Substance: 40mg Nandrolone

Phenylpropionate & 60mg Nandrolone Decanoate per ml.

In females, dosages above 15 mg./day can cause facial hair, deepening of the voice, clitoral hypertrophy, and acne.

Danabol / Dianabol (Methandienone) additional information

Proviron (Mesterolone), 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 Proviron is included.

Effective Dose: 20-50 mg/day.

 - You must not take Roaccutane if you are pregnant.

Product Description: Cialis (Tadalafil)

Testosterone is usually attached to an ester (i.e. when you buy testosterone propionate, the subject of this profile, you are buying testosterone with a propionate ester attached). The ester determines how long it takes your body to dispose of the steroid in question, and propionate is the shortest ester available with a testosterone base (of course, testosterone suspension has no ester). There are enzymes, called esterases, in your body which have the function

of removing the ester from steroids, and leaving you with just the steroid molecule with the ester cleaved off. Depending on how heavy the ester chain is, that determines how long it takes the esterase to remove it. And that amount of time determines how long the drug stays active in your body. Great, right? Not really...see, the ester takes up "room" in the injection. Check out this chart:

Obtaining DNP and Making Capsules

The strangest thing however, taking into account that Primo is still a DHT (or rather DHB) derivative, is that it is quite easy on the system androgenically as well. Women use

methenolone often, usually the tabs, and find little virilisation symptoms in short term use of methenolone. Long-term use may induce some acne and a deepening of the voice however. Methenolone is also not overly suppressive of the HPT axis (endocrinal axis for the production of natural testosterone). These are both the result of DHB's 1,2-double bond, which, analog to the parent structure boldenone, reduces the androgenic binding by 50% as opposed to DHT.

Tell your health care professional if you are taking any other prescription or nonprescription medicine. If you are taking tamoxifen to reduce the risk of breast

cancer, it is especially important that your health care professional know if you are taking the following:

Important information about Rohypnol

Reductil works like other appetite suppressants on the market by increasing the amount of serotonin and catecholamine in the brain. Serotonin and catecholamine are two important chemicals that control mood and appetite. When levels of serotonin and catecholamine are raised, your appetite decreases.

The propionate ester used with this compound will extend its activity for only a few days. With such a short duration of effect, injections need to be repeated at

least every 3 or 4 days in order to maintain a consistent level of hormone in the blood. Factoring this in with its low strength (50 mg/ml), men will generally inject a full 2 ml ampule of Masteron (100 mg) every two or three days. The weekly dosage therefore lands in the range of 200-350 mg, a level more than sufficient to receive good results. We also should mention that while some women do profess to using this item before a show, it is much too androgenic in nature to recommend. Virilization symptoms can result quickly with its use, making Masteron a very risky item to experiment with. If attempted, the dosage should

be limited to no more than 25 to 50 mg each week. The female athlete would be further served by increasing the number of days between injections to prevent buildup of steroid in the body. In this case, Masteron can perhaps be administered once every 7 days.

10 mg tablets are yellow square tablets, with "10" imprinted on one side and "BD" separated by a score imprinted on the reverse, sealed in foil pouches of 100 tablets.

Tprop. Eifelfango 10, 25 mg/ml; Eifelfango G

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) (17). 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 (18). 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 (20). Testicular atrophy (shrunken balls) may also occur; HCG used intermittently throughout a cycle can prevent this. (21) 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.

Virormone 25, 50 mg/ml; Paines & Byrne GB

Cytomel® is the popularly recognized brand name for the drug liothyronine sodium. This is not an anabolic steroid but a thyroid hormone. It is used medically to treat cases of thyroid insufficiency, obesity, certain metabolic disorders and fatigue. Specifically this drug is a pharmaceutical preparation of the natural thyroid hormone triiodothyronine (T-3). When administered, Cytomel® increases

the patient's metabolism. The result is an increased rate of cellular activity (noted by a more rapid utilization of carbohydrates, fats and proteins). Bodybuilders are particularly attracted to this drug for its ability to burn off body excess fat. Most often utilized during contest preparation, one can greatly decrease the amount of stored fat without being forced to severely restrict calories. To this end Cytomel® is commonly used in conjunction with Clenbuterol and can produce extremely dramatic results. This combination has become very popular in recent years, no doubt responsible for many "ripped" on-stage physiques.

It is also noted by many that when thyroid hormones are taken in conjunction with steroids, an increased anabolic effect can be seen (noticeably greater than if the steroids are used alone). This is likely due to faster utilization of proteins by the body, increasing the rate for new muscle accumulation.

Androlic / Anadrol increases the number of red blood cells, allowing the muscle to absorb more oxygen. The muscle thus has a higher endurance and performance level. Although anadrol is not a steroid used in preparation for a competition, it does help more than any other steroid during dieting to maintain the muscle

mass and to allow an intense workout.

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-muscular 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 over 3 weeks time. A long-acting testosterone ester may be the best for all your mass-building needs, but it's not an easy product to use. Nolvadex and Proviron will come in very handy in

such cases and post-cycle. HCG and Clomid or Nolvadex will be required as well to help restore natural testosterone.Frequency of side effects is probably highest with this type of product.

by Patrick Arnold - Viagra works by increasing the effects of nitric oxide (NO), a substance that serves many key functions in biological processes throughout the body. One of the most well known and important functions of NO is the dilation of blood vessels. This allows greater blood flow to the muscles, which of course can be valuable to an athlete during competition.

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).

Day 1: 20 mcg

This medicine is a phosphodiesterase inhibitor used to treat sexual function problems such as impotence or erectile dysfunction. In combination with sexual stimulation, this medicine works by helping the blood flow into the penis to achieve and maintain an erection. This medicine is not intended

for use in women or children. This medicine will not protect against sexually transmitted diseases including HIV infection. Use "safe sex" practices such as latex condoms.

Boldenone is very common in the precontest arena for two main reasons. First off, there is a low amount of aromitization and secondly there is very little water retention while taking equipoise. This makes equipoise a good precontest steroid. Boldenone is well known to give a good increase in the pumps you get while working out. This is caused from the increase in red blood cells that you will experience while taking this steroid. It is also

well known to help cause a dramatic increase in appetite. When taken with a good mass building steroid like dianabol, this is a sure formula for successful gains in muscle mass.

Apnea, hypotension, and cardiac arrest have been reported following parenteral administration of benzodiazepines to the elderly, severely ill patients, or patients with compromised respiratory function. Respiratory depression also has occurred in these patients during benzodiazepine therapy, occasionally resulting in death.

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.

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.

Clomid tablets, containing clomiphene citrate, is a non steroidal ovulatory stimulant.

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.

As an aromatase inhibitor, Arimidex's mechanism of action — blocking conversion of aromatizable steroids to estrogen — is in contrast to the mechanism of action of anti-estrogens such as clomiphene (Clomid ®) or tamoxifen (Nolvadex ®), which block estrogen receptors in some tissues, and activate estrogen

receptors in others. During a cycle, if using Arimidex, there is generally no need to use Clomid as well, but (as mentioned in the section on Clomid) there may still be benefits to doing so.

Stanozolol, possible side effects

Mesterolone is an orally active, 1-methylated DHT. Like Masteron, but then actually delivered in an oral fashion. DHT is the conversion product of testosterone at the 5-alpha-reductase enzyme, the result being a hormone that is 3 to 4 times as androgenic and is structurally incapable of forming estrogen. One would imagine then that mesterolone would be a perfect drug to enhance strength and

add small but completely lean gains to the frame. Unfortunately there is a control mechanism for DHT in the human body. When levels get too high, the 3alpha hydroxysteroid dehydrogenase enzyme converts it to a mostly inactive compound known as 3-alpha (5-alpha-androstan-3alpha,17beta-diol), a prohormone if you will. It can equally convert back to DHT by way of the same enzyme when low levels of DHT are detected. But it means that unless one uses ridiculously high amounts, most of what is administered is quite useless at the height of the androgen receptor in muscle tissue and thus mesterolone is not particularly suited, if

at all, to promote muscle hypertrophy.

Given all of this information, there are nonetheless more things to know before you undertake your first DNP cycle. The following tips and tricks gathered from personal experience and consultations with users are presented for your aid:

It is also important to remember that the use of an injectable testosterone will quickly suppress endogenous testosterone production. It is therefore good advice to use a testosterone stimulating drug like HCG and/or Clomid®/Nolvadex® at the conclusion of a cycle. This should help the user avoid a strong "crash" due to

hormonal imbalance, which can strip away much of the new muscle mass and strength. This is no doubt the reason why many athletes claim to be very disappointed with the final result of steroid use, as there is often only a slight permanent gain if anabolics are discontinued incorrectly. Of course we cannot expect to retain every pound of new bodyweight after a cycle. This is especially true whenever we are withdrawing a strong (aromatizing) androgen like testosterone, as a considerable drop in weight (and strength) is to be expected as retained water is excreted. This should not be of much concern; instead the user should focus

on ancillary drug therapy so as to preserve the solid mass underneath. Another way athletes have found to lessen the "crash", is to first replace the testosterone with a milder anabolic like Deca-Durabolin®. This steroid is administered alone, at a typical dosage (200-400mg per week), for the following month or two. In this "stepping down" procedure the user is attempting to turn the watery bulk of a strong testosterone into the more solid muscularity we see with nandrolone preparations. In many instances this practice proves to be very effective. Of course we must remember to still administer ancillary

drugs at the conclusion, as endogenous testosterone production will not be rebounding during the Deca therapy. Cypionate can still be found on the black market in good volume.

This medicine is a phosphodiesterase inhibitor used to treat sexual function problems such as impotence or erectile dysfunction. In combination with sexual stimulation, this medicine works by helping the blood flow into the penis to achieve and maintain an erection. This medicine is not intended for use in women or children. This medicine will not protect against sexually transmitted diseases including HIV infection. Use "safe sex" practices

such as latex condoms.

Many have speculated as to what makes Anapolon so troublesome in terms of estrogenic side effects. Some have suggested that it has progestational activity, similar to nandrolone, and Anapolon is not actually estrogenic at all. Since the obvious Anapolon side effects of both estrogens and progestins are very similar, this explanation might be a plausible one. However we do find medical studies looking at this possibility. Anapolon (Oxymetholone) is also a very potent androgen. This trait tends of Anapolon to produce many pronounced, unwanted androgenic side effects.

Testosterone

suspension is an injectable preparation containing unesterfied testosterone in a water base. Among athletes, testosterone suspension has a reputation of being an extremely potent injectable, often ranked highest among the testosterones. Very fast acting, testosterone suspension will sustain elevated testosterone levels for only 2-3 days. Athletes will most commonly inject "suspension" daily, at a dosage of 50-100 mg.

Benzodiazepines belong to the group of medicines called central nervous system (CNS) depressants (medicines that slow down the nervous system). Some benzodiazepines are used to relieve anxiety.

However, benzodiazepines should not be used to relieve nervousness or tension caused by the stress of everyday life. Some benzodiazepines are used to treat insomnia (trouble in sleeping). However, if used regularly (for example, every day) for insomnia, they usually are not effective for more than a few weeks.

For athletes who wish to maintain a "natural" status in competition, the tablets are quite well-suited as detection chances for the acetate-form are quite slim. However tests have improved and quite a number of metabolites1 of methenolone can be detected with a simple urine sample. But an English study documented

that there is a liability in eating methenolone contaminated meats2, which could provide a possible defense if found out. One could always claim they ate the meat of a chicken or cow injected with methenolone since the test concluded eating such meat does not improve performance, but can deliver positive tests for several methenolone metabolites almost 24 hours after ingestion. That's for those of you seeking a viable defense against a possible methenolone-positive.

Proscar dosage

Tell your doctor or pharmacist: about all other medicines you are taking, including non-prescription medicines; if you are a frequent

user of drinks with caffeine or alcohol; if you smoke; or if you use illegal drugs. These may affect the way your medicine works. Check before stopping or starting any of your medicines.

Andriol is actually contained in a natural ester base, one, which is very easy on the body. This product's advantageous properties are similar to other testosterones in that it promotes rapid strength and weight gains. It, like other testosterones, promotes the storage of glycogen as well as ATP. Andriol does not seem to exhibit the degree of LH and FSH suppression that is seen with other testosterones and androgens.

Each 10ml

multidose vial contains 50mg per ml. Vials have yellow coloured flip-off caps with have Stanabol stamped on them.

Do not let anyone else take your medicines.

What do diazepam tablets do?

Winstrol comes in 50 mg/cc, 2 mg/tab or 5mg/tab. Winstrol Depot is manufactured by Winthrop in USA and by Zambon in Europe. Winstrol depot is very popular anabolic steroid and is a derivative of DHT. It is a relatively low androgenic steroid which does not seem to aromatize. It can be toxic to the liver in excessive dosages. Very few user report water retention or any other side effects. It is a popular all purpose

steroid; many stack with Primobolan depot for cutting, others stack it with testosterone for size and strength gains. Women often use winstrol depot but occasionally it can cause virilization, even at low dosages. Users report that the muscle gains they make are solid, they are well retained after the drug use is discontinued. Athletes also find that the injectable version is far superior to the oral. Dosages range from 3-5 ccs per week for men, 1-2 ccs in women. Oral dosages are usually in the area of 16-30 mg per day for men, 4-8 mg for women.

Nitrates are also found in recreational drugs such as amyl nitrate or nitrite

("poppers"). If you are not sure if any of your medications contain nitrates, or if you do not understand what nitrates are, ask your healthcare provider or pharmacist.

Driving and using machines:

If it were around in the United States, it's popularity would be comparable to oral Dianabol. Effective dosages seem to be in the area of 200 mg a day taken in divided dosages. Andriol is a safe oral steroid that does not suppress gonadotrophins.It is absorbed through the small intestine into the lymphatic system, no burden to the liver it is a natural ester added to a synthetic derivative which will

nor change liver enzymes. No testicular shrinkage, no reduction on in spermatogenesis will occur with reasonable dosages. Cholesterol triglycerides and total lipids tend to be reduced with long term use of Andriol as opposed to elevated with most oral steroids.

Average Dose: Men 75 mg every day or two days

The history of Cialis cannot be discussed without mentioning Pfizer's drug, Viagra. The FDA's approval on March 27, 1998, led this prescription drug, Viagra, to a ground breaking success in just the first year of introduction as Pfizer sold drugs worth over a billion dollars. However, things changed considerably

for the giant of erectile dysfunction drugs when the FDA also approved Levitra on August 19, 2003, and Cialis on November 21, 2003. In 1993 the drug company Icos began studying IC351, which is a PDE5 enzyme inhibitor, and this is basically the process through which the erectile dysfunction drugs work. In 1994, Pfizer scientists discovered that sildenafil citrate, which is a white crystalline powder that temporarily normalizes erectile function of the penis by blocking an enzyme known to inhibit the production of a chemical that causes erections, caused the heart patients that were participating in a clinical study of

a heart medicine to have erections. Although the scientists were not testing the chemical compound IC351 for erectile dysfunction, the compound seemed to have a side effect which could potentially be worth millions, if not billions of dollars. Soon Icos received its very first patent in 1994 on IC351, and the clinical trials of phase 1 took place in 1995. In 1997, phase 2 clinical studies began and Icos performed its first study on patients with erectile dysfunction. Phase 2 lasted about two years, and after that phase 3 began.

Unlike most oral steroids, which are Class II steroids giving most of their anabolic effect

by means other than the androgen receptor (AR), it seems that oxandrolone probably does have good binding to the AR, and is therefore a Class I steroid, while having little other effect. By itself it is considered to be a weak anabolic.

As with all Testosterone products, Sustanon is a strong anabolic with pronounced androgenic activity. It is most commonly used as a bulking drug, providing exceptional gains in strength and muscle mass. Although it does convert to estrogen, as is the nature of Testosterone, Sustanon injectable is noted as being slightly more tolerable than cypionate or enanthate. As stated throughout

this book, such observations are only issues of timing however. Blood levels of Testosterone are building more slowly, so side effects do not set in as fast. For equal blood hormone levels however, Testosterone will break down equally without regard to ester. Many individuals may likewise find it necessary to use with this steroid an antiestrogen, in which case a low dosage of Nolvadex or Proviron would be appropriate. Also correlating with estrogen, water retention should be noticeable. This is not desirable when the athlete is looking to maintain a quality look to the physique, so this is certainly not an idea drug for contest

preparation.

Generic Name: Orlistat

Anabolic steroids may cause children to stop growing. In addition, they may make male children develop too fast sexually and may cause male-like changes in female children.

Each 10ml multidose vial contains 75mg per ml. Beginning in May, 2005, new flip-off tops are purple coloured and have Trenabol stamped on them. Older vials have a white coloured generic flip-off top.

The normal daily dosage taken by athletes is 10-30 mg/day. To prevent estrogenic side effects normally 10 mg/day is sufficient, a dosage which also keeps low the risk of reducing the effect

of simultaneously taken steroids. Often it is sufficient if the athlete begins this preventive intake of Nolvadex three to four weeks after the first intake of anabolic steroids. Athletes who have tendencies toward gynecomastia, strong water retention, and increased fat deposits with steroids such as Dianabol, Testosterone, Anadrol 50, and Deca-Durabolin usually take 20-30 mg/day The combined application of Nolvadex 20-30 mg/day and Proviron 25-50 mg/day in these cases leads to excellent results. The same is true for athletes who are in competition, and for women. Women, however, should do without the intake of Proviron or at

least reduce the dose to one 25 mg tablet per day.

Evidence suggests that GABA receptors are heterogeneous with many different subtypes, which may account for the various effects of GABA receptor agonists and benzodiazepines. Midazolam, for example, has twice the affinity for benzodiazepine receptors than diazepam. The antianxiety action of benzodiazepines may be a result of their ability to block cortical and limbic arousal following stimulation of the reticular pathways while muscle relaxation properties are mediated by inhibiting both mono-and polysynaptic pathways. Benzodiazepine can also depress muscle and motor

nerve function directly. Animal studies of the anticonvulsant actions suggest that benzodiazepines augment presynaptic inhibition of neurons, thereby limiting the spread of electrical activity, although they do not actually inhibit the abnormally discharging focus.

There is no need for an anti-estrogen as Winny may have such a property of its own and does not aromatize at any rate. The only counter-indication with Winny would perhaps be an anti-hypertensive if you use for a longer stack. Be sure to get liver values checked if you use for longer than 6 weeks on end. There is no real use for Clomid or Nolva post-cycle

for Winny specifically since there is no post-cycle aromatisation to cause negative feedback. That makes whatever gains you made on Winny quite easy to maintain.

The use of HCG (Human Chorionic Gonadotropin) and/or Clomiphene Citrate/Tamoxifen Citrate may also be beneficial at the conclusion of use in order to ensure balance in the hormone system. Although it remains active in the body for approximately two to three weeks, injections are typically taken at least every 10 days. An effective dosage for most ranges from 250mg - 500mg every 7 to 10 days. Genesis Meds offers this product in a 10ml vial, 250mg/ml.