Oral Dianabol was reported to be a highly effective mass AAS which provided impressive weight and strength gains. Most users experienced a 2-4 LB
bodyweight increase per week with heavy water retention. With higher dosages gynecomastia (bitch tits) was a common negative side effect. Obviously much of this was avoided by those who reported co-addministration of Proviron and/or Novladex. When stacked with a nandrolone, some gyno problems seemed to lessen.
This was probably due to Nandrolones aromatization to a weaker estrogen called Norestrogen and the resulting mild anti-estrogenic effect that results in moderate dosage administration. Methandrostenlone becomes active in 1-3 hours with a half-life of about 3.5-4.5 hours. For this reason, dosages were spread through out the day to maintain blood serum concentrations at an elevated state. Massive dosages just were not necessary since a single 10-mg dose has increase androgen anabolic activity 5 times over normal with a correlating reduction in natural cortisol activity of 50-70%. Males using 5mg per 25-LBS of body weight broken into 3-5 equal dosages throughout the day have experienced impressive results. At dosages above 50 mg per day, results were not progressively quantitative. Most first time AAS users who used a daily dosage of 20-30mg daily experience significant results over a 4-6 week period. Women should not utilize Methandrostenolone but a surprising number did report the inclusion of the drug in AAS protocols. For those who insisted, no more than 10-mg daily for 3-4 weeks stacked with a very low androgenic product minimized masculization type negative side effects. Side effects such as increased liver values (toxicity) “usually” returned to normal within a short period of time after use was discontinued. High blood pressure, elevated heart rates, gyno, heavy water retention, and acne were all frequent reported negative side effects of Methandrostenlone use. Some literature on this drug supports DHT- like activity. Finasteride “usually” prevented this effect as well as possible prostate enlargement.
Denothon heavily suppresses natural testosterone production within only 10 days after continuous administration begins (dose dependent). Most note a sense of well being during use of this drug. Significant strength and weight loss follows discontinued use due to the loss of excessive water and HPTA suppression. So retained gains were only fair post-cycle. My personal experiences with this drug have led me to believe that no athlete should have ever stacked high dosage protocols of Denothon with Anadrol-50 or Methyltestosterone. It is a liver killer combo. A last note: Injectable Denothon did not have anywhere Nera as dramatic effects when utilized in its intended method. However, the injectable is orally active and as such was reported to be commonly used in this manner by filling gel-caps with the desired amount/dosage and subsequent ingestion. This is probably due to the fact that oral administration of a c17-alkylated AAS results in increased liver production of IGF-1. I have also learned that it was best to avoid Russian Methandrostenlone. (It commonly contains a large amount of unconverted methyltestosterone).
Manufacturer :Python Pharma LABS
Form : Oral
Molecule : Stanozolol
Volume :100 tabs
Recommended dosage :10mg/capsules
Stanathon, is a synthetic anabolic steroid derived from Dihydrotestosterone that is used in both oral and injectable form. It was developed by Winthrop Laboratories (Sterling Drug) in 1962. Unlike most injectable anabolic steroids, Stanathon is not esterified and is sold as an aqueous suspension, or in oral tablet form Stanathon is used in medicine to treat a condition known as hereditary angioedema which is characterized by occasionally recurring swelling in different parts of the body. This condition occurs due increased water retention in the body of the affected individuals. It has also been used to treat anaemia, a disorder characterized by decreased red blood cells in the body. Veterinarians may prescribe the drug to improve muscle growth, red blood cell production, increase bone density and stimulate the appetite of debilitated or weakened animals.
Also known under the name of Stanathon , Winstrol molecule or in the bodybuilding jargon as Winny. It can also be taken for lean mass gain, for a weight loss diet or a slimming. Everything will depend on how it will be used and the product (s) to combine with it. Alone it does not demand recovery because it does not aromatize and is not suppressive.
Stanathon is a moderate anabolic and low androgen steroid. This means that it produces muscle mass and medium strength gains.
However, the mass gained through Winstrol has the advantage of being of good quality and durable as this gain is not due to the soda hydro retention, as is the case for many anabolic.
Winstrol is used by bodybuilders primarily in slimming cycles because it significantly reduces water retention and fat. It can also be taken for lean mass gain, and for a weight loss diet. All depends on the dosage and its association with one or more other products.
However as this is a fairly moderate product, it is often used in mix with stronger anabolics that offset its lack of anabolic properties and guarantee a higher mass gain.
Combined with products like Primobolan, Masteron, Clenbuterol or T3 Cytomel for a slimming or in combination with testosterone, or an oral steroid such as Dianabol for an increase in power and lean mass gain, this product does not cause water retention or excessive weight gain.
Be careful anyway, it is alkyl alpha and thus toxic to the liver (liver protection). Alone it does not demand recovery because it does not aromatize.
Manufacturer: Python Pharma LABS
Used at a normal and advisable dosage, the moleculea Oxandrolone Oxanthon does not disturb the hormonal cycles, or metabolism because it aromatizes only slightly. The Oxandrolone causes fat burning and thus firmer muscles and optimization of powerlifting.
Oxandrolone, also known as Oxandrin, is an oral synthetic anabolic steroid, which is a derivative of Dihydrotestosterone. It was first synthesized by Raphael Pappo while at Searle Laboratories, now Pfizer Inc., under the trademark Oxanthon, and introduced into the United States in 1964. Its practical use is to promote weight gain after weight loss following extensive surgery, chronic infections, or severe trauma, and in some patients. Oxandrolone is also used to counter the protein catabolism associated with prolonged administration of corticosteroids, and for the relief of the bone pain frequently accompanying osteoporosis. It is also used as part of treatment for HIV/AIDS.
Oxandrolone is widely used by bodybuilders and athletes specialized in weightlifting and powerlifting. This steroid offers important gains in strength without gaining body weight. Oxandrolone is also one of the leading steroids in therapeutic steroidal treatment. It treats the fighting muscle wasting diseases or osteoporosis, and other conditions. This steroid is ideal for bulking purposes and it is commonly used during cutting phases of training. Oxandrolone is often used for cutting cycle or pre-contest period. It helps enhancing great effects on both abdominal and visceral fat elimination, which makes it very useful for those who compete in bodybuilding and stay in a weight class. Oxandrolone is very popular and efficient among female athletes. It is a very beneficial steroid for women and it works the same as it works for men.
Oxandrolone is widely used due to its exceptionally small level of androgenicity accompanied by moderate anabolic effect. Although oxandrolone is a 17-alpha alkylated steroid, its liver toxicity is very small as well. It can be combined with many steroids, like Nandrolone Decaonate, Methandrostenolone and various Testosterone compounds (Cypionate, Enanthate, Propionate)
(Oxandrolone) is an anabolic steroid which resembles closely the male hormone Testosterone. The steroid is a derivative of DHT (Dihydrotestosterone) made by substituting the second carbon atom of the molecular formulae with an oxygen atom and thus resulting to a molecular formula represented as.
Oxanthon comes in the form of a capsule and is consumed orally. When ingested, the steroid inhibits the production of Testosterone by suppressing the functions of the gonads and of the pituitary glands. Once the steroid acts as the Testosterone more masculine biased actions are often taken up by the body. The ingestion of the steroid usually affects two hormones in the body; the luteinizing hormone and the follicle stimulating hormone of the pituitary.
The Oxandrolone causes fat burning and thus firmer muscles and optimization of strength. Users looking for a mass gain will take it in “stack”, ie combine it with another product more anabolic, as the Oxandrolone does not provide mass gain.
Oxanthon is considered as a weak steroid that is slightly androgenic such that it has very minimal side effects on the growth of children. When the drug is administered in small doses, the side effects or contraindications are limited. Most concern is shown when men use the steroid as it affects the production of testosterone.
Oxydrolone is an anabolic steroid used to treat anemia, aplastic anemia, myelofibrosis, or hypoplastic anemia caused by chemotherapy.
has unusually strong androgenic effects. It can provide a huge increase in strength and mass in a very short time. Given that it has a considerable ability to retain water in the body, increases muscle mass are usually thick, with typical swollen appearance of muscle. It is used mainly in volume period, when it acts as a growth accelerator with a strong pump-effect and helps to maintain great level of strength on a high level for most of the workout. Moreover, it has strong regenerative effect. Many athletes also use it to protect joints at high load.
Oxymetholone is derived from dihydrotestosterone (DHT). That is, oxymetholone is basically a modified dihydrotestosterone. Other compounds belonging to the group of anabolic steroids are derived from DHT stanozolol, methenolone, drostanolone, oxandrolone as well as several others. Oxymetholone differs from DHT by the addition of a methyl group attached to the carbon at the 17 position, and the 2-hydroxymethyl group is attached to the first carbon on cycloalkane ring. These changes allow the oxymetholone to remain active in muscle tissue, where the dihydrotestosterone is normally disposed. The enzyme responsible for the degradation of dihydrotestosterone in muscle tissue is called 3-hydroxysteroid dehydrogenase. With the above chemical modifications, the enzyme does not react with oxymetholone. This allows the compound to stay active in the muscle tissue, and provide a very strong effect. Oxymetholone has anabolic strength in the value of 320 (more than 3 times the force of testosterone, which has an anabolic power of 100 value).It has also been found to have lower androgen strength (value of 45) compared to testosterone (value 100).
One of the unique and mysterious features of oxymetholone is that, while a derivative of dihydrotestosterone, it has a very high level of estrogenic activity. Dihydrotestosterone derivatives should not be able to convert to estrogen by the enzyme aromatase, and thus do not cause any estrogenic effects, but it’s different with oxymetholone. Oxymetholone is also well known to cause excessive water retention, bloating, gynecomastia, and other estrogenic effects in the body, although it does not convert to estrogen.It is believed that in some tissues it acts like an estrogen. It is necessary to note that all potential users understand that although Oxymetholone is a derivative of dihydrotestosterone, they cannot expect a solid and quality gains that are typical of other DHT derivatives. Estrogenic effects of oxymetholone cannot be combated by means of aromatase inhibitors because of the fact that it is not capable of converting into estrogen.
Oxymetholone belongs to a group of anabolic-androgenic steroid with the most harmful effects.Many directly associate this substance with liver cancer. It can cause liver failure, which is initially manifested in elevated values, but later the prolonged use of this substance leads to liver damage. Among the estrogenic side effects is the emergence of gynekomatic. The high retention of salt and water increases the blood pressure. Oxymetholone has significant impact on reducing the production of testosterone. It increases the number of red blood cells. Part of the active substance is converted to dihydrotestosterone (DHT); therefore some individuals may experience severe acne and hair loss. Other side effects may be headache, nausea, stomach pain, vomiting, insomnia and diarrhoea. While taking oxymetholone often paradoxical situation arises when a bodybuilder is gaining weight and strength, but does not feel particularly well. It strongly affects the conversion of carbohydrates into glycogen. In case of insufficient intake of carbohydrates it may induce a state of hypoglycemia. Greater level of aggression is attributed to increased levels of androgens and still rises at simultaneous application of large doses of testosterone. It leads to changes in the values %u200B%u200Bof HDL (good) and LDL (bad) cholesterol. Gains from the substance tend to disappear fairly quickly after discontinuation.
The first studies on oxymetholone liver toxicity in AIDS patients, have shown a harmful effect in the dose of 40 and 80 mg but not in a dose of 20 mg daily.(Detection of liver toxicity of steroids, however, is now generally problematic because it is deduced based on responses of steroid with certain enzymes and their subsequent concentration.) W. Llewellyn cites in his book Anabolics 2006 another interesting study that describes the side effects of oxymetholone on a group of older men (65-80 years), who received 50 or 100 mg of oxymetholone per day for 12 weeks. It was shown that in both groups oxymetholone significantly reduced HDL cholesterol levels, but the burden on the liver (the measurement of the activity of liver enzymes AST and ALT) surprisingly occurred only in the group receiving 100 mg / day, and even in this case it was not dramatic.
It is one of the few anabolic-androgenic steroids, which abused dose is significantly lower than the so-called therapeutic dose, commonly used in the treatment process. The package leaflet usually indicates a therapeutic dosage of 1-5 mg per kg body weight. Available information suggests that athletes due to the high toxicity of the substance opt for the optimal dose to be 50-100 mg per day. Its half-life (biological half-life) is 8-9 hours. Obviously, only short-term abuse of this substance should be considered (maximum 3-5 weeks) because the receptors that react to this substances do so only for a short period. However, as oxymetholone causes a significant reduction in the level of natural androgens, after discontinuation the vast majority of gains are lost. Quality PCT is therefore a necessity.
Athletes take oxymetholone primarily as a “starter” substance at the beginning of the injection cycle, the effect of which is slow (e.g. with testosterone, nandrolone, methenolonom, boldenone).Separate use of oxymetholone does not make sense, because the results are hardly sustainable. Studies show that the substance stays in the urine for 50-60 days.
Manufacturer : Python Pharma LABS
Volume :50 tabs
Recommended dosage :20-30mg/day
Methyl-1-testosterone (M1T) was first researched in 1962.The 60s was actually an extremely active time for steroid research.There were literally hundreds of different anabolic agents that were being actively studied and pursued by drug companies.M1T had a very favorable ratio of anabolic to androgenic effect, so there was much promise with this compound.But like many other steroids being studied at this time, it was not selected to be developed as a medicine.There were only a select few agents that were given the money for full studies and eventual release.For no clear reason M1T was not selected and it lay dormant in the medical books for forty years.M1T reemerged in 2003 when it was introduced as a “dietary supplement” in the United States. Since it was relatively unknown, it was not specifically listed in the 1991 law controlling anabolic steroids. This allowed the company Legal Gear to manufacture it legally.M1T however did not last long. On January 20, 2005 a new law came into effect banning many new compounds including M1T.
Methyl-1-testosterone is the methylated version of the steroid 1-testosterone. It is a DHT derivative. It cannot convert to DHT or estrogen.M1T is 910-1600% as anabolic and 100-200% as androgenic as methlytest. There is a structural modification that allows the compound to survive the first pass through the liver. This is what makes it extremely orally bioavailable but also liver toxic.
Cycles / Dosages:
A typical dose for M1T would range from 10mg per day to 30mg per day depending on experience. It is extremely powerful and extremely liver toxic. Due to this it is not recommended to run a cycle for more than 2-4 weeks. Many users will start at a lower dose and taper up depending on side effects and results. It is very possible to add 15-20lbs on a 2-4 week cycle of M1T. Users will often stack injectables such as testosterone with an M1T cycle.
Regardless, if you stack it or not, N2Guard must be run while on M1T to protect the liver. A PCT (post cycle therapy) will absolutely need to be run since M1T will suppress natural testosterone production. When run on its own, a mini-PCT will suffice due to the short length. I would recommend something like a 4 week PCT with the following:
HCGenerate– 5 caps per day
Clomid – 25mg per day
N2Guard 7 caps per day
We have already discussed liver toxicity but there are other side effects that come with the use of M1T.Probably the most common and toughest to deal with is lethargy. Users may become extremely fatigued throughout the day while using this compound. It is the reason many people will keep their dose closer to the 10mg per day mark.
Another side effect which is common with many oral steroids is elevated blood pressure. This is not something to take lightly. In addition, a side effect similar to one that comes with anavar is possible nosebleeds. It is not known why this happens with M1T use but it has been reported.
Other possible side effects include muscle cramps (lower back, calves), lack of sex drive, increase in sex drive, HPTA suppression, hair loss for those prone to male pattern baldness, BHP or increased size of prostate, aggressiveness, headaches, irritability, insomnia, and a decrease in appetite. The nice thing is that M1T does not aromatize, so there is no risk of estrogen related side effects.
The half-life of Methyl-1-testosterone is similar to most oral steroids but slightly longer. It is reported to be between 9-12 hours. There are still some people that will argue that the true half-life is 48 hours based on effects after usage is ceased. It is best to split the dose into 2 per day but 1 will work if it is necessary.
M1T is one of the most potent and toxic oral steroids ever created. The only way to find this product now is on the black market manufactured by underground labs. If you are looking to pack on some serious mass and strength then this compound will definitely do the job. It is also great since there is no water retention. The main thing to keep in mind is that the side effects can be tough to tolerate even for experienced PED users. All precautions must be taken to keep yourself safe and it should never be run by someone not in tip-top shape.
Manufacturer : Python Pharma
Volume : 100 tabs
Recommended dosage : 50-150mcg/day
Clenbuterol HCL is an oral anabolic steroid with multiple goals: in addition to keeping the increase of muscle mass, this steroid also causes thermogenesis and accelerates fat burning. Clenbuterol the oral version of Ventipulmin and it is distinguished from all other orals anabolic steroids.
Clenbuterol, commonly called Clen, is neither a steroid not a hormone but it is a very popular supplement among athletes and bodybuilders alike.
Athletes and bodybuilders use the drug due to its thermogenic and anti-catabolic effects. This is down to its ability to slightly increase the body’s core temperature, thereby raising calorie (energy) expenditure. It is thought that a 1°F increase yields around a 5% increase in maintenance calories burned. Studies on livestock suggest that Clenbuterol also has anabolic properties.
Clenbuterol exerts further action promoting fat burning, it helps burning fat without the need to make a diet by slightly increasing the body temperature, thus prompting the body to use fat as fuel.
Clenbuterol represents a sympathomimetic amine used by sufferers of breathing disorders as a decongestant and bronchodilator. People with chronic breathing disorders such as asthma use this as a bronchodilator to make breathing easier. It is most commonly available as the Hydrochloride salt, Clenbuterol Hydrochloride. Clenbuterol is approved for use in some countries, via prescription only, as a bronchodilator for asthma patients. Recently the drug has been publicized for l use as a weight-loss drug, similar to usage of other sympathomimetic amines such as Ephedrine.
Besides being used as a fat loss medication Clenbuterol Hydrochloride compounds are also quite popular for athletes involved in body-building, power-related, and even endurance sports. Besides being a fat burner it is also very useful as a drug in preparation for competitions and during a cutting cycle. Clenbuterol also exhibits and extremely long half-life in the body, which is measured to be approximately 34 hours long. This makes steady blood levels easy to achieve, requiring only a single or twice daily dosing schedule at most. This of course makes it much easier for the patient to use, and may tie in to its high compliance rate.
clenthon is mainly considered among bodybuilders as a weight loss drug and it also has smooth muscle relaxant properties. Clenbuterol have an anabolic effect on human muscles, and it may also increase fat metabolism. It has the property endure cardio sessions for long periods of time. This effect also lends itself greatly to athletes who are trying to cut fat in order to get into contest shape and besides all that it is a very efficient breathing assistant. Clenbuterol Hydrochloride products are also attractive for their pronounced thermogenic effects, which lead to a more efficient weight loss process, but at the end of a cycle with these compounds the human body temperature returns to normal. Caution is advised when employing the use of Clenbuterol in conjunction with other adrenoceptor agonists as side effects are likely to be cumulative.
Manufacturer :Python Pharma
Molecule :liothyronine sodium
Volume :100 tabs
Recommended dosage :100-200mcg/day
Cytomel (liothyronine sodium) is a product for a slimming cycle. This product acts on the thyroid. Great product for weight loss. In this case, combine it with clenbuterol. It is important to take this product during the morning with an empty stomach.
Liothyronine is a form of thyroid hormone used in medicine to treat hypothyroidism and myxedema coma. It is often sold under the brand name Cytomel. Liothyronine acts on the body to increase the basal metabolic rate, effect protein synthesis and increase the body’s sensitivity to catecholamines. The thyroid hormones are essential to proper development and differentiation of all cells of the human body. These hormones also regulate protein, fat, and carbohydrate metabolism, affecting how human cells use energetic compounds.
Bodybuilders use this compound to burn off fat and give them a better look. Liothyronine Sodium increases the patient’s metabolism. The result is an increased rate of cellular activity with a more rapid utilization of carbohydrates, fats and proteins. Bodybuilders and athletes are particularly attracted to this drug for its ability to burn off body excess fat. Most often utilized during contest preparation, one can greatly decrease the amount of stored fat without being forced to restrict calories. It is often used in conjunction with Clenbuterol and can produce extremely dramatic results. This combination has become very popular in recent years, and it was also noted that when thyroid hormones are taken in conjunction with steroids, an increased anabolic effect can be seen due to faster utilization of proteins by the body, increasing the rate for new muscle accumulation.
Liothyronine substances are also is used for suppressing production of thyroid stimulating hormone in patients with goiters and for testing how well the thyroid gland is functioning. The doses of Liothyronine Sodium should be increased gradually; the product should be taken with precaution by women. Taking Liothyronine for too long and/or at too high a dosage can result in a permanent thyroid deficiency. Optimal liothyronine doses are different for each patient and vary depending on the patient’s age, weight, symptoms, blood levels of thyroid hormone and underlying conditions such as heart disease.
T3-Cytomel (liothyronine sodium) is a product for a dry or weight loss cycle. This product acts on the thyroid. Great product for weight loss. Box of 100 tabs, 25 mcg / tabs.
For a lean mass cycle, this product combines very well with Dianabol ou Anabol,, or Androlic.
As part of a weight loss cycle, this product is combined with Testosterone to avoid losing too much muscle mass, and Winstrol or Primobolan or Primabolan.
This product is also excellent for losing weight; in that case, combine it with Clenbuterol.
You must first take this after fasting in the morning.
This product should be taken for a minimum of 8 weeks and a maximum of 12 weeks.
Dosage: 1-2tablets (100-200 mcg) per day.