PHARMA DRO P100: Drostanolone Propionate 100 from Pharmacom Labs

Analytic testing performed by Janoshik.

RESULTS

1. Qualitative analysis: the sample contains the active ingredient: Drostanolone Propionate.
2. Quantitative analysis showed the content of active ingredient: 101.92 mg/mL.

Analysis conducted: 15 June 2023

PHARMA TEST E300: Testosterone Enanthate 300 from Pharmacom Labs

Analytic testing performed by Janoshik.

RESULTS:

1. Qualitative analysis: the sample contains the active ingredient: Testosterone Enanthate.
2. Quantitative analysis showed the content of active ingredient: 319.55 mg/mL.

Analysis conducted: 15 June 2023

PHARMAPRIM 200 – 200 mg/mL Primobolan Enanthate – is Now Available in the Basicstero Store. Methenolone (also known as primobolan) was described in 1960. Squibb Company began producing injectable drug in 1962. Methenolone originally was prescribed in case of muscle loss after operations, infections, long-term illnesses, aggressive therapy with corticoids or malnutrition, and in some cases, it was used to treat osteoporosis and breast cancer. Methenolone was commonly used to promote weight gain in infants, weighing less than normal, without any side effects. Methenolone is an anabolic steroid, modification of dihydrotestosterone (DHT) with weak androgenic activity and a moderate anabolic effect.

A notable trait of methenolone is that it can firmly bind to androgen receptors, stronger than testosterone. This trait makes primobolan to be a good fat burner.

Primobolan does not convert into estradiol; thereby you can take it without the risk of developing estrogenic side effects (gynecomastia, water retention).

Methenolone is one of most safe steroids on the market, hence women, elderly athletes and youth often find this steroid the best one to improve their physique and avoid side effects.

Overall, methenolone being one of the safest anabolic steroids available on the market is at the same time a rather weak compound and needs time to show affects at its best. Results of primobolan will be seen, if the drug is used at least 10 weeks and in stack with other steroids. Primobolan is well suited for cutting cycles when a mass gain is not the main goal.

Both 200 mg/mL and 100 mg/mL preparations of this legendary classic are available at: basicstero.ws/injectableline/primobolan

Primobolan Information: Primobolan Description (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Primobolan® Depot is an injectable version of the steroid methenolone. This is the same constituent in Primobolan® orals (methenolone acetate), although here an enanthate ester is used to slow the steroid's release from a site of injection. Methenolone enanthate offers a similar pattern of steroid release as testosterone enanthate, with blood hormone levels remaining markedly elevated for approximately 2 weeks. Methenolone itself is a moderately strong anabolic steroid with very low androgenic properties. Its anabolic effect is considered to be slightly less than Deca-Durabolin® (nandrolone decanoate) on a milligram for milligram basis. Methenolone enanthate is most commonly used during cutting cycles, when lean mass gain, not a raw mass increase, is the main objective.

History (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methenolone was first described in 1960. Squibb introduced the drug (as methenolone enanthate) to the U.S. prescription drug market in 1962, sold for a very short time in the U.S. under the brand name of Nibal® Depot. Rights to the drug were given to Schering in West Germany (now Bayer) that same year, and Nibal® Depot soon disappeared from the U.S. market. Schering would sell methenolone enanthate under its new and ultimately most recognizable brand name, Primobolan® Depot. During the 1960s and '70s Primobolan® Depot was available mainly in Europe, including such countries as Switzerland, Italy, Germany, Austria, Belgium, France, Portugal, and Greece.

Schering maintained patent control over methenolone enanthate until the late 1970s. Before its patents expired, Schering had rigorously protected its intellectual property rights against any potential infringement, even in the U.S. market, where the company had not been marketing Primobolan Depot. Although methenolone enanthate has not been available for commercial sale in the United States for decades, it has technically retained its status as an FDA approved drug.

Primobolan Depot is typically prescribed as a lean tissue building anabolic agent, often used in cases where body wasting has occurred secondary to an operation, prolonged infection, wasting disease, aggressive corticosteroid administration, or convalescence. Some clinicians also prescribe this agent for treating osteoporosis, sarcopenia (the natural loss of muscle mass with aging), certain cases of chronic hepatitis, and breast carcinoma (usually as a secondary medication following other therapies). The steroid has also been used to promote weight gain in underweight premature infants and children in clinical studies, and was able to do so effectively and without signs of toxicity or undesirable effects. Athletes have long favored the combined strong anabolic, weak androgenic, and non-estrogenic nature of this drug, which makes it very desirable for building lean muscularity without side effects.

Although Primobolan Depot demonstrated a good record of clinical safety, by the 1990s Schering had grown to be a multinational pharmaceutical giant, and was inevitably forced to reexamine its global steroid offerings in light of public concerns about sports doping. Primobolan Depot would be voluntarily withdrawn from most of the countries that had originally sold it. Today, the brand is sold in just a handful of countries including Spain, Turkey, Japan, Paraguay, and Ecuador. In spite of its limited supply, Bayer has remained (nearly) the exclusive producer of methenolone enanthate in the human drug business worldwide. In recent years, however, methenolone enanthate has shown up in a small number of other preparations, most from underground or export-only companies.

Structural Characteristics (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methenolone is a derivative of dihydrotestosterone. It contains one additional double bond between carbons 1 and 2, which helps to stabilize the 3-keto group and increase the steroid's anabolic properties, and an additional 1-methyl group, which gives the steroid some protection against hepatic metabolism. Primobolan Depot makes use of methenolone with a carboxylic acid ester (enanthoic acid) attached to the 17-beta hydroxyl group. Esterified steroids are less polar than free steroids, and are absorbed more slowly from the area of injection. Once in the bloodstream, the ester is removed to yield free (active) methenolone. Esterified steroids are designed to prolong the window of therapeutic effect following administration, allowing for a less frequent injection schedule compared to injections of free (unesterified) steroid.

Side Effects (Estrogenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methenolone is not aromatized by the body, and is not measurably estrogenic. Estrogen-linked side effects should not be seen when administering this steroid. Sensitive individuals need not worry about developing gynecomastia, nor should they be noticing any appreciable water retention with this drug. The increase seen with methenolone should be quality muscle mass, not the smooth bulk that often accompanies steroids open to aromatization. During a cycle, the user should additionally not notice strong elevations in blood pressure, as this effect is also related (generally) to estrogen and water retention. Methenolone is a steroid most favored during cutting phases of training, when water and fat retention are major concerns, and sheer mass not the central objective.

Side Effects (Androgenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Although classified as an anabolic steroid, androgenic side effects are still possible with this substance. This may include bouts of oily skin, acne, and body/ facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Methenolone is still a very mild steroid, however, and strong androgenic side effects are typically related to higher doses. Women often find this preparation an acceptable choice, observing it to be a very comfortable and effective anabolic.

Side Effects (Hepatotoxicity) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methenolone is not considered a hepatotoxic steroid; liver toxicity is unlikely. Studies have failed to produce appreciable changes in markers of hepatic stress when the drug was given in therapeutic levels.

Side Effects (Cardiovascular) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL cholesterol values and increase LDL cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependent on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Methenolone should have a stronger negative effect on the hepatic management of cholesterol than testosterone or nandrolone due to its non-aromatizable nature, but a much weaker impact than c-17 alpha alkylated steroids. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce cardiovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.

Side Effects (Testosterone Suppression) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotropic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention. At a moderate dosage of 100-200 mg weekly, methenolone should offer measurably less testosterone suppression than an equal dose of nandrolone or testosterone, due to its non-aromatizable nature. If used for less than eight weeks, hormonal recovery should not be a protracted experience.

For more information about Basicstero.ws - the Direct from Pharmacom Labs Store! please see the post here on steroidwiki.com at: https://steroidwiki.com/forum/topic/994-pharmacom-labs-officials-and-our-basicsterows.html

Basicstero's 2023 "SUMMER CHILL" PROMO! Pay with cryptocurrency and get FREE bonuses as follows:

• $100 of FREE bonus items for orders over $200.
• $300 of FREE bonus items for orders over $500.
• $600 of FREE bonus items for orders over $800.
• $800 of FREE bonus items for orders over $1000.

Bonuses are picked during the ordering process and shipped together with the main order. No promo code is needed. This promo is valid for orders from the International Warehouse (W1) only! Please plan accordingly for international transit times.

In case of seizures/lost-packs only items that were paid for are reshipped, not free bonuses (please understand this means promo free bonus items are not included in a reship). If you need discreet shipping please select the "Discreet Shipping" option during the check-out process on the "Address" page when you enter your order. Pharmatropin GH is not participating in this promotion. Nothing new with these terms and conditions - just the typical rules for many Basicstero promos.

Be sure to stay up-to-date with all the latest Promotions, News, and Announcements by checking the ”News” section on the Basicstero site.

Chill this Summer and Look Good with some new Gains from Basicstero!

For more information about Basicstero.ws - the Direct from Pharmacom Labs Store! please see the post here on steroidwiki.com at: https://steroidwiki.com/forum/topic/994-pharmacom-labs-officials-and-our-basicsterows.html

Basicstero's MEMORIAL PROMO DAYS!

The United States celebrates Memorial Day to remember and honor those who gave their lives while serving in the United States Armed Forces. Many people also consider it the start of the summer season, with cookouts, chilling on beaches, outdoor training, and a lean pumped up athletic body.

Place your order from the Domestic Warehouse and get FREE bonuses as follows: $100 bonus for orders over $200 $200 bonus for orders over $300 $500 bonus for orders over $500

A list of various items available to be selected as bonuses, which you can add to your order, is automatically offered in a step during the check-out process.

MEMORIAL PROMO DAYS is for orders from the US Domestic Warehouse (W2) only! Bonuses are picked during the ordering process and shipped together with the main order. No promo code is needed. Estimated shipping time from W2 is about 5–10 days from the time payment is confirmed.

Nothing new with these terms and conditions – just the typical rules for Basicstero promos.

Be sure to stay up-to-date with all the latest Promotions, News, and Announcements by checking the "News" section on the Basicstero site.

DROLOS – The New SUPERDROL Product from Pharmacom Labs! – is Now Available in the Basicstero Store.

Methyldrostanolone is scientifically known as Superdrol and it is arguably the most effective and potent oral anabolic steroid to be utilized over the last decade. Superdol is very similar to Masteron, with the only difference being that Masteron though is lacking an ester chain. The name Superdrol is a combination of the words “super” and “anadrol." Superdrol is an awesome steroid for bulking, though some bodybuilders also use it as part of their cut as it yields very dry and hard gains with no bloating or water retention. It was created back in the 1950s by doctors who were looking to create a drug to destroy tumors. Sadly, this wasn’t achievable, but they did find that the oral steroid promoted huge increases in lean muscle mass and strength. However, Superdol wasn’t released until 2005.

The active steroidal hormone in Superdrol is Methyldrostanolone. It is a structurally altered form of Drostanolone, with an added methyl group at the 17th carbon position. There is also an added methyl group at the carbon 2 position. These changes ramp-up the anabolic potential of this drug, giving it an anabolic rating of 400.

Effects: • Increases muscle mass. • Improves recovery. • Improves athletic performance.

This Powerful Oral-Line product is currently offered as 10 mg tablets available at: basicstero.ws/oral-steroids/drolos

Superdrol Information:

Superdrol Description (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone, also known as methasteron, is a potent oral anabolic steroid that was never sold as a prescription drug. In structure, this steroid is a close derivative of drostanolone (Masteron). The only difference in this case is the addition of a c-17 alpha methyl group, a modification that gives this steroid high oral bioavailability. The two agents remain very comparable, however. Both methyldrostanolone and drostanolone are nonaromatizable, so there is no difference in the estrogenicity of these two steroids, and both steroids retain favorable anabolic to androgenic ratios. Lab assays do put Superdrol ahead here, however, showing it to possess 4 times the anabolic potency of oral methyltestosterone while displaying only 20% of the androgenicity (a 20:1 ratio, compared to 3:1 ). The exact real-world relevance of these figures remains to be seen, however. Methyldrostanolone is favored by athletes for its moderate anabolic properties, which are usually accompanied by fat loss and minimal androgenic side effects.

History (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone was first described in 1959.1 This steroid was developed by the international pharmaceuticals giant Syntex, alongside such other wellknown anabolic agents as drostanolone propionate and oxymetholone. Unlike rostanolone and oxymetholone, however, this steroid (at least in its basic form) was never released as a medicinal product. It was only sold for a brief period of time as a modified hormone called dimethazine. Dimethazine is made from two molecules of methyldrostanolone that are bonded together, which are later metabolically separated to yield free methyldrostanolone. So while technically methyldrostanolone itself was never sold as a prescription agent, we can say that the drug was one utilized medicinally (for more information see the Roxilon drug profile). Otherwise, the methyldrostanolone molecule remained an obscure research steroid only, and was never itself approved for use in humans. Methyldrostanolone was released in early 2005 as an over the counter "grey market" anabolic steroid in the United States. The drug was being sold without restrictions as a nutritional supplement product, barring some minimum age disclaimers by the manufacturer. No State or Federal laws identify this drug as an anabolic steroid, which remove the legalities associated with being a Class Ill controlled substance like other steroids. This is simply due to the fact that methyldrostanolone was not in commerce at the time such laws were written, and was unknown to lawmakers. It was never legal to sell as a dietary supplement, however, and in late 2005 the FDA angrily acknowledged methyldrostanolone was being sold on the sports supplement market. In early 2006, the FDA sent letters to the manufacturer and a distributor demanding it be pulled from commerce. Superdrol has since been discontinued.

Structural Characteristics (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is a modified form of dihydrotestosterone. It differs by: 1) the addition of a methyl group at carbon 17-alpha, which helps protect the hormone during oral administration, and 2) the introduction of a methyl group at carbon-2 (alpha), which considerably increases the anabolic strength of the steroid by heightening its resistance to metabolism by the 3-hydroxysteroid dehydrogenase enzyme in skeletal muscle tissue.

Side Effects (Estrogenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals. Since estrogen is the usual culprit with water retention, methyldrostanolone instead produces a lean, quality look to the physique with no fear of excess subcutaneous fluid retention. This makes it a favorable steroid to use during cutting cycles, when water and fat retention are major concerns.

Side Effects (Androgenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Although classified as an anabolic steroid,androgenic side effects are still possible with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Methyldrostanolone is a steroid with relatively low androgenic activity relative to its tissuebuilding actions, making the threshold for strong androgenic side effects comparably higher than with more androgenic agents such as testosterone, methandrostenolone, or fluoxymesterone. Note that methyldrostanolone is unaffected by the 5-alpha reductase enzyme, so its relative androgenicity is not affected by the concurrent use of finasteride or dutasteride.

Side Effects (Hepatotoxicity) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is a cl 7-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage of the drug entry into the bloodstream following oral administration. Cl 7-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances life-threatening dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain. Note that although no human data can be found to make reference of, doses of 1 0 mg and 20 mg per day have been sufficient to produce high elevations of liver enzymes in consumers, as reported by private lab test results. Also, a small number of serious adverse events relating to liver toxicity have been reported with the use of this substance. The use of a liver detoxification supplement such as Liver Stabil, Liv-52, or Essentiale Forte is advised while taking any hepatotoxic anabolic/androgenic steroids.

Side Effects (Cardiovascular) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL cholesterol values and increase LDL cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Methyldrostanolone has a strong effect on the hepatic management of cholesterol due to its non-aromatizable nature, structural resistance to liver breakdown, and route of administration. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce card iovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.

Side Effects (Testosterone Suppression) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration (Men) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methydrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. An effective dosage of methyldrostanolone for physique- or performance-enhancing purposes seems to begin in the range of 10-20 mg per day, taken for no longer than 6 or 8 weeks. At this level it seems to impart a measurable muscle-building effect, which is usually accompanied by fat loss and increased definition. Don't expect to gain 30 pounds on this agent (its name, which is short for "Super Anadrol," is more marketing than reality), but many do walk away with more than 10 pounds of solid muscle gain when using this agent alone. In determining an optimal daily dosage, some do find the drug to be measurably more effective when venturing up to the 30 mg range. Potential hepatotoxicity should definitely be taken into account with such use, however. To avoid further escalating liver strain, 20 mg daily of methyldrostanolone is sometimes stacked with a nontoxic injectable steroid, such as testosterone for massbuilding phases of training, or nandrolone or boldenone for more lean tissue gain and definition, instead of simply increasing the dosage. The drug also works well in cutting cycles, where its lack of estrogenicity is highly favored. Often it is combined here with a non-aromatizable injectable steroid like Primobolan or Parabolan.

Administration (Women) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. In the athletic arena, an effective oral daily dosage would fall around 2.5 mg per day, taken in cycles lasting no more than 4-6 weeks to minimize the chance for virilization. The main point of contention with females is probably going to be the 10 mg product, which is far too high to use. Application would require splitting contents up into 4 separate doses. As with all steroids, virilization is still possible.

DROLOS – The New SUPERDROL Product from Pharmacom Labs! – is Now Available in the Basicstero Store.

Methyldrostanolone is scientifically known as Superdrol and it is arguably the most effective and potent oral anabolic steroid to be utilized over the last decade. Superdol is very similar to Masteron, with the only difference being that Masteron though is lacking an ester chain. The name Superdrol is a combination of the words “super” and “anadrol." Superdrol is an awesome steroid for bulking, though some bodybuilders also use it as part of their cut as it yields very dry and hard gains with no bloating or water retention. It was created back in the 1950s by doctors who were looking to create a drug to destroy tumors. Sadly, this wasn’t achievable, but they did find that the oral steroid promoted huge increases in lean muscle mass and strength. However, Superdol wasn’t released until 2005.

The active steroidal hormone in Superdrol is Methyldrostanolone. It is a structurally altered form of Drostanolone, with an added methyl group at the 17th carbon position. There is also an added methyl group at the carbon 2 position. These changes ramp-up the anabolic potential of this drug, giving it an anabolic rating of 400.

Effects: • Increases muscle mass. • Improves recovery. • Improves athletic performance.

This Powerful Oral-Line product is currently offered as 10 mg tablets available at: basicstero.ws/oral-steroids/drolos

Superdrol Information:

Superdrol Description (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone, also known as methasteron, is a potent oral anabolic steroid that was never sold as a prescription drug. In structure, this steroid is a close derivative of drostanolone (Masteron). The only difference in this case is the addition of a c-17 alpha methyl group, a modification that gives this steroid high oral bioavailability. The two agents remain very comparable, however. Both methyldrostanolone and drostanolone are nonaromatizable, so there is no difference in the estrogenicity of these two steroids, and both steroids retain favorable anabolic to androgenic ratios. Lab assays do put Superdrol ahead here, however, showing it to possess 4 times the anabolic potency of oral methyltestosterone while displaying only 20% of the androgenicity (a 20:1 ratio, compared to 3:1 ). The exact real-world relevance of these figures remains to be seen, however. Methyldrostanolone is favored by athletes for its moderate anabolic properties, which are usually accompanied by fat loss and minimal androgenic side effects.

History (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone was first described in 1959.1 This steroid was developed by the international pharmaceuticals giant Syntex, alongside such other wellknown anabolic agents as drostanolone propionate and oxymetholone. Unlike rostanolone and oxymetholone, however, this steroid (at least in its basic form) was never released as a medicinal product. It was only sold for a brief period of time as a modified hormone called dimethazine. Dimethazine is made from two molecules of methyldrostanolone that are bonded together, which are later metabolically separated to yield free methyldrostanolone. So while technically methyldrostanolone itself was never sold as a prescription agent, we can say that the drug was one utilized medicinally (for more information see the Roxilon drug profile). Otherwise, the methyldrostanolone molecule remained an obscure research steroid only, and was never itself approved for use in humans. Methyldrostanolone was released in early 2005 as an over the counter "grey market" anabolic steroid in the United States. The drug was being sold without restrictions as a nutritional supplement product, barring some minimum age disclaimers by the manufacturer. No State or Federal laws identify this drug as an anabolic steroid, which remove the legalities associated with being a Class Ill controlled substance like other steroids. This is simply due to the fact that methyldrostanolone was not in commerce at the time such laws were written, and was unknown to lawmakers. It was never legal to sell as a dietary supplement, however, and in late 2005 the FDA angrily acknowledged methyldrostanolone was being sold on the sports supplement market. In early 2006, the FDA sent letters to the manufacturer and a distributor demanding it be pulled from commerce. Superdrol has since been discontinued.

Structural Characteristics (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is a modified form of dihydrotestosterone. It differs by: 1) the addition of a methyl group at carbon 17-alpha, which helps protect the hormone during oral administration, and 2) the introduction of a methyl group at carbon-2 (alpha), which considerably increases the anabolic strength of the steroid by heightening its resistance to metabolism by the 3-hydroxysteroid dehydrogenase enzyme in skeletal muscle tissue.

Side Effects (Estrogenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals. Since estrogen is the usual culprit with water retention, methyldrostanolone instead produces a lean, quality look to the physique with no fear of excess subcutaneous fluid retention. This makes it a favorable steroid to use during cutting cycles, when water and fat retention are major concerns.

Side Effects (Androgenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Although classified as an anabolic steroid,androgenic side effects are still possible with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Methyldrostanolone is a steroid with relatively low androgenic activity relative to its tissuebuilding actions, making the threshold for strong androgenic side effects comparably higher than with more androgenic agents such as testosterone, methandrostenolone, or fluoxymesterone. Note that methyldrostanolone is unaffected by the 5-alpha reductase enzyme, so its relative androgenicity is not affected by the concurrent use of finasteride or dutasteride.

Side Effects (Hepatotoxicity) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is a cl 7-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage of the drug entry into the bloodstream following oral administration. Cl 7-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances life-threatening dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain. Note that although no human data can be found to make reference of, doses of 1 0 mg and 20 mg per day have been sufficient to produce high elevations of liver enzymes in consumers, as reported by private lab test results. Also, a small number of serious adverse events relating to liver toxicity have been reported with the use of this substance. The use of a liver detoxification supplement such as Liver Stabil, Liv-52, or Essentiale Forte is advised while taking any hepatotoxic anabolic/androgenic steroids.

Side Effects (Cardiovascular) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL cholesterol values and increase LDL cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Methyldrostanolone has a strong effect on the hepatic management of cholesterol due to its non-aromatizable nature, structural resistance to liver breakdown, and route of administration. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce card iovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.

Side Effects (Testosterone Suppression) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration (Men) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methydrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. An effective dosage of methyldrostanolone for physique- or performance-enhancing purposes seems to begin in the range of 10-20 mg per day, taken for no longer than 6 or 8 weeks. At this level it seems to impart a measurable muscle-building effect, which is usually accompanied by fat loss and increased definition. Don't expect to gain 30 pounds on this agent (its name, which is short for "Super Anadrol," is more marketing than reality), but many do walk away with more than 10 pounds of solid muscle gain when using this agent alone. In determining an optimal daily dosage, some do find the drug to be measurably more effective when venturing up to the 30 mg range. Potential hepatotoxicity should definitely be taken into account with such use, however. To avoid further escalating liver strain, 20 mg daily of methyldrostanolone is sometimes stacked with a nontoxic injectable steroid, such as testosterone for massbuilding phases of training, or nandrolone or boldenone for more lean tissue gain and definition, instead of simply increasing the dosage. The drug also works well in cutting cycles, where its lack of estrogenicity is highly favored. Often it is combined here with a non-aromatizable injectable steroid like Primobolan or Parabolan.

Administration (Women) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. In the athletic arena, an effective oral daily dosage would fall around 2.5 mg per day, taken in cycles lasting no more than 4-6 weeks to minimize the chance for virilization. The main point of contention with females is probably going to be the 10 mg product, which is far too high to use. Application would require splitting contents up into 4 separate doses. As with all steroids, virilization is still possible.

DROLOS – The New SUPERDROL Product from Pharmacom Labs! – is Now Available in the Basicstero Store.

Methyldrostanolone is scientifically known as Superdrol and it is arguably the most effective and potent oral anabolic steroid to be utilized over the last decade. Superdol is very similar to Masteron, with the only difference being that Masteron though is lacking an ester chain. The name Superdrol is a combination of the words “super” and “anadrol." Superdrol is an awesome steroid for bulking, though some bodybuilders also use it as part of their cut as it yields very dry and hard gains with no bloating or water retention. It was created back in the 1950s by doctors who were looking to create a drug to destroy tumors. Sadly, this wasn’t achievable, but they did find that the oral steroid promoted huge increases in lean muscle mass and strength. However, Superdol wasn’t released until 2005.

The active steroidal hormone in Superdrol is Methyldrostanolone. It is a structurally altered form of Drostanolone, with an added methyl group at the 17th carbon position. There is also an added methyl group at the carbon 2 position. These changes ramp-up the anabolic potential of this drug, giving it an anabolic rating of 400.

Effects: • Increases muscle mass. • Improves recovery. • Improves athletic performance.

This Powerful Oral-Line product is currently offered as 10 mg tablets available at: basicstero.ws/oral-steroids/drolos

Superdrol Information:

Superdrol Description (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone, also known as methasteron, is a potent oral anabolic steroid that was never sold as a prescription drug. In structure, this steroid is a close derivative of drostanolone (Masteron). The only difference in this case is the addition of a c-17 alpha methyl group, a modification that gives this steroid high oral bioavailability. The two agents remain very comparable, however. Both methyldrostanolone and drostanolone are nonaromatizable, so there is no difference in the estrogenicity of these two steroids, and both steroids retain favorable anabolic to androgenic ratios. Lab assays do put Superdrol ahead here, however, showing it to possess 4 times the anabolic potency of oral methyltestosterone while displaying only 20% of the androgenicity (a 20:1 ratio, compared to 3:1 ). The exact real-world relevance of these figures remains to be seen, however. Methyldrostanolone is favored by athletes for its moderate anabolic properties, which are usually accompanied by fat loss and minimal androgenic side effects.

History (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone was first described in 1959.1 This steroid was developed by the international pharmaceuticals giant Syntex, alongside such other wellknown anabolic agents as drostanolone propionate and oxymetholone. Unlike rostanolone and oxymetholone, however, this steroid (at least in its basic form) was never released as a medicinal product. It was only sold for a brief period of time as a modified hormone called dimethazine. Dimethazine is made from two molecules of methyldrostanolone that are bonded together, which are later metabolically separated to yield free methyldrostanolone. So while technically methyldrostanolone itself was never sold as a prescription agent, we can say that the drug was one utilized medicinally (for more information see the Roxilon drug profile). Otherwise, the methyldrostanolone molecule remained an obscure research steroid only, and was never itself approved for use in humans. Methyldrostanolone was released in early 2005 as an over the counter "grey market" anabolic steroid in the United States. The drug was being sold without restrictions as a nutritional supplement product, barring some minimum age disclaimers by the manufacturer. No State or Federal laws identify this drug as an anabolic steroid, which remove the legalities associated with being a Class Ill controlled substance like other steroids. This is simply due to the fact that methyldrostanolone was not in commerce at the time such laws were written, and was unknown to lawmakers. It was never legal to sell as a dietary supplement, however, and in late 2005 the FDA angrily acknowledged methyldrostanolone was being sold on the sports supplement market. In early 2006, the FDA sent letters to the manufacturer and a distributor demanding it be pulled from commerce. Superdrol has since been discontinued.

Structural Characteristics (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is a modified form of dihydrotestosterone. It differs by: 1) the addition of a methyl group at carbon 17-alpha, which helps protect the hormone during oral administration, and 2) the introduction of a methyl group at carbon-2 (alpha), which considerably increases the anabolic strength of the steroid by heightening its resistance to metabolism by the 3-hydroxysteroid dehydrogenase enzyme in skeletal muscle tissue.

Side Effects (Estrogenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals. Since estrogen is the usual culprit with water retention, methyldrostanolone instead produces a lean, quality look to the physique with no fear of excess subcutaneous fluid retention. This makes it a favorable steroid to use during cutting cycles, when water and fat retention are major concerns.

Side Effects (Androgenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Although classified as an anabolic steroid,androgenic side effects are still possible with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Methyldrostanolone is a steroid with relatively low androgenic activity relative to its tissuebuilding actions, making the threshold for strong androgenic side effects comparably higher than with more androgenic agents such as testosterone, methandrostenolone, or fluoxymesterone. Note that methyldrostanolone is unaffected by the 5-alpha reductase enzyme, so its relative androgenicity is not affected by the concurrent use of finasteride or dutasteride.

Side Effects (Hepatotoxicity) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone is a cl 7-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage of the drug entry into the bloodstream following oral administration. Cl 7-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances life-threatening dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain. Note that although no human data can be found to make reference of, doses of 1 0 mg and 20 mg per day have been sufficient to produce high elevations of liver enzymes in consumers, as reported by private lab test results. Also, a small number of serious adverse events relating to liver toxicity have been reported with the use of this substance. The use of a liver detoxification supplement such as Liver Stabil, Liv-52, or Essentiale Forte is advised while taking any hepatotoxic anabolic/androgenic steroids.

Side Effects (Cardiovascular) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL cholesterol values and increase LDL cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Methyldrostanolone has a strong effect on the hepatic management of cholesterol due to its non-aromatizable nature, structural resistance to liver breakdown, and route of administration. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce card iovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.

Side Effects (Testosterone Suppression) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration (Men) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methydrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. An effective dosage of methyldrostanolone for physique- or performance-enhancing purposes seems to begin in the range of 10-20 mg per day, taken for no longer than 6 or 8 weeks. At this level it seems to impart a measurable muscle-building effect, which is usually accompanied by fat loss and increased definition. Don't expect to gain 30 pounds on this agent (its name, which is short for "Super Anadrol," is more marketing than reality), but many do walk away with more than 10 pounds of solid muscle gain when using this agent alone. In determining an optimal daily dosage, some do find the drug to be measurably more effective when venturing up to the 30 mg range. Potential hepatotoxicity should definitely be taken into account with such use, however. To avoid further escalating liver strain, 20 mg daily of methyldrostanolone is sometimes stacked with a nontoxic injectable steroid, such as testosterone for massbuilding phases of training, or nandrolone or boldenone for more lean tissue gain and definition, instead of simply increasing the dosage. The drug also works well in cutting cycles, where its lack of estrogenicity is highly favored. Often it is combined here with a non-aromatizable injectable steroid like Primobolan or Parabolan.

Administration (Women) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.): Methyldrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. In the athletic arena, an effective oral daily dosage would fall around 2.5 mg per day, taken in cycles lasting no more than 4-6 weeks to minimize the chance for virilization. The main point of contention with females is probably going to be the 10 mg product, which is far too high to use. Application would require splitting contents up into 4 separate doses. As with all steroids, virilization is still possible.