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Winstrol Depot

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Centrino Laboratories (Thailand)
5 Vials x 10ml. [50mg./ml.] Total 2500mg		 CS Balkan Pharmaceuticals (Moldova)
15 Amps x 1ml. [50mg./ml.] Total 750mg		 Balkan Pharmaceuticals (Moldova)
100 Tabs x 10mg Total 1000mg

Winstrol Depot (StanoJect, Stanozolol, Stanabol, Stromba, StrombaJect)

Winstrol (Winstrol Depot, oral Winstrol) is a brand name of very popular anabolic steroid called Stanozolol, which is a derivative of DHT (dihydrotestosterone). It has low androgenic ratio and thus low possibility of aromatization and estrogen-related side effects.

It’s primarily usage in bodybuilding is cutting (relief) Tables of Cycles. However, Winstrol is widely used not only by bodybuilders but also by non-bodybuilding athletes such as runners, cyclists, football players, soccer or hockey players and fighters of all kinds (kick-boxers for instance); i.e. in the sports where you have to be swift but not too heavy, because it provides you with lean mass and improves your strength without gaining excessive muscles.<

Stanozolol is one of the chemicals, which allowed amazing results to famous runner and simply exceptional athlete Ben Johnson. This substance provided him with a noticeable gain in muscle mass and relief, which could be perfect even for professional bodybuilder.

So, Winstrol is a very effective steroid when used properly. It is important to distinguish between two forms of Winstrol-Stanozolol, first is long-acting injectable version called Winstrol depot. Second is short-acting oral one (Winstrol oral). Winstrol depot is more effective and thus preferred by most athletes.

The main usage of Winstrol (Winstrol Depot) in bodybuilding is preparation for a competition. When complemented by a proper calorie-rich and protein-rich diet, Winstrol Depot provides the muscles with firmness and elasticity. Unfortunately, due to its low androgenic component, it is unable to protect the athlete from damages to muscle tissue. The absence of androgenic effect is compensated by stacking with Parabolan. The combination of injectable Winstrol 50 mg per day and Parabolan 2-3 amps / week is "a combination of top championships".<

Winstrol is good not only for preparation for a competition, but also in the bulking phase. Due to low water retention rapid weight gains with Winstrol are unlikely to occur. It provides rather moderate amount of lean and dry mass, which preserves after the cycle is over.

Injections of Winstrol in certain muscle groups are gaining in popularity because athletes have noticed that this leads to an accelerated growth of the affected muscles.

Dosage and usage

Injectable version is just slightly more efficient than the oral one and it’s not being destroyed by the liver. Because of this oral Winstrol requires a little bit higher dosages, however, most of athletes underdose it due to gastrointestinal pain and increased liver values – oral Winstrol is liver-toxic. So, here is where the myth of superiority of injectable Winstrol comes from. People simply can’t take equal dosages of oral version. Common dosage of oral Stanozolol is 15-30 mg/ED, daily dosage should be split on two parts – in the morning and evening during a meal, drink a liquid along with it.

Feature of the injectable Winstrol Depot is that its substance is dissolved in the water and not oil unlike most of other steroids. Therefore, intervals between injections with Winstrol Depot must be shorter comparing to other oil-based steroids like Primobolan, Deca-Duraboline, SuStanon, Parabolan, etc. because its lifetime is much shorter. Practice has shown that Winstrol Depot should be administered at least twice a day and the best results are observed at a daily dose of 50mg. (300-350 mg/week). Milder dosage is 50 mg/EOD (150 mg/week)

Inject deep in muscles and constantly rotate the spots. However, if athlete wants to promote particular muscle group injections should be done into it.

Winstrol Stacking

Winstrol (Stanozolol) is all-purpose steroid, however, we should admit that in first turn it’s a cutting agent for bodybuilder and it plays rather limited role in bulking cycles. The main reason for using it in non-cutting cycles is that in limited dose it can lower SHBG, which, in turn, increases the amount of free testosterone in the body
Depending on the level of the athlete, one usually takes 50 mg of long-acting Winstrol /ED or EOD and Parabolan 76 mg/ every 1 – 3 days. Although there is no scientific evidence in favor of special interaction between Winstrol Depot and Parabolan, it’s very likely that a synergistic effect appears basing on real-world evidence. Other steroids that well stack with Winstrol during pre-competition (cutting) cycle are Masterolone, Boldenone, Halotestin, Oxandrolone (anavar), Testosterone propionate, Primobolan and human growth hormone (:HGH

Bodybuilders who want to build up strength and mass often combine Winstrol injectable with Dianabol, Anadrol 50 (Anapolon, Oxymetholone), Testosterone,(long-acting) and Deca-Durabolin. With the combination of Anadrol 50 100 mg/ED, 50 mg Winstrol depot 50 mg/ED and 400 mg of Deca / week athlete is slowly coming to the ambitious results.

Aged athletes and steroid novices can achieve good progress with Winstrol depot and Deca-Durabolin or Winstrol depot and Primobolan

Cycle 0:

Winstrol depot 50 mg/ED is a cutting stack. Some people may do 50 mg/ED, it’s more aggressive.

Cycle 1:

Winstrol 100-150 mf/week + Primobolan Depot (Methenolone Enanthate) 200-300 mg/week for 6 weeks as a cutting phase AFTER regular deca-dianabol cycle

Cycle 2

Oxandrolone (anavar) 20-30 mg/ED + Winstrol 150 mg/week + clenbuterol 120 mg/ED for 12 weeks;
prabolan 152-228 mg/week for the first 8 weeks; Proviron (Masterlone) 300 mg/week + Cytomel T3 increase from 25 to 100 mg / week during weeks 9-12

Cycle 3

Winstrol 150 mg/w + Parabolan Depot 152 mg/w

Cycle 4

Winstrol (150 mg/w) + Dianabol (20-30 mg/ED) + Testosterone Propionate (150 mg/w) for 8-10 weeks + Clenbuterol at the end

Cycle 5

Winstrol 50-100 mg/w + Deca-Durabolin 300-200 mg/w

Cycle 6

Winstrol oral 40-60mg/ED + Boldabol (Equipoise) 100-200 mg/w

Cycle 7

Winstrol + Trenbolone + Clenbuterol – relief cycle for novices.

Cycle 8

Primobolan Depot (Methenolone Enanthate) 200-300 mg/w + Winstrol 150-300 mg/w + Anavar (Oxandrolone) 20-60 mg/ED + Clenbuterol + PCT (Tamoxifen (Nolvadex) and HCG) – relief for advanced users

Cycle 9

Boldenone Undecylenate 300 mg/w + Winstrol oral 40 mg/ED + Nandrolone Decanoate (Phenilpropionate) 300 mg / w – relief for advanced users

Detection time

Oral Stanozolol – 3 weeks

Injectable Stanozolol (Winstrol depot) – 3 months

Side effects and PCT (Post Cycle Therapy) with Winstrol

Only small number of athletes report water retention or other negative effects. However, one should be aware that oral Winstrol can be toxic to the liver in excessive dosages.

Other non-androgenic side effects, which might occur are: headaches, muscle spasms, in rare cases high blood pressure can occur. The possibility of liver damage in the form of injectable Winstrol is very small, but still in high doses may increase the liver values.

Because the Winstrol Depot is dissolved in the water, injection, in common is more painful comparing to oil-based gear and have to be taken more frequently. This leads to another negative effect – scar tissue on the often injection spots, which cause athletes t inject not only into buttocks but also to shoulders, legs or even calves. Athletes wishing to avoid this take Winstrol Depot twice a week for 2-3ml. This decreases effectiveness but decreases pain and prevents scar tissue appearance.

As with most of other steroids, Winstrol suppresses natural hormonal levels although not to that extension as many others. Running testosterone in a cycle containing Winstrol helps to avoid possible sexual dysfunction.
After Winstrol cycle is over it’s necessary to do PCT: First week: 40mg of tamoxifen or 100mg clomiphen/ED or combo of both. One-two more weeks: 20mg of tamoxifen or 50mg clomiphen or combo of both.

Female usage

It’s one of the few substances, which could be used more or less safely by females in low dosages because it has more anabolic properties than androgenic ones. But occasionally Winstrol can cause virilization, even this small androgenic component may, become noticeable for women with a dose of only 50 mg per week. And troubles are almost guaranteed for female athletes with a dosage of 100 mg / week. Despite Winstrol moves out quickly, it can cause undesired accumulation of androgens in the female body, which cause virilization effects such as deep voice, hair growth, hypersexuality, etc. (something similar happens to some of natural brunettes). However, ambitious female athletes still use it 50 mg / EOD disregarding all side effects.
Normally, female athlete can tolerate around 5-10mg of Stanosolol per day, which perfectly fits for oral Winstrol usage

Winstrol fakes

Due to popularity of Winstrol there are many fakes on the market. The first thing to mention is that British Dragon Winstrol depot and Stanozolol (oral Winstrol) is no longer manufactured since they got busted, It might be still in circulation till the end of 2011 but anything with manufacture date after 2008 is a fake.

Brief description of Stanozolol:

Activity: 48 hours
Classification: Anabolic / Androgenic Steroid
Dose: Men 25-100 mg / day
Acne: Rare
Water Retention: Rare
High Blood Pressure: Rare
Hepatotoxicity: Yes, it is 17-Alpha alkalized
Aromatization: No, it is a derivative of DHT
DHT Conversion: No
Decrease HPTA function: Weak

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Viagra

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50-mg,
100-mg tablets.

General

VIAGRA is an oral medication for erectile dysfunction (ED). It helps most men with ED improve their erections. That means they are able to achieve harder erections.

Getting an erection is only half the story.

Maintaining an erection is just as important as getting one. VIAGRA can help with both. This can lead to a more satisfying sexual experience with your partner.

Who can take VIAGRA?

VIAGRA has an established safety profile of over 9 years. It has been shown to work safely and effectively in men with ED. This includes:

  • Men of all ages
  • Men who have difficulty all the time or just some of the time
  • Men with other health issues such as high blood pressure, diabetes, and depression

Find out if VIAGRA is right for you. Speak to your doctor. He can tell you if you have ED. And can recommend an effective treatment.

Sildenafil citrate, sold under the name Viagra is the first of a new group of medication which allows adequate sexual stimulation, relaxes the blood vessels of the penis and helps erection. Sildenafil tablet should be taken once a day. The time necessary for Sildenafil to exercise its action is about half an hour. The effect is maintained for about four hours.

The effect is only obtained with a satisfactory sexual stimulation.

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Ventolase

Buy Albuterol/Ventolin, Salbutamol

Albuterol/Ventolin, Ventolase, Salbutamol
Glaxo Smith Kline (UK)
300 Tabs x 0.04mg Total 12mg

Ventolase (Clenbuterol, Albuterol/Ventolin, Salbutamol)

Details:
hemical Name: Albuterol Sulfate
Drug Class: Beta-Agonist

Albuterol (Salbutamol) as a much better alternative to clenbuterol due to lesser side effects. Albuterol is a (relatively) selective beta-2 adrenoreceptor agonist, just like Clenbuterol. Clen is simply too harsh on most people; they get too jittery, too shaky, and too anxious. It’s a lot to go through to burn some fat.

Albuterol produces a much “cleaner” type of stimulant effect than Clenbuterol. I don’t know how to really describe this other than to say that the “Clen-shakes” just aren’t as bad with Albuterol in addition, I’m able to focus better on my work when I use Albuterol, while with Clenbuterol I’m stimulated but not really focused. But even though Albuterol produces a much cleaner stimulant-type feeling in most people, the main question is “How well does it burn fat”? As far as fat-burning stimulants go, how does it stack up to Clenbuterol? Lets face it, most people are really only concerned with the end results, right? Well, at least in me and the people I’ve worked with, Albuterol seems to produce significantly better results than Clen in terms of fat burning effects and it produces them just a bit more quickly too. This makes sense, if you think about it.

Albuterol is often thought of as a “shorter acting” version of Clen and, to draw an analogy, when we look at the steroids which are shorter acting versions (think about comparing something like Testosterone Propionate vs Cypionate, or NPP vs Deca-Durabolin) – they typically produce more dramatic results a bit quicker than their long acting cousins. I’m finding the same thing to be true with Albuterol. When we take a look at a medical study examining Clenbuterol vs. a beta-2 agonist which has an even longer half life (“Salmeterol”), we see that Clen out performs it in terms of anabolic effects. So I think it would only be logical to assume that something that was a shorter acting beta-2 agonist than Clen would likely outperform it, right? Let me just restate that, to make sure we’re all on the same page, ok? Clenbuterol outperforms longer acting beta-2 agonists, in terms of anabolic effects. Albuterol is a beta-2 agonist with a shorter acting effect than Clenbuterol. Therefore, it’s only logical that Albuterol is going to be more anabolic than Clen, right? Ok, let’s move on

To understand how Albuterol works, first we need to take a look at the Beta adrenergic system. This system is comprised of something called adrenoreceptors, and the most well known (to bodybuilders anyway) of the adrenoreceptors are the beta receptors. Beta receptors are embedded in the cell’s outer phospholipid membrane, and are stimulated by all the really popular stimulants ephedrine, Clenbuterol, etc… These receptors can further be divided into three subtypes: 1, 2, & 3, (of which we are primarily concerned with type-2, because the type-3 variety seems to primarily be less relevant in humans than in other animals, and because Albuterol doesn’t stimulate the type-1 receptor). There also exists a type of receptor known as an alpha receptor, which isn’t relevant here, but warrants a brief explanation. Alpha receptors differ from beta receptors in that they are activated at significantly lower catecholamine levels than are the beta receptors. A catecholamine is simply an organic compound that affects the sympathetic nervous system. For example, dopamine, norepinephrine and epinephrine are all catecholamines.

We are, mostly concerned with Beta-2 receptors, because those are what we see stimulated with Albuterol. It should come as no surprise to anyone who has used Clenbuterol as well as Albuterol is that when you stimulate your beta receptors, it causes something called vasodilatation (increased blood flow). Stimulation of these receptors also stimulates the break down of fatty acids into the blood stream for use as fuel, which causes a reduction in stored fat. Of course, this increased blood flow also comes with an increased heart rate. This explains how Beta-2 adrenergic stimulation can also increase your body temperature a bit however this isn’t something that’s too noticeable on a thermometer most people will feel a bit hotter, and some will even break a sweat (I fall into the latter category). Beta-agonists work to do this by increasing heat production in the cell’s owerhouse, the mitochondria, which will also increase your basal metabolic rate, and decrease your appetite. Not too many people feel hungry after a whopping dose of stimulants.

There is also some evidence that Beta-Agonists are anabolic (more properly, however, this would actually be anti-catabolic). This is because Beta-agonists also act to initiate a hormonal cascade that involves the activation of a compound called cAMP (basically: cyclic-Adenosine Monophosphate). After this, cAMP activates calpistatin that is the inhibitor of calpain. Calpain works to degrade protein in skeletal muscle (among other functions). Therefore, we already saw that how stimulation of beta 2 receptors have the ability to increase energy expenditure and free up body fat to be used as fuel, and now we have some understanding of how that stimulation can also have the potential to be anti-catabolic as well . Now that we’re all on the same page regarding the beta-adregenic system, and what sorts of effects we can expect when we stimulate it with beta-2 agonists lets take a more specific look at Albuterol, and why I think it’s such a great compound.

When we take a look at Albuterol’s ability to burn fat, it’s clear that it has the ability to aid fat loss in both normal as well as obese men . That’s not very different from Clenbuterol, in any way. However, in my personal experience with it, I think that Albuterol really outperforms Clen in areas of strength gains as well as for athletic purposes .lets take a look at my claim and see how Albuterol performs in humans In one study, subjects were given Albuterol and performed 9 weeks of isokinetic knee extensions (there was also a group who performed the same exercise routine but were not given Albuterol). The Albuterol group, predictably, had better strength gains than the non-Albuterol group (only a therapeutic dose was given). In my own experience, strength gains with Albuterol are much better and seen more quickly than I see them with Clen. In fact, while I don’t particularly experience much of a performance enhancing effect from Clen in the gym; on the other hand I see strength gains and muscular improvements within the first couple weeks of using Albuterol. Of course, this is likely a pure anabolic effect and probably not easily explained as a simple “enhanced” anti-catabolic effect, and likely can’t be explained away with the Calpain idea you read about earlier.

I still think that I can take a pretty good shot at explaining why Albuterol is anabolic, though. strong body of evidence exists to suggest that Albuterol influences the release of cAMP. As you may know, cAMP also plays an important role in mediating certain catecholamines secreted by the adrenal medulla have an inhibitory effect on muscle dependent protein degradation, but in addition, norepinephrine released from adrenergic terminals may actually increase the rate of protein synthesis(not just decrease the rate of their degradation) in oxidative muscles, thereby leading to increased protein accretion (representing a true anabolic effect). That’s most likely the way that we receive part of the anabolic effect from Beta-stimulation. Another way is perhaps through the beta-adrenergic stimulated lowering of “Interleukin-6” from fat cells (long story ). Anecdotally, Clenbuterol and ephedrine have both shown themselves capable of temporarily increasing strength, and I would bet most beta-agonists have this effect, but I don’t think has been shown as conclusively in the medical literature as it has been with Albuterol.

Albuterol has been shown to increase muscle size (3-6) as well as strength and endurance (*while people have anecdotally reported that Clen seems to lower their aerobic capacity. Clenbuterol has a disadvantage when compared with Albuterol in the area of strength gains, probably due to the act that it use-dependently inhibits action potential firing in skeletal muscle fibers, which is not directly caused by inherent Beta-2 stimulant activities . I think that’s the best quasi-scientific explanation I Again, my own personal experience and that of my research assistant(s) would also seem to strongly support this claim all of us have gotten leaner, bigger and stronger with the use of Albuterol, while with Clen, we got more ripped but not really stronger (and certainly not much bigger). Anecdotally, we’ve seen Clenbuterol fall a bit flat when people use it for anabolic effects, although in animals it would appear to be highly anabolic, though human studies are a bit shaky (ha!) in this area.

One of the things I really like about Albuterol is that it has the potential to actually be used on my cycle to make it safer by improving my lipid profile (cholesterol) or during PCT to help get my cholesterol levels back in check. This is because Albuterol shows significant benefits to cholesterol as it works to lower total cholesterol, specifically LDL (the bad stuff) while at the same time elevating HDL (the good stuff).

In my own particular case, cholesterol never seems to be an issue, but now that I’m working with Oasis for HRT, it’s certainly in my best interests to show up every three months with nice looking blood work.

So now is the part you’ve been waiting for (*or the part you skipped to, ignoring the rest of the article whatever ). How much of this should you take, and how often? Well, I can tell you that I have found the best results by working my way up from 4mgs taken once a day, up to 4-8 mgs taken 3x a day. I know that some people will think that 24ms a day of this stuff is going to be too much (it is, after all, a stimulant). But I can tell you that I have a pretty good tolerance for stimulants (I’ve taken up to 200 mcg/day of Clenbuterol, and some other pretty hefty stimulants that I probably shouldn’t mention in polite company). Most people are going to find their sweet spot at about 4mgs of Albuterol 3x a day or so women will probably take about half that dose, and be fine with it. I think that Albuterol is about to become very popular, very soon and I, for one, am looking forward to seeing less of my old Clen article around the ‘net, and more of this one.

For oral dosage form (syrup, tablets):
Adults and children older than 12 years of age—2 or 4 milligrams (mg) taken 3 or 4 times per day.
Your doctor may increase your dose as needed up to a maximum of 32 mg per day, divided and given 4 times per day

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Turanabol

buy Turanabol Balkan Pharma
 CS Balkan Pharmaceuticals Ltd. (Moldova) Tabs x 10mg

Oral Turanabol (Turanol, Turinabol, Chlordehydromethyl-testosterone)

Androgenic effect of the drug in pretty poor (6 out of 100), but in combination with anabolic effect (54 out of 100), Turanabol become extremely effective drug. For instance, dianabol has androgenic effect 43/100 and anabolic effect 90/100, but, in turn, dianabol has much more side effects and unacceptable for performance sportsmen such as runners or cyclists. With Turanabol you won’t have problems with enlarged breasts, excessive estrogen or watery, puffy outlook like with dianabol.

The drug turinabol (turanabol) was invented in Eastern Germany and was first used in medical practice in 1965. A year later it was fully applied in the sport. At the beginning the users were only men, but since 1968 a new drug was introduced for the preparation of females. The use of oral Turinabol has been thoroughly documented. A secret document dated 1973 indicates that the outcome for women in the shot put increased by about two meters (!) due to the using of only two oral turinabol tabs (10 mg/tab) daily for 11 weeks. The results were raising along with dosage and duration of use. In 1972 oral turinabol usage in Eastern Germany spread over many other sports where speed and strength were needed besides athletics, where it was initially introduced.

Turinabol effects

Here is a small table, which clearly shows oral turinabol effects on improving the results of the athletes.

Men Women

Shot put 4,5-5 m 2,5-5 m

Discus Throw 10-12 m 6-9 m

Hammer Throw 6-10 m 4-8 m

Javelin 8-15 m 6-12 m

Running at 400 m 45 sec 48 sec

Impressive, isn’t it?

Turanabol – What is it?

Oral turinabol is actually a version of methandrostenolone with extra chlorine atom in the fourth position. Hence the official name of turinabol is 4-chloro-alpha-Dihydromethyltestosteron. This upgrade has made the drug practically non-aromatized. Even more, turinabol metabolites very quickly leave the body, making huge advantage against the threat of doping tests.

Like the vast majority of oral AAS oral turinabol is 17-alpha alkylated, thus is potentially harmful to the liver. However, negative impact on the liver was not reported even after prolonged use.

Oral turinabol sufficiently resembles methandrostenolone not only on the structure of the molecule but the action of both drugs is also very similar. Turinabol produces less gains, but this is "quality", lean mass and also it produces less side effects. Despite turinabol does not aromatize and is quite mild drug, prolonged usage may cause the suppression of secretion of endogenous testosterone but at much lesser extent comparing to methandrostenolone (dianabol) and it’s easily rejuvenated.

Oral turinabol and injectable turinabol in bodybuilding

The difference between oral and injectable turinabol is like with most of other steroids. Oral is easier to take but in theory it may be harmful to the liver, so one can sustain higher dosages of injectable version. Furthermore, injectable is slightly more detected. But, in general, this is a matter of personal preferences.

In bodybuilding turinabol can be called a rookie. Not surprising – in the past "pharmacological king" in Eastern Europe used to be relatively cheap methandrostenolone (dianabol). All turinabol smuggled from Eastern Germany was captured by light athletics coaches. Western Europe and USA even did not know that such product exists, at least no bodybuilders reported they ever used it. Situation changed not that long ago when this very useful drug has been given a second chance and had a stunning success on US market and short after that in all other countries.

What are the reasons of this success? At-first turinabol notably raises power. Secondly, as has been said, oral turinabol quickly leaves the body and not found in the urine within 6-8 days after end of usage. We have not heard about any positive doping tests for turinabol. However, it may be because such tests are simply not being made nowadays.

A positive feature of the drug can be considered as giving hardness to the muscles without any significant accumulation of water. Experience shows that using of turinabol is almost mandatory in contest preparation stacks. Also it copes with the task of protection of muscle mass against destruction after bulking cycles.

There is another feature of turinabol – it’s a «sex drug». This steroid fairly rapidly increase libido for men, sometimes too much, so desire of sex prevail over desire for trainings 🙂 This property, as well as the ability just slightly inhibit the production of endogenous testosterone, makes it useful drug to take in moderate doses between the cycles of "heavy" AAS to maintain sex-drive.

Dosage and usage

Turanabol is mostly used to build lean body mass and strength without water retention, which often occurs with Daianabol and testosterone. The results with Turanabol straightly depends on the daily dosage, which normally varies between 20 to 100 mg. Athletes below 90 kgs experience no side effects at 20 mg daily and more heavy athletes easily adopt 40 – 50 mg daily.

When administered 50 mg/ED it significantly increases dry muscle mass, strength, and all of this without water retention, which can cause serious side effects due to estrogenic activity. Because of these characteristics, Turanabol is very effective product for powerlifters. In order to increase the results at the end of the course it is recommended to combine this drug with Parabolan (200 mg every week) or with Stanozolol (150 mg every week). This is very good pre-competition combo as well. The above combination allows us to construct a relief and build muscle without any additional fat-burners and guaranteed against side effects such as gynecomastia, and excessive estrogen.

In light athletics dosage is following: body weight in pounds divided by 10. For bodybuilders dosage is: body weight in kilograms divided by 1.5-2 (normally it’s 1.5 times more than your daily dianabol dosage).

Product could be applied once a day in the morning or split on two applications – morning and evening.

Stacking

It’s good for performance sportsmen, powerlifters or bodybuilders on cutting stacks. But if serious fat-burn needed, it won’t help because it’s a steroid, not pure fat-burner.

1) Turanabol 35 mg/ ED for three weeks at the end of Deca-Durabolin cycle to make a relief

2) Turanabol 50 mg/ED for 6 weeks with Parabolan Depot (200 mg / w) and / or :stanozolol: (150 mg /w) at the end of cycle for 2-3 weeks (possibly from the beginning of cycle)

3) Turanabol standalone cycle 50 mg/ED for 6 weeks. Lean mass / pre-competition stack.

4) During preparation stacks Turinabol is often combined with Trenbolone, Oxandrolone or :stanozolol:. Very good results are obtained by combination with testosterone propionate.

5) The combination of oral Turinabol + Oxandrolone is too weak, it can be recommended only for women.

6) You can use oral and injectable turinabol during mass-gaining cycle in various combinations, for example with testosterone, Nandrolone Decanoate or a combination thereof, instead of Methandrostenolone (Dianabol). It is recommended for those athletes who want to get quality muscles.

PCT is needed after most of these courses

Detection time

There is a big controversy on this matter. There are some sources, which tells that turinabol depot is detectable up to 18 months and oral turinabol is detectable up to 12 months in worst-case scenario. Some other people on the forums tell that 6-8 weeks in more than enough. However, we cannot understand where they all took such huge and unreliable numbers from. Doping tests rarely shows chlordehydromethyl-testosterone indeed and it was widely used in 60es and 70es so there is a good evidence that real detection times are much shorter. Most likely this mistake happened because athletes used some long-living substances like deca long with it. Or, maybe, these sources misrepresent turinabol with the same deca, we have seen some product descriptions, supposedly made for turanabol but after reading we understood they were just copypasted from deca descriptions, stupid, isnt’ it? Also, just as brain-storming: YES, it quickly leaves the body and not detectable in the urine tests, but probably modern blood tests can detect it for longer time, especially when using injectable turinabol.

So, it’s difficult to be absolutely sure, but we stick to the idea that Oral turinabol moves out of the body within 5-8 days after the end of cycle (if this was turanabol standalone cycle up to 100-150 mg/ ED) and any urine doping test shows negative results. Ok, if the risks of testing is too high and you are too nervous about it, discontinue turanabol 2 weeks before the contest to feel certain. 2 months is most likely sufficient evenfor injectable turinabol and sophisticated blood tests.

Another positive thing is that nowadays doping tests do not include turinabol at all, because it is considered to be a drug, which came out of usage after decease of Eastern Germany. Unfortunately, with its growing popularity one day it may change back as it happened with genabolom (norboleton) during Olympic Games 2000.

Side effects and PCT (Post Cycle Therapy) with Turanabol

Side effects of this drug depends on dosages or personal characteristics of an athlete. Women usually experience virilization side effects from prolonged use of the drug at dosages of above 20 mg per day. For men side effects occur very rarely as the estrogenic activity of the drug is quite low. Six weeks cycle makes no negative effects at all, nut normally one can use it even longer.

When doing 20 mg daily, endogenous testosterone production starts being suppressed after ten days. However, it goes down only to 60-70% (for instance dianabol suppresses it to 30-40%), which is the reason of quick rejuvenation afterwards. Just 5 days after the cycle is over, natural testosterone production normalizes. 7 days after the cycle, endogenous testosterone production may even become higher (!!!) than before the cycle.

High dosages of oral turanabol version may lead to increasing of liver values, thus some protection like Liv-52 is needed. However, this is not a case when using injectable turanabol.

Other side effects such as gynecomastia, water retention, high blood pressure, acne, gastrointestinal pain, and uncontrolled aggressive behavior are highly unlikely.

Increased libido during cycle occurs for both sexes.

PCT is not absolutely necessary if used standalone but desirable if used more than 20 mg daily. In this instance Clomiphene (Clomid) is preferred to Nolvadex (tamoxifen citrate). Do 3 tabs (150 mg) of Clomiphene for the 1st day after the cycle, and 2 tabs/ED for two more weeks (you may reduce to 1 tab/ED at the end of PCT)

Female usage

Oral Turinabol is relatively safe drug for women in dosages no more than 20 mg daily and if used for no longer than 4-5 weeks. According to many studies under such conditions it does not cause virilization effects.

Combination of oral turinabol + oxandrolone well suits for females.

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Trenabol

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TrenaJect / Trenbolone Acetate / Trenol-75 / Trenbolone Enanthate

Trenbolone is nandrolone derivative. It has several commonly used esters, trenbolone acetate is the most well-known, trenbolone enathate is the most soft for usage and very similar by it’s effects to Parabolan Depot (Trenbolone Cyclohexahydrobenzylcarbonate). This substance is very powerful Class I steroid with strong androgenic properties and no aromatization sides. Trenbolone acetate half-life is around one-two days. Also, it increases IGF-1 levels in the blood thus leading to muscle hyperplasia.

It’s important during pre-competition cycles. However, it shows fat-burn properties only with non-aromatized drugs like methenolone, oxandrolone or drostanolone and stanozolol.

Dosage and usage

A good dosage for the beginners and advanced users is 50 mg daily. For sportsmen who are 10 and more kgs. over natural limits preferred dosage is 100 mg daily.

Oral parabolan (Trenbolone cyclohexahydrobenzylcarbonate) dosage should be no less than 75 mg, preferably 100-125 mg.

Stacking

Trenbolone is not fat-burner but very strong androgenic anabolic steroid, which is three times stronger mg per mg comparing to testosterone. This is true, however, only to androgenic activities. To obtain good anabolic effects a Class II steroid such as Dianabol or Anadrol should be added to the stack.

Trenbolone has a unique property of effective standalone usage but it’s also well stacks with many other drugs, in such case dosage may be reduced accordingly. It’s mass-gaining effects are less than testosterone, so test is the first choice to stack for a bulking cycle. In veterinary trenbolone is often combined with estradiol for fast muscle growth. For definition, one should add stanozolol and exclude any aromatized drugs i.e. exclude estradiol.

Trenbolone + Dianabol / Anadrol (Anadrol 50 / Anapolon 50) or testosterone is for mass-gaining cycle

Trenbolone + drostanolone (Masteron) / :stanozolol: is for pre-competition (definition) cycle

Trenbolone Acetate detection times

5 months

Side effects and PCT (Post Cycle Therapy) with Trenbolone

Androgen-related sides like oily skin, aggressive behavior, acne and hair loss may occur.

17-alpha alkylated trenbolone version is called methyl-rienolone, it’s no longer manufactured due to extremely bad impact on the liver. Trenbolone acetate, enanthate and cyclohexylmethylcarbonate (parabolan) side effects are quite low.

Despite of some rumors, it has no negative effects on kidneys. Decrease in aerobic capacity is the most common complaint with Trenbolone acetate, it’s less visible with enanthate version.

There are reports of sexual dysfunction (which can be subsided if you stack Trenbolone with testosterone) and gynocomastia. Gynocomastia symptoms include bloating and an increase in breast tissue. On the opposite note, it’s not necessarily a great choice for women because it can have strong virilization effects on women.

It can also lower thyroid levels, so it’s important to take a T3 to minimize the effects of this. Coughs, insomnia and night sweats and decreased cardiovascular capacity are also common.

PCT is strongly recommended.

Female usage

If you are a woman, using tren is a horrible idea. Way too androgenic.

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Man Sexual Health – Titanic-K2 Capsule

Titanic-K2 is a herbal alternative of Viagra, with growing popularity over the world due to the lack of side effects and relatively cheap price. It is manufactured by Sun Laboratories (P) Ltd., India

One Titanic K2 capsule restores your loss vigor and vitality itself provides you complete sexual satisfaction. This does not cause any adverse effects its high quality ,this medicine and after using it, you shall find it more effective than what it sold for .We are of the firm belief that one Titanic K2 itself shall make you ,your own admirer.

Dosage

1 Capsule 2 hour before desire or as directed by physician. No more than one capsule per day.

Avoid intoxicants, allopathic sex stimulant and overeating while using this medicine

Contains

  • Withania Somnifera Extracts 240mg, Terminalia Arjuna Extracts 100mg
  • Asparagus adscendens Extracts 100mg, Crocus Staivus 50mg, Abhrak Bhasam (Rastantra Sar) 50mg,
  • Siddha MakraDhwaj Bhasam (Bhaishajya Ratnawali) 50mg,
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Number of Capsules 6

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Testosterone Propionate

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Testosterone Propionate, Testabol Propionate, PropioJect

General

Testosterone propionate is a common oil-based injectable testosterone. The added propionate extends the activity of the testosterone but it is still comparatively much faster acting than other testosterone esters such as Cypionate and Enanthate. While cypionate and enanthate are injected weekly, propionate is most commonly injected at least every third day to keep blood levels steady. For strength and muscle mass gains, this drug is quite effective.

With propionate, androgenic side effects seem somewhat less pronounced than with the other testosterones, probably due to the fact that blood levels do not build up as high. Users often report less gyno trouble, lower water retention and commonly claim to be harder on prop than with the others.

This however is still a testosterone and, as with all testosterone products, androgenic side effects are unavoidable.

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Testosterone Cypionate

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Testosterone Cypionate (CypioJect, Testabol)

General

Testosterone is the major and most important male androgen in the body, which carries many important functions, one of them is muscle growth. This makes testosterone the first steroid for bodybuilding. There is simply nothing more powerful. One may ask then – why other steroids still exist? The answer is that although testosterone is number one – it’s not ideal and still has certain disadvantages and different gear fill their own unique niches.

Cypionate aromatizes easily; like other testosterones do, making water retention a problem for many users. It is only moderately toxic to the liver but can cause a marked disturbance, in the body

One should be aware that when you cease using long-acting gear its effects as well as side-effects still take place for 3-4 weeks, so short-living forms are easier to watch and control.

Testosterone aromatizes easily (i.e. part of it is being converted to estradiol). But more important point is that besides estrogen testosterone easily converts to dihydrotestosterone (DHT) thus increasing its androgenic properties (action on the prostate, body hair growth, increasing libido, unfortunately DHT is almost inactive in muscle cells).

In simple words, when you take testosterone your existing muscle cells are growing by themselves and also they are producing new cells, which results in substantial muscle gains and increase in power. New muscle fibers normally appear when high dosages used. Besides this, there are also many other positive factors (general feeling of well-being, improved immune system, increased libido, etc.), as well as side effects, which we should consider.

The effectiveness of testosterone depends on the amount of certain enzymes in the body. For testosterone, as well as for nandrolone, a "critical" enzyme is a 5-Alpha-Reductase. Especially important this enzyme is for long-acting esters of both steroids. The increased amount of 5-Alpha-Reductase leads to accelerated conversion of testosterone to dihydrotestosterone (DHT). The latter is good for increasing libido, but not to build muscle. As you recall, in muscle fibers DHT is practically inactive (unlike in the skin and prostate). In addition, DHT is not so bad as anti-estrogen, but at high level this is not good for muscle gains (on one hand you try to kill estrogen to avoid side effects, on other hhand, estrogen helps to build muscle size). Therefore, testosterone and nandrolone are not ideal agents for athletes with elevated level of 5-Alpha-Reductase enzymes. How to find out your 5-Alpha-Reductase level? Either by taking special medical tests or by carefully watching your body reaction on different steroids

Dosage and usage

Inject every 5-7 days (more frequent shots will slightly increase the effect) , preferably into big muscles like upper leg or buttocks. Rotate injection spots to prevent inflammation.

Stacking

Testosterone is very powerful substance by itself to allow standalone cycles. So 500-1000mg of testosterone enanthate or cypionate (both are long-acting) will produce notable results over 8 or better 10 weeks cycle whether used in combo or standalone. 12 week stacks also often takes place since this product is non-toxic. Testosterone has so many different activities that other steroids serves merely as an additional supplement. However, stacking is necessary if athlete have serious goals. It helps to reduce the quantity of testosterone and thus negative side effects by adding some milder substances like Primobolan Depot (Methenolone Enanthate), Nandrolone Decanoate (Deca-Durabolin) or Boldabol (Equipoise).

Testosterone is in fact an ideal partner for any other steroid because of its action on androgen receptor in muscle cells and it’s possible to combine it virtually with everything. The best results, however, are achieved when testosterone enanthate is combined with Nandrolone Decanoate esters, Methandrosterolone or Anadrol/Anapolon (Oxymetholone). Combination of testosterone enanthate + Nandrolone Phenilpropionate + Methandrosterolone provides bulking "super action". Stacking of testosterone enanthate with Trenbolone or Boldabol (Equipoise) produces great results as well.

Common length of testosterone enanthate cycles is 8-10 weeks, sometimes 12 weeks.

A popular "mass" stack is 500 mg of testosterone enanthate / week + 400 mg of Nandrolone Decanoate (Deca-Durabolin) / week and strong PCT – you need anti-estrogen during and after cycle and you need to boost natural production afterwards.

For those who are looking for milder bulking stack – the same testosterone dosage in combination with primobolan 400-600 mg/week is an option. It makes cycle much safer although gains will be also lower because primobolan has lower anabolic properties comparing to deca, it’s main advantage is non-aromatization. As we already mentioned low estrogen level leads to lower mass gains although the gains you receive will be more lean and dry. Another disadvantage is high price of Primobolan. PCT and anti-estrogen are still needed as always with testosterone.

Third option is testosterone enanthate with Boldabol (Equipoise) 200-400 mg/week, which is stronger than deca (nandrolone) and has lower side-effects. This is still bulking stack, however, boldenone provides more lean and dry mass gains, which is similar to positive effects of primobolan, although much stronger. Furthermore, boldenone promotes appetite, which is often suppressed by usage of testosterone thus making your nutrition more effective.

As it was mentioned before, you can stack testosterone virtually with everything, but nandrolone, primobolan and boldenone are the best options for bulking cycles. As for other gear – you should consider what kind of effect they can add. For instance oxandrolone (anavar) will add some strength and might be used in pre-competition cycle when bulking is not necessary. If you are looking only for mass – you may simply increase testosterone dosages and no need to add other compound UNTIL side effects will prevail. Only after this it worth stacking (or if you are looking for milder cycle from the beginning). To explain this thought read following example. For instance, someone wants purely bulking cycle. He tried once, did 250 mg/week and was not satisfied with the results. What to do next time? Not ideal decision would be 250 mg of test in combo with 400 mg of deca. Ideal and simple decision 500 mg of testosterone /week. Another example, someone is looking for a moderate bulking cycle. Not too weak, not with a lot of side effects as well but rather something on the middle. A possible solution is 250 mg of testosterone/week and 200 mg of boldenone/week with PCT, of course. Hopefully you understood what author means.

Some other cycle examples

Nomal cycle:
500 mg testosterone enanthate/week +
Turanabol (Turinabol) or Anavar (Oxandrolone) 40-50 mg / day

Pre-competition cycle for advanced users, 8 weeks. Start with testosterone enanthate and testosterone cypionate 400 mg/week each, decrease smoothly to 100 mg on the last week. At the same time do Anavar (Oxandrolone) starting from 80 mg / day and decrease by 10 mg every week until you reach 10 mg/day on the last week. For amateur users dosages of testosterone starts 200 mg/week and fall down to 25 mg/w on the last week with the same dosage of anavar, although on my opinion this is extreme case.

"Super" stack for PRO:
Anadrol/Anapolon (Oxymetholone) 100-150 mg / ED for 8 weeks +
Nandrolone Decanoate (Deca-Durabolin) 400 mg/week for 7 weeks, decrease dosage on last two weeks +
Testosterone Enanthate 500-1000 mg (peak on the mid) for 10 weeks +
Testosterone Cypionate 400-800 mg / week (peak on the mid) +
Dianabol 50-20 mg on weeks 8-11.

Anti-estrogen is needed starting from week 2 or 3 till the end and HCG is needed on weeks 4-5 and 9-11, 5000 IU / week. Tamoxifen/Clomiphen is still needed after the cycle to boost natural hormone production, HCG will just smoothen this downfall.

Detection times

It has long detection time as most of testosterones, especially long-acting ones. Doping tests can find it up to three months after the cycle.

Side effects and PCT (Post Cycle Therapy) with testosterone Enanthate

Since testosterone is easily aromatized, its use in high doses may cause side effects such as water retention, acne, female-pattern fat deposits, and gynecomastia ("bitchy tits"). But for most athletes these problems start at high doses of the drug – from 1 gram (1000mg) per week or more. Therefore, it is advised to take some anti-estrogen like Arimidex (Anastrozole), Proviron (Masterlone), Tamoxifen (Nolvadex) or Clomiphene (Clomid). At dosages of 500-600 mg per week, side effects are normally low, but some people are more prone (more sensitive) to these side effects than others, so if problems arise, do 1 tab of :clomiphen: 50mg or tamoxifen 20mg until problem disappear.

The conversion of testosterone to DHT means a risk of such androgen-related side effects as baldness and prostate enlargement. Again, this only applies to high dosages or to the people with high level of 5-alpha-reductase enzyme.

The use of testosterone, even at doses of more than two grams (2000mg) a week not infringe either the liver or other organs. Recovery of natural testosterone production after a cycle is normally quick and successful.

PCT: 25-50mg of arimidex / day OR 25-50 mg of proviron / day during the cycle. Normally 25 mg is just fine but in case of "heavy" cycles dosages up to 100 mg of proviron might be required. Actually, it’s better to use Proviron (Masterlone) instead of Arimidex (Anastrozole) along with the testosterone injections since it increases volume of free testosterone in the blood thus promoting gains. Athlete should also consider the following thing – estrogen converted from androgen plays very important role in muscle gains. Thus, more anti-estrogen you use – there are less estrogen-related side effects but also less gains. So, you have to find experimentally what suits the best to your body. People who worry more about gains should use minimal dosage of anti-estrogen, people who worry more about estrogen level should use higher one.

Some people are more concerned about androgen-related side effects such as deep voice, baldness, prostate hypertrophy. These ones should do 1 tab / ED of a product named finasteride (brand names propecia, proscar, fincar, etc.), which blocks 5-alpha-reductaze and thus conversion of testosterone into more aggressive androgenic substance DHT. Again, one should find a balance. DHT is more powerful androgen, maybe 300% stronger than testosterone and it’s positive effects increases along with unwanted side effects. Also, keep in mind that if you are more concerned about androgen-related side effects, you should not use Proviron, which is in fact very similar to :DHT:. Better use Arimidex (Anastrozole) as anti-estrogen in that case.

As you may see, all these things – testosterone, dihydrotestosterone, estrogen and androgen levels, estrogen blockers, etc. are highly related and dependant on each other so there is no single advice for everyone, you should consider what is more important exactly for you and choose appropriate anti-estrogen and dosage basing on it.

When the cycle is over, natural testosterone production is severely suppressed and needs to be restored, otherwise much of gains will be lost and also you’ll have problems with libido and shrinkage of testicles, which is especially true for long cycles. Many bodybuilders of 70es, when steroid science was not so developed felt all these side effects and became big and fatty or small and tiny or had heart problems (heart is also a muscle) which leaded to all these horror stories and prohibition of steroids in many countries. Fortunately, now we all know how to make it safe. Using Human Chorionic Gonadtropin (HCG, Pregnyl) and Tamoxifen (Nolvadex) (nolvadex, cymoplex, cytotam) / Clomiphene (Clomid) (clomid, fertomid) plays key role in Post Cycle Therapy. Let’s say 40 mg (2 tabs 20 mg) of Tamoxifen equals 150 mg (3 tabs 50 mg) of Clomiphene). People still argue, what is more effective. Many people believe tamoxifen is better during cycle and Clomiphene (Clomid) is better after it. However, there are also opposite opinions, so if you are in doubts combine tamo+clom during PCT after the cycle is over.

One should start HCG injections on the last week of cycle and do 1500-3000 IU every 5-7 days depending on testosterone dosages during the cycle. HCG serves as an alternative to natural LH, it will boost testosterone production in the body thus restoring size of testicles back to normal. HCG should be used for 2-4 weeks in total. However, it does not eliminate the problem but serves just as a "bridge" between the cycle and post-cycle healers – Tamoxifen (Nolvadex)/Clomid. Although it "orders" to the body to start producing testosterone, this is not "natural" production. In fact it even suppresses natural production of the hormone, and usage of HCG should be stopped two weeks before you finish Tamoxifen (Nolvadex) / Clomiphene (Clomid).

Using HCG is strictly advisable, but if you don’t have it, just start with higher then described below clomiphene/tamoxifene dosages, let’s say 3-4 tabs/ED for two weeks.

Two weeks after the cycle (if HCG has been used) start doing 2 tabs of tamoxifen 20 mg or 3 tabs of clomiphene 50 mg or combination of both for two weeks. After this, do two more weeks with 1 tab of tamoxifen or two tabs of clomiphene daily.

A conclusion: Arimidex or Proviron fight estrogen during cycle, tamoxifen and clomid finish this job and also boost natural testosterone production. HCG helps to smoothen critical testosterone production downfall right after the cycle.

Female usage

Amazingly, in medical practice testosterone enanthate is widely used in treatment of females and even children with certain pathologies. The only common thing between all these people is low testosterone level in the blood.

But it is strictly not advisable for females with normal testosterone level to use testosterone injections for sport-related purposes. External testosterone will simply lead to virilization effects, so women in bodybuilding should stay away from it. There are different ethers like testosterone undecanoate, which fit well for them.

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Androgel (Testogel, Cernos gel, Testosterone gel sachets)

General

Androgel (Testogel, Cernos gel, Testosterone gel) by Bayer Schering comes in boxes containing 10 or 30 sachets 5 g each (50 mg of testosterone inside), totally  500-1500 mg of active substance.

Androgel is used for treatment of low Testosterone levels in men in easy and convenient way by replacing natural hormone. Such decease is called hypogonadism and it may have a serious negative impact on the quality of men’s life (especially elderly men) and are commonly associated with a decrease in libido, lean body mass and bone density, as well as an increase in visceral fat, and disturbances in well-being and mood. Transdermal 1% hydroalcoholic Testogel restores testosterone levels to normal range and had a statistically proven, significant positive effect on lean body mass and body composition.

Dosage and usage

Cutaneous use only. Androgel contains native Testosterone in a clear and colorless formulation which is absorbed by the skin within a few minutes after the morning application to the upper arms, shoulders and abdomen, without leaving any residue. The Testosterone passes from the gel through the skin and follows into the bloodstream at a steady rate. The recommended dose is 5 g of gel (i.e. 50 mg of testosterone) applied once daily approximately the same time to maintain steady level. The serum testosterone concentration remains very reliably within the normal range for 24 hours after application.

Even if toying with higher dosages, you should not aply more than 10 g per day. “More” is not always “better”. The adjustment should be achieved by 2.5 g of gel steps. The gel should be administered by the patient himself, onto clean, dry, healthy skin. Allow drying for at least 3–5 minutes before dressing. Do not shower for at least six hours after applying Testogel to make it fully utilized by the body.

Androgel helps to control the symptoms of your condition, but does not cure it. Therefore, you must use Testogel every day throughout the life. In general, testosterone-replacement therapy is indicated for all men over 40, starting from the small dosage and increasing with the age. However, one should do it only in accordance with doctor’s advice basing on proper tests. Some people may have sufficient endogenous testosterone levels for longer period of time, some others may still want to have a child, so use any medications including Testogel wisely.

Stacking

Hey, this is not for bodybuilding. No stacking, standalone usage is just fine for testosterone-replacement therapy.

Side effect and PCT

This is testosterone and Androgen-related side effects might be an issue in theory. However, due to weak action most of these effects are possible to neglect. However, prolonged use of testosterone containing products may result in aromatization process and thus estrogen related side effects such as growing breast and conversion to DHT reslting in destroying of hair follicles. Both of these processes are coming even naturally, that’s why many elderly men lost their hair and have “bitchy tits”  without using any testosterone. Possible answer to that might be using low-dosages of propecia (finasteride) and tamoxifen citrate.

It may lead to increasing hematocrit levels, which is not bad thing for stamina but dangerous because of increased blood viscosity, especially for elderly men.

Another possible and very important  side is decreased sperm count, which may affect fertility.

There are also some others, do not get frightened, this is just minor possibility, most of people do not experience anything of it.

Possible local side effects

  • erythema
  • acne
  • dry skin

Possible systemic side effects

  • prostatic disorders
  • gynecomastia
  • mastalgia
  • dizziness
  • hyper- and paresthesia
  • amnesia
  • mood disorders
  • hypertension
  • diarrhea
  • alopecia
  • polycythemia
  • increased serum lipids

Other known adverse drug reactions of treatments containing testosterone are:

  • prostatic changes and progression of sub-clinical prostatic cancer
  • urinary obstruction
  • pruritus
  • arterial vasodilatation
  • nausea
  • cholestatic jaundice
  • changes in liver function tests
  • increased libido
  • nervousness
  • myalgia and
  • during high dose prolonged treatment
  • electrolyte changes
  • oligospermia and priapism

Doping control

Athletes should note that the active substance, testosterone, may produce a positive reaction in antidoping tests.

Indications

Testosterone treatment for confirmed male hypogonadism. Not advisable to use in the sport, especially bodybuilding because it’s too weak component, better use injectable testosterones like sustanon with more effect for the same money.

Contraindications

Cases of known or suspected cancer of the prostate or breast, known hypersensitivity to testosterone or to any other constituent of the gel, skin conditions prohibiting the topical application of medication. Planning to have a children (usage must be ceased some months before it and proper PCT like clomiphene citrate used)

Androgel must not be used by children under the age of 18 years because it may destroy natural hormone production and woman due to high risk of androgen related side effects, especially masculinisation (virilization).

Special warnings and precautions

Exclusion of risk of pre-existing prostatic cancer, monitoring of the prostate gland and breast. Regular monitoring of serum calcium concentrations is recommended in cancer patients at risk of hypercalcemia (and associated hypercalciuria), due to bone metastases. Androgel may cause edema with or without congestive cardiac failure in patients suffering from severe cardiac, hepatic or renal insufficiency. In this case, treatment must be stopped immediately. Androgel should be used with caution in patients with ischemic heart disease. Testosterone may cause a rise in blood pressure and should be used with caution in patients with hypertension. Beside laboratory tests of the testosterone concentrations in patients on long-term androgen treatment the following laboratory parameters should be checked periodically: hemoglobin, hematocrit (to detect polycythemia), liver function tests. Androgel should be used with caution in patients with epilepsy and migraine as these conditions may be aggravated.

Androgel may quicken the growth of existing prostatic tumours and benign prostatic hyperplasia (enlargement of the prostate gland). It may also increase the risk of breast cancer in males. Before treatment, your doctor should conduct tests to check that you do not have existing prostate or breast cancer.

If you use Androgel over long periods of time, you may develop an abnormal increase in the number of red blood cells in the blood (polycythaemia) and thus increase blood viscosity. Take aspirin to treat this side effect, stronger oral anticoagulants are not needed unless prescribed by a doctor.

Testogel is not indicated for use in children and has not been evaluated clinically in males under 18 years of age. Pregnant women must avoid any contact with Androgel application sites. This product may have adverse virilizing effects on the fetus. Testogel is no treatment for male impotence or sterility. For further details refer to the package insert or contact your local Bayer HealthCare Pharmaceuticals organization.

You should leave a gap of 6 hours between applying Androgel and having intimate physical contact to prevent passing of the testosterone to the female. You should also wear clothing such as a T-shirt to cover the gel application area and/or have a shower or bath beforehand. You should also follow these precautions before coming into close contact with children. If a woman or child does come into contact with Testogel, thoroughly wash the area of skin exposed to the gel with soap and water.

Female usage of testogel

Not advisable due to the risk of masculinisation (virilization).

Storage

Keep Androgel in a cool dry place where the temperature stays below 25°C. Do not store it or any other medicine in the bathroom, near a sink, or on a window-sill. Do not leave it in the car. Heat and dampness can destroy some medicines.

Pharmacologically inactive ingredients

Carbomer 980, isopropyl myristate, ethanol 96%, sodium hydroxide, purified water.

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