods of official sale and use on the pharmaceutical drug market, although briefly. Trenbolone Acetate’s life on the pharmaceutical market was short lived in the 1970s, while Parabolan reigned briefly during the 1990s. It was not long until they were pulled from the market and their status as human-use prescription drugs stripped. Trenbolone Enanthate, on the other hand, would surface much later on in 2004 as an underground lab (UGL) product, made by British Dragon and sold as Trenabol. British Dragon was the first to manufacture and offer this ester of Trenbolone, dosed at 200mg/ml, and eventually manufactured a full line of Trenbolone based products that were all underground products for sale on the black market. None were FDA-approved, manufactured by pharmaceutical companies, or sold in pharmacies.

Trenbolone Enanthate was never approved for either human or veterinary use, and is still to this day strictly an underground origin product that is only manufactured by underground laboratories. It is impossible to find any pharmaceutical grade Trenbolone Enanthate that is made to pharmaceutical standards and meant for human use. Its popularity is only as big as it currently is due to its popularity growth and boom on the black market and is extremely common among bodybuilders and athletes, probably because it is one of the few convenient long-acting Trenbolone esters. By the time Trenbolone Enanthate arrived on the scene, the vast majority of Trenbolone users were utilizing the Acetate ester, and still remains the most common form of Trenbolone even today. Although the original British Dragon laboratories shut down in 2006 and underwent a law enforcement bust, the legacy of Trenbolone Enanthate continues today and countless other underground labs continue to manufacture it, ensuring a steady and guaranteed supply on the black market.

What Is Trenbolone Enanthate?

As previously mentioned, Trenbolone Enanthate is a long ester variant of the hormone Trenbolone. Trenbolone, being a derivative of Nandrolone (the base hormone in Deca-Durabolin), is a 19-nor anabolic steroid. 19-nor compounds are characterized by their lack of a 19th carbon on the steroid structure, which also brings Trenbolone the classification of a progestin as well. Through it’s modifications from Nandrolone, it introduces two double-bonds between carbons 11 and 9, and it is this chemical modification that effectively makes Trenbolone totally immune to aromatization (conversion into Estrogen) by way of the aromatase enzyme as well as increasing the strength at which Trenbolone binds to the androgen receptor[2]. That is to say that Trenbolone will not produce any estrogenic side effects alone, and that it is an extremely potent and very strong anabolic steroid with an anabolic:androgenic ratio of 500:500. Compared to Testosterone, this is staggering, as Testosterone expresses an anabolic:androgenic ratio of 100:100. Hence, we can see how and why Trenbolone is five times the strength of Testosterone. Its chemical modifications also allow it a stronger resistance to metabolism in the body, allowing even more maximization of its anabolic capabilities in muscle tissue. Lastly, Trenbolone Enanthate possesses the enanthate ester, affixed at the 17-beta hydroxyl group on the steroid structure. This, as mentioned many times already, slows the release rate and also extends Trenbolone’s half-life in the body to approximately 7 – 10 days.

As a result of its chemical modifications, there is little question as to why Trenbolone Enanthate is so popular and effective among bodybuilders and athletes. Because of its unique characteristics, Trenbolone Enanthate is quite versatile in terms of its capabilities of use. It can literally be utilized for any goal: bulking, lean mass gaining, cutting (fat loss), strength gaining, and other goals perhaps more specific to different sports. Trenbolone Enanthate is commonly utilized in longer cycles due to its longer half-life and slower activity in the body. Because of the long Enanthate ester, users will typical inject Trenbolone Enanthate approximately twice per week, with each administration spaced evenly apart. For example, an injection on Sunday and an injection on Wednesday would suffice. If an individual is utilizing 400mg/week of Trenbolone Enanthate, 200mg would be injected on Sunday and the following 200mg would be injected on Wednesday.

How Does Trenbolone Enanthate Work and How Is It Best Used?

Because Trenbolone Enanthate exhibits a half-life of approximately 7 – 10 days and is presently more common than its other long-ester counterpart Parabolan, it provides many users who are mostly needle-shy or find frequent injections inconvenient with a more convenient form of Trenbolone to use. In contrast with Trenbolone Acetate, which requires every other day injections at the very least, Trenbolone Enanthate requires administration only twice per week with each injection spread evenly apart (Monday and Thursday, for example). Because Trenbolone is considered an intermediate-advanced level anabolic steroid, the majority of users of this compound are usually well aware of the ins and outs of it.  Many intermediates making their first step to Trenbolone will prefer Trenbolone Enanthate due to the convenience of less frequent injections. However, the disadvantage to this is the fact that Trenbolone is an anabolic steroid that is extremely powerful and does carry with it some potential side effects unseen with any other compounds. It has therefore been labelled as a ‘harsh’ anabolic steroid, and beginners to Trenbolone who are wondering which form to use might want to opt for Trenbolone Acetate instead. The reason being that the faster half-life of Trenbolone Acetate ensures that blood levels of Trenbolone rise quickly and fall quickly as well, ensuring a fast clearance from the body should any issues arise and the user wishes to stop. With Trenbolone Enanthate, two weeks is what is required before Trenbolone is completely clear of the body, during which time undesirable side-effects might persist.

It is therefore the prerogative of the individual to use this information and decide for themselves whether the convenience of less frequent injections is indeed worth the risk of having to wait two weeks before the drug is clear from the body if any undesirable effects arise. If the user is a well-experienced user of Trenbolone that already understands their body’s reaction, this decision should already be made.

It is important to understand that with long-estered anabolic steroids like Trenbolone Enanthate, the time required for the hormone to reach peak and optimal circulating blood plasma levels is considerably longer than short-estered variants. For example, many individuals report experiencing significant strength gains and/or physique changes by the second or third week with Trenbolone Acetate, but Trenbolone Enanthate might require upwards of 4 – 6 weeks (depending on the individual as well) before the hormone noticeably “kicks in”. Because of the long Enanthate ester, the hormone slowly reaches optimal levels over a period of a few weeks as each dose builds upon the last. Of course, those who wish to speed up this process can always decide to frontload. However, be aware that there are both benefits as well as risks/downsides to such a practice, and frontloading should thoroughly be researched and contemplated before doing so. This is especially true with a compound such as Trenbolone, and is doubly especially true if the user is a first-time Trenbolone user.

In general, 

Trenbolone Enanthate is what would be considered the advanced Trenbolone user’s Trenbolone. However, this is not to say that plenty of well-experienced Trenbolone veterans won’t utilize Trenbolone Acetate – many do, and many tend to stick with Trenbolone Acetate exclusively forever without touching Tren Enanthate. The take-home point here is that Trenbolone Enanthate use is much more common among experienced users rather than bare beginners to Trenbolone, who will most often elect to use Trenbolone Acetate due to the short half-life and therefore relatively quick clearance from the body. This is usually a security precaution in the event that the first-time user encounters a bad experience on Trenbolone and wishes to stop more abruptly than stopping Trenbolone Enanthate would.

Tren is best utilized with other similar compounds, but it is absolutely essential that some form of Testosterone be run with it, even if only for the sake of health. It might be a wise idea to limit the amount and/or dosage of aromatizable androgens used with it, as some times the Estrogen-related side effects can be exacerbated when high levels of a progestin is utilized in a high-Estrogen environment. Normally it is Testosterone Enanthate that is commonly combined in cycles with Trenbolone Enanthate, for very obvious reasons.

Trenbolone Enanthate Side Effects

Trenbolone is an anabolic steroid, and as such, it carries with it all of the typical side effects that are common among all anabolic steroids and more. “And more” refers to the additional unqiue side effects common to Trenbolone that are often discussed within the bodybuilding community (and frequently carried out of proportion) attached to very ridiculous and mostly-exaggerated horror stories.

Because Trenbolone does not aromatize into Estrogen at any dosage, there is zero risk of Estrogen-related side effects with Trenbolone alone. Estrogen Trenbolone Enanthate side effects are literally nonexistent. However, it is advised to closely monitor the dosage of aromatizable compounds run with it (i.e. Testosterone, Dianabol, etc.) as an Estrogen-rich environment in the body often leads to additional Trenbolone Enanthate side effects and complications due to complex hormonal pathways in the body that is related and linked between Estrogen, progestins, Prolactin, and the aromatase enzyme. Often times if an individual experiences Estrogen-related side effects during Trenbolone use, it is not the result of Trenbolone itself, but of the other compounds the individual is using alongside it.

Androgenic side effects are indeed a concern and definitely included as a part of the list of Trenbolone Enanthate side effects, as Trenbolone exhibits an adrogenic strength rating of 500. This means it is 5 times the androgenic strength of Testosterone. However, the up-side to this factor is that Trenbolone does not convert into any stronger androgenic metabolites in the body (unlike Testosterone, which is reduced into Dihydrotestosterone in the body). Therefore, any androgenic capabilities resultant from Trenbolone are what can be expected on average throughout its use. Individuals must take care to monitor and watch for androgenic side effects such as: increased aggression, irritability, acne (as a result of increased oil secretion on the skin), potential for male pattern baldness (if one possesses the genetics for it), and benign prostatic hyperplasia (enlargement of the prostate). Note that 5-alpha reductase inhibitors such as Proscar, Finasteride, Dutasteride, and Propecia do nothing to reduce or eliminate the androgenic Trenbolone Enanthate side effects.

There should be no concern for liver issues (hepatotoxicity) with Trenbolone Enanthate, as it is an injectable anabolic steroid that avoids the first pass through the liver. However, negative alteration of cholesterol and other cardiovascular concerns and issues can be a problem, as is the case with most, if not all anabolic steroids. Trenbolone Enanthate side effects also bring with it the typical HPTA suppression/shutdown that is common of all anabolic steroids. Therefore, users should either limit themselves to shorter cycles or ensure to engage in a proper PCT (Post Cycle Therapy) protocol following use, lest the secondary hypogonadism develops as a result of neglect in this area.

Trenbolone Enanthate side effects that are unique to Trenbolone itself include profuse perspiration (sweating), especially at night in bed for as of yet unknown reasons. Coughing fits that are normally more heavily associated with Trenbolone Acetate are very rarely reported or seen with Trenbolone Enanthate, though it still remains a possibility (dubbed the ‘tren cough’). The cough seems to occur more with Trenbolone Acetate rather than with the Enanthate variant, possibly because the incidence and severity of the cough have much to do with the rate of release of Trenbolone into the body. The true roots and cause of the ‘tren cough’ are currently not fully understood, but some valid and accurate hypotheses include the fact that Trenbolone itself causes varying degrees of anaphylactic reactions in the bronchial pathways, as well as some of the compound seeping into punctured capillaries/veins during the injection, which irritate the lungs. In the case of oil entering the bloodstream through capillaries/veins, this can occur with any oil-based anabolic steroid as well, which also results in coughing fits during or shortly after injection.

Finally, a small note should be made about one of the most commonly discussed Trenbolone Enanthate side effects: its seeming capability to induce larger amounts of aggression, anger, and impatientness in some users. Although there is a massive lack of clinical evidence to support the anecdotal claims that Tren exhibits this in some or most of its users, it is therefore the most important point of this whole profile to send the following message out to anyone willing to use Trenbolone in any form: those who have problems with their temper or patience must at all costs take responsible action and avoid the use of Trenbolone. If the use of Trenbolone Enanthate is too alluring, ensure to learn to exhibit self-control when one’s anger, temper, or lack of patience arises in any situations. It is irresponsible to utilize an anabolic steroid as potent as Trenbolone while knowing full well all of its potential effects, and allow oneself to get into serious trouble as a result of uncontrolled anger, and veer off blaming the anabolic steroid they had used as opposed to themselves for exercising poor self-responsibility. Trenbolone is a drug, and a very powerful androgenic anabolic hormone to be respected. Respect the hormone and it will respect you.

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V.Med - Bulk Mix Hybrid One 600mg (Super Bulk)

V.Med - Bulk Mix Hybrid One 600mg (Super Bulk)

V.MED BULK MIX 

HYBRID ONE 600MG

10ML

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