(Normethandrolone)
Orgasteron, also known by its chemical name Normethandrolone, is an anabolic-androgenic steroid (AAS) that has been used in the past for a variety of medical purposes. It is a synthetic derivative of testosterone, modified to enhance its anabolic properties (muscle building) and reduce its androgenic effects (characteristics related to male sexual development and maintenance).
History of Orgasteron
Orgasteron, known chemically as Normethandrolone, represents a unique chapter in the history of anabolic-androgenic steroids (AAS). Its development and use are marked by the typical trajectory of therapeutic application, followed by controversy due to misuse and doping in sports, much like other steroids of its era. However, digging into its history and related incidents reveals a broader narrative about the evolution of performance-enhancing drugs and society’s response to them.
Development and Medical Use
Orgasteron was developed in the 1960s as a synthetic anabolic steroid with the intent to offer the benefits of increased muscle mass and strength, reduced recovery times, and improved red blood cell production, with fewer androgenic side effects than testosterone. Its medical applications were initially promising, offering potential treatments for conditions like muscle wasting diseases, certain forms of anemia, and to help maintain body mass in patients with chronic illnesses.
The Shift to Performance Enhancement
Despite its medical benefits, Orgasteron, like many AAS, quickly gained attention in the athletic and bodybuilding communities for its potential to enhance physical performance and appearance. Its use became widespread among athletes seeking an edge in competition, leading to its eventual ban by sports authorities worldwide. This shift from therapeutic use to performance enhancement marked a turning point in the perception and regulation of AAS, including Orgasteron.
Controversies and Unusual Incidents
One of the more unusual and controversial aspects of Orgasteron’s history involves its role in the early days of steroid testing and regulation. As testing methods were in their infancy, some athletes turned to compounds like Orgasteron, believing they were less detectable or could be masked more easily than other steroids. This cat-and-mouse game between athletes seeking to evade detection and regulatory bodies striving to catch up contributed significantly to the development of more sophisticated anti-doping technologies and policies.
In some cases, athletes who were caught using or associated with Orgasteron faced not only bans and disqualification but also significant damage to their careers and reputations. These incidents served as high-profile examples of the broader ethical and health debates surrounding AAS use, bringing to light issues of fairness, health risks, and the integrity of competitive sports.
Regulatory Response and Legacy
The response to the misuse of Orgasteron and other AAS was a significant increase in regulation and control. This included classifying these substances as controlled drugs in many countries, developing more rigorous testing protocols, and instituting harsher penalties for violations. The history of Orgasteron is thus closely tied to the evolution of sports ethics and anti-doping efforts worldwide.
Practical use
Orgasteron, with its chemical identifier as noremthandrolone, serves as the pill-based variant of nandrolone, widely recognized within the bodybuilding community through names such as Deca Durabolin or Nandrolone Phenylpropionate (NPP). Deca Durabolin, an injectable form of nandrolone, is distinguished by its long-lasting decanoate ester, whereas NPP, through its phenylpropionate ester, offers a more transient effect.
With its significant anabolic capabilities and minimized androgenic effects, Orgasteron becomes an excellent supplement within an established steroid regimen, owing to its gentler characteristics. Like its nandrolone counterparts, it’s notably effective in stimulating appetite. Deca Durabolin, another well-regarded anabolic androgenic steroid (AAS), is acclaimed for its role in preventing muscle degeneration among HIV patients.
Orgasteron stands out for being approximately five times more anabolic than oral testosterone derivatives, albeit with a significantly lower androgenic profile. Nonetheless, it exhibits pronounced progestational activity, meaning it targets not just estrogen but also progesterone receptors within the body. This dual action can offer temporary relief for joint discomfort but may also introduce several adverse effects, as detailed below.
Estrogen can be a concern
The potential progestational risks associated with Orgasteron necessitate the use of a reliable aromatase inhibitor (AI), such as aromasin or letrozole, alongside possible prolactin inhibitors (cabergoline or pramipexole).
Its prowess extends to muscle-building and anti-catabolic effects, and it’s less commonly known for increasing IGF-1 in muscle tissues. As with all AAS, it enhances red blood cell count, improves nutrient delivery to muscles, and aids in post-exercise recovery. For a comprehensive understanding of Orgasteron’s benefits, one might refer to articles on Deca Durabolin.
Side Effects
Being an orally active form of nandrolone, Orgasteron is a 17-alpha-alkylated (17AA) substance, making it more strenuous on the liver compared to its injectable counterpart, Deca Durabolin. Therefore, individuals with pre-existing liver conditions should exercise caution. It’s advised against combining Orgasteron with other potent oral steroids, such as halodrol or anadrol, to prevent jaundice symptoms. The use of liver-protective supplements, like N2Guard, is highly recommended with any oral steroid to safeguard the liver and other organs.
Due to its progestin nature, Orgasteron can stimulate progesterone receptors, potentially leading to gynecomastia, especially when used with testosterone, enhancing estrogenic effects. Thus, employing an AI is crucial.
The infamous “deca dick,” a term for reduced libido, is a risk due to norethandrolone’s suppression of dihydrotestosterone (DHT). However, this can be mitigated by incorporating a DHT derivative compound into the stack.
Additional side effects include increased blood pressure, cholesterol imbalance, and other lipid issues. Unmanaged estrogen levels can trigger a cascade of problems like insomnia and water retention, emphasizing the importance of strict estrogen control.
User Results
Orgasteron users often report quick gains in mass and strength, albeit not as rapidly as with other orals like halo or anadrol, which are also more side-effect-prone.
Interestingly, some have found temporary relief for joint problems with Orgasteron, though it’s advised against using nandrolone derivatives for joint issues due to potential long-term complications post-use.
Half Life
Norethandrolone has a half-life of approximately 14 hours, offering a stark contrast to Deca Durabolin’s 14-day half-life, facilitating a quicker recovery post-cycle.
Doses
Produced by international underground labs in 2.5, 5, and 10 mg tablets, the recommended dosage for men is 10-30mg daily for 6-8 weeks, ideally as a cycle kickstarter. Women may also use it, but should limit their intake to no more than 5mg daily for up to 4 weeks, mindful of potential androgenic effects.
Combining norethandrolone with liver-safe DHT derivatives like masteron, winstrol, or proviron is advised.
Other Names
In various regions, Orgasteron (norethandrolone) is also known as Orgaseone, Matdonal, Lutenin, Methalutin, and by its generic labels, methylnandrolone and methlnortestosterone.
Summary
Orgasteron’s versatility in both bulking and cutting cycles makes it a notable compound in the realm of bodybuilding. Its ability to significantly enhance muscle mass at higher doses places it in a category similar to Deca-Durabolin, making it an excellent choice for those looking to gain size and strength. When integrated into bulking cycles alongside testosterone variants such as enanthate, cypionate, and propionate, Orgasteron synergizes well, enhancing the anabolic environment and promoting substantial muscle growth. The inclusion of Trenbolone and Dianabol further amplifies these effects, creating a potent combination for maximizing mass and power gains.
On the flip side, Orgasteron’s utility is not limited to just bulking phases. When the goal shifts towards cutting—reducing body fat while preserving lean muscle mass—Orgasteron demonstrates remarkable adaptability. By stacking it with anabolic steroids known for their favorable effects on lean muscle retention and fat loss, such as Anavar, Primobolan, Winstrol, and Oral Turinabol, Orgasteron contributes to a refined, muscular physique. This combination facilitates the shedding of excess body fat while ensuring that muscle catabolism is minimized, a crucial balance during calorie-restricted phases.
The strategic use of Orgasteron in cutting cycles helps in maintaining strength levels, a common challenge when in a caloric deficit. Anavar and Winstrol, in particular, provide complementary benefits by enhancing muscle hardness and vascularity, attributes highly valued in the cutting phase. Meanwhile, Primobolan’s mild nature and Oral Turinabol’s ability to promote lean muscle gains without excessive water retention make them excellent partners for Orgasteron, ensuring that the bodybuilder can achieve a lean, defined appearance without the bulkiness associated with off-season cycles.
However, it’s critical to approach the use of Orgasteron and its stacking with other anabolic steroids with caution. The potential for adverse health effects, the need for precise dosing, cycle planning, and post-cycle therapy cannot be overstated. Ensuring liver health, managing cholesterol levels, and monitoring hormonal balance are essential considerations to mitigate the risks associated with steroid use. Consulting with healthcare professionals and conducting thorough research before embarking on any steroid cycle is imperative for safeguarding health while pursuing bodybuilding goals.