ANASTROVER® 1mg (Arimidex) 100 tabs/1mg Price:55 EUR
ANASTROVER® 1mg (Arimidex) 25 tabs/1mg Price:19 EUR
Manufacturer: Vermodje, Moldova
Pharmaceutical name: Anastrozole
Pack: 100 tabs (1 mg/tab)
Anastrover is an post cycle steroid, its active substance is Anastrozole and is made by Vermodje.
Anastrover is a potent and selective non-steroidal aromatase inhibitor indicated for the treatment of advanced breast cancer in post-menopausal women with disease progression following tamoxifen therapy. Many breast cancers have estrogen receptors and growth of these tumors can be stimulated by estrogens. In post-menopausal women, the principal source of circulating estrogen (primarily estradiol) is conversion of adrenally-generated androstenedione to estrone by aromatase in peripheral tissues, such as adipose tissue, with further conversion of estrone to estradiol. Many breast cancers also contain aromatase, the importance of tumor-generated estrogens is uncertain. Treatment of breast cancer has included efforts to decrease estrogen levels by ovariectomy premenopausally and by use of anti-estrogens and progestational agents both pre- and post-menopausally, and these interventions lead to decreased tumor mass or delayed progression of tumor growth in some women. Anastrover is a potent and selective non-steroidal aromatase inhibitor. It significantly lowers serum estradiol concentrations and has no detectable effect on formation of adrenal corticosteroids or aldosterone.
Anastrover is the first in a new class of third-generation selective oral aromatase inhibitors. It acts by blocking the enzyme aromatase, subsequently blocking the production of estrogen. Since many forms of breast cancer cells are stimulated by estrogen, it is hoped that by reducing amounts of estrogen in the body the progression of such a disease can be halted. This is the basic premise behind Nolvadex, except this drug blocks the action and not production of estrogen. The effects of Anastrover can be quite dramatic to say the least. A daily dose of one tablet can produce estrogen suppression greater than 80 % in treated patients. With the powerful effect this drug has on hormone levels, it is only to be used (clinically) by post-menopausal women whose disease has progressed following treatment with Nolvadex (tamoxifen citrate). Side effects like hot flushes and hair thinning can be present, and would no doubt be much more.
For the steroid using male athlete, Anastrover shows great potential. Up to this point, drugs like Nolvadex and Proviron have been our weapons against excess estrogen. These drugs, especially in combination, do prove quite effective. But Anastrover appears able to do the job much more efficiently, and with less hassle. A single tablet daily, the same dose use clinically, seems to be all one needs for an exceptional effect (some even report excellent results with only 0.25 mg daily). When used with strong, readily aromatizing androgens such as Dianabol or testosterone, gynecomastia and water retention can be effectively blocked. In combination with Propecia (finasteride), we have a great advance. With the one drug halting estrogen conversion and the other blocking 5-alpha reduction , related side effects can be effectively minimized. Here the strong androgen testosterone could theoretically provide incredible muscular growth, while at the same time being as tolerable as nandrolone. Additionally the quality of the muscle should be greater, the athlete appearing harder and much more defined without holding excess water.
ANDROVER® 100 tabs/50mg Price:55 EUR
Pack: 100 tablets (50 mg/tab)
Pharmaceutical Name: Oxymetholone
Androver(Anadrol) by Vermodje is an oral steroid which contains 50mg of the hormone Oxymetholone.A few common nicknames for this substance are "A-50", "Anandrol 50" and "A-bombs". Oxymetholone is a very good drug for promoting massive gains in both strength and size. This steroid is very anabolic and will promote an increase in red blood cell count and appetite. The steroid was originally designed as a form of treatment for patients suffering from diseases which cause the body to waste away, such as HIV.
A lot of bodybuilders consider this drug to be the strongest oral that there is for sheer mass gain.After usage of this hormone, bodybuilder’s growth in their muscle mass in very short time, for example about 10-15 pounds in just 14 days.It is important to note that some of this mass will be from water bloat caused by the steroid.While Anadrol is a DHT derived compound and therefore can’t convert directly to estrogen, it still is known for many estrogenic related side effects. Some have speculated that A-50 somehow triggers the body’s natural estrogen receptors into overdrive. Stronger anti-estrogens such as Letrozole and Exemestane have been shown to greatly suppress the body’s estrogen levels and can both be very effective in keeping these types of side effects to a minimum while using Oxymetholone.
Anapolon is a very fast acting steroid and bodybuilders usually begin to notice its effects towards the end of the first week. Because of this, Oxymetholone can make a great kickstart to any bulking cycle. It is important to note that A-50 can be liver toxic if not used responsibly. Bodybuilders are urged to keep cycles of this steroid short, preferably 6 weeks or less, and to keep doses to 100mg or less daily.
While Oxymetholone will increase appetite in proper doses, this drug has been known to decrease appetite, making it difficult to eat, if abused in higher doses. Some users of this steroid also report headaches. Clearly this is a serious substance that should be treated with respect, but if used properly can be a very useful tool in achieving goals.
Those looking to cycle with Oxymetholone will typically use it the first 3-6wks of a cycle that also includes an injectable form of Testosterone. For even more superior mass gains, bodybuilders may choose to add another injectable such as Deca or Tren to the cycle. In these cases, mass and strength gains are sure to be nothing less than dramatic. Oxymetholone will shut down the body’s ability to produce testosterone naturally, therefore making a PCT with Nolvadex(Tamoxifen citrate),Clomid and HGH is recommend.
BOLDEVER® 200mg/ml 10ml Price:30 EUR
Product Name: Boldever Boldenone Undecylenate (Equipoise)
Price 10ml vial 200mg/ml
Active Substance: Boldenone Undecylenate
Active Life: 7-10 days
Suggested Use: 300-600mg
Water retained: 20% compared to testosterone
Liver toxicity: NO
DHT Conversion: No, the NOR-DHT
Own inhibition test: Moderate
Boldenone Undecylenate (Equipoise)
Boldenone undecylenate is a very effective steroid for humans offering the athlete interesting characterisitics which other steroids simply do not have. Boldenone has a high anabolic effect coupled with a distinct androgenic component. Boldenone has a very favorable effect on the organisms nitrogen balance so that the main effect consists of a distinctly increased protein synthesis in the muscle cell. This results in a gain in lean body mass with very little water bloating. Boldenone undecylenate is not a rapid mass builder, but will provide a slow but steady gain of strength and quality muscle mass. The most positive effects of this drug are seen when it is used for longer cycles, usually lasting at least 10 weeks in length. The muscle gained should not be the smooth bulk seen with androgens, but instead a very defined and solid look. Since water bloat is not contributing greatly to the diameter of the muscle, much of the size gained on a cycle of Boldenone undecylenate can be retained after the drug has been discontinued.
How to Use:
Boldenone steroid has very low aromatizing properties and as such makes it an ideal steroid for pre contest preparation. Athletes that stack equipoise with Winstrol (Stanozolol) notice an increase in muscle hardness for pre-contest. Boldenone undecylenate can also be used as a mass building steroid. Boldenone has been noted to stimulate appetite. This stimulus coupled with increased calorie intake creates a rapid gain in quality muscle mass. Boldenone steroid has a long half life and can be injected once per week. Higher doses are more efficient spread out throughout the week. Many athletes opt for every other day injections for convenience and to reduce the risk of getting an abscess. Effective doses are usually between 200mgs/week and 600mgs/week for men and between 50mgs/week and 100mgs/week for women.
Boldenone undecylenate has been shown to increase red blood cells. Although this is common with most steroids – Boldenone appears to do this at a higher rate. Boldenone will suppress your natural hormones so pairing it with a testosterone injection is recommended. Oily skin, acne, increased aggression and hair loss are all possible with this compound. Women find this drug quite comfortable, virilization symptoms usually unheard of when taken at low doses. Although this drug is relatively mild, it still has a depressive effect on endogenous testosterone levels, therefore a proper post cycle therapy HCG and Clomid/Nolvadex is needed at the conclusion of each cycle.
Suggested Equipoise Stack:
Effective steroids to stack equipoise with include Testosterone Enanthate, Cypionate or Sustanon and an oral steroid - Dianabol or Anadrol.
For pre contest preparation one can stack equipoise with Winstrol injectable, Trenbolone Acetate and Testosterone Propionate has been very effective amongst athletes.
Price: 17.5 EUR
Pharmaceutical name: Clenbuterol Hydrochloride
Pack: 100 tabs (40 mcg/tab)
Active Life: Up to 68 hours
Average Dose: Men 100-140 mcg/day; Women 80-100 mcg/day
Clenbuterol is a widely used bronchodilator in many parts of the world. The drug is most often prepared in 20mcg or 40mcg tablets, but it is also available in syrup and injectable form. Clenbuterol belongs to a broad group of drugs knows as sympathomimetics. These drugs affect that sympathetic nervous system in a wide number of ways, largely mediated by the distribution of adrenoceptors. There are actually nine different types of these receptors in the body, which are classified as either alpha or beta and further subcategorized by type number. Depending on the specific affinities of these agents for the various receptors, they can potentially be used in the treatment of conditions such as asthma, hypertension, cardiovascular shock, arrhythmias, migraine headaches and anaphylactic shock. The text Goodman and Gillman's The Pharmacological Basis of Therapeutics Edition does a good job of describing the diverse nature in which these drugs affect the body:
Most of the actions of catecholamines and sympathomimetic agents can be classified into seven broad types: (1) peripheral excitatory action on certain types of smooth muscles such as those in blood vessels supplying the skin, kidney, and mucous membranes, and on the gland cells, such as those of the salivary and sweat glands; (2) a peripheral inhibitory action on certain other types of smooth muscle, such as those in the wall of the gut, in the bronchial tree, and in blood vessels supplying skeletal muscle; (3) a cardiac excitatory action, responsible for in increase in heart rate and force of contraction; (4) metabolic actions, such as an increase in the rate of glycogenolysis in liver and muscle and liberation of free fatty acids from adipose tissue; (5) endocrine actions, such as modulation of the secretion of insulin, rennin, and pituitary hormones; (6) CNS actions, such as respiratory stimulation and, with some of the drugs, an increase in wakefulness and psychomotor activity and a reduction in appetite; and (7) presynaptic actions that result in either inhibition or facilitation of the release of the neurotransmitters such as such as norepinephrine and acetylcholine."
The drug clenbuterol is specifically a selective beta-2 sympathomimetic, primarily affecting only one of the three subsets of beta-receptors. Of particular interest is the fact that this drug has little beta-1 stimulating activity. Since beta-1 receptors are closely tied to the cardiac effects of these agents, this allows clenbuterol to reduce reversible airway obstruction (and effect of beta-2 stimulation) with much less cardiovascular side effects compared to nonselective beta agonists. Clinical studies with this drug show it is extremely effective as a bronchodilator, with a low level of user complaints and high patient compliance. Clenbuterol also exhibits an extremely long half-life in the body, which is measured to be approximately 34 hours. 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. In spite that clenbuterol is available in a wide number of other countries however; this compound has never been approved for use in the United States. The fact that there are a number of similar, effective asthma medications already available in this country may have something to do with this, as a prospective drug firm would likely not find it a profitable enough product to warrant undergoing the expense of the FDA approval process. Regardless, foreign clenbuterol preparations are widely available on the U.S. black market.
In animal studies, clenbuterol is shown to exhibit anabolic activity, so it is obviously an attractive trait to the athlete. This compound is additionally a known thermogenic, with beta-2 agonists like clenbuterol shown to directly stimulate fat cells and accelerate the breakdown of triglycerides to form free fatty acids. Its efficacy in this area makes clenbuterol a very attractive, and today almost mandatory, pre-contest drug. Those interested in this drug are most often hoping it will impart a little of both benefits, promoting the loss of body fat while imparting strength and muscle mass increases. But as was well pointed out by a review published in the August 1995 issue of Medicine and Science in Sports and Exercise, the possible anabolic activities in humans are very questionable, and based only on animal data using much larger doses than would be required for bronchodilation. With such reports there has been a lot of debate lately as to whether or not clenbuterol is really anabolic at all. Some seem to swear by the fact that it builds muscle regardless, firmly sticking by "clen" as a great off-season or adjunct anabolic. To others such reports are confirmation that athletes have wasted valuable time and money on drugs that do not work as they are intended to by the user. This debate continues today, with many still using clenbuterol as a potential anabolic. With this in mind athletes will tailor their dosage and cycling of this product individually depending on which of the two "possible" results are more desired, and how much side effects are to be tolerated. The possible side effects of clenbuterol include those of other CNS stimulants, and include such occurrences as shaky hands, insomnia, sweating, increased blood pressure and nausea. These side effects will generally subside after a week or so of use however, once the user becomes accustomed to the drug. One would typically start a cycle by gradually increasing the dosage each day until a desired range is established. This process will minimize the unwanted side effects seen from the drug; which otherwise might be dramatic if a large dose is administered from the onset. Men generally end up in the range of 2-8 tablets per day, although some people do claim to tolerate even higher dosages. Women get by on less, generally 2-4 tablets daily. Very quickly, the drug will elevate the body temperature. The rise is not usually dramatic, perhaps a half of a Cegree or so, sometimes a little more. This elevation is due to your body burning excess energy (largely from fat) and is usually not uncomfortable. Now that it is working, the number of consecutive days clenbuterol can be used is believed to be dependent on the goal of the individual. To be clear, the athletic benefits of this drug will only last for a limited time and then diminish, largely due to beta-receptor down regulation. When using it for fat loss. the primary effect of the drug, it seems to work well for approximately 4-6 weeks. During this period users will want to constantly monitor their body temperature. We are assured clenbuterol is working by the temperature elevation. Once the temperature drops back to normal, clenbuterol is no longer exhibiting a thermogenic effect. At this point increasing the dosage would not be very effective, and a break for at least a few weeks should be taken before it is used again effectively. If one is looking for strength gains, clenbuterol appears to be effective for a much shorter period of time, around 3-4 weeks. This may be due to an absence of real anabolic effect, with the strength gain seen with clenbuterol possibly due only to the stimulant properties of the drug (similar to the strength boost seen by Ephedrine users). Again however, this is still debated.
Many competitors also find the fat burning effect of clenbuterol can be further enhanced by additional substances. When combined with thyroid hormones, specifically the powerful Cytomel, the thermogenic effect can become extremely dramatic. This can be to a point that the athlete could shred exceptional amounts of extra fat during contest preparations, without a dramatic restriction in calories. Such a mix can be further used during a steroid cycle, eliciting a much harder look from the anabolics. These cutting agents can often greatly inhibit extra fat storage during the cycle, even when using strong aromatizing androgens. A clenbuterol/thyroid mix is also common when using growth hormone, further enhancing the thermogenic and anabolic effect of this therapy.
CLOMIVER® 100 tabs/50mg Price:39 EUR
Clomiver (Clomiphene Citrate) 100 tabs x 50 mg Package: 100,25 Tabs x 50 mg.
Each tablet contains 50 mg Clomiphene citrate.