This drug is unique (so far as I know) in that 5a -reductase,

the enzyme which converts testosterone to the more-potent DHT, actually converts nandrolone to a less-potent compound. Therefore this AAS is somewhat deactivated in the skin, scalp, and prostate, and these tissues experience an effectively-lower androgen level than the rest of the body. Therefore, for the same amount of activity as another drug at the androgen receptors (ARs) in muscle tissue, Deca gives less activity in the scalp, skin, and prostate. Thus, it is the best choice for those particularly concerned with these things.

Testosterone levels decrease as we age with level dramatically falling at 50-60

years of age(18). Low test levels leads to loss of muscle mass and strength, gains in fat and loss of sex drive (18). So it is a good idea to replace testosterone with an outside source. Supplementing testosterone in older adults with sub-optimal levels may prevent or delay Alzheimer´s disease and other cognitive diseases, protect nerves, regenerate motor units, improves mood, memory, appetite, sex drive, improve bone mass and decrease the risk of heart attack and stroke(19) (20)(21)(22). This shows that test replacement significantly improves quality of life and may be a good option for middle-aged men. Caution

should be taken when using higher dosages because of an increased risk of adverse side effects.(23)

Side effects like hot flashes, menstrual irregularities and a variety of complications with the reproductive system are all possible.

Testosterone Heptylate Theramex leads to a strong protein synthesis in the muscle cell and promotes recovery to a high degree. Athletes report an enormous pump effect during the workout and a noticeable appetite increase after only days of intake. The gains usually consist of solid muscle since the water retention that occurs during intake is usually lower than with

enantathe and cypionate. Competing bodybuilders and athletes normally become puffy be-cause of the testosterone injections should give Testosterone Heptylate Theramex a try.

Be aware that 1.0 ml of insulin contains one hundred International Units (100 IU), 0.1 ml of insulin contains ten (10) IU and 0.01 ml contains one (1.0) IU. So take care in measuring out your insulin ….it is very concentrated!

So why else may you keep such a high proportion of what you gained on ´var? Well, I think it may be due to it´s relatively light impact on the HPTA, which brings me to my final point; Bonavar

will not totally shut down your HPTA, especially at lower doses (unlike testosterone, which will eventually do this even at a 100mg dose, or deca which will do it with a single 100mg dose). This could be due, at least partly, to the fact that Bonavar doesn´t aromatize (convert to estrogen).

Cialis ® is a treatment for men with erectile dysfunction. This is when a man cannot get, or keep a hard, erect penis suitable for sexual activity.

4-androstene-3-one, 17beta-ol

CIALIS is not for everyone. If you take nitrates, often used for chest pain (also known as angina), or alpha-blockers

(other than Flomax 0.4 mg once daily), prescribed for prostate problems or high blood pressure, do not take CIALIS. Such combinations could cause a sudden, unsafe drop in blood pressure. Don't drink alcohol in excess (to a level of intoxication) with CIALIS. This combination may increase your chances of getting dizzy or lowering your blood pressure. CIALIS does not protect a man or his partner from sexually transmitted diseases, including HIV.

Trenabol 75 is a fast-acting injectable steroid with a great effect on protein metabolism. Trenbolone is one of the best effective anabolic compounds, promoting protein

synthesis, as well as creating a positive nitrogen balance. It is an appetite stimulant and improves the conversion of proteins. In laboratory tests, it has been demonstrated that trenbolone increases protein and decreases fat deposition. It has proven to be an excellent product for promoting size and strength in the presence of adequate protein and calories, promotes body tissue building processes, and can reverse catabolism.

Do not let anyone else take your medicines.

The third reason for the popularity of Anavar is that oxandrolone does not influence the body's own testosterone production.

This special feature of Anavar can be explained by the fact that the oxandrolone is not converted into estrogen.

Potential side effects such as palpitations, tremors, irregular heartbeat, dizziness, restlessness, nervousness, and excessive perspiration occur mostly during the first few days of intake. Those who in-crease their dosages slowly and evenly over several days as suggested usually have few problems with Triacana. Toward the end of the intake period a step-by-step reduction in the daily tablet dosage is better than abruptly discontinuing the substance. In summary one can say that Triacana is a

(mild) alternative to the strong L-T3 thyroid hormone compounds such as Cytomel or Thybon with their strong side effects. It has only a lower lipolytic effect but can be taken over a prolonged period of time. Mistakes made during the intake are forgiven with Triacana rather than with Cytomel. Ambitious bodybuilders and athletes who are able to responsibly use strong medication choose Cytomel; persons who, however, fear side effects, who do not know much, or believe that "more is better," should select Triacana.

Currently, DNP is the most powerful weapon against fat loss in the bodybuilder's arsenal;

however, this does not necessarily mean that it is right for everyone or is by any means safe. The possibility also exists that PGF2 may be better for some people, particularly when taking the fact that it may kill fat cells into consideration. However, the guidelines given here will allow the user unrivaled fat loss, and will do so quite safely provided that precautionary measures are taken. While certainly quite dangerous, it is nonetheless the most effective tool available today for the loss of bodyfat.

"Over time, the drug causes the estrogen receptor on cells to change and form a pocketlike structure

that allows other proteins to bind there. The proteins action somehow changes the cell's reaction to Tamoxifen. Theres more to the article but this is the essence of it. Probably you will find something in your papers as it from the Associated Press Newswire. But just in case - thought you should be made aware."

There is any significant proof that shows roaccutane is damaging the sperm. Very low levels of isotretinoin are present in the semen of men who are using roaccutane but this amount is too little to affect your partner's unborn baby. The important thing is not to sharing your drugs with someone else

especially with women.

If you take more Cialis ® than you should:

As the body reaches full maturation, the endogenous levels of GH are substantially diminished. After this, GH is still present in the body but at a substantially lower level where it continues to aid in protein synthesis, RNA and DNA reactions and the conversion of body fat to energy. By introducing an exogenous source of this hormone, athletes are hoping to promote these effects, causing the body to deposit more muscle tissue while at the same time reducing body fat stores.

Phentermine Storage

Effects were seen

in one animal species that might indicate impairment of fertility. Subsequent studies in man suggest that this effect is unlikely in humans.

Additional: HCG/Pregnyl

Is available in 10-20mcg tablets or in the .016 mg/gram Ventapulmin Vet variety. Clenbuterol is known as a sympathomimetic. These hormones are taken to mimic adrenaline and noradrenaline in the human body. Clenbuterol is a selective beta-2 agonist that is used to stimulate the beta-receptors in fat and muscle tissue in the body. Clenbuterol exhibits most of its effects on the stimulation of both type 2 and 3 beta-receptors. Clenbuterol is

really one of bodybuilding's most misunderstood performance enhancement drugs. It is true that it is effective in helping to burn bodyfat but it is often been stated that clenbuterol is effective in causing anabolic gains and has in times even been compared to some of the weaker anabolic steroids. Books such as the World Anabolic Review, 1996, by P. Grunding and M. Bachmann state incorrectly that, "its effects, however, can by all means be compared to those of steroids. Similar to a combination of Winstrol Depot and Oxandrolone...." These statements are inaccurate and misleading to say the least. A lot

of these claims as to the anabolic effects of clenbuterol are derived from studying the effects of clenbuterol on livestock. Clenbuterol is effective in increasing muscle mass and decreasing fat loss in animals.

When administered, HCG raises serum testosterone very quickly. A rise in testosterone first appears about 2 hours after injecting HCG. The second peak occurs about 2 to 4 days later. HCG therapy has been found to be very effective in the prevention of testicular atrophy as well as to use the body's own biochemical stimulating mechanisms to increase plasma testosterone levels during training. Some steroid

users find that they have some of their best strength and size gains while using HCG in conjunction with steroids. This may well be due to the fact that the body has a high level of natural androgens as well as the artificial steroid hormones at that time. The optimal dosage for an athlete using HCG has never been established, but it is thought that a single shot of 1000 to 2000 IU per week will get the desired results. Cycles on HCG should be kept down to around 3 weeks at a time with an off cycle of at least a month in between. For example, one might use the HCG for 2 or 3 weeks in the middle of a cycle, and

for 2 or 3 weeks at the end of a cycle. It has been speculated that the prolonged use of HCG could repress the body's own production of gonadotrophins permanently. This is why short cycles are the best way to go. The side effects from HCG use include gynecomastia, water retention, increased sex drive, mood alterations, headaches, and high blood pressure. HCG raises androgen levels in males by up to 400% but it also raises estrogen levels dramatically as well, This is why it can cause gynecomastia. Other side effects seen from HCG use include "morning sickness like" symptoms (nausea and vomiting). There have been

no cases of overdose complications with the use of HCG nor have there been any associated carcinomas, liver or renal impairment.

The body's own production of testosterone is considerably reduced since anadrol has an inhibiting effect on the hypothalamus, which in turn completely reduces or stops the release of GnRH (gonadotropin releasing hormone). For this reason the intake of testosterone-stimulating compounds such as HCG and Clomid is absolutely necessary to maintain the hormone production in the testes.

Body weight;

Medications similar to testosterone that are taken by mouth for a long

time may cause serious damage to the liver or liver cancer. Testosterone gel has not been shown to cause this damage. Testosterone may increase the risk of developing prostate cancer. Talk to your doctor about the risks of taking this medication. Testosterone gel may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.

• It improves on hot flashes- (58%)

It is important to stress that a cycle should last no longer than 6 weeks and it should never be halted abruptly. As slowly as the dosage was built up it should also be lowered, one tablet every

3-4 days. Taking Cytomel® for too long and/or at too high a dosage can result in a permanent thyroid deficiency. After doing such, one might need to be treated with a drug like Cytomel® for life. It is also a good idea to first consult your physician and have your thyroid function tested. An undiagnosed hyperfunction would not mix well with the added hormone. An athlete should also be sure never to purchase an injectable form of the drug. It is generally an emergency room product, much too powerful for athletic use. Since T-3 is the most powerful thyroid hormone athletes are using, this is generally not the starting

point for a beginner. Before using such a powerful item, it is a good idea to become familiar with a weaker substance. The highly popular Triacana is very mild, allowing the user much more latitude (from severe side effects) than Cytomel®. An in-between point is Synthroid (synthetic T-4), still weaker in action than Cytomel®. Once the user is ready however, the fat burning effect of this hormone can be extremely dramatic.

Stanozolol: Description

50-100 mg/day seems is a sufficient dosage for athletes. Clomid is usually taken with fluids after meals. If several tablets are taken it is recomended that they

be administered in equal doses distributed throughout the day. The duration of Clomid intake should not exceed 10 to 14 days. Most athlets begin with 100 mg/day taking one 50 mg. tablet every morning and evening after meals. After the fifth day the dosage is often reduced to only one 50 mg tablet per day.

For competitive bodybuilders Cytomel is an almost unmissable aid in contest preparation, along with clenbuterol and non-aromatizing steroids such as stanazolol, trenbolone, methenolone and so forth...

"Long R3 IGF-1 is signifacantly more potent than IGF-1. The enhanced potency is due to the decreased binding

of Long R3 IGF-1 to all known IGF binding proteins. These binding proteins normally inhibit the biological actions of IGF's."

Women with a dosage of up to 100 mg/week usually experience no major problems with Deca Durabolin. At higher dosages androgenic-caused virilization symptoms can occur, including deep voice (irreversible), increased growth of body hair, acne, increased libido, and possibly clitorishypertrophy. Since most female athletes get on well with Deca a dose of Deca 50 mg+/week is usually combined with Anavar 10 mg+/day. Both compounds, when taken in a low dosage, are only slightly androgenic

so that masculinizing side effects only rarely occur. Deca, through its increased protein synthesis, also leads to a net muscle gain and Anavar, based on the increased phosphocreatine synthesis, leads to a measurable strength gain with very low water retention. Other variations of administration used by female athletes are Deca and Winstrol tablets, as well as Deca and Primobolan's tablets. Since Deca-Durabolin has no negative effects on the liver it can even be used by persons with liver diseases. Exams have shown that a combined application of Dianabol / Deca increases the liver values which, however, return to normal

upon discontinuance of the 17-alpha alkylated Dianabol and continued administration of Deca. Even a treatment period with Deca over several years could not reveal a damage to the liver. For this reason Deca combines well with Andriol (240-280 mg/day) since Andriol is not broken down through the liver and thus the liver function is not influenced either. Older and more cautious steroid users, in particular, like this combination.

Bodybuilders and powerlifters, in particutar, like Oxandrolone for three reasons. First, Oxandrolone causes a strong strength gain by stimulating the phosphocreatine synthesis in the

muscle cell without depositing liquid (water) in the joints and the muscles. Powerlifters and weightlifters who do not want to end up in a higher weight class take advantage of this since it allows them to get stronger without gaining body weight at the same time. The combination of Oxandrolone and 20-30 mg Holotestin daily has proven to be very effective since the muscles also look harder. Similarly good results can be achieved by a simultaneous intake of Oxandrolone and 120-140 mcg Clenbuterol per day. Although Oxandrolone itself does not cause a noticeable muscle growth it can clearly improve the muscle-developing

effect of many steroids. Deca-Durabolin , Dianabol (D-bol) and the various testosterone compounds, in particular, combine well with Oxandrolone to achieve a "mass buildup" because the strength gain caused by the intake of these highly tissue-developing and liquid-retaining substances results in an additional muscle mass. A stack of 200 mg Deca-Durabolin/week , 500 mg Testoviron Depot/week, and 25 mg Oxandrolone/day leads to a good gain in strength and mass in most athletes. Deca-Durabolin has a distinct anabolic effect and stimulates the synthesis of protein; Oxandrolone improves the

strength by a higher phosphocreatine synthesis; and Testoviron Depot inereases the aggressiveness for the workout and accelerates regeneration.

Start with no more than 5 IU (0.05 ml) of this short acting/ regular insulin preparation and increase the dose gradually over a period of one week, to a dose no higher than 20 IU (0.20 ml) per day. Doses above this will expose you to progressively greater risk and most body builders who use insulin believe there is no advantage in taking doses higher than this. Anecdotal evidence amongst bodybuilders suggests increased doses leads to excess bodyfat accumulation.

Melting Point (ester): 21C

Chronic use of Rohypnol can result in physical dependence and the appearance of withdrawal syndrome when the drug is discontinued. Rohypnol impairs cognitive and psychomotor functions affecting reaction time and driving skill. The use of this drug in combination with alcohol is a particular concern as both substances potentiate each other's toxicity.

The side effects of Provironum in men are low at a dosage of 24 tab-lets/day so that Provironum, taken for example in combination with a steroid cycle, can be used comparatively without risk over several weeks. Since Provironum

is well-tolerated by the liver, liver dysfunc-tions do not occur in the given dosages. For athletes who are used to acting under the motto "more is better" the intake of Provironum could have a paradoxical effect. The most common side effect of Provironum is a distinct sexual overstimulation and in some cases continuous penis erection. Since this condition can be painful and lead to possible damages, a lower dosage or discontinu-ing the compound are the only sensible solutions. Female athletes should use Provironum with caution since possible androgenic side ef-fects cannot be excluded. Women who want to give

Provironum a try should not take more than one 25 mg tablet per day. Higher dosages and periods of intake of more than four weeks considerably increase the risk of virilization symptoms. Female athletes who have no dif-ficulties with Provironum obtain good results with 25 mg Provironum/ day and 20 mg Nolvadex/day and, in combination with a diet, re-port an accelerated fat breakdown and continuously harder muscles.

Substance: 40mg Nandrolone Phenylpropionate & 60mg Nandrolone Decanoate per ml.

It is first important to understand why there the results obtained from this drug seem to vary so much. A logical

factor in this regard would seem to be the price of this drug. Due to the elaborate manufacturing techniques used to produce it, it is extremely costly. Even a moderately dosed cycle could cost an athlete between $75-$150 per daily dosage. Most are unable or unwilling to spend so much, and instead tinker around with low dosages of the drug. Most who have used this item extensively claim it will only be effective at higher doses. Poor results would then be expected if low amounts were used, or the drug not administered daily. If you cannot commit to the full expense of an HGH cycle, you should really not be trying

to use the drug. The average male athlete will usually need a dosage in the range of 5 to 10 I.U. per day to elicit the best results. On the low end perhaps 2 to 6 I.U. can be used daily, but this is still a considerable expense. Daily dosing is important, as HGH has a very short life span in the body. Peak blood concentrations are noted quickly (2 to 6 hours) after injection, and the hormone is cleared from the body with a half-life of only 20-30 minutes. Clearly it does not stick around very long, making stable blood levels difficult to maintain. The effects of this drug are also most pronounced when it is used for longer

periods of time, often many months long. Some do use it for shorter periods, but generally only when looking for fat loss. For this purpose a cycle of at least four weeks would be used. This compound can be administered in both an intramuscular and subcutaneous injection. "Sub-Q" injections are particularly noted for producing a localized loss of fat, requiring the user to change injection points regularly to even out the effect. A general loss of fat seems to be the one characteristic most people agree on. It appears that the fat burning properties of this drug are more quickly apparent, and less dependent

on high doses.

Propecia comes as a tablet, containing 1 mg finasteride, to take by mouth.

by Bill Roberts - Proviron, an anabolic steroid, is particularly interesting. I suspect that it not only acts as an antiaromatase but in an unknown DHT-like anti-estrogenic manner. This might involve estrogen receptor downregulation for example. In any case, aromatase inhibition and/or Clomid don’t seem to give the same effect on appearance and muscle hardness as when Mesterolone (Proviron)is included.

by Bill Roberts - Nolvadex is very comparable to Clomid, behaves in the same manner in all tissues,

and is a mixed estrogen agonist/antagonist of the same type as Clomid. The two molecules are also very similar in structure.

Usage: Average dose is 50-100 mg a day.

Tell your doctor if you are pregnant or if you intend to become pregnant. Tamoxifen should not be used to reduce the risk of breast cancer if you are pregnant of if you intend to become pregnant. Tamoxifen use in women has been shown to cause miscarriages, birth defects, death of the fetus, and vaginal bleeding.

Women should not use Omnadren under any circumstances.

lightheadedness or fainting spells

Harifin

side effects

Stacking and Use:

Because of the risk of birth defects, there are strict rules for the females who could get pregnant to use Roaccutane.

Trenbolones chemical structure makes it resistant to the aromatize enzyme (conversion to estrogen) thus absolutely no percentage of trenbolone will convert to estrogen. Trenbolone administration would not promote estrogenic side effects such as breast tissue growth in men (gynecomastia, bitch tits) accelerated fat gain, decline in fat break down and water retention trenbolone. Trenbolone is also resistant to the 5- alpha-reductase enzyme, this enzyme

reduces some steroid hormones into a more androgenic form, in trenbolones case however this does not matter, trenbolone boasts an androgenic ratio of 500, it can easily cause adverse androgenic side effects in any steroid.com members who are prone cases of hair loss, prostate enlargement, oily skin and acne have been reported. Unfortunately trenbolones potential negative side effects do not end there. Trenbolone is also a noted progestin: it binds to the receptor of the female sex hormone progesterone (with about 60% of the actual strength progesterone). In sensitive steroid.com members this can lead to bloat and breast

growth worse still, trenbolones active metabolite17beta-trenbolone has a binding affinity to the progesterone receptor (PgR) that is actually greater than progesterone itself. No need to panic though, the anti-estrogens letrzole or fulvestrant can lower progesterone levels, and combat any progestenic sides. The use of a 19-nor compound like trenbolone also increases prolactin&. bromocriptine or cabergoline are often recommended to lower prolatin levels. Testicular atrophy (shrunken balls) may also occur; HCG used intermittently throughout a cycle can prevent this. It is also wise for Tren users to closely monitor their

cholesterol levels, as well as kidney function and liver enzymes, as Tren has the potential to negatively affect all of those functions. Trenbolone, being a powerful progestin, will also shut down natural testosterone production which even a relatively small dose and keep the testosterone level suppressed for an extended period of time, this can lower libido and cause erectile dysfunction (fina dick). It is essential that you always stack trenbolone with testosterone.

There is no use for alternate drugs since it does not aromatize, is quite mild and the gains are fairly easy to maintain, so post-cycle use of

clomid or Nolvadex is not warranted.

Cialis ® belongs to a group of medicines called phosphodiesterase type 5 inhibitors. Following sexual stimulation Cialis ® works by helping the blood vessels in your penis to relax, allowing the flow of blood into your penis. The result of this is improved erectile function. Cialis ® will not help you if you do not have erectile dysfunction. It is important to note that Cialis ® does not work if there is no sexual stimulation. You and your partner will need to engage in foreplay, just as you would if you were not taking a medicine for erectile dysfunction.

The side effects from HCG use include gynecomastia, water retention, and an increase in sex drive, mood alterations, headaches, and high blood pressure. HCG raises androgen levels in males by up to 400% but it also raises estrogen levels dramatically as well. This is why it can cause a real case of gynecomastia if dosages get too elevated for that person. Another side effect seen from HCG use is morning sickness (nausea and vomiting).

Anadrol information

Xenical, possible side effects

Xenical, possible side effects

First of all, and this will come as no surprise to many people, Bonavar

(oxandrolone) is quite mild on your liver. It´s probably the mildest oral steroid available today. Dosages of up to 80mgs/day are easily tolerated by most men, and most side effects often found with other steroids are not common with ´var. For this reason, Bonavar is frequently the steroid of choice for many top level female bodybuilders and other athletes.

Testosterone Propionate

Longer intake of anadrol and/or higher doses can cause a yellow discoloration of fingernails, eyes, or skin. The liver enzyme gamma-GT also reacts sensitively to the oxymetholone, causing it to elevate. If high

dosages of anadrol are taken over a long period, there is an increased risk that the described liver changes could end up damaging the liver. During the intake of Androlic / Anadrol 50, the liver values as well as the LDH/HBDH quotient, should always be checked by a competent physician. Oxymetholone is the only anabolic/androgenic steroids which has been linked with liver cancer.

The highly androgenic effect of anadrol stimulates the regeneration of the body so that the often feared "over training" is unlikely to occur.

The side effects associated with Equipoise® are generally mild. The structure

of boldenone does allow it to convert into estrogen, but it does not have an extremely high affinity to do so. To try and quantify this we can look toward aromatization studies, which suggest that its rate of estrogen conversion should be roughly half that of testosterone's. The tendency to develop a noticeable amount of water retention with this drug would therefore be slightly higher than that with Deca-DurabolinO (with an estimated 20A°/a conversion), but much less than what would be expected with a stronger agent such as Testosterone. While one does still have a chance of encountering an estrogen related side effect

as such when using this substance, it is not a common problem when taken at a moderate dosage level. Gynecomastia might theoretically become a concern, but is usually only heaved of with very sensitive individuals or (again) those venturing high in dosage. Should estrogenic effects become troublesome, the addition of Nolvadex® and/or Proviron® should of course make the cycle more tolerable. An antiaromatase such as Cytadren® or Arimidex® would be stronger options, however probably not indicated with a mild drug as such.

Supplementation

Loeffler: Cypiotest L/A (MX) - 250 mg/ml

Nandrolone Decanoate is unique in that 5a -reductase, the enzyme which converts testosterone to the more-potent DHT, actually converts nandrolone to a less-potent compound. Therefore this AAS is somewhat deactivated in the skin, scalp, and prostate, and these tissues experience an effectively-lower androgen level than the rest of the body. Therefore, for the same amount of activity as another drug at the androgen receptors (ARs) in muscle tissue, Deca gives less activity in the scalp, skin, and prostate. Thus, it is the best choice for those particularly concerned with these things.

Packaging: 1 bottle (5 ml/amp).

This is another one of the popular ones. Next to Deca and D-bol the third most abused substance among athletes is stanozolol, as documented by the many positive drug tests. Among them the case sprinter Ben Johnson, who was stripped of his Gold Medal in the 100 meter dash in the 1988 Olympics. But since then the number of positives has grown exponentially. In bodybuilding Shawn Ray's positive in the 1990 Arnold Schwarzenegger Classic (a brief stint the IFBB had with drug testing). Ray was the winner of that event, but Canadion pro Nimrod King was also shown to have stanazolol metabolites in his urine.