Tuesday, August 30, 2016

News 12 Investigates: How Long Steroids Can Stay In Your System??


Edit: Shenzhen OK Biotech Technology Co., Ltd. (SZOB)    Date: Aug 30, 2016
Our own investigation a day after the District Attorney's office decides not to charge any Richmond County deputies with steroid abuse.
Sheriff Richard Roundtree says the deputies under investigation voluntarily submitted to a GBI drug test for steroids and none tested positive.
The deputies were tested for steroids about 40 days after the investigation started. But the question remains, would a steroid still show up on a drug test that much later?
"How long does an anabolic steroid stay in your system?" News 12's Christie Ethridge asked Georgia Regents Senior Athletic Trainer Tim McLane.
"That's a good question. 'Cause it depends on which ones you've used, what method of delivery you've used, how long you've cycled and used it," McLane said.
"It all depends" is the best answer we could get when it comes to finding out if a certain anabolic steroid would show up on a drug test at least 40 days after use.
In a news conference Monday, the Sheriff assured us it would."The steroids that were in question had a life cycle of up to 30 days, I'm sorry I mean 3 months or 90 days if not cycled. So, we were well within that time period that we felt comfortable that any traces would still be in their system," Sheriff Roundtree said.
In an interview with investigators, Brandon Paquette said he sold steroids to fellow deputies."Anywhere from 2-4 bottles each time being testosterone, winstrol, or equipoise," Paquette told investigators.The DA's findings name at least eight different kinds of steroids, either found in Paquette's car or mentioned in his interviews.
McLane says the 300 and 400 listed in the report naming the steroid "Testo-Ject C300" and "Teste-Ject 400" indicates how concentrated the steroid is. His pharmaceutical references show the ones listed there are much stronger than anything that would be used medically.
"Dose levels 100-200 mg/ml, so anytime you're starting to get up to 300-400mg/ml on some of those, those aren't even recommended therapeutic uses," McLane said.
All the deputies Paquette named volunteered to take a drug test, but it was 40 days after the investigation started.
Research shows some drugs like winstrol taken orally can cycle out in as little as three weeks.
"That's why it used to be a real popular oral form, because you could pee it out in three to four weeks," McLane said.
McLane says other steroids stay in your system for a long time.
As a general rule, he says injectibles get into your system quicker but stay there longer, whereas tablets taken orally take longer to get absorbed but are flushed out faster.
He says, as a guess, a drug screen would probably show something for most steroids, even 40 days later.
"That stuff stays in your system a long time. Think about what its purpose is. It's there to produce growth in different organs and stuff in the body, so it's there for a while," he said.

Monday, August 29, 2016

How Previous Steroid Use Could Give A Boost For Entire Athletic Career

Co., Ltd. (SZOB)    Date: Aug 29, 2016
     
They were caught doping. Now they’re clean. Should athletes who have used performance-enhancing drugs be given a second chance?
Leading up to his widely anticipated faceoff against Usain Bolt in the men’s 100-metre final on Sunday, U.S. sprinter Justin Gatlin, who has twice been caught using banned substances, defended his participation in the Rio Olympics.
“At the end of the day, I’ve served the time,” Gatlin, who was suspended for four years for having elevated testosterone levels in 2006, told the Associated Press. “I’ve dealt with that punishment. I’ve moved forward.”
But even when athletes quit cheating, the effects of doping can have long-lasting consequences that extend beyond the damage to their reputations. According to experts who study muscle physiology, the use of anabolic steroids may lead to changes in the body that last for the duration of one’s athletic career, and potentially even a lifetime.
The critical issue is how anabolic steroids (of which the most commonly used by athletes is a synthetic form of testosterone) affect what’s known as muscle memory. Muscle memory is believed to be the reason why people who work out seem to bounce back quickly in fitness, regaining muscle strength and size, even after taking a break. There are a few possible explanations for how it works.
Unlike other cells in the body, muscle fibres don’t divide, explains Stuart Phillips, a professor in the department of kinesiology at McMaster University in Hamilton. Rather, they rely on a population of cells, called satellite cells, that help regenerate and repair muscle fibres.
Anabolic steroids spark a dramatic surge in these satellite cells, says Phillips, who is the Tier 1 Canada Research Chair in skeletal muscle health. “It really switches them on,” he says. “You become very, very efficient at repairing your muscles. So people who take steroids are able to tolerate higher volumes of work, they’re able to put muscles under greater stress, and then recover much faster.”
Once they increase in number, these satellite cells remain for a very long time, effectively for the rest of an athlete’s career, Phillips says. Thus, he says, unlike other banned substances such as stimulants, which provide a boost that lasts only as long as the drug stays in the body, anabolic steroids continue to give athletes an advantage over their competitors, even years after they’ve stopped doping.
“If you’re caught taking anabolic steroids, I think it should be a lifetime ban,” he says.
At the University of Olso, physiology professor Kristian Gundersen also believes doping has an enduring effect on muscle memory, but he suggests another mechanism is at work. Most cells in the body have only one nucleus, which can be thought of as the command centre of a cell. But muscle fibre cells have multiple nuclei, Gundersen explains. Each nucleus can only serve a certain volume of muscle, so when you’re trying to build more muscle, your satellite cells help deliver more nuclei to the muscle fibre, he says. Thus, having more nuclei means having a greater ability to grow bigger and stronger muscles.
Once they’re there, Gundersen says, these extra nuclei remain in the muscle. And that’s where anabolic steroids provide a long-term advantage.
In a 2013 study on female mice, Gundersen and his team found even brief exposure to the anabolic steroid testosterone propionate allowed the rodents to regain muscle mass far more quickly months afterward, compared with those that never received the steroids.
Even though the rodents’ muscles shrank back to normal when the researchers stopped administering testosterone, three months later, a period Gundersen suggests may be roughly equivalent to 15 years in human terms, the mice that received testosterone showed 30-per-cent growth in muscle after six days of strength exercise. Those that weren’t given testosterone had 6-per-cent growth.
Although this research was done on lab animals and with a “highly artificial procedure,” Gundersen says, “the mechanisms are very basic, and I would be very surprised if it wasn’t similar in humans.”
He notes other research on humans indicates the half-life of muscle cell nuclei is at least 15 years.
Gundersen adds this effect on muscle memory may not only have implications for banned substances in sports, but also for transgender athletes. The International Olympic Committee adopted new guidelines early this year to allow transgender athletes to compete without undergoing sex reassignment surgery, which they were required to have had under previous guidelines.
“When it comes to strength-related types of competitions, I think one has to be very careful,” Gundersen says. Even if trans female athletes no longer produce testosterone, he suggests, they may still have muscle memory. “I think it’s not unlikely that they will have an advantage.”

Friday, August 26, 2016

Oral Nandrolone Phenylpropionate NPP Durabolin Powder CAS 62-90-8

Oral Nandrolone Phenylpropionate NPP Durabolin Powder CAS 62-90-8

Quick Detail:
Nandrolone Phenylpropionate
Ordering notes: 10g sample, 100g mimimum order
Trusted steroid powder source:Shenzhen China
Leading supplier:Top quality steroid legit source at Shenzhen Shijingu
Cas number:62-90-8
Trusted oringin: Shenzhen China
Molecular formula is C28H44O3
molecular weight 424
Melting Point (base): 122-124C
Purity:99.18%
Drug Class: Injectable steroid, bodybuilding steroid, bulking steroids
Character:White Or White-off Crystalline Powder
Oil-based injection: 200mg/ml, 250mg/ml, 300mg/ml
Effective Dose (Men): 200-600mgs/week (2mg/lb of Bodyweight)
Effective Dose (Women): 50-100mgs/week
Description:
Nandrolone phenylpropionate is one of the most popular injectable steroids. It is basically Deca, with a shorter ester ( phenylpropionate instead of decanoate ester found in deca durabolin or nandrolone decanoate), resulting in quicker release into the bloodstream. Although its shorter ester means it will require more frequent injections than decanoate, the positive side is that the amount of effective nandrolone in the blood and its levels are more easilly contollable. It's popularity is likely due to the fact that nandrolone exhibits significant anabolic effects with minimal androgenic side effects.
Applications:
Below are some example cycles using
Testosterone/Deca/Dianabol is a superb combination with this goal in mind, two examples of which are shown below:
(Novice)
Testosterone (Enanthate/Cypionate/Sustanon) 500mg pw, weeks 1-11
Deca 400mg pw, weeks 1-10
Dianabol 25mg ed, weeks 1-4
(Intermediate)
Testosterone (Enanthate/Cypionate/Sustanon) 750mg pw, weeks 1-11
Deca 600mg pw, weeks 1-10
Dianabol 35mg ed, weeks 1-4
Due to the sometimes excessive water retentive properties of Dianabol, it makes it a poor choice of
 compound in cycles 
where the user is looking to shed fat. Cardiovascular activity will feature heavily during periods of cutting 
and these 
endeavours will be greatly hampered by the water retention and the painful 'pumps' that often ensue
Competitive Advantage:
We have enough stock, so we can delivery in time when receive the payment
Special disguised packages
The most professional express
Favorable prices
Efficient After-sale service
Rich experience and various safety routes for you to choose

Wednesday, August 24, 2016

Gym steroid use has impact on memory

Gym steroid use has impact on memory

People using anabolic steroids to improve muscle growth and sporting performance are far more likely to experience issues with their memory, according to new research from Northumbria University.

In some specialist gym user groups -- such as bodybuilders and weightlifters -- it is estimated that as many as 38% take steroids. Dr Tom Heffernan from the University's Department of Psychology therefore aimed to examine whether the long-term use of high doses of anabolic-androgenic steroids within a sporting context might affect everyday memory.

He assessed almost 100 males aged 18-30 who were regular gym users. Half of the group used steroids and half did not.

The results, which are published in The Open Psychiatry Journal, revealed that those using steroids had significantly more deficits in their prospective and retrospective memory functioning, as well as their mental executive function, compared to non-users.

Steroid users were 39% more forgetting in terms of prospective memory -- the process of remembering to do something you had planned to do in the future, such as remembering to pay a bill before it is due or to take medication at a certain time.

They were also 28% more forgetting when recalling past memories or previous facts, known as retrospective memory, and demonstrated a 32% difference in their mental executive function compared to non-users. Executive functioning is a term used to describe a number of cognitive processes that help an individual to pay attention, coordinate information and plan and execute tasks. A compromised executive function is likely to lead to confusion and poor planning, while reduced prospective memory ability leads to forgetfulness.
While a previous study from Harvard University found deficits in visuo-spatial memory in long-term steroid users, this is the first study to explore the impact that steroid use in a sporting context has on memory for everyday activities.

Dr Heffernan explained: "The non-medical use of anabolic-androgenic steroid use came to the forefront in the 1960s when elite athletes and bodybuilders used the drugs to promote muscle growth and improve performance levels. Since the 1980s many millions of individuals worldwide have used such steroids in a sporting context, which has now become much more widespread within non-competitive recreational sports circles.

"Overall the health-related risks of long-term steroid use are fairly well documented but we know much less about what the everyday consequences of their use may be.

"Our findings suggest that long-term use of anabolic-androgenic steroids has a significant impact on an individual's everyday memory and ability to remember. This could affect many spheres of life, including interpersonal, occupational, educational and health-related aspects, given the ubiquitous nature of everyday remembering.

"This, combined with the work of Professor Pope at Harvard, should provide the impetus for much needed future work in this area."

The paper, titled "Everyday memory deficits associated with anabolic-androgenic steroid use in regular gymnasium users" is published in the latest edition of The Open Psychiatry Journal and can be found online 


Tuesday, August 23, 2016

Deca-Durabol / Nandrolone Decanoate / Durabolin 200mg/ml DECA 250mg/ml Raw Gear Bulk Anabolic Steroids

Deca-Durabol / Nandrolone Decanoate / Durabolin 200mg/ml DECA 250mg/ml Raw Gear Bulk Anabolic Steroids

STEROID NAMES: Deca Durabolin, Decabolic, Hybolin Decanoate, Nandrobolic, Neo-Durabolic, Retabolin, Nandrolone decanoate, Deca-Durabolin, Decabolic, Deca 100, NandroJect 100
ACTIVE SUBSTANCE: Nandrolone decanoate
Description:
While Deca, as it’s often simply called can be used when dieting, bulking is and will always remain its primary purpose but to truly reap any reward use must necessarily remain long in duration; if you recall this is one very slow acting steroid. Most will find 8-12 weeks to be the minimal with 12 weeks being far more optimal and16 weeks of total use being the best but it is recommended you start with 8-12 weeks to ensure you react well; however, most all will find this to be a very well-suited and highly well-tolerated anabolic steroid. Even so and it is often out of fear of the unknown, many will supplement with Deca-Durabolin for very short periods of time but remember,
as it takes a good 4 weeks to really see any results these short bursts of use will almost always prove to be useless.
There is truly no set in stone dosing for this hormone; therapeutic dosing can range and vary quite a bit but most will find 100mg per week to be enough to see joint relief associated with the hormone and 200mg per week to be the minimum dose if one desires any type of noticeable anabolic effect. While 200mg per week will assuredly provide growth most will find 400mg per week to be far more optimal and generally a well-tolerated dose; yes, you can go higher but remember it is important to keep your testosterone in-line and increase the testosterone accordingly with the increases of Deca. For those that want more of a bump 600mg per week can be used safely but this dose in some has proven to be a little harsh and is not recommended for any beginner; most beginners and even many veterans will find 400mg per week to be all the Nandrolone they ever really need.
Recipe for DECA 160mg/ml @250ml
40 grams Nandrolone Decanoate
162.5 ml sesame oil
12.5ml BA 5%
37.5ml BB 15% 
Recipe for DECA 50 ml @ 200 mg/ml 
10 grams Nandrolone Decanoate
32.50 ml sesame oil
2.5ml BA 5%
7.50ml BB 15%
1. Raw Steroid Powder
Testosterone enanthate, Testosterone propionate, Testosterone cypionate, Testosterone Sustanon, Nandrolone Decanoate, Trenbolone Acetate, Trenbolone Enanthate, Boldenone Undecylenate, Drostanolone Propionate, Methenolone Enanthate, Oxymetholone, Oxandrolone, Stanozolol, Dianabol, Tamoxifen Citrate, Sildenafil citrate
2. Injectable steroids as below.
Test prop        100mg/ml      200mg/ml 
Test e             250mg/ml      300mg/ml     400mg/ml       500mg/ml    600mg/ml
Test cyp          200mg/ml      250mg/ml     300mg/ml
Sustanon         200mg/ml      250mg/ml     300mg/ml       400mg/ml    
Deca               200mg/ml      250mg/ml
Equipoise        200mg/ml      300mg/ml
Tren ace         100mg/ml       200mg/ml
Tren en          100mg/ml       200mg/ml 
Masteron        100mg/ml       150mg/ml
Primobolone   100mg/ml
Supertest        450mg/ml    
Anomass        400mg/ml  
Ripex             225mg/ml  
Tritren           180mg/ml

Prenatal steroids reduce risk of brain bleeding in preemies, Stanford study finds

Prenatal steroids reduce risk of brain bleeding in preemies, Stanford study finds

Prenatal steroid treatment reduces by half a premature baby's risk for a severe form of brain hemorrhage after birth, a study from the Stanford University School of Medicine has found.

The research, on nearly 26,000 premature infants, demonstrated that the benefit applies even to the earliest born preemies, who can be overlooked as potential candidates for this steroid treatment.

The study will be published online March 24 in the Journal of Perinatology. The senior author is Henry Lee, MD, assistant professor of pediatrics. The lead author is Julia Wei, who was a graduate student at the University of California-Berkeley School of Public Health when the study was conducted.

The researchers evaluated steroid treatments that were originally developed to mature fetal lungs before premature birth. Studies from the 1990s and early 2000s suggested that these steroids also protect preemies' brains, but the Stanford team was unsure if the benefit held in the context of modern neonatal care. The team also wondered about extremely premature babies, a population that had not been enrolled in the original clinical trials evaluating the effects of steroids on lung maturation.

"When steroids first came out, they were being used only in babies born at 26 weeks of pregnancy or older," said Lee, who is also a neonatologist at Lucile Packard Children's Hospital Stanford and Stanford Children's Health. "But we've now been able to show that even in babies born as early as 22 to 24 weeks, steroid treatment has a very strong benefit for the brain. This may expand the group of babies we would recommend using steroids for."

Potentially fatal hemorrhages
Current recommendations from the National Institutes of Health suggest giving steroids to mothers likely to deliver between 24 and 34 weeks of pregnancy, Lee noted.

The study evaluated intraventricular hemorrhage, in which bleeding occurs in the spaces around the brain where cerebrospinal fluid normally circulates. Intraventricular hemorrhages can increase the risk of death, and babies who survive them may develop neurologic problems such as hydrocephalus, cerebral palsy and mental retardation.

The researchers analyzed data on 25,979 infants born between 2007 and 2013. The data were drawn from the California Perinatal Quality Care Collaborative, which collects information about nearly all California births for preterm neonates. Infants were included in the study if they arrived between 22 and 32 weeks of pregnancy and weighed less than 3.3 pounds at birth. A normal pregnancy lasts 40 weeks.

Among the infants studied, 87 percent were born to mothers who received steroids in anticipation of a premature delivery. The risk of all types of intraventricular hemorrhage was one-third lower in babies of mothers who received prenatal steroids than in those whose mothers didn't receive prenatal steroids. For the most severe forms of IVH, the risk was cut in half. The drop in risk was statistically significant for babies born between 22 and 29 weeks of pregnancy, but not for those born at 30 weeks or later, the study said.

"We speculate that steroids may accelerate the maturation of blood vessels in the brain and make them stronger," Lee said. "That may make the baby less vulnerable to rapid shifts in blood pressure, which could otherwise cause bleeding similar to a stroke."

Condition now less common in preemies

The rate of intraventricular hemorrhage in premature babies has declined since the 1980s, Lee noted. "That change is probably not due to only one thing, but more to our overall awareness of how to take better care of the baby before and after birth," he said. For example, in addition to using prenatal steroids more often, doctors and nurses also keep premature babies' heads in a stable position during the first few days of life, and attempt to avoid dramatic shifts in preemies' blood pressure.

"It's helpful to know that prenatal steroids are an impactful component to our strategy to prevent these potentially devastating hemorrhages," Lee said. He thinks the new finding will be welcome news not just for other physicians but also for the parents of preemies.

"When I talk with these parents, I'm often describing risks and potential complications for their baby," he said. "It helps to be able to talk not just about risks but also about proven therapies -- to say, 'Here is a therapy that we have found to be very beneficial.'"

Monday, August 22, 2016

Human Growth Hormone

Human Growth Hormone

How to Use Human Growth 
Hormone (hGH) for Fat Loss
trenbolone-www.ok-biotech.comQ:“How can I use GH for fat loss? How about for mass gain, and what would be the differences if any in use?”
A: The first consideration really in GH use for fat loss is dosage. Individual tolerance of GH can vary widely, but broadly speaking, most can use up to 14 IU total per week without development of neuropathy (numbness, weakness, or pain from nerve compression due to growth of cartilage.) Some can tolerate much more, a few cannot tolerate even this amount. So far as I know everyone can tolerate at least 7 IU per week, and nearly everyone 10.5 IU/week, or an average of 1.5 IU/day.
As might be expected, the higher the weekly dose the greater the benefit on fat loss.
There’s a wide range of theories on timing of doses. I’m not persuaded by any of them and have seen good results from any of a wide range of methods. My inclination is that best results are from at least 1x/day per use, rather than for example taking 4 IU every two days. However, difference in fat loss results from individuals, or differences in the same individual at different times, are large enough and the difference between protocols seems small enough that I won’t insist that the at-least-daily use is better for fat loss. It does seem so to me, however.
I don’t think there’s importance in GH timing with regard to meals. Morning may be better than evening or later in the day due to possibly providing less suppression of natural GH production; at any rate results seem a little better this way. If wishing to time the injection after a workout, this also is a well-proven method.
If wishing to be in best condition by a particular date, it usually proves acceptable to increase dosage by 50% in the two weeks before that date. While that dosage may be above the acceptable long-term dosage, the time period is short enough that neuropathy usually doesn’t develop, and if it does it will prove reversible, again due to the short time period.

Thursday, August 18, 2016

Oral Turinabol CAS: 2446-23-3

Oral Turinabol

Oral Turinabol CAS: 2446-23-3


Oral-Turinabol (dehydrochloromethyltestosterone) is an oral anabolic steroid which is interesting principally for reasons other than its unexceptional performance. It can however meet some specific needs.

What Is Oral-Turinabol?

Oral Turinabol is, to some extent, enigmatic and prone to misunderstanding.

It is not simply a tablet version of injectable Turinabol, or an alkylated version of it. Nor, despite claims, is it an anabolic steroid developed specifically for doping. That claim results from confusion with mestanolone.

Structurally, it is Dianabol with an added chlorine at the -4 position, which has the predictable advantage of preventing aromatization.

Caution must be taken however when trying to arrive at conclusions about anabolic steroids from structure. Substituting an atom or chemical bond makes large changes to the entire shape rather than affecting only a single point. This can result in changes in properties beyond the predictable. An example would be if one tried to predict the properties of Dianabol from its structural relation to boldenone (they are the same except for the 19-methylation of Dianabol.) While the methylation does provide the predictable oral bioavailability, in actuality Dianabol’s other properties are such that one can’t reasonably call “oral boldenone.”

In the case of Oral Turinabol, due to the above structural relation to Dianabol it’s commonly called a dry version of it. Now if this were true though, one could tell no difference between using OT alone and using Dianabol plus aromatase inhibitor. There is considerable difference in practice however.

OT must be considered its own compound rather than simply as a dry Dianabol. That said, this popular description is not a bad first approximation. Simply be aware of its limitations.

History Of Oral Turinabol

Ordinarily in anabolic steroid profiles I don’t discuss history of the drugs, but here it’s worth making an exception.

OT received an East German patent in 1961 and was soon approved as a prescription drug. At the time, there was wide medical belief that anabolic steroids were useful for recovery from surgery, burns, or nearly any condition that caused substantial loss of bodyweight. Newly developed anabolic steroids were considered suitable even for women and children, as it was thought that synthetic modifications dissociated androgenic from anabolic effects.



In 1966, use of OT for athletic doping began. This drug became the principal cause of the obvious virilization of East German female athletes of the era, despite the theoretical belief in separation of effects. Women did not respond as the theories from rat testing had predicted.

Why did the East Germans choose this specific compound for athletic doping? The reason does not seem to be from superior performance to Western anabolic steroids, or from drug testing concerns. That did not become an issue until much later. And a particularly favorable side-effect profile seems unlikely as the reason, as no other anabolic steroid has such a thoroughly documented track record for adverse effect on health.

A key doping advantage of OT for the East Germans was that it was locally produced. This provided easy availability, economy, and secrecy. And it was effective enough, especially for female athletes (but then again, every anabolic steroid is.)

The fact that its bad side effect profile made it quite harmful to the athletes was irrelevant to the East German Communist regime. Many lives were destroyed, at least in the judgment of the unknowing female doping victims.

Why mention all this? First, this history has created a mystique, whether warranted or not. And second, it has provided us with a great deal of toxicological information. Last, one should be sure that if choosing the drug, the decision is not simply from the mystique. Being the old East German doping drug of choice should be irrelevant to whether an athlete or bodybuilder should choose it today. Instead it should be considered in terms of its positive and negative effects. Among available anabolic steroids, OT offers nothing outstanding here, though it’s certainly usable.

Dosing Of Oral Turinabol For Men

When Oral Turinabol is used in an anabolic steroid cycle, less than 20 mg per day will be an almost unnoticeable addition to a stack, or will be a very weak cycle if used alone. There is little point in exceeding 50 or 60 mg/day, as added anabolic effect will be small if any. And adverse side effects of excessive muscle pumps and/or blood pressure elevation are often at a tolerance limit at this point, while becoming excessive past it.

I don’t recommend combining OT with other oral anabolic steroids. Instead, when using OT and wishing to increase anabolism, one or more injectables should be added rather than another oral. A sufficient reason for this is that results are much better from combining an injectable rather than any other oral (with possible exception of oxandrolone.) Another reason is that at effective doses of OT, hepatotoxicity is already as high as can be considered reasonable. Another alkylated steroid should not be added.

Still another reason to not combine OT with other oral anabolic steroids in a stack with injectables is this: If Dianabol or Anadrol are included in the stack, then there’s no reason to also include OT. It will do nothing anabolically that they will not.

Oral Turinabol can be used alone with significant results for novice steroid users or for experienced users who have experienced losses and are regaining. However in general I don’t recommend oral only cycles, and this is no exception.

When using OT, dosing is preferably divided to twice per day, although once per day is acceptable.

Oral Turinabol For Women?

East German female athletes took OT at 5-15 mg per day for two to six weeks at a time. Aside from obvious virilization, many of these female athletes also suffered liver disease, heart disease, infertility, psychiatric issues, and even death. Oral Turinabol is proven not to be a safe anabolic steroid for women. I am not saying these consequences are inevitable, but rather that it’s a proven fact that the incidence rate of such consequences is very substantial.

Risk will exist for some women at doses less than 5 mg/day as well.

Nearly any anabolic steroid is better choice for women than OT.

Summary

Oral Turinabol is of interest mostly for its history, not its performance. When chosen, dosing range should be 20-60 mg/day, taken either once per day or preferably twice. It is usable by men, although there are better choices. OT is a very poor choice for women.


Wednesday, August 17, 2016

Cialis (Tadalifil)

Cialis (Tadalifil)

Cialis (Tadalafil) CAS: 171596-29-5


Cialis (Tadalifil citrate), a phosphodiesterase type 5 inhibitor, is used to treat erectile dysfunction (ED) and decreased libido in males.  Cialis works by aiding relaxation of blood vessels and increasing blood flow in the penis during sexual arousal, resulting in improved erectile function.  Cialis is much longer lasting than Viagra.  Effects can be felt anywhere between 36-48 hours.

Background

The FDA approved Cialis as a medicine for ED on November 21, 2003. It is available through prescription for those who are diagnosed with impotence.  In 1998, ICOS Corporation, and Eli Lilly and Company, began manufacturing Cialis, which is available orally in 5mg, 10mg and 20mg tablets.  It is also widely available by many research companies and underground labs.

Action

Tadalafil improves erectile function significantly, possibly increase testosterone through increased sexual activity, and is very safe.

There are limited side effects associated with its use.  The most common side effects are headache, upset stomach, back pain, and muscle aches, and usually subside with in a few hours.

Technical Data

In a six month study on men with erectile dysfunction ranging from mild to severe, 20 mgs of Cialis or placebo was administered to subjects as needed.  It was discovered that Tadalafil improved ED compared to placebo.  Ability to achieve erection and sucessful intercourse was 73% greater in those reciving Cialis verses the placebo group (1). Cialis was administered three times per week for an extended period of time, it was found to be extremely safe and very limited side effects were experienced, if any (1).

Cialis was also linked to increased testosterone levels in a one month study where testosterone levels were found to be significantly higher at the end of the month, due to increased sexual activity(2).

User Notes

How ironic. Some of the compounds which can be used to make men more physically attractive to women (Deca, Tren, etc…) can cause sexual dysfunction. Even more ironic is that many of the compounds which make them more attractive to us (Beer, Whiskey, etc…) can also do this.

Cialis is useful for these occasions…or during PCT when sexual dysfunction may occur.

Tadalifil citrate is the chemical name of active ingredient in Cialis. Cialis is a registered trademark of Lilly ICOS LLC in the United States and/or other countries.

References

1.A 6-month study of the efficacy and safety of tadalafil in the treatment of erectile dysfunction: a randomised, double-blind, parallel-group, placebo-controlled study in Australian men. Int J Clin Pract. 2005 Feb;59(2):143-9.
2.Type V phosphodiesterase inhibitor treatments for erectile dysfunction increase testosterone levels. Clin Endocrinol (Oxf). 2004 Sep;61(3):382-6.



Tuesday, August 16, 2016

Trenbolone will be soon used for hormone replacement therapy

Trenbolone will be soon used for 
hormone replacement therapy
Trenbolone is a steroid that is taken by bodybuilders for many years. Unfortunately, this drug has never been considered to be an effective drug for clinical purposes. It isn't approved for human usage by the U. S. Food and Drug Administration (FDA). Trenbolone has been demonized many times by media. A lot of articles have announced that this medication is quite dangerous. 
But recent studies have shown opposite facts. It is supposed that common attitude to this medicine can be soon changed. 
Joshua Yarrow and his colleagues from the University of Florida claim that this medicine can be taken as testosterone for hormone replacement therapy. The experts point out that it is an appropriate alternative preparation to testosterone for the purpose mentioned above. Results of studies conducted by these experts have been published in the American Journal of Physiology – Endocrinology and Metabolism. 
Moreover, the specialists assure that trenbolone enanthate has even some priorities over testosterone for certain persons. Bodybuilders know and support the statements linked with this product. It is known that testosterone aromatases. As for trenbolone, it is turned neither to estradiol, nor to dihydrotestosterone (DHT). That's why trenbolone doesn't lead to unwanted symptoms related to estrogen and DHT. 
Joshua Yarrow says about the studies led by him and his colleagues. Castrated rats have been given trenbolone enanthate. Even reduced dosages of this medication have enhanced their muscle size and kept bone mineral density. There have not seen such side reactions, as prostate enlargement or polycythemia in these lab rats. 
But too increased dosages of testosterone enanthate were required to cause the same anabolic effects in muscles as were caused by reduced dosages of trenbolone enanthate. But such negative consequences, as enlargement of prostate and increased hemoglobin accompanied the increased measures of testosterone enanthate. It is supposed by the researchers that trenbolone acts like selective androgen receptor modulators, causing anabolic effects in muscles and bones without androgenic adverse reactions. 
Professional competitive bodybuilders prefer taking trenbolone several weeks before competitions because it causes fat loss. Moreover, the studies have shown that the same measures of trenbolone have stronger lipolytic effects than those of testosterone. It has been determined that more trenbolone a person administers, the greater the fat loss is produced. 
Since trenbolone lacks aromatization, it is commonly taken together with such steroids, as testosterone, Dianabol or with another aromatizable steroid. The lack of aromatization leads trenbolone to disability to be used alone for testosterone replacement therapy. The non-aromatizable characteristic of this medicine is responsible for just partial protective effect of bones. 
Nevertheless, it is possible to make conclusion that additional studies are needed in order to apply trenbolone for hormone replacement therapy.