Information om vanliga steroider.

TRENBOLONE ACETATE

Reported Characteristics

Pharmaceutical Name: Trenbolone
Chemical Name:17beta-acetoxy-3-oxoestra-4,9,11-triene
Cutting/Bulking:cutting
Anabolic Rating: 500
Active-Life: About 2-3 days
Drug Class: High Androgenic/Anabolic Steroid (for injection)
Dosage: 75-150mgs Every Day to Every other Day
Acne: Yes
Aromatization: No
Water Retention: No
High Blood Pressure: Possible
DHT Conversion: No
HPTA Suppression: High
Liver Toxic: No (However it can be kidney-toxic)
Average Price: 700-900kr /10ml vial


Trenbolone Acetate has an active-life of about 2 days, but in most other ways resembles Parabolan (See Profile: PARABOLIN). Many who have used Trenbolone in it's various forms and esters agree that the acetate ester produces the best results, and this is certainly not counterintuitive. With shorter esters, you get more actual Trenbolone in your body, and less ester.

It is often used pre-contest for its rapid hardening abilities and unquestionable fat metabolizing qualities. Since it is highly androgenic and does not aromatize, it makes a perfect pre-contest drug. It remains anti-anti-anabolic (not a typo) even in a reduced calorie environment, such as dieting. Amazingly clean, quality mass gains were experienced from , especially when this drug is stacked with testosteron, as well as Masteron, Winstrol or .Anavar.

Trenbolone Acetate can, unfortunately, be potentially kidney toxic. To combat this, fluid intake is often increased when using Trenbolone of any kind. Trenbolone has a very high binding ability to androgen receptor-sites. This means it is very potent even in small doses, and is very lypolytic (fatburning), and even has a CNS stimulatory effect, thus increasing strength without increasing bodyweight much. Strength to weight ratio's often go through the roof with Trenbolone Acetate use. This may help explain the insomnia experienced while on Tren also. Finally, users have also noted that paradoxically, while tren reduces your thyroid levels, sweating increases quite a bit.


Trade Name:

TRENABOL (British Dragon)
Tren A finns också från en uppsjö andra underground tillverkare.

TRENABOL 200 (TRENBOLONE ENANTHATE)
Trenabol 200


(Trenbolone Enanthate)
Chemical structure: 17-beta-Hydroxyestra-4,9,11-trien-3-one
Cutting/Bulking: Both
Anabolic Rating:500
Active-Life: 8 days
Drug Class: Anabolic/Androgenic Steroid
Average Reccomended Dosage: 200-600mgs/week
Acne: Possible
Water Retention: No
High Blood Pressure: Possible
Decreases HPTA function:
Aromatization:No
Liver Toxicity: (no, possible renaltoxicity, though)
DHT conversion: No
Estrogen Conversion:No
Average Price:
Comments:

This product is produced by British Dragon, which is a registered pharmaceutical company out of Thailand. In addition, it is produced by several underground labs. Trenbolone Enanthate has an active-life of about 8 days, making it the longest lasting Trenbolone product available on the market. Typically, bodybuilders administer this compound 1-2x a week, in divided doses..

Most bodybuilders who have tried both Trenbolone Enanthate and Parabolan consider Trenbolone Enanthate to be equally effective, dispite Parabolan's cult popularity. The drug is often used for pre-contest purposes, due to its hardening effects and lypolytic ( fat metabolizing) qualities. This drug is possibly the most highly androgenic and anabolic compound, which does not aromatize, in circulation today. It remains reasonably anabolic even in a reduced calorie environment. This is due to it's anti-anti-Anabolic effects, which it exerts on the anti-anabolic hormones in your body. Those hormones limit your anabolic potential, and Trenbolone is probably the steroid with the most profound effect on fighting those hormones. Users of Trenbolone Enanthate report highly enhanced strength gains and post-training recovery, as well as quality mass gains

Trenbolone Enanthate can be kidney toxic, users have typically reported very dark urine when using Trenbolone. This is easily combatted by increasing fluid intake to a gallon+/day and . Gynocomastia is not a usually a problem with Trenbolone since the drug can convert to estrogen. Trenbolone is, hower, a progestin, which means it can amplify the effects of any estrogen in your body, including estrogen occuring from administration of other anabolics. Also, being a progestin, it can cause prolactin levels in your body to become elevated, causing possible sexual dysfunction. Ergo, testosterone is always reccomended in a cycle containing Trenbolone, to combat possible sexual dysfunction..

Trenbolones (and most 19-nor test compounds, in general) have a very high affinity for androgen receptor-sites. This is probably partly how it exerts it's lypolytic effects. Also, due to this very high affinity for the receptor site, many athletes find that stacking it with steroids with low receptor binding abilities is preferential, and for this reason Winstrol often finds its way into a cutting cycle with Trenbolone enanthate, while Anadrol or Dianabol is often used with it for bulking. However, in both cutting as well as bulking cycles, testosterone administration is necessary with Trenbolone Enanthate, to avoid sexual dysfuncion.




TRADE NAMES:
TRENABOL 200 200mg/ml (British Dragon)
Tren Enathate finns också från en uppsjö andra underground tillverkare.

CYTOMEL (T-3/Triiodothyronine/Liothyronine Sodium)
Reported Characteristics

Drug Class: Synthetic thyroid hormone.
Average Reported Dosage: 25-150 MCG daily.
Noted Comments: Significant suppression of Thyroid function during use.
Cytomel is the synthetic form of T-3/L-triiodothyronine and was a commonly known trade or brand name among athletes. T-3/L-triiodothyronine is used as a form of thyroid hormone therapy mostly in Europe. Most bodybuilders favored this drug over synthetic forms of T-4/L-thyroxine due to its vastly superior activity level. An advantage of T-3/L-triiodothyronine administration over T-4/L-thyroxine was the lack of dependence upon the liver enzyme responsible for T-4/T-3 conversion. During diet restricted periods the liver naturally decreases the liver enzyme levels as a control measure to prevent metabolic rate induced starvation. Just as the liver increases production of this enzyme in response to elevated calorie intake it also reduces levels in response to decreased calorie intake. Remember that T-4 /L-thyroxine is only 20% as active as T-3/L-triiodothyronine.

The abuse of synthetic T-3/L-triiodothyronine will result in severe suppression of natural (endogenous) thyroid function. This is especially true of this drug because it actually circumvents the normal thyroid hormone manufacturing process the body utilizes to produce endogenous forms as required. Simplified this is because T-3/Ltriiodothyronine is the most potent thyroid hormone so the body shuts down each level required for production to try to reduce circulatory T-3/L-triiodothyronine levels. Of course this does not reduce the level if the hormone is being administered exogenously (from outside the body).

Since long term use of T-3 /L-triiodothyronine will lead to thyroid function suppression the issue of rebound should be briefly discussed. It is commonly stated that synthetic thyroid hormone abuse will lead to permanent thyroid gland dysfunction. Though it is definitely a physiological possibility, I have not yet found a case study to support this statement. However, there is a common occurrence of thyroid gland/function rebound in natural endogenous thyroid hormone production. It seems that it was common for individuals to realize an "increase" in endogenous thyroid hormone production of 120-130 % within 3-15 days after drug discontinuance. This means an individual would commonly see an increase in their thyroid hormone production of 20- 30% above their normal pre-drug administration levels, in many cases.

Normalt pris: 7-10kr per 50mcg.

ANDRIOL (TESTOSTERONE UNDECANOATE)

Reported Characteristics

Pharmaceutical Name: Testosterone Undecanoate
Chemical Name:4-androstene-3-one-17b-ol
Cutting/Bulking: Cutting
Anadolic Rating:100
Active -Life: Less than 8 hours
Drug Class: Androgenic/Anabolic Steroid (Oral)
Average Reported Dosage: Men (only) 240-320 mg daily, Women Not Reccomended
Acne: Low
Water Retention: No
High Blood Pressure: Rare (Dosage related)
Liver Toxic: Low
DHT Conversion: Significant in higher dosage administration
Decreases HPTA functions: Low, except in higher reported dosages (above 320mg)
Aromatization: Low-moderate.
Average Price: N/A
Andriol is one of two versions of orally active testosterone (the other being methyltestosterone). Wheras Methyltestosterone is (as you can tell from the name) a methylated version of testosterone, Andriol uses a very unique (and often inneffective) delivery method. Andriol is simply Testosterone Undecanoate in oleic acid (an oil), which is encapsulated. Currently the formula includes castor oil and propylene glycol laurate instead of oleic acid, but that is simply to increase the shelf life. Once ingested, the testosterone undecanoate is absorbed through the mucosal cells in the small intestine which is part of the lymphatic system of your body. This Testosterone Undecanoate then has the Undecanoate Ester cleaved off by your body's esterases, and what you are left with (hopefully) is roughly 25mgs of testosterone which was put into your body orally, but not passed through your liver (which would usually be a liver-toxic process). As a comparison, Methyltestosterone is passed through your liver and is generally thought to be one of the most liver-toxic steroids on the market. To further give a reference for this compound, Methyltestosterone will also give you roughly 25mgs of testosterone per tablet. Some testosterone, whether you inject it or ingest it orally will be converted into DHT (dihydrotestosterone) by the 5-Alpha-Reducatas enzyme. DHT has a high affinity for androgen receptors, which is why many DHT-based compounds are exceptionally good cutting agents. Andriol converts to DHT at a reasonably high rate, and thus does not aromatize into estrogen at a high rate like other testosterone. The reasons behind this are still less than clear. However, this is good news to athletes who can obtain (and afford) Andriol, because generally water retention is much lower as is gynocomastia. As it has minimal estrogen conversion, the HTPA (hypothalamic pituitary testes axis) is not affected through this mechanism, and therefore Andriol may not suppress natural (endogenous) androgen (testosterone) production.

Although generally testosterone is considered a stand alone compound, Andriol is generally not used alone, and when it is, the results can be disappointing. This is probably due to the relatively inconshstent effects of using the lymphatic system to deliver testosterone. In a cycle containing other, stronger, compounds, it can provided a mild anabolic additive effect at dosages of 200(+) mg daily. Since Andriol is quickly excreted through urine release, the drug is generally taken 3-6 times daily, in equally divided doses, to maintain adequate levels of it in the blood.

Typically, Andriol would be used in a stack with some other form of testosterone (injectable) as well as perhaps another oral. Andriol will not have any liver-toxicity, so this is one of the few orals which can be used in conjunction with another one. It is most often used with another form of testosterone and a high anabolic agent like Deca Durabolin, Primobolan Depot, or Equpoise. Those compounds are generally run at around 400mgs/week, while the Andriol comes in at around 200mgs daily. as reported as a mildly Androgenic / Anabolic steroid that was best used in stacks for its excellent compatibility at dosages of 240-320 mg daily. It has also been found that while gains from Andriol are not as dramatic as with other steroids, they would appear to be somewhat more permanent and easily maintained.

TRADE NAMES

ANDRIOL 40-MG GEL CAPS
ANDROGEN 40 MG CAPS
PANTESTON 40 MG CAPS
RESTANDOL 40 MG CAPS
UNDESTOR 40 MG CAPS
VIRIGEN 40 MG CAPS

DECA-DURABOLIN (NANDROLONE DECANOATE)


Reported Characteristics

Pharmaceutical Name:Nandrolone Decanoate
Chemical Name:19-nor-testosterone
Cutting/Bulking:Both
Anabolic Rating: 125
Active-Life: 14-16 days
Drug Class: Anabolic/Androgenic steroid
Average Reported Dosage: Men 400-600mg weekly, Women 50-100mg weekly
Acne: Possible
Water Retention: Some
Decreases HPTA function: Severe
High Blood Pressure: No.
Aromatization: Low, converts to less active norestrogens
Liver Toxic: No
DHT Conversion: No, converts to NOR- DHT
Noted Comments: Highly anabolic/moderate androgenic effects
Average Price: 80-100kr för 2ml 100mg/ml. (Dvs 200mg)
Nandrolone Decanoate is a very anabolic and slightly androgenic form of 19-nortestosterone A very prominent positive nitrogen balance is realized with administration of this product. And since nandrolone promotes nitrogen storage, growthand repair in hard-trained muscles will bemore pronounced than normal. In addition, a noted effect by many athletes polled was that most of them experienced a joint healing effect during Deca cycles. Since aromatization was low, in 400-600-mg weekly dosages, and fatburning was high due to the high affinity to the androgen recepror that Deca has, anti-estrogens were not typically necessary to avoid gyno and other estrogen induced side effects.

Commonly used doses for men were in the area of 400-600mg weekly, and dosages over 400 mgweekly caused more water retention, while women seemed to do well with 100mgs/week. In fact, women have consistently reported very respectable lean mass and strength gains at dosages of only 50-100 mg weekly. Virilizing effects usually were avoided by single weekly injections of 50-100 mg nandrolone decanoate. Men, however would need to stack Deca with testosterone in order to have more appreciable weight gains, and avoid sexula dysfunction. Unfortunately, this compound is detectable for up to a year and a half after administration, so drug tested athletes should avoid it.

TRADE NAMES

DECA DURABOLIN 250mg/ml (British Dragon)
DECA-DURABOLIN 200mg/2ml vial (Norma Greece)
DECA-DURABOLIN (Organon)
ANABOLINE 50-MG/ML
ANDROLONE- D 200 200-MG/ML
DECA DURABOLIN 25-MG/ML DECA DURABOLIN 50-MG/ML
DECA DURABOLIN "100" 100-MG/ML
DECA DURABOLIN 200-MG/ML
ELPIHORM 50MG/ML
EXTRABOLINE 50MG/ML
HYBOLIN DECANOATE 50,100MG/ML
JEBOLAN 50MG/ML
NANDROLONE DECANOATE 50,100, 200MG /ML
NANDROBOLIC L.A. 100MG/ML
NEO-DURABOLIC 100,200,/ML
NUREZAN 50MG/ML
RETABOLIL 25MG/ML RETABOLIL 50MG /ML
DECANANDROLEN 200 200MG/ML
STEROBOLIN 50MG/ML
TURINABOL DEPOT 50MG/ML
ANABOLICAN 25ML/ML 10, 50ML
NORANDREN 50 50MG/ML 10,50ML

Oral-Turinabol is an oral steroid which was developed during the early 1960's.

OT has a predominantly anabolic effect which is combined with a relatively low androgenic component. On a scale of 1 to 100 the androgenic effect is very low -only a 6- and the anabolic effect is 53. (In comparison: the androgenic effect of Dianabol is 45 and its anabolic effect is 90.) Oral-Turinabol thus has milligram for milli-gram a lower effect than Dianabol. It is therefore not a steroid that causes a rapid gain in strength, weight, and muscle mass. Rather, the achievable results manifest themselves in a solid muscle gain and, if taken over several weeks, also in a good strength gain. The athlete will certainly not get a puffy look as is the case with Test-osterone, Dianabol, and Anadrol 50. The maximum blood concen-tration of Oral-Turinabol when taking 10, 20 or 40 mg/day is 1.5 -3.5 or 4.5 times the endogenous testosterone concentration (also see Dianabol). This clearly shows that the effectiveness of this compound strongly depends on the dosage.


In our experience bodybuilders take 8-10 tablets of 5 mg, that is 40-50 mg/day. Many enthusiastically report good results with this dosage: one builds a solid muscle mass, the strength gain is worthwhile seeing, the water retention is very low, and the estrogen-caused side effects are rare. Not without good reason OT is also popular among powerlifters and weightlifters who appreciate these characteristics.

Due to its characteristics OT is also a suitable steroid both for men and women in competitions. A usually very effective stack for male bodybuilders consists of 50 mg OT/day, 228 mg Parabolan/week, and 150 mg Winstrol Depot/week. Those who have brought their body fat content to a low level by dieting and/or by using fatburning substances (e.g. Clenbuterol, Ephedrine, Salbutamol, Cytomel, Triacana), will find that the above steroid combination will manifest itself in hard, sharply-defined but still dense and full muscles. No enlarged breasts, no estrogen surplus, and no watery, puffy-look-ing muscle system. If OT were available on the U.S. black market for steroids, bodybuilders, powerlifters, and weightlifters would go crazy for this East German anabolic.

OT enjoys a great popularity since it is quickly broken down by the body and the metabolites are excreted relatively quickly through the urine. The often-posed question regarding how many days before a test OT can be taken in order to be "clean" is difficult to answer specifically or in general. We know from a reli-able source that athletes who only take OT as a steroid and who, in part, take dosages of 10- 15 tablets/day, have discontinued the com-pound exactly five days before a doping test and tested negative. These indications are supported by the fact that even positive urine analyses have rarely mentioned the names Oral-Turinabol or chlordehydromethyl-testosterone.

The potential side effects of OT usually depend on the dosage level and are gender-specific. in women, depending on their predisposi-tion, the usual virilization symptoms occur and increase when dos-ages of more than 20 mg per day are taken over a prolonged time. In men the already discussed reduced testosterone production can rarely be avoided. Gynecomastia occurs rarely with OT Since the response of the water and electrolyte household is not overly dis-tinct athletes only rarely report water retention and high blood pressure. Acne, gastrointestinal pain, and uncontrolled aggressive behavior are also the exception rather than the rule with OT An increased libido is reported in most cases by both sexes. Since the substance chlordehydromethyltestosterone is I 7-alpha alkylated the manufacturer in its package insert recommends that the liver func-tion be checked regularly since it can be negatively affected by high dosages and the risk of possible liver damage cannot be excluded. Thus OT is also a steroid that can be taken without interruption for long intervals. Studies of male athletes who over a period of six weeks were given 10 mg OT/day did not show any indications of health-threatening effects.

DHT Conversions
Decreases HPTA Function
Aromatization

Skulle vara fint att få dessa m fl. ord/termer förklarade. Tror inte att alla nybörjare har ett hutt om vad de betyder. Bara ett förslag.

Sen antar jag att du ändrat lite med priserna så att de stämmer mer överlag med våra priser här i Sverige? Tycker det såg ut så iaf.

DHT conversion = Om steroiden konverterar till DHT en variant av testosteron
HPTA = En steroids påverkan på HPTA (de körtlar/organ som är inblandade i testosteronproduktion). Dvs om dom minskar testosteronproduktionen.
Aromatization = En steroids benägenhet att konvertera (aromatisera) till östrogen.