Winstrol (stanozolol) is a relatively

low androgenic steroid which does not seem to aromatize. Winstrol can be toxic to the liver in excessive dosages. Winstrol is a popular all purpose steroid; many stack with Primobolan or Parabolan for cutting, others stack it with testosterone for size and strength gains. Women often use winstrol but occasionally it can cause virilization, even at low dosages. Winstrol gives a solid muscle gain and an overproportionally strong strength, which usually remains after use of Winstrol is discontinued.

The optimal dose for this purpose lies between 200 and 600 mg/week. Scientific research has shown that best results can

be obtained by the intake of 2 mg/pound body weight. Those who take a dose of less than 200 mg/week will usually feel only a very light anabolic effect which, however, increases with a higher dosage. The anabolic and consequent buildup effect of deca, up to a certain degree, depends on the dosage. In the range of approx. 200 to 600 mg/week, the anabolic effect increases almost proportionately to the dosage increase. If more than 600 mg/week are administered, the relationship of the positive to the negative effects shifts in favor of the latter. In addition, at a dosage level above 600 mg/week, the anabolic effect no longer

increases proportionately to the dosage increase, so that 1000 mg/week do not guarantee significantly better results than 600 mg/week. Most male athletes experience good results by taking 400 mg/week. Steroid novices usually need only 200 mg/week. Deca Durabolin works very well for muscle buildup when combined with Dianabol (D-bol) and Testoviron Depot. The famous Dianabol (D-bol)/Deca stack results in a a fast and strong gain in muscle mass. Most athletes usually take 15-40 mg Dianabol (D-bol)/day and 200-400 mg Deca/week. Even faster results can be achieved with 400 mg Deca/week and 500 mg Sustanon/week. Athletes report

an enormous gain in strength and muscle mass when taking 400 mg Deca/week, 500 mg Sustanon/week, and 30 mg Dianabol (D-bol)/day.

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

Xenical (Orlistat) additional information:

The anti-estrogenic properties of Provironum© are not unique to this compound. A number of steroids have in fact demonstrated similar activity. Dihydrotestosterone and Masteron (2methyl-dihydrotestosterone) for example have been successfully used as therapies for gynecomastia and breast cancer

due to their strong anti-estrogenic effect. It has been suggested that nandrolone may even lower aromatase activity in peripheral tissues where it is more resistant to estrogen conversion (the most active site of nandrolone aromatization seems to be the liver). The antiestrogenic effect of all of these compounds is presumably caused by their ability to compete with other substrates for binding to the aromatase enzyme. With the aromatase enzyme bound to the steroid, yet being unable to alter it, and inhibiting effect is achieved as it is temporarily blocked from interacting with other hormones.

Tablets are orange

square tablets, with "10" imprinted on one side and "BD" separated by a score imprinted on the reverse, sealed in foil pouches of 50 tablets.

CLONAZEPAM

This drug has good binding to the androgen receptor, but in muscle tissue most of it never reaches the androgen receptor because it is enzymatically converted to the diol. Thus, it is not an effective anabolic. It is somewhat effective as an anti-gyno agent, however, and appears to reduce estrogenic bloating if that problem exists.

Active Life: Less than 16 hours.

Viagra should be used with caution by individuals with

anatomical deformation of the penis and by individuals who have conditions which may predispose them to priapism.

To some extent, nandrolone aromatizes to estrogen, and it does not appear that this can be entirely blocked by use of aromatase inhibitors ¨C indeed, aromatase may not be involved at all in this process (there is no evidence in humans that such occurs) with the enzyme CYP 2C11 being in my opinion the more likely candidate for this activity. In any case, Cytadren, an aromatase inhibitor, has not been found effective in avoiding aromatization of nandrolone.

The claim that Omnadren has

a duration effect of "a good 2-3 weeks" is somewhat misleading since the half life of the longest lived component is only about 5 days. There is of course some effect 2 or 3 weeks after injection, but relatively little.

How Taken

Clomiphene Citrate is typically prescribed for women to aid in ovulation. In men, the application of Clomid causes an elevation of follicle stimulating hormone and luteinizing hormone. As a result, natural testosterone production is also increased.

• Magnesium (1500mg)*
• Vitamin C (3000mg in divided doses)*
• Vitamin E (1200 IU in divided doses)*

• Glutathione (200mg in divided doses)***)
• NAC (various amounts)**
• T3 (dose according to personal preference)**
• Calcium (2000mg not taken with the Magnesium)
• 5-HTP (if not on antidepressant medication) (various amounts)****
• Meridia, Redux, or Fenfluramine (various amounts)****
• Hydroxycitric Acid (particularly in the evenings to curb cravings)****
• Pyruvate (2-6g/day in divided doses)
• Glycerol (3 tbsp/day in divided doses)
• Alpha-Lipoic Acid (500-1000mg daily in divided doses)

Key:

Guess what? Dumb people

shouldn´t use steroids at all, especially testosterone!

T Jenapharm (o.c.) 25 mg/ml; Jenapharm G

Methenolone is not used all that often by experienced users. It makes a good product as an alternative to Deca or EQ in a cutting stack, because it has similar properties but does not aromatize and does not have progestagenic activity. But those at least slightly versed will prefer boldenone over methenolone as its more potent gram for gram. Its quite mild, so its not as prone to cause your standard side-effects. This too makes it quite popular with beginners. Methenolone was quite popular during the

70's in stacks with Methandrostenolone. Some of the all-time greats of bodybuilding were quite fond of this stack.

Decongestants can cause interactions with Phentermine, you should avoid other drugs that may increase your heart rate. Inform your online physician about any medications that you use. If you take high blood pressure medicine or MAO inhibitors your doctor might not prescribe you Phentermine. Your doctor might chose to put you on a different medication so do your self a favor and let them know about any other types of weight loss medicines you take to help prevent drug interactions.

Myasthenia

gravis

Although Sustanon does not aromatize excessively when taken in a reasonable dosage many people, in addition, also take an antiestrogen such as Nolvadex and/or Proviron to prevent possible estrogen-linked side effects.

• It improves skin texture (71%) and skin elasticity ( 71%)

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

Day 14: 80 mcg

Chemical Structure: tri-iodio-thyronine (T3)

The trick of using Clenbuterol successfully seems to be avoiding receptor downgrade which occurs

rapidly with the use of this beta agonist. In fact, one clinical study showed downgrade at receptor as much as 50% experienced after using Clenbuterol for as little as 18 days consecutively. The same study showed that attenuation can be avoided if Clenbuterol is taken in a '2 day on' then '2 day off' pattern. Athletes using Clenbuterol in this manner have reported much greater results than those who use the product continualy which seems to support the theory that attenuation can be at least partially avoided by staggering the dosage. Athletes have also made a habit of cycling Clenbuterol in an effort to minimize side effects

as well as prevent receptor downgrade. Average cycle length on Clenbuterol is 8-10 weeks with a 4-6 week off period.

Nolvadex C&K (Tamoxifen) blocks the effects of the estrogen hormone in the body. Nolvadex C&K is used to treat breast cancer in women or men but tamoxifen may also be used to treat other kinds of cancer, as determined by your doctor.

The increased aggressiveness is caused by the resulting high level of androgen and occurs mostly when large quantities of testosterone are injected simultaneously with the use of anadrol.

As far as adding products, no ancillaries are

needed, but its highly recommended that this is only used when anabolic/androgenic steroids are also being used. First of all the extra free calories work with the steroids to enhance results, but also because an increased level of thyroid hormones can be extremely catabolic and the use of anabolic compounds to counter muscle loss is a requirement here.

The chance of finding real Trenabol Depot on the black market is around 5%. That is the reason why we take a chance and claim that only very few of you who read this book will have ever held an original Trenabol Depot in your hand, let alone injected one. Those

who have not tried the originals simply cannot take part in this discussion. As to the effect, the difference between the real French Trenabol Depot and the fakes circulating on the black market is gigantic.

Precautions

IGF prevents insulin from transporting glucose across cell membranes. As a result the cells have to switch to burning off fat as a source of energy.

Type of insulin: short acting insulin preparations are considerably safer than long acting preparations because with short acting types, it is much easier to avoid hypoglycemia with adequate food intake. With the non-medical use of

longer acting insulin preparations, a person is at real risk of experiencing hypoglycemia late in the day, particularly in between meals, during or after exercise and when asleep. Regardless of this advice, some people are in reality using a mixture of short and long acting insulin preparations and exposing themselves to unnecessary increased risk.

For use in cycles with testosterone, I don't think it is bad at all. One simply doesn't want less DHT than normal. As the amount of testosterone in the system increases, the amount of finasteride needed to keep levels down to normal increases. I consider 5 mg/day reasonable

at the gram per week level, and proportionally less at lower dosages of testosterone.

Although the side effects of propionate are similar to the ones of enanthate and cypionate these, as already mentioned, occur less frequently. However, if there is a predisposition and very high dosages are taken, the known androgenic-linked side effects such as acne vulgaris, accelerated hair loss, and increased growth of body hair and deep voice can occur. An increased libido is common both in men and women with the use of propionate. Despite the high conversion rate of propionate into estrogen gynecomastia is less common

than with other testosterones. The same is true for possible water retention since the retention of electrolytes and water is less pronounced. The administration of testosterone stimulating compounds such as HCG and Clomid can, however, also be advised with propionate use since it has a strong influence on the hypothalamohypophysial testicular axis, suppressing the endogenous hormone production. The toxic influence on the liver is minimal so that a liver damage is unlikely (see also Testosterone Enanthate).

Xenical (Orlistat) additional information:

This drug is classified as a beta-2 adrenergic agonist. Clenbuterol

is a bronchiodilator. This drug is banned by the FDA although it is used outside the US by asthma patients. The reason although it is fairly anabolic, and it promotes the burning of fatty acids through brown fat burning. Clenbuterol is a little scary because of some other side effects including the following: tremors, sweating, sleeplessness, rapid heartbeat, etc. These side effects vary in people. Some people aren’t affected at all. This drug comes in tablets of 20 mcg (micrograms not milligrams ). Dosages are normally between 20-120 mcg for bodybuilders that use this. It should be taken in a 2 days on /2days off

fashion because this drug becomes ineffective for its anabolic properties after 18 successive days of use. The receptor sites seem to be non-responsive for anabolic purposes if taken continuously, but brown fat-burning will continue past the 18 day period. It shouldn’t be used this way for more than 12 weeks. After 12 weeks, the drug should be discontinued for a couple of months.

by Bill Roberts - Topically (on the scalp itself) it is of some effect in minimizing further loss. In combination with Nizoral and spironolactone (which smells awful, by the way) it can actually reverse loss moderately.

Tamoxifen also

may be used to reduce the risk of developing breast cancer in women who have a high risk of developing breast cancer.

This special feature has two positive characteristics for the athlete. First, based on the special combination effect of the compounds, Sustanon, milligram for milligram, has a better effect than Testosterone enanthate, cypionate, and propionate alone. Second, the effect of the four testosterones is time-released so that Sustanon goes rapidly into the sytem and remains effective in the body for several weeks. Due to the propionate also included in the steroid, Sustanon is effective after one day

and, based on the mixed in decanoates, remains active for 3-4 weeks.

Since l mg corresponds to exactly 2.7 I.U. the 5mg solution of the compound Humatrope by Lilly contains exactl 13.5 I.U. of Somatropin. The 10 mg solution of the Protropin compound by the Genentech therefore contains 27 I.U. of Somatropin. In American powerlifting and bodybuilding circles Humatrope is usually preferred over Protropin. The reason is that Humatrope is synthesized from a chain of 191 amino acids and thus is identical to the amino acid sequence of the human growth hormones. Protropin, on the other hand, consists of 192 amino acids, one

amino acid too many. This might be the explanation for why more antibodies are developed with Protropin than with Humatrope. growth hormones are on the doping list but they are not yet detectable during doping tests.

by Bill Roberts - Primobolan Depot is a Class I steroid working well at the androgen receptor but which apparently is ineffective in non-AR-mediated anabolic effects. It is most closely compared to Deca Durabolin , requiring a little higher dosage to achieve the same anabolic effect, but since it is pleasant to use at doses considerably higher than what is pleasant for nandrolone esters, it can achieve

higher maximal effectiveness. That is, provided that one can afford it a gram per week of Primobolan Depot can be costly. 400 mg/week should be considered a reasonable minimum dose.

Anadrol 50 is the U.S. brand name for oxymetholone, a very potent oral androgen. This compound was first made available in 1960, by the international drug firm Syntex. Since oxymetholone is quite reliable in its ability to increase red blood cell production (and effect admittedly characteristic of nearly all anabolic/androgenic steroids), it showed particular promise in treating cases of severe anemia. For this purpose it turned out to

be well suited, and was popular for quite some time. But recent years have brought fourth a number of new treatments, most notably the non-steroidal hormone Epogen (erythropoietin). This item is shown to have a much more direct effect on the red blood cell count, without the side effects of a strong androgen. Financial disinterest finally prompted Syntex to halt production of the U.S. Anadrol 50 in 1993, which was around the same time they decided to drop this item in a number of foreign countries. Plenastril from Switzerland and Austria was dropped; following soon was Oxitosona from Spain. Many Athletes feared Anadrol

50 might be on the way out for good. But new HIV/AIDS studies have shown a new light on oxymetholone. These studies are finding (big surprise) exceptional anti-wasting properties to the compound and believe it can be used safely in many such cases. Interest has been peaked, and as of 1998 Anadrol 50 is again being sold in the United States. This time we see the same Anadrol 50 brand name, but the manufacturer is the drug firm Unimed. Syntex continues to market & license this drug in a number of countries however (under a few different brand names).

Many athletes also claim that they enjoyed significant gains

in muscle mass while using clenbuterol. There is no doubt that clenbuterol has an anabolic effect in animals but there are, though, no scientific evidence this also is true in humans. The same goes for the strong anticatabolic effect of clenbuterol, meaning it decreases the rate at which protein is reduced in the muscle cell, consequently causing an enlargement of muscle cells.

Nolvadex is used to treat breast cancer in women or men. Tamoxifen may also be used to treat other kinds of cancer, as determined by your doctor.

Dromastolone di-Propionate is a synthetic derivative of dihydrotestosterone,producing

effective anabolic, promoting protein synthesis as well as creating a positive nitrogen balance in humans,since it is a derivative of dihydrotestosterone it causes the dromastolone not to aromatize in any dosage and thus, it cannot be converted into estrogens.

Sleep apnea (temporary stopping of breathing during sleep) — Benzodiazepines may make these conditions worse

In his book, Anabolics 2002, Bill Llewellyn says that Cytomel is not a drug to start off on, and that use of milder drugs like T4 (Synthroid) or triacana can help ease a person into the use of T3. I'm inclined to disagree here however.

Triacana is weak compound and I find of little use. Its not easily found anymore and not cheap either. T4 is basically similar to Cytomel except that its weaker. Something that users normally compensate with higher doses and sends them down a similar lane as simply using cytomel. Agreed, cytomel is NOT a drug for beginners, but with adequate research, experience with diet and some self-control, I don't see why cytomel shouldn't be the first thyoid compound used. But for recreational users looking for a fatburner, I still suggest using clenbuterol over cytomel for all intents and purposes. Cytomel is much more powerful, but

clenbuterol is a lot safer for use. The results are easier to maintain with clenbuterol as well. Negative feedback in the thyroid may decrease natural levels of T3 in the body, causing a decrease of metabolic rate after coming off a cycle of T3. That can cause a rebound effect during which a lot of weight is gained back.

Uses:

As with all testosterone injectables, one can expect a considerable gain in muscle mass and strength during a cycle. Since testosterone has a notably high affinity for estrogen conversion, the mass gained from this drug is likely to be accompanied by a discernible level of water retention.

The resulting loss of definition of course makes cypionate a very poor choice for dieting or cutting phases. The excess level of estrogen brought about by this drug can also cause one to develop gynecomastia rather quickly. Should the user notice an uncomfortable soreness, swelling or lump under the nipple, an ancillary drug like Nolvadex® should probably be added. This will minimize the effect of estrogen greatly, making the steroid much more tolerable to use. The powerful antiaromatases Arimidex®, Femara, or Aromasin are yet a better choice. Those who have a known sensitivity to estrogen may find it more

beneficial to use ancillary drugs like Nolvadex® and Proviron® from the onset of the cycle, in order to prevent estrogen related side effects before they become apparent.

The recommended dosage of Propecia is 1 mg once a day, to be taken with or without meals.

Difficulty in swallowing (in children) or

Diazepam is a long-acting oral and parenteral benzodiazepine. Diazepam is similar to chlordiazepoxide and clorazepate in that all three generate the same active metabolite. Diazepam is used orally for the short-term management of anxiety disorders and acute alcohol withdrawal, and as a skeletal

muscle relaxant. Parenterally, it is indicated as an antianxiety agent, sedative, amnestic, anticonvulsant, skeletal muscle relaxant, anesthetic adjunct, and as a treatment for alcohol withdrawal. In addition to treating status epilepticus, diazepam has recently been shown effective in preventing recurrence of febrile seizures.I Although diazepam has been the benzodiazepine of choice for status epilepticus, recent evidence indicates that lorazepam may be more beneficial because it provides longer control of seizures and produces less cardiorespiratory depression. Diazepam was approved by the FDA in November 1963. Phase III

data for a rectal formulation of diazepam in the treatment of acute repetitive seizures was completed April 1995. The NDA for the rectal formulation (Diastat) is expected to be filed in 1995. Diazepam is a schedule IV controlled substance.

If overdose of anadrol is suspected, contact your local poison control center or emergency room immediately.

Although dianabol has many potential side effects, they are rare with a dosage of up to 20 mg./day. Danabol / Dianabol causes a considerable strain on the liver and high dosages or use of over a longer period of time, is liver-toxic. Even a dosage of only 10 mg./day

can increase the liver values but after discontinuation of the drug, however, the values return to normal.

Injectable steroid nandrolone decanoate is compound came around early in the wave of commercial steroid development, first being made available as a prescription medication in 1962.

Lowered blood pressure

Clomid (Clomiphene citrate) additional information

If a hereditary predisposition exists Dianabol can also accelerate a possible hair loss which again can be explained by the high conversion of the substance into dihydrotestosterone. Another disadvantage is that, after discontinuance

of the compound, a considerable loss of strength and mass often occurs since the water stored during the intake is again excreted by the body. In high dosages of 50+ mg/day aggressive behavior in the user c occasionally be observed which, if it only refers to his workout, can be an advantage. In order to avoid uncontrolled actions, those who have a tendency to easily lose, their temper should be aware of this characteristic when taking a high D-bol dosage. Despite all of these possible symptoms Dianabol instills in most athletes a "sense of well-being anabolic" which improves the mood and appetite and in many users,

together with the obtained results, leads to an improved level of consciousness and a higher self-confidence.

Being moderately androgenic, Methandienone is really only a popular steroid with men. When used by women, strong virilization symptoms are of course a possible result. Some do however experiment with it, and find low doses (5mg) of this steroid extremely powerful for new muscle growth. Whenever taken, Methandienone (dianabol) will produce exceptional mass and strength gains. It's effectiveness is often compared to other strong steroids like testosterone and Anadrol 50, and it is likewise a popular choice

for bulking purposes. A daily dosage of 20-40mg is enough to give almost anybody dramatic results. Some do venture much higher in dosage, but this practice usually leads to a more profound incidence of side effects. It additionally combines well with a number of other steroids. It is noted to mix particularly well with the mild anabolic Deca-Durabolin. Together one can expect an exceptional muscle and strength gains, with side effects not much worse than one would expect from Dianabol alone. For all out mass, a long acting testosterone ester like enanthate can be used. With the similarly high estrogenic/androgenic properties

of this androgen, side effects may be extreme with such a combination however. Gains would be great as well, which usually makes such an endeavor worthwhile to the user. As discussed earlier, ancillary drugs can be added to reduce the side effects associated with this kind of cycle.

Proviron© is also not a c17 alpha alkylated compound, an alteration commonly used with oral anabolic/androgenic steroids. Not using this structure in the case of Proviron© removes the notable risk of liver toxicity we normally associate with oral dosing. We therefore consider this a "safe" oral, the user having no need to worry

about serious complications with use. This steroid in fact utilizes the same 1-methylation we see present on Primobolan© (methenolone), another well tolerated orally active compound. Alkylation at the one position also slows metabolism of the steroid during the first pass, although much less profoundly than 17 alpha alkylation. Likewise Proviron© and Primobolan© are resistant enough to breakdown to allow therapeutically beneficial blood levels to be achieved, although the overall bioavailability of these compounds is still much lower than methylated oral steroids.

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.

There is no research to site on exactly what dosage would be the most appropriate for a steroid user.

Logic woul dictate that the typically prescribed amount of Proscar / Propecia, a single 1mg tablet per day, would most likely be sufficient. In clinical trials the effect of just a single tablet is clearly dramatic. But if after a while the androgenic content of the cycle is still perceived as too high, increasing the number of tablets of Propecia per day or perhaps switching to the stronger Proscar (5mg tablet) may be necessary. This is also a relatively expensive compound, so it can become quite costly as the dosage of Proscar / Propecia increases, it is probably best to keep the dosage of Proscar at the lowest effective

amount. Cost may not be the only basis for such a decision, as DHT is believed to affect the nervous & reproductive system in many beneficial ways. By minimizing this conversion we not only face the possibility of interference with sexual functioning, but might also be inadvertently lessening the level of strength gained during testosterone therapy (this being tied to the actions of DHT on the neuromuscular system). A "use only when necessary" position should likewise be taken in regard to Proscar.

Use clenbuterol with caution in hypersensitive and diabetic individuals and in individuals with latent

or clinically recognized angle closure glaucoma, coronary artery disease, congestive heart failure, prostatic hypertrophy, hyperthyroidism, urinary retention.

Check with your doctor as soon as possible if any of the following side effects occur:

Keep Clomid in a tightly closed container and out of reach of children. Store Clomid at room temperature and away from excess heat and moisture (not in the bathroom).

Rather than waiting to the end of a workout, many athletes prefer to inject their insulin dosage 30 minutes before their training session is over and then consume a carbohydrate drink immediately

following the workout. This will make the insulin more efficient at bringing glycogen to the muscles, but it will also increase the danger of hypoglycemia. Some athletes will even inject a few IUs before lifting to improve their pump. This practice is extremely risky and best left to athletes with experience using insulin. Finally, some athletes like to inject insulin upon waking in the morning. After the injection, they will consume a carbohydrate drink and then have breakfast within the next hour. Some athletes find this application of insulin very beneficial for putting on mass, while others will tend to put on excess

fat using insulin in this way.

Halotestex (fluoxymesterone) is an oral derivative of the male hormone testosterone. Unlike testosterone, halotestex does not convert to estrogen. Therefore, estrogen-related side effects such as fat deposition, water retention, and gynecomastia do not occur. Halotestex has powerful androgenic properties. It is particularly noted for increased strength without significant additional weight gain. Side effects include aggression, oily skin, and virilization. Halotestex is considered to be very toxic to the liver, and thus must be used with caution and for short durations only.