You may get drowsy or dizzy. Do not drive, use machinery, or do anything

that needs mental alertness until you know how diazepam affects you. To reduce the risk of dizzy and fainting spells, do not stand or sit up quickly, especially if you are an older patient. Alcohol may increase dizziness and drowsiness. Avoid alcoholic drinks.

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.

Additional comments:

DESCRIPTION: Stanabol is very popular anabolic steroid and is a derivative of DHT. Dosages for Stanabol 50 range from 3-5 cc per week for men, 1-2 cc in women.

Minor side effects with diazepam include:

Although Dianabol has many potential side effects, they are rare with a dosage of up to 20 mg/day. Since Dianabol is 17-alpha alkylated it causes a considerable strain on the liver. In high dosages and over a longer period of time, Dianabol is liver-toxic. Even a dosage of only 10 mg/day can increase the liver values; after discontinuance of the drug, however, the values return to normal. Since

Dianabol quickly inereases the body weight due to high water retention, a high blood pressure and a faster heartbeat can occur, sometimes requiring the intake of an antihypertensive drug such as Catapresan. Additive intake of Nolvadex and Proviron might be necessary as well, since Dianabol strongly converts into estrogens and in some athletes causes gynecomastia ("bitch tits") or worsens an already existing condition. Because of the strongly androgenic component and the conversion into dihydrotestosterone. Dianabol has significant influence on the endogenous testosterone level. Studies have shown that the intake of 20 mg

Dianabol/day over 10 days reduces the testosterone level by 30-40% (3). This can be explained by Dianabols distinct antigonadotropic effect, meaning that it inhibits the release of the gonadotropic FSH (follicle stimulating hormone) and LH (luteinizing hormone) by the hypophysis. 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 exereted by the body. In high dosages of 5O mg+/ day aggressive behavior in the user can 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.

A suitable dosage of Anavar for a male athlete is 0.125 mg./pound of body weight per day. Women should not take more than about half of that dosage, though. Anavar is normally

taken two to three times daily after meals thus assuring an optimal absorption of the oxandrolone.

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.

I’m not sure where to begin. This study has the potential to completely change the way we age.

Oral contraceptives can increase the effects of diazepam because they inhibit oxidative metabolism, thereby increasing serum concentrations

of concomitantly administered benzodiazepines that undergo oxidation. Patients receiving oral contraceptive therapy should be observed for evidence of increased response to diazepam.

Oxandrolone has often been used as a growth-promoting agent in the therapy of boys with growth delays in adolescence. Oxandrolone is also used in treating girls affected with Turner's syndrome, another growth-delay ailment. In obese individuals, oral oxandrolone has been shown to decrease subcutaneous abdominal fat more than Testosterone enanthate or weight loss alone, and it also tended to produce favorable changes in visceral

fat.

The drug is moderately effective at doses of 400 mg/week. The long half-life of nandrolone decanoate makes it unsuited to short alternating cycles, but suitable for more traditional cycles, with a built-in self-tapering effect in the weeks following the last injection.

Nolvadex C&K is also useful during a diet since it helps in the burning of fat. Although tamoxifen has no direct fatburning effect its antiestrogenic effect contributes to keeping the estrogen level as low as possible. Nolvadex C&K should especially be taken together with the strong androgenic steroids Dianabol and Anadrol

, and the various testosterone compounds.

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.

Roche Valium (Diazepam) is an antianxiety agent (benzodiazepine), used primarily for short-term relief of mild to moderate

anxiety. It may also be used to treat symptoms of acute alcohol withdrawals, to help control epilepsy, or to relieve muscle spasms.

Endogenous testosterone levels can be a concern with Deca-Durabolin, especially after long cycles. It is therefore mandatory to incorporate ancillary drugs at the conclusion of therapy. An estrogen antagonist such as Clomid or Nolvadex is therefore commonly used for a few weeks. These both provide a good level of testosterone stimulation, although they may take a couple of weeks to show the best effect. HCG injections could be added for extra reassurance, acting to rapidly

restore the normal ability of the testes to respond to the resumed release of gonadotropins. For this purpose one could administer three injections of 2500-50001.U., spaced five days apart. After which point the antagonist is continued alone for a few more weeks in an effort to stabilize the production of testosterone. Remember not to begin post cycle therapy (PCT) until after Deca has been withdrawn for around three weeks. Deca stays active for quite some time so the ancillary drugs will not be able to exhibit their optimal effect when the steroid is still being released into the bloodstream. The major drawback for competitive

purposes is that in many cases nandrolone metabolites will be detectable in a drug screen for up to a year (or more) after use. This is clearly due to the form of administration. Esterified compounds have a high affinity to stay stored in fatty tissues. While we can accurately estimate the time frame it will take for a given dose to enter circulation from an injection site, we cannot know for sure that 100% of the steroid will have been metabolized at any given point. Small amounts may indeed be stubborn in leaving fatty tissue, particularly after heavy, longer-term use. Some quantity of nandrolone decanoate

may therefore be left to sporadically enter into the blood stream many months after use. This process may be further aggravated when dieting for a show, a time when body fat stores are being actively depleted (possibly freeing more steroid). This has no doubt been the cause for many unexpected positives on a drug screen. The fact that nandrolone has been isolated as the "hands-off" injectable for the drug tested athlete is most likely due to its popularity (and therefore common appearance on drug screens). The same risk would of course hold true for other long chain esterified injectables such as Equipoise,

and Primobolan.

The normal recommended dose for Reductil is one 10 mg or 15 mg tablet a day at least one hour before your eat.

Mesterolone is an oral alkylated steroid. If used primarily as an anti-aromatase drug, using it throughout a longer cycle (10-12 weeks) of injectables may elevate liver values a little bit, though much, much less than one would expect with a 17-alpha-alkylated steroid. Eventhough instead of inhibiting gains, mesterolone may actually contribute to gains. So that's a bit of a shame. Its not quite as toxic since its not alkylated in the same fashion, but at the 1 position, which

reduces hepatic breakdown, but not like 17-alpha alkylation. The reason for the change of position I assume, is because alkylating at the 17-alpha position has been shown to reduce affinity for sex hormone binding proteins. This would in turn decrease its ability to free testosterone. Nonetheless the delivery rate is quite good. Its taken daily in 50-100 mg doses.

What VIAGRA Does Not Do:

Possibly the most exciting thing I read about Teslac is that it has been PROVEN (!) to be an effective and safe treatment for Gynocomastia(3) (development of breasts in male mammary glands& often ineloquently referred to as

"bitch tits" in gym-speak). So yeah, if you get a bit of Gyno on a cycle, you may want to include Teslac in your PCT for both the (very good) reasons I revealed above, as well as it´s potential to treat your gyno.

The first study I looked at (1) showed that Teslac increases testosterone (by 47%) and it´s precursor androstenedione (70%) levels in the body. In the second study I looked at, it raised testosterone levels in men up to 290ng/dl (almost enough to bring you from 0 test to the lowest end of normal/acceptable range), as well as raising LH (leutenizing hormone) levels, and even FSH (Follicle

Stimulating Hormone) levels slightly (2). So as you can see, not only is this stuff not suppressive of your natural hormones, it actually stimulates your body to produce more testosterone as well as the hormones which produce it.(2) As for it´s ability to halt aromatization, it has been shown to reduce it by 90-95%, with regards to decrease in the overall rate, in some instances (7). In another third study, Aromatase inhibition by testolactone, at a dose of 500 mg twice daily (so a total of 1,000mgs/day) for 4 weeks lowered circulating estradiol (E2) levels by roughly 1/3rd and enhanced the secretion of follicle-stimulating

hormone and testosterone by approximately the same amount (1/3rd each)(6). Basically, we´re looking at pretty decent reductions in both aromatization, as well as reduction in total estrogen floating around your body. So far, we have seen that, in different studies it has been shown to increase LH as well as FSH, respectively, and in addition it raises testosterone levels and lowers estrogen levels in all of the studies we´ve examined. Raising FSH, LH, and testosterone while lowering estrogen is a pretty good deal considering most steroids lower endogenous (natural) production of the first three,

and raise estrogen.

The mixture of the testosterones (30mg propionate, 60mg phenylpropionate, 60mg isocaproate, 100mg decanoate) are time-released to provide an immediate effect while still remaining active in the body for up to a month. As with other testosterones, Sustanon is an androgenic steroid with a pronounced anabolic effect. Therefore, athletes commonly use Sustanon to put on mass and size while increasing strength. However, unlike other testosterone compounds such as Cypionate and Enanthate, the use of Sustanon leads to less water retention and estrogenic side effects. This characteristic is extremely beneficial

to bodybuilders who suffer from gynecomastia yet still seek the powerful anabolic effect of an injectable testosterone. The decreased water retention also makes Sustanon a desirable steroid for bodybuilders and athletes interested in cutting up or building a solid foundation of quality mass. Dosages of Sustanon range from 250 mg every other week, up to 2000 mg or more per week. These dosages seem to be the extremes. A more common dosage would range from 250 mg to 1000 mg per week. Although Sustanon remains active for up to a month, injections should be taken at least once a week to keep testosterone levels stable.

A steroid novice can expect to gain about 20 pounds within a couple of months by using only 250-500 mg of Sustanon a week. Sustanon is a fairly safe steroid, but in high dosages, some athletes may experience side effects due to an elevated estrogen level. With dosages exceeding 1000 mg a week, it is probably wise to use an anti-estrogen such as Nolvadex or Proviron. The use of Sustanon will suppress natural testosterone production, so the use of HCG or Clomid may be appropriate at the end of a cycle. Sustanon 250 is a good base steroid to use in a stack. Athletes interested in rapid size and strength gains find that Sustanon

stacks extremely well with orals such as Anadrol and Dianabol. On the other hand, Sustanon also stacks well with Parabolan, Masteron, and Winstrol for athletes seeking the hard, ripped look.

Clenbuterol

Kamagra is a discreet pill for the treatment of male erectile dysfunction, often called impotence. it is a real breakthrough treatment that can help many man who have erectile dysfunction to get and keep an erection when they are sexually aroused.

Packaging: 1000 mg in 10 ml.

IGF also mimic's insulin in the human body. It makes muscles more sensitive to insulin's effects, so if you are

a person that currently uses insulin you can lower your dosage by a decent margin to achieve the same effects, and as mentioned IGF will keep the insulin from making you fat.

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).

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.

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.

Testosterone Cypionate is a single-ester,

long-acting form of testosterone. Due to the length of its ester (8 carbons) it is stored mostly in the adipose tissue upon intra-musuclar injection, and then slowly but very steadily released over a certain period of time. A peak is noted after 24-48 hours of injection and then a slow decline, reaching a steady point after 12 days and staying there for over 3 weeks time. Of course most users of anabolics will not find adequate benefit in the use of this steady-point dose, so this product is normally injected once a week, making the very lowest dose higher than half the peak dose at any given time. This is roughly

the starting blood level as well. A long-acting testosterone ester is a must-have in any mass-building cycle. As such this is a very decent product.

 - The medicine is likely to pass into your milk and your baby so you must not take Roaccutane if you are breastfeeding.

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).

The old practice of slowly tapering off your dosage is totally ineffective at raising testosterone levels. Without ancillary drugs, run away cortisol levels

will likely strip much of the muscle that was gained during the cycle. If HCG and Clomid/Nolvadex are used properly, the person should be able to maintain a considerable amount of new muscle mass. Before going off, some alternately choose to first switch over to a milder injectable like Deca-Durabolin. This is in an effort to harden up the new mass, and can prove to be an effective practice. Although a drop of weight due to water loss is likely when making the switch, the end result should be the retention of more (quality) muscle mass with a less pronounced crash. Remember ancillaries though, as testosterone production will

not be rebounding during Deca therapy.

Day 6 - Day 12: 120 mcg

A last note about injectable Winny is : shake before use. Its called an aqueous solution, but the Winny being a steroid is not particularly polar, meaning it doesn't dissolve in the water. When the stuff sits, it will accumulate at the bottom of the vial. A good way to recognize the real stuff as well. So shake before you draw it into a syringe or mix it before you drink it, and perhaps even stir it again once in the syringe prior to injection.

Triolandren 20 mg/ml; Ciba Geigy CH

Theoretically, Restandol (Andriol) should build

up muscle and mass, in combination with noticeable water retention, in a fast and reliable way, similar to the tested injectable Testosterone Sustanon and Testoviron Depot. Unfortunately, this is not the case. Some athletes who work out for a competition store too much water due to their use of the injectable testosterone, resulting in smooth muscles. However, if they still do not want to give up Testo, they should at least not have the estrogen-linked complications caused by taking up to 240 mg Restandol (Andriol)/day and be able to reduce the water retention. In this phase, the estrogen level must be kept as low as possible,

otherwise the best diet will be useless. The intake of Restandol (Andriol) makes sense in this case and usually brings acceptable results. Otherwise, Restandol (Andriol) is a drug better used by hobby-bodybuilders.

Other examples of glucose or other high Glycemic index carbohydrate preparations which you can use include: glucose tablets, glucose powder mixed in a small volume of water, barley sugar, or other sweets or if these are not immediately available, a sugar containing cordial, soft drink or plain sugar dissolved in water. This should be followed by an adequate low Glycemic index carbohydrate meal to

prevent further hypoglycemia since the insulin levels are likely to remain high for some hours after the high Glycemic index carbohydrates are used up (metabolized) in the body.

Do not take Roaccutane...

Dose: 2500IU to 5000IU/week.

A typical daily dosage of Tamoxifen for men is in the range of 10 to 30mg, the chosen amount obviously dependent on the level of effect desired. It is advisable to begin with a low dosage and work up, so as to avoid taking an unnecessary amount. The time in which Tamoxifen is started also relies on individual needs of the user. If an athlete with a known sensitivity to

estrogen is starting a strong steroid cycle, Tamoxifen should probably be added soon after the cycle had been initiated. If estrogen is probably not going to be a major problem during the cycle (but will likely be after), this substance is administered around the time exogenous steroid levels will drop.

Foods with a low G.I. produce a slower, smaller but more sustained increase in blood glucose levels. Examples of such low G.I. foods are pasta, varieties of high amylose rice, barley, instant noodles, oats, heavy grain breads, lentils, and many fruits such as apples and dried apricots. Low G.I foods are advantageous

if consumed at least two hours before an event. This gives time for this food to be emptied from the stomach into the small intestine. Since these foods are digested and absorbed slowly from the gastro-intestinal tract, they continue to provide glucose to muscle cells for a longer period of time than moderate or high G.I. foods, particularly towards the end of an event when muscle glycogen stores may be running low. In this way, low G.I. foods can increase a person's exercise endurance and prolong the time before exhaustion sets in.

Always use a sterile needle and syringe every time and a clean injecting technique

(e.g. don't touch the needle or the skin where you are going to inject, with your fingers and don't breathe on or cough over the injection site before or after injecting).

Steroid novices should not (yet) use Trenabol Depot. The same is true for women; however, there are enough female athletes who do not care since the female organism reacts to the androgenic charge and the strong anabolic effect of Trenabol Depot with distinct gains in muscles and strength, especially from a female point of view. Thus the entire body has a harder and more athletic look. Trenabol Depot without a doubt is an enticing product for ambitious

female athletes. In the end everything depends on your personal willingness to take risks, ladies. The fact is that the standards on the national and international competition scenes in female bodybuilding have achieved levels which cannot be reached without the administration of strongly androgenic steroid compounds. A combination well liked by female bodybuilders consists of 76 mg Trenabol Depot/week, 20 mg Winstrol tablets/day, and 100 mcg Clenbuterol/day Women who do not in-ject more than one ampule of Trenabol Depot per week and who limit the period of intake to 4-5 weeks can mostly avoid or minimize virilization

symptoms. Female athletes who are overdoing it or who are sensitive to the androgenic part of trenbolone hexahydrobencylcarbonate can be confronted with some unpleas-ant surprises after several weeks of use: acne, androgenically caused hair loss on the scalp, irregular menstrual cycles, missed periods, much higher libido, aggressiveness, deep voice, chtorial hypertrophy, and increased hair growth on face and on the legs. The last three side effects are mostly irreversible changes.

Day 6 - Day 12: 120 mcg

The side effects of Durabolin are few. Water retention, high blood pressure, an el-evated estrogen level,

and virilization symptoms occur less often with Durabolin than with Deca-Durabolin. Female athletes therefore take Durabolin in weekly intervals since, due to its short duration of effect, no undesirable concentration of androgen takes place. They achieve good results with 50 mg Durabolin/week, 50 mg Testosterone Propionate every 8 -10 days, and 8-10 mg Winstrol/day, or 10 mg Oxandrolone/day. Three to four day intervals between the relative injections are to be observed. Durabolin is one of the safest non-toxic steroids offering satisfactory results. Durabolin has no negative effect on the liver function so it can even

be taken in cases of liver disease. Side effects occur only in rare cases and in persons who are extremely sensitive. Virilization symptoms in women such as huskiness, deep voice, hirsutism, acne, and increased libido are possible but occur only rarely if reasonable dosages are taken at reasonable intervals. Men usually experience no symptoms with Durabolin. Since the release of gonadotropins in the hypophysis is inhibited, there is a chance that the body's own testosterone production in a male athlete will be lower when the compound is taken over a prolonged time and in excessive doses.

The clearance and/or elimination

of many drugs are reduced in the elderly. Delayed elimination can either intensify or prolong the actions of adverse reactions of the drug. Benzodiazepines have been associated with falls in the elderly and the consumer advocate group, Public Citizen, has recommended these drugs not be used in the elderly.

The second use is in enhancing the potency of testosterone. Testosterone in the body at normal physiological levels is mostly inactive. As much as 97 or 98 percent of testosterone in that amount is bound to sex hormone binding globulin (SHBG) and albumin, two proteins. In such a form testosterone is

mostly inactive. But as with the aromatase enzyme, DHT has a higher affinity for these proteins than testosterone does, so when administered simultaneously the mesterolone will attach to the SHBG and albumin, leaving larger amounts of free testosterone to mediate anabolic activities such as protein synthesis. Another way in which it helps to increase gains. Its also another part of the equation that makes it ineffective on its own, as binding to these proteins too, would render it a non-issue at the androgen receptor.

• It improves memory- 62%

Drug Class: Highly Anabolic/Androgenic Steroid.

The popularity of Provironum© amongst bodybuilders has been increasing in recent years. Many experienced bodybuilders have in fact come to swear by it, incorporating it effectively in most markedly estrogenic cycles. Due to high demand Provironum© is now very easy to obtain on the black market. Most versions will be manufactured by Schering. In many instances this item is obtained via mail order, and here can sell for less than .50 per tab. This drug is packaged in both push-through strips and small glass vials, so do not let this alarm you. There is currently no need to worry about authenticity with this drug, as no counterfeits

are known to exist. If money and availability does not prevent it, Arimidex© is actually a much better choice than Provironum© though. This drug was designed specifically as an antiaromatase, and works much more effectively than anything else we have available. Since this item is extremely expensive however, Nolvadex© and Provironum© will no doubt remain to be the "standard" antiestrogen regimen among athletes.

Dianobol has a half-life time of only 3.2-4.5 hours. Meaning that you should take dianobol twice a day to enjoy a rich content in the blood stream.

5mg tablets are pink pentagon shaped tablets,

with snake&arrow imprinted on one side.

Timetable of Effects and Symptoms

Overdose

Effective Dose: 1-2 tabs/day.

Androlic / Anadrol is the most harmful oral steroid and its intake can cause many considerable side effects. Most users can expect certain pathological changes in their liver values after approximately one week. An increase in liver values of both the enzymes GOT and GPT also called transaminases, often cannot be avoided, which are indications of hepatitis, i.e. a liver infection. Those who discontinue oxymetholone will usually show normal values within two months.