Oral Products

Stanozolol 10 mg 100 tablets

Chemical Name:

  • 17α-Methyl-17β-hydroxy-[5α]-androst-2-eno[3,2-c]pyrazole
  • Formula C21H32N2O
  • Anabolic activity index 320%
  • Androgenic activity index 30%

Stanozolol (also known as winstrol) is a 17-alpha-alkylated derivative of dihydrotestosterone (DHT) with low androgenic qualities yet highly anabolic. It was first developed in 1962 by American global pharmaceutical company Sterling-Winthrop Laboratories to increase lymphocyte count and CD8+ cell numbers, but to decrease CD4+ and CD3+ in postmenopausal women using it for osteoporosis. This effect would plausibly be useful for treatment of autoimmune disorders. Winstrol is useful in treatment of hereditary angioedema. It also influences some immunological processes.

Now stanozolol is produced for sale in two forms: tablets and injections. Stanozolol is the second most widely used oral steroid, succeeded in popularity only by methandienone. Stanozolol tablets have a short life time (about 9 hours) as compared against injectable stanozolol. The injectable version of stanozolol differs from other injectable anabolic steroids in being an aqueous suspension of fine particles of steroid, instead of being an oil solution of an esterified compound. For this reason, it has unusual pharmacokinetics which do not follow the classic half-life pattern. Instead, there is a sustained effect which slowly tapers. The duration of action is probably at least a week. Individual particles of stanozolol may remain at the injection site for extended periods of time. However, La Pharma managed to create an oil-based version of stanozolol, which can be mixed with all other oil and has no flaws of the suspension. All three forms are characterized by good bioavailability.

Although stanozolol is a DHT based compound, its activity is much milder than this androgen in nature. As DHT derivative Stanozolol can`t convert into estradiol, hence aromatase inhibitors are not required when taking this compound. As a result stanozolol does not cause water retention. On the contrary, it possess a diuretic effect. So, instead of bulk look winstrol produces a lean, quality look without excess subcutaneous water retention. This makes it an excellent steroid to use throughout cutting cycles, when getting rid of superfluous water and fat as well as strongly defined, hard looking muscularity are a major goal. Due to its features stanozolol is highly regarded among athletes of strength/speed sports like track and field.

As for bodybuilders, stanozolol has one interesting peculiarity demanded among them. It consists in the profound ability to lower sex hormone-binding globulin (SHBG) level resulting in efficiency growing of other steroids in stack with it. In particular, it raises the amount of biologically active free testosterone circulating in the blood. For this reason it is advisable always to use stanozolol in stack with testosterone. Another one reason for this is as follows: winstrol may be more prone than other anabolic steroids to increasing tendon brittleness. This happens due to winstrol`s possibility to dry out the joint fluid, which can lead to joint pain and damages. Also both stanozolol forms: tablets and injections have been noted to provoke adverse changes in cholesterol levels. Hence, monitoring of the lipid profile of the body (blood works) during cycle is advisable.

To summarize, stanozolol is generally recommended for athletes having sufficient muscle bulk, but wishing to improve endurance and increase muscle relief and hardness.

ACTIVE HALF-LIFE

CLASSIFICATION

DOSAGE

ACNE

9 hours

Anabolic steroid

Men 20-50 mg/day

Yes

WATER RETENTION

HBR

HEPATOXITY

AROMATIZATION

No

Perhaps

Yes

No

Clenbuterol 40 mcg 100 tablets

Chemical Name:

  • 1-(4-amino-3,5-dichlorophenyl)-2-(tert-butylamino)ethanol
  • Formula C12H18Cl2N2O
  • Anabolic activity index not a steroid
  • Androgenic activity index not a steroid36-48 hours

Clenbuterol is not an anabolic steroid, but rather a stimulant that belongs to a classification of compounds known as sympathomimetics. Clenbuterol’s original use as a medicine in the prescription drug market was (and still currently is) as a bronchodilator in the treatment of asthma. Upon activation of beta-2 receptors in the cell lining of the bronchial tubes, it initiates bronchial dilation (the opening and expanding of the airways) in the lungs, nose, and throat.

In bodybuilding clenbuterol is most commonly utilized in cutting, pre-contest, and fat loss cycles. Clenbuterol can bind to receptors on fat cells and initiate lipolysis. This effect involves its interaction with beta-2 adreno-receptors in fat tissue.

One important point to note is that through continued consistent use, clenbuterol will downregulate beta-2 receptors in the body in response to its stimulation of those receptors, and it occurs very quickly. The manifestation of this effect is diminished fat loss during use until the fat loss reaches a complete stop. There are two methods of remedying this effect. The first is to introduce time off from use of the drug for at least 2 weeks. The second is through the use of Ketotifen, an anti-histamine drug that is known for upregulating beta-2 receptors.

Clenbuterol is not an anabolic steroid, it does not express or exhibit any of the known side effects that are associated with anabolic steroid use. Instead, clenbuterol expresses side effects that are common to all drugs and compounds in the stimulant class.  Perhaps the most unique of clenbuterol side effects is the commonly reported side effect of muscle cramping. The cause of this is through Clenbuterol’s depletion of taurine in the body. Taurine, alongside magnesium, potassium, and sodium, play very crucial roles in the regulation of bioelectrical nerve impulses and signals that govern the contraction and relaxation of all muscle tissue types. When taurine is depleted, involuntary and often intense and painful muscle contractions that lead to cramps can result. Supplementation with taurine at 2.5 – 5 grams per day can mitigate this side effect.

Clenbuterol may adversely affect the cardiovascular system and raises heart rate and blood pressure. Please take this into account prior to using it.

Other common clenbuterol side effects include tremors, insomnia, sweating, and nausea. 

In order to achieve any significant amount of fat loss, the maximum Ņlenbuterol dosage should be no more than 120 – 160 mcg per day (for males). 

WARNING: The dosage must be slowly ramped up to the maximum dosages mentioned. The initial starting dosage should not exceed 20-40 mcg for the first 2-4 days, after this the clenbuterol dosage is increased by another 20 mcg and so on. Titration downwards is not necessary when ending clenbuterol use.

Clenbuterol exhibits a half-life of approximately 37 hours, so all Clenbuterol dosages should ideally be consumed at once in the morning. There is no requirement to spread the clenbuterol dosages throughout the day, and this would in fact cause worse insomnia and sleep disturbances.

ACTIVE HALF-LIFE

CLASSIFICATION

DOSAGE

ACNE

36-48 hours

Sympathomimetic, beta-2 receptor agonist

20-120 mcg/day

No

WATER RETENTION

HBR

HEPATOXITY

AROMATIZATION

No

Yes

No

No

Methandienone 10 mg 100 tablets

Chemical Name:

  • 17α-Methyl-17β-hydroxyandrost-1,4-dien-3-one
  • Formula C20H28O2
  • Anabolic activity index 200%
  • Androgenic activity index 50%

Methandienone (also known as methandrostenolone, Dbol, dianabol) is an orally-effective anabolic steroid originally developed in Germany and released in the US in the early 1960s by Ciba Specialty Chemicals. This is a derivative from testosterone, one of the most popular steroid compounds in the world and the second steroid (after testosterone) ever produced. Methandienone promotes dramatic increases in protein synthesis, glycogenolysis, and muscle strength over a short space of time.  

It also has the effect of decreasing the steroid's affinity for sex hormone binding globulin. As a result, methandrostenolone is significantly more active than an equivalent quantity of testosterone, resulting in rapid growth of muscle tissue. However, the concomitant elevation in estrogen levels - a result of the aromatization of methandrostenolone - results in significant water retention. Hence, do not forget to perform blood works and use an aromatase inhibitor.

In summary, this is a very good drug, and a potent tool for quick gains or retaining gains when used properly and safely.

ACTIVE HALF-LIFE

CLASSIFICATION

DOSAGE

ACNE

5-6 hours

Anabolic steroid

Men 20-50 mg/day

Yes

WATER RETENTION

HBR

HEPATOXITY

AROMATIZATION

High

Yes

Yes

High

Oxymethalone 50 mg 100 tablets

Chemical Name:

  • 17α-Methyl-2-hydroxymethylene-17β-hydroxy-[5α]-androstan-3-one
  • Formula C21H32O3
  • Anabolic activity index 320%
  • Androgenic activity index 45%

Oxymetholone (also known as anapolon or anadrol) is a very drastic synthetic steroid, 17-alpha-alkylated modification of dihydrotestosterone. It was developed for the treatment of osteoporosis and anaemia, as well as to stimulate muscle gain in malnourished and debilitated patients. Oxymetholone has been approved by the American Food and Drug Administration (FDA) for use in humans. Later there where created non-steroidal drugs that effectively could treat anaemia and osteoporosis; because of this anapolon lost his popularity and by 1993 Syntex decided to cease the production of the drug, as well as other manufacturers did.  

By its performance parameters oxymetholone is most similar to methandienone.  As with methandienone, it provokes not only active muscle bulking, but also a significant increase in power performance. However, a large part of the gained weight is because of water retention in the body, which can lead to high blood pressure on cycle.  

Thanks to its ability to influence the level of hemoglobin and to increase the blood volume in the body, oxymetholone may cause an extremely strong pumping effect by athletes, which consequently complicates the training process, because muscles get sore almost immediately after the first heavy set.  

Oxymetholone is a derivative of dihydrotestosterone, which gives it a chemical structure that does not aromatize. Despite the fact that oxymetholone does not directly convert to estradiol, it itself has pronounced estrogenic properties. It should be remembered that because of this peculiarity only antiestrogens would be able to combat with estrogenic side effects, but not aromatase inhibitors, because aromatase is not involved into the process.  

Some suggest that oxymetholone`s estrogenic activity relates to the progestogenic one, like with nandrolones. Side effects may be similar. However, medical studies have shown that oxymetholone does not possess any progestogenic activity. 

 

ACTIVE HALF-LIFE

CLASSIFICATION

DOSAGE

ACNE

8 hours

Anabolic steroid

Men 50 - 100

Yes

WATER RETENTION

HBR

HEPATOXITY

AROMATIZATION

High

Yes

Yes

Yes

Halotestin 10 mg 100 tablets

Chemical Name:

  • 9-Fluoro-17α-methyl-11β,17β-dihydroxyandrost-4-en-3-one
  • Formula C20H29FO3
  • Anabolic activity index 1900%
  • Androgenic activity index 850%

Halotestin is an anabolic steroid with a very strong androgenic activity, derived from methyltestosterone. The clinical purpose of fluoxymesterone consisted originally in the treatment of male hypogenitalism, delayed puberty in men, and in the treatment of breastneoplasms in women. 

Due to its specific fluoxymesterone is mainly used by athletes to enhance the power performance, muscle hardness and aggression without increasing the overall weight; it is used as well in box and other combat sports. In bodybuilding fluoxymesterone is used rarely, because it does not promote significant muscle bulking.

Fluoxymesterone does not aromatize and does not convert to estradiol; however, this is a very potent androgen. Female athletes should stay away from the drug. 

Fluoxymesterone has an interesting feature: it activates erythropoiesis (production of red blood cells) and enhances the branching of the capillary network in muscles, and as result of improved blood supply significantly increases strength and endurance.  


ACTIVE HALF-LIFE

CLASSIFICATION

DOSAGE

ACNE

9 hours

Anabolic steroid

Men 10-40 mg/day

Yes

WATER RETENTION

HBR

HEPATOXITY

AROMATIZATION

No

Perhaps

High

No

T3Cytomel 25 mcg 100 tablets

Chemical Name:

  • (2S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid
  • Formula C15H12I3NO4

Triiodothyronine, also known as T3, is a thyroid hormone, that greatly affects almost every physiological process in the body, including growth and development, metabolism, body temperature, and heart rate.

This hormone is involved in many cellular functions including the metabolism of carbohydrates, fats and proteins. When an individual is no longer producing enough of this hormone on his own, such as when suffering from hypothyroidism, the metabolism does not function properly. When suffering from hypothyroidism, the individual will find body fat gain to be very common and fat loss becomes extremely difficult. The individual also often experiences a loss of energy and even hair loss in some cases. By supplementing with T3 this provides the body with the thyroid hormone it needs and the problem is solved.

It generally only takes a low dose of T3 to treat hypothyroidism. This will not necessarily promote enhanced fat loss, but it should return the metabolism back to proper working order. However, many performance enhancing athletes enjoy using triiodothyronine to in fact enhance direct fat loss. The use of Triiodothyronine alongside a calorie restricted diet will promote significant and accelerated fat loss. While effective, generally this type of use cannot be recommended without the use of anabolic steroids. Due to the necessarily higher doses needed to promote enhanced fat loss and due to the depletion of ATP (Adenosine triphosphate), this can promote lean tissue loss. The body will take whatever it needs from wherever it can get it to meet its energy demands. For this reason, an anabolic protectant is normally advised when supplementing with T3 for this purpose.

Effects

T3 increases the basal metabolic rate and, thus, increases the body's oxygen and energy consumption.

Protein

T3 stimulates the production of RNA Polymerase I and II and, therefore, increases the rate of protein synthesis. It also increases the rate of protein degradation, and, in excess, the rate of protein degradation exceeds the rate of protein synthesis. In such situations, the body may go into negative ion balance.

Glucose

T3 potentiates the effects of the β-adrenergic receptors on the metabolism of glucose. Therefore, it increases the rate of glycogen breakdown and glucose synthesis in gluconeogenesis.

Lipids

T3 stimulates the breakdown of cholesterol and increases the number of LDL receptors, thereby increasing the rate of lipolysis.

Heart

T3 increases the heart rate and force of contraction, thus increasing cardiac output, by increasing β-adrenergic receptor levels in myocardium. This results in increased systolic blood pressure and decreased diastolic blood pressure. The latter two effects act to produce the typical bounding pulse seen in hyperthyroidism.

Before taking this drug, we strongly recommend to perform a blood work and find out your TSH, T4, T3 serums!

It is also important to stress that a cycle should last no longer than 6 weeks and it should never be halted abruptly. As slowly as the dosage was built up it should also be lowered, 15-25 mg every 3-4 days. 


ACTIVE HALF-LIFE

CLASSIFICATION

DOSAGE

ACNE

1 day

Thyroid hormon

25-75 mcg/day

No

WATER RETENTION

HBR

HEPATOXITY

AROMATIZATION

No

Yes

No

No

Oxandrolone 10 mg 100tablets

Chemical Name:

  • 17α-Methyl-17β-hydroxy-2-oxa-[5α]-androstan-3-one
  • Formula C19H30O3
  • Anabolic activity index   400 %
  • Androgenic activity index   24 %

Oxandrolone (also known as anavar) is an oral 17-alpha-alkylated steroid, modification of dihydrotestosterone. It was firstly synthesized for the treatment of debilitated HIV-infected patients, for persons with Turner syndrome, anaemia, for bones strengthening and recovery from burns. 

Oxandrolone does not yield to aromatization and is not estrogenic itself.  This drug is beloved by athletes, who prepares for competition in strength and endurance sports, where lean muscle without water and fat are needed. Oxandrolone cycle won`t help athletes gain colossal muscle volumes; however, it is a perfect compound for getting rid of fat and giving the body a more relief look. 

Despite the fact that anavar is 17-alpha-alkylated, it causes gentle toxic impact on the liver. Researches have shown that taking oxandrolone at 20 mg per day for twelve weeks did not cause statistically important raise in AST and ALT. So, oxandrolone side effects show very rare, though oxandrolone results are also not significant. It is probably the mildest and safest oral steroid available today for sale, hence, it is perfect for the first acquaintance with anabolic steroids. 

ACTIVE HALF-LIFE

CLASSIFICATION

DOSAGE

ACNE

9 hours

Anabolic steroid

Men 30-50 mg/day

Rarely

WATER RETENTION

HBR

HEPATOXITY

AROMATIZATION

No

No

Low

No