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Wednesday 02, Jul 2014

  Sonnen Fired From FOX Sports And UFC Broadcasting Positions

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Former UFC fighter Chael Sonnen has been fired by the UFC and FOX Sports organizations from his broadcast positions. This announcement was made after Sonnen failed a second random test given by the Nevada Athletic Commission (NAC) on June 5.

Sonnen’s first failed test was on May 24 after which he announced his retirement. Sonnen was scheduled to fight UFC light heavyweight Wanderlei Silva at UFC 175 but announced his retirement after his failed test in May.

FOX and the UFC released a joint statement to announce that the UFC Tonight co-host was terminated. It was revealed that the UFC and FOX Sports organizations announced the termination of their respective broadcasting services agreements with analyst Chael Sonnen. It was added that this decision comes in light of Sonnen failing a second test conducted by the Nevada Athletic Commission for banned substances in June and Sonnen was previously under temporary suspension by the Nevada Athletic Commission for failing an initial test conducted in May.

In his MMA career, Sonnen has failed three drug tests with the first being after his 2010 title fight against Anderson Silva in Oakland. The MMA fighter was suspended by the California athletic commission but made false claims to have his suspension reduced.

In May this year, Sonnen tested positive for two prohibited substances and voluntarily admitted to a third banned drug after a random drug test administered on May 24 in Las Vegas. His second failed test this year was confirmed by blood and urine samples given at another random drug test that was administered on June 5 in Portland. In his first random test, Sonnen tested positive for Anastrozole and Clomiphene, which are used to provide relief to men with hypogonadism. Sonnen also claimed he used Human Chorionic Gonadotropin (hCG). In his second test, he failed for Human growth hormone (hGH) and recombinant human erythropoietin (EPO) that are prohibited by the World Anti-Doping Agency.

Anastrozole (also known as Arimidex) is used as an on-cycle support drug to treat side effects of excess estrogens, which are usually associated with the use of harsh and aromatizable steroids. This post cycle therapy drug blocks the action (and not the production) of estrogen. On the other hand, Clomiphene citrate (also called Clomid) is used by athletes during the recovery phase of steroid cycles to restore the production of naturally-occurring hormones, including Testosterone, and prevent side effects of excess estrogens.

According to WADA’s description of human growth hormone, hGH is known to act on many aspects of cellular metabolism and is also necessary for skeletal growth in humans and the major role of hGH in body growth is to stimulate the liver and other tissues to secrete insulin-like growth factor (IGF-1) that stimulates production of cartilage cells, resulting in bone growth and also plays a key role in muscle and organ growth.

Sonnen now claims that the second failed test is because of the prescribed medications. He remarked the Commission is aware of other prescribed medications he was taking and he will not challenge their allegations. Sonnen remarked he will cooperate with the Commission and look forward to having a dialogue about how fighters who transition off Testosterone replacement therapy can avoid violating any rules.

pdf_iconDownload in PDF: Sonnen Fired From FOX Sports And UFC Broadcasting Positions

Saturday 09, Jun 2012

  Arimidex Cycle

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Amateur and professional sportsmen, especially those in muscle building and professional bodybuilding, need to always be on their toes. Their place in individual or team sports is never assured and this is the reason why they try using steroids and performance enhancing drugs. However, it is essential for them to have a clear and complete knowing about the advantages and disadvantages of these drugs so that they do not end up abusing them, deliberately or inadvertently. In this piece of information, we would be accessing information on Arimidex.

Also known as Anastrozole and Liquidex, Arimidex is an antiestrogen that is used by sportsmen on serious and aromatizable steroids to control or avoid estrogenic side effects such as oily skin or acne. Scientifically, Arimidex is continually recommended by physicians for the treatment of postmenopausal women patients with hormone receptor-positive early breast cancer.

A popular steroid cycle with Arimidex (Arimidex Cycle) as the post cycle therapy drug is as follows:

Week Dianabol Deca Durabolin Nolvadex Arimidex Sustanon 250
1 30 mg every day 200 mg every week 250 mg every week
2 30 mg every day 300 mg every week 250 mg every week
3 30 mg every day 300 mg every week 20 mg every day 250 mg every week
4 40 mg every day 400 mg every week 20 mg every day 250 mg every week
5 40 mg every day 400 mg every week 20 mg every day 250 mg every week
6 40 mg every day 300 mg every week 20 mg every day 250 mg every week
7 200 mg every week 20 mg every day 250 mg every week
8 20 mg every day 250 mg every week
9 20 mg every day 250 mg every week
10 1 mg every day 250 mg every week
11 1 mg every day 250 mg every week
12 1 mg every day 250 mg every week

From the category of 3rd generating discerning oral aromatase inhibitors, Arimidex is also used to recover the production of organic testosterone (the male sex hormone) as testosterone production gets disrupted when aromatizable or severe anabolics are used during a steroid cycles.

Friday 04, May 2012


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Arimidex, also known as Anastrozole and Liquidex, is one of the most popular antiestrogens for professional athletes on anabolic steroids and performance enhancing drugs. This oral aromatase chemical is mainly recommended for adjuvant treatments of postmenopausal females with hormone receptor-positive early breast cancers.

In the world of professional sports that is generally dominated by use of steroids and performance improving medications, Arimidex performs an important part in managing or avoiding excess estrogen creation that could have otherwise led to adverse reactions such as greasy skin, acne, liquid storage, and gynecomastia.

Arimidex, from the class of 3rd generation selective oral aromatase inhibitors, is a commonly used drug during androgenic hormone or testosterone replacement treatments for hypogonadal men.

Arimidex is also considered a better choice than antiestrogens such as Clomid and Nolvadex as the two medications (Clomid and Nolvadex) are meant for decreasing estrogenic activity in the body or delay the development of cancer malignancy but Arimidex prevents the aromatase compound to prevent the level of estrogen. This antiestrogen is usually used with Propecia (Finasteride) to boost benefits as Arimidex stops development of estrogen while Finasteride stops transformation of androgenic hormone or testosterone to dihydrotestosterone (DHT) besides decreasing the serum attention of DHT and unwanted androgenic results such as hair loss.

When Arimidex is used with Finasteride by athletes on highly aromatizable steroids, athletes can easily obtain amazing muscular profits with a reduced possibility of oily skin, acne, and liquid storage to boast of an attractive and lean appearance. Arimidex is also an effective selection for helping the levels of muscular strength and profits besides decreasing the incident of injuries.

Scientific studies, in the past, have recommended that Arimidex is useful in helping the amount of androgenic hormone or testosterone in the system and these profits could be as much as 60 percent with just 7 days of use. The recommended dose of Arimidex for men is 0.5-3.0 mg per day. The standard dose of Arimidex for females is 1.0 mg per day. Arimidex amounts are generally taken two to six times a day at equal durations because of its short active life.

Wednesday 28, Mar 2012


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The risk of estrogenic side effects is often one of the biggest factors why some sportsmen tend to avoid anabolic steroids and performance enhancing drugs. This obviously means that their performance fells short compared to performances delivered by steroid-using sportsmen population. However, Arimidex can help in getting rid of all side effects of estrogens in quick time besides restoring testosterone levels in the body.

Also known as Anastrozole and Liquidex, Arimidex is a powerful antiestrogen that can easily restore or improve the production of naturally occurring testosterone besides reducing or eliminating the formation of excess estrogens by as much as 98 percent. The fact that only 1 mg of Arimidex is required to bring these dramatic results means that there is everything for a sportsman to win and nothing to lose by trusting this non-steroidal aromatase inhibitor.

The active ingredient in Arimidex tablets is Anastrozole and the list of inactive ingredients includes lactose, magnesium stearate, hydroxypropylmethylcellulose, polyethylene glycol, povidone, sodium starch glycolate, and titanium dioxide. Medically, this drug is recommended for treating postmenopausal women patients with hormone receptor-positive early breast cancer. Arimidex belongs to the category of 3rd generation selective oral aromatase inhibitors and is chemically described as 1,3-Benzenediacetonitrile, a, a, a’, a’-tetramethyl-5-(1H-1,2,4-triazol-1-ylmethyl).

Sportsmen commonly use Arimidex with Propecia (Finasteride) as Propecia prevents the conversion of testosterone to dihydrotestosterone and preventing male pattern baldness while Arimidex takes care of estrogen formation. It can be used in doses of 0.5-3.0 mg per day though a dosage of 1.0 mg per day is common among sportsmen. Arimidex must be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F).

Tuesday 21, Feb 2012

  Testosterone Suspension

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Testosterone suspension is one of the most explored performance enhancing drugs on the Internet. The reason – this testosterone compound is the best drug for professional players preparing themselves for an intense workout or sport event. Moreover, the anabolic steroid is an affordable, efficient, and safe performance enhancing drug that can be easily purchased online, with or without a medical prescription.

Considered to be the first androgenic anabolic steroid developed and used for building strong muscle tissue, testosterone suspension has been one of the most successful given for the last many decades. Sportsmen, especially muscle builders and sports athletes, trust this testosterone mixture for its unrivaled benefits.

This anabolic steroid is second to none when it comes to improving activity of the satellite cells used to identify enhancing current muscular tissue tissues besides promoting new muscular tissues. Testosterone suspension is also beneficial for players because it has the unique capability of restoring broken muscle tissue in a short period of time. Furthermore, the effective anabolic steroid helps users lose extra weight under the buckle without losing out on strength, efficiency, and muscle tissue. If that was not all, testosterone suspension also revitalizes the processes of nitrogen storage and protein functionality besides enhancing muscular tissue firmness, vascularity, and overall body appearance.

Testosterone suspension is also efficient to secure muscle tissue against the muscular tissue spending (catabolic) glucocorticoid testosterone employed by our body for maintaining homeostasis capability in the terms of variations in regards to weather and outside environment. In addition to all these advantages, this anabolic steroid product is also critical in improving the levels of IGF-1 (insulin like growth factor-1) and red blood cells.

When applied in amounts of 350-1000 mg per week for men in oral type or 50-100 mg per day by men in injectable form, testosterone suspension produces extraordinary results that can be calculated in terms of efficiency upgrades. In order to discover the best possible benefits, players commonly collection it with efficiency boosters like Equipoise and Deca Durabolin for bulking. Use of this anabolic steroid can lead to development of estrogens and customers with a history of excess estrogen development are recommended to have antiestrogens such as Arimidex, Clomid or Nolvadex to avoid estrogen adverse reactions such as acne, oily skin, liquid retention, and gynecomastia.

Friday 20, Jan 2012

  Arimidex- Anastrozole

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If you want to use anabolic steroids but worry about estrogenic side effects, it is time that you access a clear and complete understanding about Arimidex, also known as Liquidex, A-dex, or Anastrozole. This non-steroidal drug is one of the best post cycle therapy drugs that can easily protect you from estrogenic side effects like oily skin, acne, fluid retention, or gynecomastia.

The chemical name of Arimidex is 1,3-Benzenediacetonitrile, a, a, a’, a’-tetramethyl-5-(1H-1,2,4-triazol-1-ylmethyl) and its molecular formula is C17H19N5; the active life of this drug is 42-48 hours. Arimidex is prescribed, medically, to post menopausal women with breast cancer when standard therapies such as Tamoxifen have failed to deliver results. The aromatase inhibitor, Arimidex, also has the unique ability of reducing the concentrations of blood estradiol to minimize the size and growth of cancerous tumors. It is also prescribed as part of testosterone replacement therapy to hypogonadal men afflicted with low testosterone levels.

When taken in an oral form, A-dex enters the liver where as much as 90 percent of it is broken down into inactive metabolites. One of the biggest advantages with Arimidex is that it is not excreted in the urine, which suggests that it can even be used by those with kidney impairment. Arimidex is an extremely popular antiestrogen among sportsmen and others who make use of anabolic steroids (harsh or aromatizable). It is also effective in restoring (and even promoting increases) the levels of testosterone after the same have been reduced to a considerable extent during a steroid cycle involving harsh or aromatizable steroids. The best thing about Arimidex is that it demonstrates dramatic results even at a low dose of 1 mg. It is worthwhile to note here that the ideal dose of Arimidex is 0.5 mg for the first day and thereafter the dose can be increased to 1 mg per day.

It is also important to note here that Arimidex is one of the very few antiestrogens that could be an integral of any steroid cycle, bulking or cutting, and allows steroid users to reap and even optimize the benefits of anabolic steroids and performance enhancing drugs without leading to a drop in testosterone levels or putting users in risk of estrogenic side effects. Belonging to the Class III generation selective oral aromatase inhibitors, Arimidex is not recommended for use by premenopausal females, breastfeeding or pregnant women.

Arimidex should also not be used by those with prostate or breast cancer or allergic to Arimidex or any of its active and/or inactive ingredients. The use of Arimidex should always be made after the recommended of a qualified medical practitioner and dosages must be strictly regulated and followed as per the medical advice. Under no circumstances, Arimidex should be abused or over-doses as it can lead to side effects such as dizziness. Individuals using any prescription or nonprescription medicine, herbal preparation, or dietary supplement should seek medical advice before using Arimidex as the drug may interfere with functioning of these products, leading to side effects. Since the use of Arimidex leads to dizziness, its use is not recommended for those who perform on heavy machines, vehicles, or performing or about to perform an intense activity.In order to maintain its effectiveness and shelf life, Arimidex is required to be stored at a controlled room temperature of 20-25°C (68-77°F) and must be protected against moisture, heat, direct light, and unauthorized use.

Thursday 19, Jan 2012


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Clomid is a popularly referred brand name for the drug Clomiphene or Clomifene. It is a selected estrogen receptor modulator which is known to increase the production of gonadotropins.  For this reason, it is commonly prescribed to women for improving their fertility. Clomiphene citrate is the main ingredient in this estrogen which stimulates the process of ovulation in women, thereby acting as a fertility aid. Chemically it is recognized as a 2-(4-(2-chloro-1,2-diphenylethenyl-phenoxy)-N,N-diethyl-ethanamine. Clomid is also popularly marketed as Serophene and Milophene.

Clomid intake is also common amongst athletes and bodybuilders as it restores the body’s natural testosterone levels that may have been affected by use of harsh and aromatizable steroids and also avoids the occurrence of gynecomastia in post cycle therapy. This steroid is highly effective and also an inexpensive compound. It is for this reason that it is so widely sought by bodybuilders and sportsmen all over the world.

Clomid is ideally a synthetic estrogen which possesses both agonist as well as antagonist properties. Chemically its structure and action is very similar to Nolvadex. However, when ingested in the body, Clomid minimizes the effect of natural estrogen in the body. Clinically it is believed to reduce the negative feedback of estrogen on the hypothalamus, enhancing the release of FSH and LSH. It is because of this mechanism that testosterone production in men is restored. This proves to be highly beneficial for athletes when they administer it at end of their steroid cycle because during the cycle, their endogenous testosterones are usually depressed. Once the anabolic effect from the body is removed, it is important to bring the level of endogenous testosterones back to normal as inability to do so might cause what is called a post-steroid crash.  In a steroid crash, a major loss in the size and the strength of the newly acquired muscle takes place. This is because in the absence of testosterone, the catabolic cortisol hormone becomes dominant. Administration of Clomid at this point, helps avoiding this crash.

For women, the best time to use it is around the contest time when the adjustment of estrogen levels is required. Women should intake this steroid only under the supervision of a physician as excessive intake may increase fat loss as well as muscularity. In some cases, it might cause troubled effects such as poor vision. However, this may take place only when dosages become exceedingly high.

For men, the best dosage is 50 to 100 mg per day. Its administration brings testosterone production to normal levels within the period of 4 to 6 weeks. The regime followed by professionals is 100 mg from day 1 to 11 and 50 mg from days 12 to 21. The restoration of testosterone levels is however, gradual. To achieve an immediate effect, Clomid is often ingested with Human Chorionic Gonadotropin (HCG) for the first two weeks after the anabolic steroid intake is discontinued. This combined intake also aids in restoring the normal ability of the testicles’ responsiveness to endogenous LH. After HCG’s administration along with Clomid is stopped, the user may continue to take Clomid for a certain period. It must be mentioned here that the use of HCG should not exceed more than 2-3 weeks as it may it may initiate the negative feedback inhibition on the hypothalamic-pituitary axis. Also Clomid intake in injectable form has an effect more long lasting in an ancillary drug program. It is also observed that if HCG and Clomid are taken periodically in a steroid cycle, the natural testosterone level can be prevented from reducing. Usage of strong androgens should be avoided for a prolonged period of time. Some bodybuilders take these drugs alternatively, sometimes even after long intervals for the fear of losing their effectiveness if taken together.

Another drug that is widely used in combination with Clomid is Proviron. Proviron is an oral DHT which considerably lowers the aromatase activity in the body, thereby raising the estrogen to androgen ratio. Clomid’s association with Proviron has been proved to be extremely effective. However, it can also be combined with certain specific inhibitors such as Aromasin, Femara, and Arimidex.

A factor that makes Clomid such a popular drug is that it is very safe. Bodybuilders reporting its side effects (after excessive intake) have been very few.  Some common ones include nausea, dizziness, headaches, and hot flushes. Hence over-dose is strictly not recommended. This popular estrogen is widely available in the market under a vast range of brand names. Its popular forms are tablets and injectables.

Sunday 13, Jun 2010

  Side effects of cancer treatment options can be reduced by Acupuncture

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Side effects of cancer treatment options can be reduced by AcupunctureAcupuncture can prove to be an effective yet safe treatment option when it comes to the management of common debilitating side effects of hot flashes, excessive sweating, and night sweats that are associated with breast cancer treatment. This finding was disclosed in a study that also suggested that acupuncture has no treatment side effects.

These findings were part of a first-of-its-kind study that was presented at the American Society for Therapeutic Radiology and Oncology’s 50th Annual Meeting in Boston.

Eleanor Walker, M.D., lead author of the study and a radiation oncologist at the Henry Ford Hospital Department of Radiation Oncology in Detroit, remarked that acupuncture is more durable than a drug presently used to treat symptoms of vasomotor.

Wednesday 28, Apr 2010

  Acupuncture minimizes breast cancer treatment side effects

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acupuncture-minimizes-breast-cancer-treatment-side-effectsWhen compared to conventional drug therapy, acupuncture is equally effective and long-lasting in managing the common debilitating side effects of hot flashes, excessive sweating, and night sweats that are associated with breast cancer treatment as per a study. It was also noted that acupuncture has no treatment side effects.

These findings were part of a first-of-its-kind study presented at the American Society for Therapeutic Radiology and Oncology’s 50th Annual Meeting in Boston.

Eleanor Walker, M.D., lead author of the study and a radiation oncologist at the Henry Ford Hospital Department of Radiation Oncology in Detroit, said that acupuncture is more durable than a drug presently used for treating the vasomotor symptoms.

Tuesday 11, Mar 2008

  Steroid Cycles: Trenbolone

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trenbolone finaplix finaplex1) What is Trenbolone?

Trenbolone is a 19-nor derived steroid, in the 19-nor Testosterone (Nandrolone) family. In fact, Trenbolone is structurally similar to Deca-Durabolin, differing in the fact that it has a c-9 and c-11 double bond. The c9 bond serves to prevent any aromatization (conversion) to estrogen, and thus we see far less water retention with Trenbolone when we compare it to Deca Durabolin. Unlike nandrolone however The c11 double bond also seems to increase Androgen Receptor binding quite profoundly (this may also have something to do with the c9 bond as well). This lack of estrogenic activity and powerful ability to bind to the androgen receptor combine to make Trenbolone a much more powerful androgen than Deca, however. It also virtually eliminates all water gain and makes the majority of weight gained on this drug (at least in animal studies) virtually all new, quality muscle. (1) This has been anecdotally replicated in human “studies” (read: athletes who use Trenbolone) many times over.

2) Why is trenbolone a good steroid cycle?

In general, if you run a trenbolone cycle you will need a testosterone base, it means you’ll have at least 12 weeks of trenbolone and testosterone.

Steroid Cycles: Trenbolone

Week 1-12:

300mgs of trenbolone acetate (finaplix)/week + 1000mgs of testosterone cypionate/week + 1mg arimidex/day + 0.25mgs of dostinex/day

post cycle therapy (PCT):

week 13-15:

300mgs clomid/day + 40mgs nolvadex/day + 1mg arimidex/day

week 16-18:

200mgs clomid/day + 20mgs nolvadex/day + 0.5 mg arimidex/day

week 19-21:

100mgs clomid/day + 10mgs nolvadex/day + 0.25 mg arimidex/day

week 22-25:

50mgs clomid/day

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