Primoplex

Mastaplex 100 1ml

Mastaplex 200

Stanaplex 50mg, new from Axiolabs, now available in 1ml glass ampules

Testaplex Suspension, new from Axiolabs, now available in 1ml glass ampules 100mg per ampule.

Strawberry Sildenaplex Gel

Banana Sildenaplex Gel

Pasion Fruit Sildenaplex Gel

Liquourice Sildenaplex Gel

New from Axiolabs our famous sustaplex in 1ml ampules

Testaplex C 200

Finally released from Axiolabs and due for distribution around the new year (maybe a little before) All Axiolabs oils in ampule form.

Testaplex P

Decaplex 300

Duraplex

Now available in 1ml ampules

Trenaplex A 100

Trenaplex E 200

Trinaplex 200

Trenaplex D 100

Sildenaplex (Sildenafil citrate) also known as Viagra or Kamagra, is a drug used to treat erectile dysfunction and pulmonary arterial hypertension. Sildenaplex acts by inhibiting cGMP specific phosphodiesterase type 5, an enzyme that regulates blood flow in the penis. Its primary competitors on the market are Tadalaplex (Cialis) and vardenaplex (Levitra) both produced by Axiolabs.

Taldenaplex 10

Vardenaplex (Vardenafil) is closely related in function to sildenaplex (Viagra) and Taldenaplex (Cialis). Structurally, the difference between a vardenafil molecule and the others is a methyl group and a nitrogen atom's position. Vardenaplex (Levitra)is a more targeted drug than Viagra, so it is effective at lower doses.

Important Cycle advice – we put this first as it is critically important. Don’t think you can handle more as you probably cannot. Start low to see if you can handle it because it is a strong medication start with 0.25 – 0.5 ML in the morning and inject straight into stubborn fat deposit for local fat loss. Then work your-self up to see how much still is comfortable . Never go higher then 2ML per day! Because your receptors will degrade it is best to keep the cycles short. Sample cycle: week 1: 0.5ML per day week 2: 1 ML per day then stop two weeks week 5: 0.5ML per day week 6: 1 ML per day repeat breaks and repeat usage. The compound is a 50ml vial containing a blend of Clenbuterol HCL: 40mcg/ml and Yohimbine HCL: 5.4mg/ml. AXIO - Clenbuterol & Yohimbine HCL blend The compound comes in a 50ml vial containing a blend of Clenbuterol HCL: 40mcg/ml and Yohimbine HCL: 5.4mg/ml. AXIO’s ICYPLEX is a blend of Clenbuterol and Yohimbine HCl. Clenbuterol is a ?2 adrenergic agonist with some similarities to ephedrine, but its effects are more potent and longer-lasting as a stimulant and thermogenics drug. Thermogenics are dietary supplements used to stimulate the body's burning of fat. Thermogenics increase the metabolism of the body's adipose tissue, generating heat ( thermo genesis).Old practices like exposing the body to very cold temperatures to raise Basal Metabolic Rate (BMR). This is usually done by soaking the body in icy cold water until a person can not tolerate it any longer almost to the point of inducing hypothermia. This then causes a release of thyroxin from the thyroid gland by means of the sympathetic nervous system thus raising BMR resulting in an increase in body temperature back to normal .In AXIO’s formulations we apply T3 to our CYX3 (an oral blend of t3, Yohimbine and Clenbuterol) which combines all the thermogenics properties together in one unit dose)Common thermogenics substances are Ephedra, bitter orange, capsicum, ginger and caffeine. The Clen Blend injectable unit dose was specially formulated for spot reduction of stubborn areas of fat tissue for muscle - fat desired proportions. The injected compound promotes fat loss through the adrenergic system. Spot fat reduction is a within your reach. The blend would act under conditions were other means including the use of traditional oral Clenbuterol and Yohimbine products could not provide the desirable effect. ADMINISTATION: One must start at a low dose to be on the watch for adverse side effects due to the high potency. 0, 5 ML is a recommended starting dose in the morning injected straight into the fat deposit for local fat loss. The dose must be adjusted cautiously. Never exceed 2ML per day! Because the adrenergic receptors will stop its responsiveness. Sample cycle: (Must be adopted personally) week 1: 0,5ML per day week 2: 1 ML per day then stop two weeks week 5: 0,5ML per day week 6: 1 ML per day repeat breaks and repeat usage. Axio Clen Blend (see also our oral Clen Blend with T3) contains a blend of Clenbuterol Hydrochloride and Yohimbine Hydrochloride. The blend is very potent combination of a beta and alpha antagonist.Clenbuterol and Yohimbine promote fat loss through the same adrenergic system, but the effects are achieved through different mechanisms. Clenbuterol is a known thermogenics shown to directly stimulate fat cells metabolism and accelerate the breakdown of triglycerides to form free fatty acids. The hormone glucagon released signals the breakdown of the triglycerides by hormone-sensitive lipase to release free fatty acids.Yohimbine, being an antagonist of alpha-2 receptors shifts the balance of sympathetic activity to ensure that lypolisis occurs. This increases synaptic Norepinephrine release, one of the body's own natural Lipolytic hormones. In effect, it acts as beta stimulating and alpha blocking properties, an ideal combination to stimulate fat loss. Injecting AXIO’s Clen Blend one must consider the beta-2 receptor down - regulation may/will occur, hence the need to cycle administration just as one would oral Clenbuterol. Common Uses Of Clenbuterol and Injectable Clen Post-Cycle Therapy: Clenbuterol is used post cycle to aid in recovery. It allows the user to continue eating large amounts of food, without worrying about adding body fat. It also helps the user maintain more of his strength as well as his work out intensity. Diet: Roughly the same as on cycle. Fat loss: The most popular use for Clenbuterol, it also increases muscle hardness, vascularity, strength and size on a caloric deficit. For the most significant fat loss, Clen can be stacked with T3. Diet: A high protein (1.5g per lb of bodyweight), moderate carbohydrate (0.5g to 1g per lb of bodyweight), low fat diet (0.25g per lb of bodyweight) seems to work best with Clen. Alternative to Steroids: Clenbuterol has mild steroid-like properties and can be used by non AS allowing bodybuilder to increase LBM as well as strength and muscle hardness. Diet: A moderate carbohydrate, high protein, moderate fat diet work well. Precautions: The same precautions that apply to Ephedrine must be applied to Clenbuterol, although some people find ECA - ephedrine - caffeine - aspirin stacks harsher than Clen. It should not be applied with other central nervous system stimulants such as Ephedrine. These combinations are unnecessary and potentially dangerous. Caffeine can be used in moderation before a workout for an extra energy, although its diuretic effects may shift electrolyte balance. Drink more water if one uses Caffeine. One should use Injectable Clen Blend carefully and pay attention not to inject too much as injecting Clen may be dangerous and if over administered it can cause a heart attack. Because it is injected it has a much stronger affect then tablet or liquid Clen especially due to the Yohimbine HCL present in the blend.

Testosterone suspension is an injectable preparation containing testosterone (no ester) in a water base. Although it may contain testosterone without the benefit of an ester, and contrary to popular belief, the microcrystal design of this injectable will sustain an elevated testosterone release for 2-3 days. Clearly the suspension we see today is not the basic water plus testosterone design used in the 1940"s. And since the drug will not leave circulation in a matter of hours, it is obviously useful. Among bodybuilders, "suspension" is known to be an extremely potent mass agent. It is often ranked as the most powerful injectable steroid available, resulting in an incredibly rapid gain of muscle mass and strength. This is largely due to the very fast action of this drug, as the water-based steroid will begin to enter the blood stream almost immediately after an injection is given. Unlike longer esters such as enanthate or cypionate which take weeks for blood levels to reach maximiun theraputic levels, with suspension it is just a matter of days. Clearly the anabolic effect of this testosterone will be realized much more quickly than we would expect with an oil based (esterified) preparation. It is also important to remember that 100mg of a testosterone ester is not equivalent to 100mg testosterone of pure testosterone (as in suspension). When an ester is present, its weight is obviously included in the preparation"s milligram total. Looking at Testosterone enanthate, 100mg of this compound equates to only 72mg of raw testosterone. So the bodybuilder who uses 400mg of enanthate weekly is really getting about 288mg of testosterone into his body each week. This is clearly a great increase over the endogenous testosterone level of the average male, which is in the range of 2.5 to 11 mg per day. But the general point is that during a cycle of Testosterone suspension we will often see a much more dramatic intake of testosterone on average than is typically utilized with oils. Each 10ml Vial contains 100mg/ml testosterone

Mastaplex is a synthetic derivative of dihydrotestosterone, displaying a potent androgenic effect that is responsible for increases in muscle density and hardness and a moderate anabolic effect that creates a positive nitrogen balance in humans and promotes protein synthesis. Since it is a derivative of dihydrotestosterone, dromastolone does not aromatize in any dosage and thus it cannot be converted into estrogen. Therefore, estrogen-related water retention is eliminated. Mastaplex combines the fast-acting propionate form with the longer acting enanthate form. Each 10ml Vial contains 50mg/ml drostanolone propionate. 150mg/ml drostanolone enanthate.

Due to the special sophisticated equipment that must fill the stanaplex50, we are unable to use the white flip caps. As a result we are currently capping the vials with a red aluminum cap. This decision was made to ensure maximum sterility and accuracy of what is inside the vial. We are waiting for more professional photos to be taken but we have added 2 additional photos of the stan settled and when it is re constituted. Substance: Stanozolol Manufactured by: Axiolabs Packaging: 1 x 10 ml (50mg/ml) Anabolic steroids such as Stanaplex are synthetic derivatives of the male hormone testosterone. Stanozolol has a pronounced anabolic effect with fewer masculinizing side effects than testosterone and some other synthetic anabolic steroids. Anabolic steroids are used in stimulating appetite and increasing weight gain, strength, and vigor. They should be used as a part of an overall program with other supportive and nutritional therapies. This is a very popular anabolic steroid, which is a derivative of dihydrotestosterone. Winstrol is a relatively low androgenic steroid which will not aromatise. It is moderately toxic to the liver. Very few users report any water retention or any other side effects while using Winstrol. It is a popular drug for cutting in a stack with Primobolan or Parabolan. When stacked with Testosterone it can be very effective for a size and strength gain. Women use the drug quite often, but it can cause virilising effects for some women even at low dosages. Most of the muscle gains made while taking the Winstrol are retained after the drug is discontinued. The injectable form is better than the oral. Many feel that the injectable must be administered at least twice a week: some take shots every day for better effects. Dosages range from 3 to 5 cc?s per week for men, 1 to 2 cc's in women. .

Primoplex 100 for intramuscular injection, contains methenolone enanthate Methenolone Enanthate is a DHT based anabolic steroid. Known under the brand name of Primoplex® in tablet or injectable form. When it interacts with the aromatase enzyme it does not form any estrogens. It is used by people who are very succeptible to estrogenic side effects, having lower estrogenic properties than Nandrolone. Methenolone is available as an injection or as an oral(primoplex). The injection is naturally regarded as having a higher bioavailability. Its an enanthate ester which is quite long-acting. Because it by-passes hepatic breakdown on the first pass, it also has a higher survival rate. The tablets are in a short-lived acetate form. Methenolone is not 17-alpha-alkylated, but 1-methylated for oral bioavailability. This reduces the stress on the liver, but also the availability. It is considered one of the safer steroids, meaning it has a very little side effects. Methenolone has no estrogenic side effects, and its effects on cholesterol levels are minimal. In doses of 200 mg or less (intramuscular) blood pressure is rarely altered. Possibly one of the safer anabolic steroids for females due to very low virilization effects in short-term usage. Of course, this is not a blanket-statement and individual results (dependent on doses and tolereance) will vary. Methenolone is also not overly suppressive of the HPTA axis, although how suppressive is debatable. For this reason, many bodybuilders use it in between steroid cycles during their "off-time" to help maintain their gains and strength. The long term safety of such a practice possibly dangerous and can lead to permanent suppression of the HPTA. Arnold Schwarzenegger is rumored to have introduced methenolone to the US bodybuilding community. Each 10ml Vial contains 100mg/ml methenolone enanthate

Mastaplex is a synthetic derivative of dihydrotestosterone, displaying a potent androgenic effect that is responsible for increases in muscle density and hardness and a moderate anabolic effect that creates a positive nitrogen balance in humans and promotes protein synthesis. Since it is a derivative of dihydrotestosterone, dromastanolone does not aromatize at any dosage and thus it cannot be converted into estrogen. Therefore, estrogen-related water retention is eliminated. Mastabol 100 is relatively fast-actiing and fast-clearing because of the attachment of the propionate ester to the base molecule. Each 10ml Vial contains 100mg/ml drostanolone propionate.

Trenaplex D 100 for intramuscular injection, contains trenbolone hexahydrobenzylcarbonate To increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate ,enanthate or Hexahydrobenzylcarbonate. Trenbolone is then produced as a metabolite by the reaction of these compounds with the androgen receptor. Bodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week.Trenbolone hexahydrobenzylcarbonate can be injected even less frequently than trenbolone enanthate. The 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record. Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone.[citation needed] Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5?-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized. Each 10ml Vial contains 100mg/ml trenbolone hexahydrobenzylcarbonate

Trinaplex E 200 for intramuscular injection contains trenbolone acetate, trenbolone hexahydrobenzylcarbonate and trenbolone enanthate. The presence of the acetate ester allows Trinaplex E 200 to display a rapid initial physiological response. The hexahydrobenzylcarbonate and enanthate esters, which release at slower rates, prolong the physiological response with a relatively flat absorption curve over the duation of the injection life-cycle. Bodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. The 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record. Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5?-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized. Each 10ml Vial contains 50mg/ml trenbolone acetate 50mg/ml trenbolone hexahydrobenzylcarbonate 100mg/ml trenbolone enanthate

Trenaplex E 200 for intramuscular injection, contains Trenbolone Enanthate. Trenbolone Enanthate is a long acting injectable steroid. To increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate ,enanthate or Hexahydrobenzylcarbonate. Trenbolone is then produced as a metabolite by the reaction of these compounds with the androgen receptor. Bodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. Due to the relatively long metabolic half-life of trenbolone enanthate dosages should be once a week. Trenbolone acetate injections are commonly split into at least once every two days. The 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record. Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5?-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized. Each 10ml Vial contains 200mg/ml trenbolone enanthate

Trenaplex A 100 for intramuscular injection, contains Trenbolone Acetate. Trenbolone Acetate is a fast acting injectable steroid. To increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate ,enanthate or Hexahydrobenzylcarbonate. Trenbolone is then produced as a metabolite by the reaction of these compounds with the androgen receptor. Bodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week. The 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record. Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5?-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized. Each 10ml Vial contains 100mg/ml trenbolone acetate

Duraplex 100 for intramuscular injection, contains nandrolone phenylpropionate Nandrolone phenylpropionate is a fast-acting form of nandrolone. Nandrolone is chemically related to the male hormone testosterone. Compared to testosterone, it has an enhanced anabolic and a reduced androgenic activity. This has been demonstrated in animal bioassays and explained by receptor binding studies. The low androgenicity of nandrolone is confirmed in clinical use. In the human, nandrolone has been shown to positively influence calcium metabolism and to increase bone mass in osteoporosis. In women with disseminated mammary carcinoma, nandrolone has been reported to produce objective regressions for many months. Furthermore, nandrolone has a nitrogen-saving action. This effect on protein metabolism has been established by metabolic studies and is utilised therapeutically in conditions where a protein deficiency exists such as during chronic debilitating diseases and after major surgery and severe trauma. In these conditions, nandrolone phenylpropionate serves as a supportive adjunct to specific therapies and dietary measures as well as parenteral nutrition, due to it's faster acting nature nandrolone phenylpropionate is preffered in situations where a faster clinical response is required over it's chemical variant nandrolone decaonate(Decaplex). Each 10ml Vial contains 100mg/ml nandrolone phenylpropionate

Equiplex 200 for intramuscular injection, contains Boldenone Undecylenate Boldenone (1,4-androstadiene-3-one-17?-ol, available as the undecylenate ester)is an anabolic steroid developed for veterinary use, mostly for treatment of horses. It is not indicated for use in humans in the US and is only available through veterinary clinics. The activity of boldenone is mainly anabolic, with a low androgenic potency. It has a very long half-life, with minimal blood levels present up to 8 weeks after discontinued use. Boldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys. The drug is commonly used in doping within bodybuilding. If intended to assist in bodybuilding, the drug is taken as part of a steroid stack of other anabolic steroids, usually with a potent androgen like testosterone as the 'base' of the stack. Boldenone has a low rate of aromatization (about 50% of Testosterone), which means it does not convert to estrogen easily and does not cause very much water retention. Many Bodybuilders will find that it is a good replacement drug for Nandrolone. It is a poor drug of choice for any athlete who will be subject to a blood test due to its long metabolic half-life. Trace amounts of the drug can easily be detected for months after discontinued use. Each 10ml Vial contains 200mg/ml boldenone undecylenate

new from Axiolabs Decaplex 300 for intramuscular injection, contains 300mg/ml of nandrolone decanoate. Nandrolone binds to the androgen receptor to a greater degree than testosterone, but due to its inability to act on the muscle in ways unmediated by the receptor, has less overall effect on muscle growth. The drug is also unusual in that unlike most anabolic steroids, it is not broken down into the more reactive DHT by the enzyme 5a-reductase, but rather into a less effective product. As such, some of the negative effects associated with most such drugs are somewhat mitigated. The positive effects of the drug include muscle growth, appetite stimulation and increased red blood cell production and bone density. Clinical studies have shown it to be effective in treating anaemia, osteoporosis and some forms of neoplasia including breast cancer, and also acts as a progestin-based contraceptive. Nandrolone is also extensively used by bodybuilders and other athletes seeking an edge in professional competition. Each 10ml Vial contains 300mg/ml nandrolone decanoate

Testaplex P 100 for intramuscular injection, contains testosterone propionate. Testosterone propionate is a male sexual hormone with pronounced, mainly androgenic action, possessing the biological and therapeutic properties of the natural hormone. In a healthy male organism, androgens are formed by the testes and adrenal cortex. It is normally produced in women in small physiological quantities. In addition to the specific action that determines the sexual characteristics of the individual, it also has a general anabolic action, manifested in enhancement of protein synthesis. Under the effect of testosterone, body weight increases and urea excretion is reduced. High doses suppress the production of hypophyseal gonadotropin, while low doses stimulate it. It has an antitumor effect on mammary gland metastases. Each 10ml Vial contains 100mg/ml testosterone propionate Also available in 50mg/ml - see Testaplex P 50 or 25mg/ml - see Testaplex P25

Decaplex 275 for intramuscular injection, contains nandrolone decanoate. Nandrolone binds to the androgen receptor to a greater degree than testosterone, but due to its inability to act on the muscle in ways unmediated by the receptor, has less overall effect on muscle growth. The drug is also unusual in that unlike most anabolic steroids, it is not broken down into the more reactive DHT by the enzyme 5a-reductase, but rather into a less effective product. As such, some of the negative effects associated with most such drugs are somewhat mitigated. The positive effects of the drug include muscle growth, appetite stimulation and increased red blood cell production and bone density. Clinical studies have shown it to be effective in treating anaemia, osteoporosis and some forms of neoplasia including breast cancer, and also acts as a progestin-based contraceptive. Nandrolone is also extensively used by bodybuilders and other athletes seeking an edge in professional competition. Each 10ml Vial contains 275mg/ml nandrolone decanoate

Testaplex E 250 injection, for intramuscular injection, contains testosterone enanthate which is insoluble in water, very soluble in ether and soluble in vegetable oils. Androgens are derivatives of cyclopentano-perhydrophenanthrene. Endogenous androgens are C-19 steroids with a side chain at C-17, and with two angular methyl groups. Testosterone is the primary endogenous androgen. In their active form, all drugs in the class have a 17-beta-hydroxy group. Esterification of the 17-beta-hydroxy group produces compounds (testosterone enanthate and testosterone propionate) which have a longer duration of action and are hydrolyzed in vivo to free testosterone. Androgens are steroids that develop and maintain primary and secondary male sex characteristics. Endogenous androgens are responsible for the normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include the growth and maturation of prostate, seminal vesicles, penis, and scrotum; the development of male hair distribution, such as beard, pubic, chest and axillary hair; laryngeal enlargement, vocal chord thickening, alterations in body musculature, and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein. Androgens are responsible for the growth spurt of adolescence and for the eventual termination of linear growth which is brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause a disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth center and termination of growth process. Androgens have been reported to stimulate the production of red blood cells by enhancing the production of erythropoietic stimulating factor. During exogenous administration of androgens, endogenous testosterone release is inhibited through feedback inhibition of pituitary luteinizing hormone (LH). At large doses of exogenous androgens, spermatogenesis may also be suppressed through feedback inhibition of pituitary follicle stimulating hormone (FSH). Each 10ml Vial contains 250mg/ml testosterone enanthate

Also known as carbergoline, cabaser and Dostinex is now available in 1mg tablets.

TAMOXIPLEX is effective in the treatment of metastatic breast cancer in women and men. In premenopausal women with metastatic breast cancer, TAMOXIPLEX is an alternative to oophorectomy or ovarian irradiation . Available evidence indicates that patients whose tumors are estrogen receptor positive are more likely to benefit from TAMOXIPLEX therapy . Adjuvant Treatment of Breast Cancer TAMOXIPLEX is indicated for the treatment of node-positive breast cancer in women following total mastectomy or segmental mastectomy, axillary dissection , and breast irradiation. In some TAMOXIPLEX adjuvant studies, most of the benefit to date has been in the subgroup with four or more positive axillary nodes. TAMOXIPLEX is indicated for the treatment of axillary node-negative breast cancer in women following total mastectomy or segmental mastectomy, axillary dissection , and breast irradiation. The estrogen and progesterone receptor values may help to predict whether adjuvant TAMOXIPLEX therapy is likely to be beneficial. TAMOXIPLEX reduces the occurrence of contralateral breast cancer in patients receiving adjuvant TAMOXIPLEX therapy for breast cancer. Ductal Carcinoma in Situ ( DCIS ) In women with DCIS, following breast surgery and radiation , TAMOXIPLEX is indicated to reduce the risk of invasive breast cancer (see BOXED WARNING at the beginning of the label). The decision regarding therapy with TAMOXIPLEX for the reduction in breast cancer incidence should be based upon an individual assessment of the benefits and risks of TAMOXIPLEX therapy. Current data from clinical trials support five years of adjuvant TAMOXIPLEX therapy for patients with breast cancer. Reduction in Breast Cancer Incidence in High Risk Women TAMOXIPLEX is indicated to reduce the incidence of breast cancer in women at high risk for breast cancer. This effect was shown in a study of 5 years planned duration with a median follow-up of 4.2 years. Twenty-five percent of the participants received drug for 5 years. The longer-term effects are not known. In this study, there was no impact of tamoxifen on overall or breast cancer-related mortality

Exemestane (Exeplex) is an oral steroidal aromatase inhibitor (but also known uniquely as an aromatase inactivator) used in the adjuvant treatment of hormonally-responsive (also called hormone-receptor-positive, estrogen-responsive) breast cancer in postmenopausal women. The aim of Exeplex is to lower estrogen levels. Exemestane is an irreversible, steroidal aromatase inactivator, structurally related to the natural substrate androstenedione. It acts as a false substrate for the aromatase enzyme, and is processed to an intermediate that binds irreversibly to the active site of the enzyme causing its inactivation, an effect also known as "suicide inhibition." In other words, the Exemestane, by being structurally similar to the target of the enzymes, permanently binds to those enzymes, thereby preventing them from ever completing their task of converting androgens into estrogen. The estrogen suppression rate for exemestane varies from 85% to 95%.

Clomiplex is commonly used by male anabolic steroid users to bind the estrogen receptors in their bodies, thereby blocking the effects of estrogen, i.e., gynecomastia. It also restores the body's natural production of testosterone. It is commonly used as a "recovery drug" and taken toward the end of a steroid cycle.

Methanoplex does not react strongly with the androgen receptor , instead relying on activity not mediated by the receptor for its effects. These include dramatic increases in protein synthesis , glycogenolysis , and muscle strength over a short space of time. . In high doses (30 mg or more per day), side effects such as gynaecomastia , high blood pressure , acne and male pattern baldness may begin to occur. The drug causes severe masculinising effects in women even at low doses. Without the administration of aromatase inhibitors such as Arimiplex , estrogenic effects will appear over time in men. Many users will combat the estrogenic side effects with Tamoxiplex or Clomid . The 17?-methylation of the steroid does allow it to pass through the liver without being broken down allowing it to be taken orally. It also has the effect of decreasing the steroid's affinity for sex hormone binding globulin , a protein that de-activates steroid molecules and prevents them from further reactions with the body. As a result, Methanoplex 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 Methanoplex - results in significant water retention. This gives the appearance of great gains in mass and strength, which prove to be temporary once the steroid is discontinued and water weight drops. Because of this, it is often used by bodybuilders only at the start of a "steroid cycle", to facilitate rapid strength increases and the appearance of great size, while compounds such as Testaplex or Decaplex with long acting esters build up in the body to an appreciable amount capable of supporting anabolic function on their own. Methanoplex 10 formula is white tablet coated in a pink protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine. The first three images are the latest product to be released both made with the same formula.

Methanoplex does not react strongly with the androgen receptor , instead relying on activity not mediated by the receptor for its effects. These include dramatic increases in protein synthesis , glycogenolysis , and muscle strength over a short space of time. . In high doses (30 mg or more per day), side effects such as gynaecomastia , high blood pressure , acne and male pattern baldness may begin to occur. The drug causes severe masculinising effects in women even at low doses. Without the administration of aromatase inhibitors such as Arimiplex , estrogenic effects will appear over time in men. Many users will combat the estrogenic side effects with Tamoxiplex or Clomid . The 17?-methylation of the steroid does allow it to pass through the liver without being broken down allowing it to be taken orally. It also has the effect of decreasing the steroid's affinity for sex hormone binding globulin , a protein that de-activates steroid molecules and prevents them from further reactions with the body. As a result, Methanoplex 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 Methanoplex - results in significant water retention. This gives the appearance of great gains in mass and strength, which prove to be temporary once the steroid is discontinued and water weight drops. Because of this, it is often used by bodybuilders only at the start of a "steroid cycle", to facilitate rapid strength increases and the appearance of great size, while compounds such as Testaplex or Decaplex with long acting esters build up in the body to an appreciable amount capable of supporting anabolic function on their own.

Stanoplex is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders. Stanoplex is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic). Stanoplex is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks. Stanoplex is used in the treatment of hereditary angioedema. Stanoplex is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud's disease, vasculitis of Behcet's disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity. The new Stanoplex 10 formula is white tablet coated in a yellow protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.

Stanoplex is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders. Stanoplex is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic). Stanoplex is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks. Stanoplex is used in the treatment of hereditary angioedema. Stanoplex is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud's disease, vasculitis of Behcet's disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity. Stanoplex 50 is white tablet coated in a yellow protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.

Fluoxymesterone (Haloplex) is an androgenic steroid that is only useful to a small select group of athletes who seeks very specific goals. Athletes tend to use it to increase strength and aggression in the gym or in competitions such as strongman contests, fighting (like boxing) or MMA. The lack of estrogenic activity makes Halotestin perfect for pre-fight usage – as weigh-ins would not be effected by water retention. Even in such an events, Fluoxymesterone usage is usually limited to mere few weeks rather then cycled like real steroids for months. Fluoxymesterone (Haloplex) has poor binding to the AR. Studies have shown the effects to be mostly non-AR mediated. However, it is considered a very toxic oral drug, and a poor choice in most bodybuilding/steroid use applications. The half life of Fluoxymesterone (Haloplex) is commonly misunderstood. The rumored belief is that 30-90 minutes is the half-life but this rumor is false, the half life of Fluoxymesterone is about 9.5 hours.

Adjunctive therapy to promote weight gain after weight loss following extensive surgery, chronic infections, or severe trauma, and in some individuals who, without definite pathophysiologic reasons, fail to gain or maintain normal weight; to offset protein catabolism associated with prolonged administration of corticosteroids; for relief of bone pain frequently accompanying osteoporosis. Also used for Catabolic illness (eg, alcoholic liver disease, burn injury). Please note that new batches of the Oxandroplex will be a darker shade of Orange. This will become the Oxandroplex permanent color. The last batch to be the yellow color will be batch# C04S12

Primoplex is indicated in the treatment of refractory deficient red cell production anemias. These may include aplastic anemia, myelofibrosis, myelosclerosis, agnogenic myeloid metaplasia, and hypoplastic anemias caused by malignancy or myelotoxic drugs. Primoplex is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders. Primoplex (Methenolone Acetate) has been used in certain countries to counteract catabolic states, for example after major trauma. Primoplex 25 is white tablet coated in a green protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.

Oxyplex(Oxymetholone) is a synthetic anabolic-androgenic steroid hormone that is structurally related to the male hormone testosterone. Synthetic androgens are used to treat a variety of conditions including hypogonadism and delayed puberty. Androgens are also used to correct hereditary angioneurotic edema, manage carcinoma of the breast, promote a positive nitrogen balance following injury or surgery, and stimulate erythropoiesis. Considerable amounts of androgens are consumed by athletes in attempts to improve athletic performance. Oxyplex is used to promote weight gain and counteract weakness and emaciation resulting from debilitating diseases, such as advanced HIV infection, and after serious infections, burns, trauma, or surgery. It is marketed as a human prescription drug for the treatment of bone marrow failure anemias and deficient red cell production anemias.

Turanaplex is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders. Turanaplex formula is white tablet coated in a peach protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.

Clenbutaplex is a ?2 adrenergic agonist with some similarities to ephedrine, but its effects are more potent and longer-lasting as a stimulant and thermogenic drug. It causes an increase in aerobic capacity, CNS stimulation, and an increase in blood pressure and oxygen transportation. It increases the rate at which fat and protein is used up in the body at the same time as slowing down the storage of glycogen. It is commonly used for smooth muscle relaxant properties. These mean that it is a bronchodilator, and tocolytic.

Thyroid hormone drugs are natural or synthetic preparations containing tetraiodothyronine (T4, levothyroxine) sodium or triiodothyronine (T3, liothyronine) sodium or both. T4 and T3 are produced in the human thyroid gland by the iodination and coupling of the amino acid tyrosine T4 contains four iodine atoms and is formed by the coupling of two molecules of diiodotyrosine (DIT). T3 contains three atoms of iodine and is formed by the coupling of one molecule of DIT with one molecule of monoiodotyrosine (MIT). Both hormones are stored in the thyroid colloid as thyroglobulin. Thyroid hormone preparations belong to two categories (1) natural hormonal preparations derived from animal thyroid, and (2) synthetic preparations. Natural preparations include desiccated thyroid and thyroglobulin. Desiccated thyroid is derived from domesticated animals that are used for food by man (either beef or hog thyroid) and thyroglobulin is derived from thyroid glands of the hog. The United States Pharmacopeia (USP) has standardized the total iodine content of natural preparations. Thyroid USP contains not less than (NLT) 0.17 percent and not more than (NMT) 0.23 percent iodine, and thyroglobulin contains not less than (NLT) 0.7 percent of organically bound iodine. Iodine content is only an indirect indicator of true hormonal biologic activity.

CYX3 (an oral blend of T3, Yohimbine and Clenbuterol) Combines the synergistic fat burning power of beta adrenergic agonists) and alpha adrenergic antagonists (Yohimbine HCl), all to add the T3 characteristics of increase the metabolic rate by increasing Thyroid efficiency. Clenbuterol - 37.5mcg T3 - 25mcg Yohimbine 5.4mg Effects and Dosage The blend is very potent combination of a beta and alpha antagonist.Clenbuterol and Yohimbine promote fat loss through the same adrenergic system, but the effects are achieved through different mechanisms. Clenbuterol is a known thermogenics shown to directly stimulate fat cells metabolism and accelerate the breakdown of triglycerides to form free fatty acids. The hormone glucagon released signals the breakdown of the triglycerides by hormone-sensitive lipase to release free fatty acids.Yohimbine, being an antagonist of alpha-2 receptors shifts the balance of sympathetic activity to ensure that lypolisis occurs. This increases synaptic Norepinephrine release, one of the body's own natural Lipolytic hormones. In effect, it acts as beta stimulating and alpha blocking properties, an ideal combination to stimulate fat loss. Administration and Use: Clenbuterol should be built up and tapered off gradually with dosage increases and decreases every 3-4 days and doses never exceeding 160 µg per day for safety measures. It is administered for periods of 2-3 weeks then discontinued for equal periods of time to prevent the body’s metabolic system the ability to adapt to the metabolic effects. For fat-burning goals Clenbuterol is often stacked with another fat-burning agent for quick effect, or alternated with another fat-burning agent by people who need to stay lean for a promote period. Usually T 3 is used for such purposes, with alternating cycles of 3 weeks each. If used together, cycles will not completely overlap!!! And a new adjustment is needed. A typical cycle for Clenbuterol might be 3 weeks, with the daily amounts being: Day1-1 tablet Day2-1 tablet Day3-1 tablet Day4-11/2 tablets Day5-11/2 tablets Day6-11/2 tablets Day7-2 tablets Day8-2 tablets Day9-2 tablets Day10-11/2 tablets Day11-11/2 tablets Day12-11/2 tablets Day13-1 tablets Day14-1 tablets Day15-1 tablets Day16-1/2tablet Day17-1/2tablet Day18-1/2tablet Day19-1/2tablet Day20-1/4tablet Day21-1/4tablet Then stopping for three weeks and recommencing. Patients should be instructed that the expected benefits of CYX 3 may only be obtained when each tablet is swallowed with plain water the first thing upon arising for the day, at least 30 minutes before the first food, beverage, or medication of the day. Even ingestion with orange juice or coffee has been shown to markedly reduce the absorption of CYX 3 To facilitate delivery to the stomach and thus reduce the potential should be instructed to swallow CYX 3 with a full glass of tap water and not to lie down for at least 30 minutes and until after their first food of the day. Patients should not chew or suck on the tablet, or retain it in the mouth for a period longer than that required for swallowing, because a potential for side effects, not to take CYX 3 at bedtime or before arising for the day Difficulty or pain upon swallowing, retrosternal pain or new or worsening heartburn), they should stop taking CYX

NEW from Axiolabs Each Tablet contains 50mg of Ephedrine HCL

A perfect blend of five testosterone compounds. The five different testosterone esters provide for different half lives. Esterization of the testosterone molecules provides for a sustained (but non-linear) release of testosterone from the injection depot into the blood plasma. While the intention of the mixed testosterone esters in Sustaplex is to provide more stable serum testosterone levels, the long-ester testosterones, such as testosterone cypionate or testosterone decanoate, provide more stable serum testosterone levels. Sustaplex is the most popular testosterone blend product among those that use anabolic steroids for muscle building purposes. Each 10ml Vial contains 30mg/ml Testosterone Acetate 50mg/ml Testosterone Propionate 50mg/ml Testosterone Phenylpropionate 90 mg/ml Testosterone Cypionate 105mg/ml Testosterone Decanoate

Tetsaplex C 200 injection, for intramuscular injection, contains testosterone cypionate which is the oil-soluble 17 (beta)-cyclopentylpropionate ester of the androgenic hormone testosterone. Endogenous androgens are responsible for normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include growth and maturation of the prostate, seminal vesicles, penis, and scrotum; development of male hair distribution, such as beard, pubic, chest, and axillary hair; laryngeal enlargement, vocal cord thickening, and alterations in body musculature and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, and phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein. Androgens are responsible for the growth spurt of adolescence and for eventual termination of linear growth, brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth centers and termination of the growth process. Androgens have been reported to stimulate production of red blood cells by enhancing production of erythropoietic stimulation factor. Each 10ml Vial contains 200mg/ml testosterone cypionate

ARIMIPLEX is indicated for adjuvant treatment of postmenopausal women with hormone receptor positive early breast cancer. ARIMIPLEX is indicated for the first-line treatment of postmenopausal women with hormone receptor positive or hormone receptor unknown locally advanced or metastatic breast cancer. ARIMIPLEX is indicated for the treatment of advanced breast cancer in postmenopausal women with disease progression following tamoxifen therapy .

Proviraplex (Mesterolone) is an androgenic/anabolic steroid with a particularly high affinity for SHBG (sex hormone binding globulin). SHBG is a protein that acts by binding to sex hormones and preventing them from interacting within the body at places like the AR (androgen receptor). Because of its high affinity with SHBG, Proviraplex' main use is to competitively bind with SHBG, freeing up more of the endogenous hormone to be active within the body. In effect, proviron acts as a 'magnifier' of the anabolic effects of steroid hormones. It also exhibits anti-aromatase activity, hence helping to prevent the conversion of certain steroids into estrogen. As a result, the intake of proviraplex whilst on a cycle of steroids, results in a 'hardening' of skeletal muscle - a look which is very popular amongst steroid users. One side effect of proviraplex is the increased frequency and severity of erections, particularly during sleep/upon waking. Although proviraplex is an orally administered steroid, and is alkylated to survive the first pass through the liver, it is considered to be almost completely non-toxic to the liver. A typical dose of proviron might be from 25-100mg daily. The new Proviraplex formula is white tablet coated in a bright blue protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.

Letroplex (Letrozole) is an oral non-steroidal aromatase inhibitor that has been introduced for the adjuvant treatment of hormonally-responsive breast cancer. Estrogens are produced by the conversion of androgens through the activity of the aromatase enzyme. Letroplex blocks production of estrogens in this way by competitive, reversible binding to the heme of its cytochrome P450 unit. The action is specific, and Letroplex does not reduce production of mineralo- or corticosteroids. In contrast, the antiestrogenic action of tamoxiplex, the major medical therapy prior to the arrival of aromatase inhibitors, is due to its interfering with the estrogen receptor, rather than inhibiting estrogen production.