Clomiphene citrate raw powder: Is it possible to get pregnancy fast by Clomiphene citrate?

 

 

What is Clomiphene citrate?

Clomiphene citrate is a non-steroidal fertility medicine. It causes the pituitary gland to release hormones needed to stimulate ovulation (the release of an egg from the ovary).

Clomiphene citrate is used to cause ovulation in women with certain medical conditions (such as polycystic ovary syndrome) that prevent naturally occurring ovulation.Clomiphene citrate may also be used for purposes not listed in this medication guide.

You know: Clomiphene citrate mechanism of action

Clomiphene citrate was recently reclassified as a selective-estrogen receptor-modulator (SERM) due to its ability to compete with estradiol for estrogen receptors at the level of the hypothalamus. Clomiphene citrate blocks the normal negative feedback of circulating estradiol on the hypothalamus, preventing estrogen from lowering the output of gonadotropin releasing hormone (GnRH). During Clomiphene citrate therapy, the frequency and amplitude of GnRH pulses increase and stimulate the pituitary gland to release more FSH and LH. In turn, FSH and LH stimulate the ovaries to develop oocyte follicles. Clomiphene citrate may allow several oocytes to develop to maturity in some patients. Estrogen produced by the maturing follicles causes the cervical mucus to thin and the endometrium to proliferate. As the estradiol from these follicles rises, the positive feedback to the pituitary causes the FSH/LH surge and is followed by mature oocyte release (ovulation). Once ovulation occurs, the corpus luteum forms, and progesterone levels rise as they do in a regular ovulatory cycle, and prepare the endometrium for implantation. Clomiphene citrate must be used before the time of normal selection of the dominant follicle in an ovulatory cycle. The "traditional" timing of Clomiphene citrate treatment is from follicular phase cycle day 5 through 9; women typically ovulate 5—10 days after the last dose of the cycle. However, earlier initiation of treatment, longer courses (i.e., up to 10 days), or higher Clomiphene citrate doses may be needed dependent on the ovulatory response of the individual woman.

Clomiphene citrate is also a weak estrogen-agonist and may interact with estrogen-receptor containing tissues, including the ovary, endometrium, vagina, and cervix. In the cervix, Clomiphene citrate can interfere with the ability of cervical mucus glands to produce thin secretions that favor sperm motility and conception. In some women, Clomiphene citrate may induce dry, thick cervical secretions. Studies are ongoing to assess the activity of Clomiphene citrate on breast tissues. The estrogenic effects of Clomiphene citrate are secondary to the primary effects on hypothalamic-pituitary-ovarian function. Clomiphene citrate exhibits no androgenic, anti-androgenic, or progestational effects, nor does it affect pituitary-thyroid or pituitary-adrenal function. After Clomiphene citrate therapy discontinuation, there is usually no continued pharmacological effect on subsequent menstrual cycles. However, in some females, spontaneous ovulation has continued.

In selected female patients, Clomiphene citrate therapy is augmented by other medications to increase the occurrence of successful ovulation or pregnancy. These medications have included: dexamethasone for hirsutism or hyperandrogenism; estradiol to offset the cervical mucus-thickening effect of Clomiphene citrate; human chorionic gonadotropin (HCG) to induce the LH-surge for ovulation; and the use of metformin or troglitazone to offset the hyperinsulinemia that occurs in some patients with polycystic ovaries. Octreotide has been used as an adjunct to Clomiphene citrate therapy in patients with polycystic ovaries in order to reduce androgen secretion, decrease LH levels, and potentially decrease the incidence of ovarian hyperstimulation. The mechanisms of action of these drugs are distinct from Clomiphene citrate and do not appear to change the pharmacokinetics of clomiphene treatment. The regimens of each of these augmenting medications requires careful monitoring and timing of administration under the prescription of a healthcare professional experienced in fertility and endocrinology.

In men with idiopathic oligospermia, Clomiphene citrate may be effective at stimulating GnRH release from the hypothalamus, thus increasing the levels of LH and FSH released from the pituitary. LH and FSH then apparently stimulate the testicles to produce testosterone and sperm. Sperm volume and density are increased; however, Clomiphene citrate may not increase sperm maturation or motility.

https://player.vimeo.com/video/244317363?badge=0

The most important information: dosage of Clomiphene citrate

Usual Adult Dose for Ovulation Induction:

50 mg orally once a day for 5 days. Therapy should be initiated on or near the 5th day of the menstrual cycle, but may be started at any time in patients without recent uterine bleeding.

If ovulation occurs and pregnancy is not achieved, up to 2 additional courses of Clomiphene citrate 50 mg orally once a day for 5 days may be administered. Each subsequent course may be started as early as 30 days after the previous course and after pregnancy has been excluded.

Most patients ovulate following the first course of therapy. However, if the patient fails to ovulate, a second course of 100 mg/day for 5 days may be given as early as 30 days following the initial course. A third course of 100 mg/day for 5 days may be given after 30 days, if necessary.

Treatments beyond three cycles of Clomiphene citrate, dosages greater than 100 mg once a day, and/or course durations beyond 5 days are not recommended by the manufacturer. However, successful pregnancies and term deliveries have been reported in women receiving up to 200 mg/day for 5 days, or extended 10-day course of therapy, or consecutive cycles of treatment beyond the 3 recommended by the manufacturer.

Usual Adult Dose for Lactation Suppression:

50 to 100 mg orally once a day for 5 days. Generally, one course of therapy is sufficient.

Usual Adult Dose for Oligospermia:

25 to 100 mg orally once a day. Therapy is generally given over a period of several months.

How should I take Clomiphene citrate?

Use Clomiphene citrate exactly as directed by your doctor. Follow all directions on your prescription label. Your doctor may occasionally change your dose to make sure you get the best results. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Your doctor will perform medical tests to make sure you do not have conditions that would prevent you from safely using Clomiphene citrate.Clomiphene citrate is usually taken for 5 days, starting on the 5th day of your menstrual period. Follow your doctor's instructions.

You will need to have a pelvic examination before each treatment cycle. You must remain under the care of a doctor while you are using this medicine.You will most likely ovulate within 5 to 10 days after you take Clomiphene citrate. To improve your chance of becoming pregnant, you should have sexual intercourse while you are ovulating.

Your doctor may have you take your temperature each morning and record your daily readings on a chart. This will help you determine when you can expect ovulation to occur.

Attention! Clomiphene citrate side effects

Get emergency medical help if you have any signs of an allergic reaction to Clomiphene citrate: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Some women using this medicine develop a condition called ovarian hyperstimulation syndrome (OHSS), especially after the first treatment. OHSS can be a life threatening condition. Call your doctor right away if you have any of the following symptoms of OHSS:

• stomach pain, bloating;
• nausea, vomiting, diarrhea;
• rapid weight gain, especially in your face and midsection;
• little or no urinating; or pain when you breathe, rapid heart rate, feeling short of breath (especially when lying down).

Stop using Clomiphene citrate and call your doctor at once if you have:

• pelvic pain or pressure, enlargement in your pelvic area;
• vision problems;
• seeing flashes of light or "floaters" in your vision;
• increased sensitivity of your eyes to light; or heavy vaginal bleeding.

Common Clomiphene citrate side effects may include:

• flushing (warmth, redness, or tingly feeling);
• breast pain or tenderness;
• headache; or breakthrough bleeding or spotting.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

How to get pregnant fast on Clomiphene citrate?

Step 1

To get pregnant fast with Clomid, you need to visit your doctor for a prescription. Doctors routinely prescribe Clomid to patients who can't get pregnant, so you shouldn't have any trouble finding one who will comply. Some doctors only prescribe Clomid if you have been trying to achieve pregnancy for a year or more. That way it shows that you are truly having issues with fertility. If you admit you have been trying to get pregnant for less time, you will probably get the "slow down, give it some time, and it will happen" speech.

Step 2

Ask for the generic of Clomid, clomiphene citrate, when you fill the prescription at the pharmacy. Clomid is probably not covered by your insurance since it's a fertility aid, so you want to save some money here and get the cheaper version. Drugs are not like clothes – the name brand and the knock off are the same exact thing. Clomiphene citrate will work just as well as Clomid so you can get pregnant fast, and it will cost between $25 and $50 a cycle, depending on your dosage. Brand name Clomid would cost much more.

Step 3

Take one pill on Day 3 through Day 7 of your menstrual cycle. (Some doctors may say to take it on Day 5 through Day 9, but most people who have success and get pregnant took Clomid on Day 3 through Day 7. Discuss it with your doctor if you're concerned, but it's really just a matter of preference. Neither will harm you.) Make sure what you are calling Day 1 of your cycle is true bleeding, not just the spotting that occurs before the full blown period starts. The most common dosage of Clomid is 50mg.

Step 4

Turn down the multiple ultrasounds to save money. Your doctor may want you to come in daily around ovulation to see how your ovaries are responding. This can be very helpful, but it is extremely expensive and again, insurance doesn't cover it. Ask politely if you can skip the ultrasounds this month due to cost. The ultrasounds won't help you get pregnant, but they will show your doctor if the Clomid is doing its job. If cost and time aren't issues, then go for it. The ultrasound tech will be able to tell you how many viable eggs you have, and the more viable eggs, the more of a chance of pregnancy.

Step 5

Have intercourse every other day starting on Day 7. Men need about 48 hours to really build up enough sperm in their systems to easily get you pregnant. They can go two days in a row ONE TIME, and then after that, the sperm will start dwindling in numbers. Having sex every day of your cycle is a bad idea and will not help you get pregnant fast. In fact, you may not get pregnant after multiple cycles if you do.

Step 6

Start checking your cervical mucus on Day 10 of your cycle to see if it's time to try to get pregnant. Cervical mucus (CM) should be wet and stringy, and of an egg white consistency. When the egg white CM (cervical mucus) starts, ovulation is imminent. Clomid has a tendency to dry up cervical mucus a little bit, so some people recommend taking Guaifenesin (Robitussin makes a product, but the generic is cheaper) each day from Day 10 to Day 16 to make the CM (cervical mucus) more favorable to sperm. It probably isn't necessary, but it can't hurt.

Step 7

Start using an ovulation predictor kit on Day 10 as well. With both the ovulation predictor kit and the CM (cervical mucus) check, you should have a very good idea of when you are ovulating, and that knowledge will help you get pregnant fast! Once the kit says you are ovulating, have intercourse that day and the next day. This is the one time you get to have sex two days in a row. Then go back to every other day for as long as you'd like (at least 8 days after the positive.)

Step 8

Take a pregnancy test on or after Day 28 if you want an accurate results. Why make yourself crazy with testing every day (even though you're dying to know!)? If you are pregnant, it will show up on a stick on Day 28. Best wishes on making your bundle of joy happen!

Clomiphene citrate review: real experience from customers

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Testosterone Sustanon 250 powder for bodybuilding: 18 secrets you should know!!!

 

 

Testosterone Sustanon 250 powder overview

Testosterone Sustanon 250 powder,the raw material of Testosterone Sustanon 250,is a kind of white powder,is a popular testosterone blend (mixture) and is without question the most popular and well known blend ever made. People usually buy high purity like 99% purity Testosterone Sustanon 250 powder,used for bodybuilding, to increase the level of Testosterone,thus enhancing your body,dosage for bodybuilding range from 300-100mg,common side effects of Testosterone Sustanon 250 powder include water retention and bloating, blood pressure elevations (as a result of the water retention), increased possible fat retention/gain, and gynecomastia.

 

What Is Testosterone Sustanon 250?

Sustanon-250 is a testosterone compound comprised of four different ester based testosterones: testosterone propionate (30 mg); testosterone phenylpropionate (60 mg); testosterone isocaproate (60 mg); and testosterone decanoate (100 mg).This is an improvement from standard testosterones such as cypionate or enanthate, which provide a shorter duration of activity. As with all testosterone products, Sustanon 250 is a very strong anabolic drug with pronounced androgenic activity. It is most commonly used in bulking cycles, providing exceptional gains in strength and muscle mass. A shorter-acting version of Sustanon, called Sustanon 100, is also made in certain areas.

A common misconception among many steroid users is that Sustanon-250 carries with it more power than other testosterone forms, this is not so, it is merely testosterone, a powerful anabolic and androgenic hormone in its own right.

Sustanon-250 was first developed by Organon in an effort to compound the perfect testosterone for the purposes of hormone replacement therapy. The idea was simple; in one single compound create a testosterone that will actively release the hormone from the point of injection up to several weeks post-injection at a steady and even rate. By creating such a compound an HRT patient could effectively keep testosterone flowing through their body and necessarily only administer the hormone once every 3-4 weeks to achieve such an end. While following such protocol would prove to be effective, as the compound was a success in this regard, maintaining stable blood levels is quite a different story and for that reason those who use Sustanon 250 for performance purposes will find frequent injections to be an absolute necessity.

 

Testosterone Sustanon 250 history

The pharmaceutical company behind Sustanon 250’s development is the Netherlands -based Organon International, which was acquired by Schering-Plough Corporation in November 2007. The anabolic steroid made its entry into the market in the 70s. The original idea that drove the makers of Sustanon 250 was to come up with a testosterone mixture that would offer greater benefits over any single testosterone product in clinical environments. Convenience was another driving force in the development of the powerful drug as fewer injections of Sustanon 250 are needed compared to mono esterified testosterone drugs such as Testosterone Propionate and Testosterone Decanoate, to name a few .

Perhaps, the most extensively used testosterone preparation by athletes and bodybuilders, Sustanon 250 has never been granted usage or sales permission in the US. Despite this it continues to be a very popular drug in the rest of the world. But what makes Sustanon 250 so popular? The answer is not its potency, which contrary to popular opinion is no more than that of single esterified preparations of testosterone. Esters appended to anabolic steroids only have the capacity to influence their release time and half-life, and do not have any direct bearing on their strength. The true reason for Sustanon 250’s success and widespread popularity is that the user stands to obtain more quantity of steroid for the same price than other testosterone preparations.

Though this anabolic steroid has enjoyed unprecedented success among athletes and bodybuilders, they were hardly the target audience the makers of Sustanon 250 had in mind while developing the drug. Instead, they were aiming for increased comfort of patients in need of medical treatment by providing them a convenient dosing schedule. Patients who are being administered Sustanon 250 don’t have to constantly worry about their dose, as one steroid injection every 21-28 days usually proves sufficient for their needs.

 

What is Testosterone Sustanon 250 powder?

Testosterone Sustanon 250 powder, the material of Testosterone Sustanon 250,a kind of White powder,many steroids products supplier usually buy high purity Testosterone Sustanon 250 powder online,make it into all kinds of brand finished Testosterone Sustanon 250,the detail of the Testosterone Sustanon 250 as below:

Name Testosterone Sustanon 250
Appearence Write powder
Assay ≧99%
Solubility: Insoluble in water or alcohol, soluble in Acetic acid, ethyl ester
Loss on drying ≤0.5%
Heavy Metal ≤10ppm
Dosage: 35-140mg
Onset time: 20 minutes
Grade:Pharmaceutical Grade

 

What’s Low Testosterone ?

Low testosterone is a term used by doctors to describe an abnormal level of the hormone testosterone. When appropriately measured, low testosterone is considered to be below 300 ng/dl in male patients, although some doctors suggest the normal range is 270 – 1070 ng/dl. Other terms for low-T include hypogonadism (primary, secondary and tertiary, depending on the cause of low-T) and testosterone deficiency (TD).Testosterone is a hormone produced by the human body. It's mainly produced in men by the testicles. Testosterone affects a man's appearance and sexual development. It stimulates sperm production as well as a man's sex drive. It also helps build muscle and bone mass.Low Testosterone can cause a range of symptoms.

One of the biggest worries faced by men with low testosterone levels is the chance that their sexual desire and performance will be affected. As men age, they can experience a number of symptoms related to sexual function that may be a result of lowered levels of this hormone. These include:

• reduced desire for sex
• fewer erections that happen spontaneously, such as during sleep
• infertility
• Physical changes

Also A number of physical changes can happen to your body if you have low testosterone levels. Testosterone is sometimes referred to as the “male” hormone. It helps increase muscle mass, leads to body hair, and contributes to an overall masculine form. Decreases in testosterone can lead to physical changes including the following:

• increased body fat
• decreased strength/mass of muscles
• fragile bones
• decreased body hair
• swelling/tenderness in the breast tissue
• hot flashes
• increased fatigue
• effects on cholesterol metabolism
• Emotional changes

In addition to causing physical changes, having low levels of testosterone can affect you on an emotional level. The condition can lead to feelings of sadness or depression. It can also degrade your overall sense of well-being. Some people have trouble with memory and concentration and experience lowered motivation and self-confidence.

 

What’s low Testosterone treatment?

Low testosterone treatment is designed to boost testosterone levels. Studies suggest this increase in testosterone can strengthen muscles, protect bones, and improve sex drive. Testosterone replacement therapy is only recommended for men who have blood levels that show low testosterone. Such treatments can have different effects from one man to another so it is difficult to predict the treatment outcomes for any one individual.

Methods of Testosterone Delivery

• Intramuscular shots
• Topical gels and patches
• Buccal patches
• Implanted pellets

 

How Does Testosterone Sustanon 250 powder Works for low Testosterone ?

As the mainly ingredient materils of  Testosterone Sustanon 250, Testosterone Sustanon 250 powder works by Stimulating the production of testosterone, increase the level of Testosterone,thus you will gain the same benefit as testosterone blends like Omnadren. All testosterone users can dramatically increase muscle mass, strength and stamina. Furthermore, testosterone, being a key component in helping to maintain muscle mass in conjunction with a calorie restricted diet, is the ideal hormone for athletes looking to reduce overall body fat. Because testosterone can prevent the buildup of hormones that cause muscle wasting, Sustanon inevitably creates a more satisfying physique due to increased testosterone levels. There are, however, risks associated with using exogenous testosterone like Sustanon. The more Sustanon you use, and the longer you use it, the more the likelihood of experiencing side effects will increase. Side effects will always be a concern with any kind of testosterone use, and this is why we recommend a good aromatase inhibitor when using testosterone supplements. You should also understand the basics of how to use testosterone responsibly if you want the desired positive effects.

 

Testosterone Sustanon 250 powder mechanism of action

Sustanon 250 is made up of four testosterone esters, each having its own action duration. With its different testosterone variants, Sustanon 250 is designed for providing a gradual release of testosterone into the blood plasma, which is helpful in bringing down the frequency of dosage. Testosterone by itself, without any esters attached has a half-life in the range of 2-4 hours. However, when esters attach themselves to this natural hormone they slow down testosterone’s release. For Sustanon 250example, with a Propionate ester attached to it, the resulting testosterone preparation has a half-life of 4.5 days, which is significantly longer than normal testosterone’s half-life. The four esters of Sustanon 250 undergo hydrolysis, i.e. are broken by the action of water, almost immediately after entering general circulation to leave the natural steroid hormone, testosterone, free in the bloodstream.

Administration of Sustanon 250 injections results in significant increase in testosterone, oestradiol, dihydrotestosterone, and androstenedione concentrations in the blood plasma. There’s also a drop in the level of SHBG (sex hormone-binding globulin). FSH (Follicle-stimulating hormone) and LH (Luteinising hormone) are returned to their expected range following the administration of Sustanon 250.

In men suffering from hypogonadism – diminished functional activity of testes – treatment with this popular Testosterone preparation results in marked improvements in testosterone-deficiency symptoms . There are several other health advantages such as increased lean-body mass and bone-mineral density. Enhanced sexual function is yet another advantage of the treatment – this includes both erectile and libido functions.

Treatment leads to a reduction in triglycerides, and serum HDL-C (High Density Lipoprotein-Cholesterol) and LDL-C (Low Density Lipoprotein-Cholesterol), while increasing hematocrit and hemoglobin, but has little to no effect on PSA (Prostate Specific Antigen). No side effects have been reported for prostate symptoms, but treatment using Sustanon 250 can increase the size of the patient’s prostate.

When administered with androgens, hypogonadal patients also suffering from diabetes show improved sensitivity to insulin. A lowering of glucose level in the bloodstream of patients has also been reported. The combination of Sustanon 250 and androgens has also proved effective in inducing masculinity in female-to-male transsexuals.  

What does Testosterone Sustanon 250 powder do?/Benefits of Testosterone Sustanon 250 powder

What Does Testosterone Sustanon 250 powder Do?

Athletes, bodybuilders and anyone else who uses Sustanon can achieve the muscle tone, strength, and size they want. Their chances of experiencing andropause will also be far less than using another exogenous testosterone product, as well. Once taken, Testosterone Sustanon 250 powder automatically converts into a very strong form of dihydrotestosterone, which is responsible for its androgenic effect. When this occurs, the body is better able to synthesize proteins than before, which facilitates muscle growth. It also allows older muscle tissue to become more developed, stronger, and larger than before. Benefiets of Testosterone Sustanon 250 powder include:

Enhanced nitrogen retention

Lean muscle tissue is comprised of 16% nitrogen. It follows that the more of this substance we retain, the greater our anabolic atmosphere will be. The point here is that when people take Sust, it enhances nitrogen retention. This is useful in bulking and cutting cycles and this is why weightlifters and bodybuilders need Sust to perform.

Improved protein synthesis

Protein synthesis is simply the process by which cells build proteins. The primary building block of muscle tissue is protein. One great benefit of “Sust” is that it increases the rate of protein synthesis and this makes it beneficial to bodybuilders and athletes.

Increased red blood cell count

Red blood cells carry oxygenated blood throughout the body. High oxygen levels in the blood help athletes perform better. In addition, high oxygen levels in the blood helps athletes recover faster. For this reason, people who buy and use Sust will experience better performance, endurance and recovery.

Inhibition of Glucocorticoid Hormones

Glucocorticoid Hormones are also called stress hormones and they promote fat storage and destroy muscle tissue. Sust combats these hormones by reducing their dominance in the body. The result is better health and more effective workout sessions.

prevent the conversion to estrogen

Like many other anabolic androgenic substances, Testosterone Sustanon 250 powder can be influenced by the aromatase enzyme, which will convert testosterone to estrogen. When you take Testosterone Sustanon 250 powder at responsible doses and for the recommended timeframe, you’ll find that estrogen conversion is quite manageable. As mentioned above, in some cases, users may need to pair Sustanon with an aromatase inhibitor like Arimidex to block the action of aromatase enzymes and prevent the conversion to estrogen.

Other benefits of Sustanon 250

This steroid is great for people who suffer from loss of libido, erectile dysfunction, lethargy, insomnia and depression. Sust improves mental clarity, helps strengthen a weakened immune system and improves mental concentration.

 

How should Testosterone Sustanon 250 powder be used?

Testosterone Sustanon 250 powder usually was made into Testosterone Sustanon 250 injection,Sustanon 250 mg Injection is a naturally occurring sex hormone in men and women. This medicine is used to treat conditions  include delayed puberty, impotence, and other hormonal imbalances.

 

Dosage of Testosterone Sustanon 250

Medical dosage of Testosterone Sustanon 250

We've already know that Sustanon 250 was originally designed and intended for use in medical application, specifically for the treatment of Testosterone deficient hypogonadal males. For the treatment of hypogonadism (or any condition resulting in Testosterone deficiency), the original medically advised Sustanon 250 doses called for a 250mg administration every 3 weeks. The very infrequent administration protocol is due to the previously explained property of Sustanon 250 whereby it will provide varying release rates and half-lives due to the blend of four different Testosterone ester types. Recall that Sustanon 250 will provide an immediate release of Testosterone over a 24 – 48 hour period (due to the short estered Testosterone variants in the mixture, such as Testosterone Propionate and Testosterone Phenylpropionate). Following this immediate release, the rest of the Testosterone is to be elevated for a period of approximately 21 days.

Beginner, Intermediate, and Advanced Sustanon 250 Dosages

There unfortunately exists very little flexibility for Sustanon 250 doses between the three tiers of users (beginner, intermediate, and advanced).

Beginner Sustanon 250 doses are in the range of 300 – 500mg weekly, which is also the standard beginner dose of any and all Testosterone cycles and this dose range should be sufficient enough to provide some dramatic gains even on the lowest number in the range given.

Intermediate users will generally make excellent progress from 500 – 750mg weekly of Sustanon 250. Advanced users will make excellent progress from the same dose range as intermediate users, and should rarely find the need to rise above this range (especially considering advanced users tend to utilize other anabolic steroids stacked with Sustanon 250).

 In any case, advanced Sustanon 250 doses tend to be in the range of 500 – 1000mg weekly, but it is important to be aware that higher doses of any anabolic steroid is not the definition of an advanced user. Often times, excessive anabolic steroid doses will lead to increased incidence of side effects and bodily harm. Very high and excessive doses are quite plainly abuse and not responsible use.

Being a Testosterone product, Sustanon 250 use as a primary anabolic in a cycle is not always necessary, and this has been touched upon lightly earlier in this profile. Often times, users (mostly intermediate and advanced users) will stack other compounds with Sustanon 250 (or any Testosterone product) and desire that only those other compounds exhibit the primary anabolic effects in the cycle. As a result, Sustanon 250 doses in this case are relegated to what is known as TRT (Testosterone Replacement Therapy) dosing schemes. The idea with running Sustanon 250 or any Testosterone product at TRT doses is to simply mimic the level of Testosterone that the body endogenously produces naturally, so as to maintain the proper normal physiological function that Testosterone provides while the user’s natural Testosterone production is shut down as a result of the anabolic steroid use in the cycle. The acceptable TRT dose range for Sustanon 250 or any Testosterone product is 100mg per week.

Female Sustanon 250 Dosage

Sustanon 250 is not recommended for females due to the strong androgenic nature of Testosterone. Instead, female athletes looking to use anabolic steroids should look elsewhere to the less potent androgenic anabolic steroids in existence. Sustanon 250 is used medically for females for the purpose of facilitating female-to-male transgender transformations. Sustanon 250 is the compound of choice for this purpose because of its strong ability to produce virilization and masculinizing effects in women. The very slow and varying release times of Sustanon 250 are also unsuitable for female athletes seeking to use anabolic steroids without a large risk of virilization.

 

Testosterone Sustanon 250 cycle

Testosterone Sustanon 250 can be used for any cycle be it bulking or cutting and as most steroid users will build their cycles around testosterone Sust can be a fine choice. Testosterone Sustanon 250 cycle are like:

For the individual who uses Sustanon-250 as part of a testosterone replacement plan 250mg every 2-4 weeks is a common dose but this will be determined by your doctor. For the performance enhancer, as a general rule of thumb 500mg of testosterone is often considered the base dosing level and is perfect for any beginner. While this is a perfect beginners dose many will find it is all they ever need no matter how advanced they become. For the hardcore, doses of 1,000mg per week are fairly common place and even beyond in bodybuilding circles, particularly those who fall in the realm of competition. Understand, when the dose increases, while the rewards may as well so do the risks associated.

You can easily find cycle of Testosterone Sustanon 250 on Internet,and choose one which fits you well.Also Many will find 12-16 week cycles of Sustanon-250 to be perfect and very well-tolerated in most cases; however, a solid post cycle therapy (PCT) plan is necessary once discontinued. Because Sustanon-250 carries long esters you will necessarily begin PCT 3 weeks after your final Sust administration which may include hCG, Nolva and/or Clomid. Those who use hCG are advised to begin use approximately ten days before Nolva/Comid for approximately ten days of use.

 

Testosterone Sustanon 250 half life

From the bodybuilding perspective, this is helpful where the bodybuilder does not know how to frontload a steroid. But if he does, frontloading a longer acting single ester will accomplish very nearly the same thing. So, a different testosterone ester product such as testosterone enanthate or testosterone cypionate can very readily be used in an anabolic steroid cycle in place of Sustanon.

The multiple esters in Sustanon result in slightly complex pharmacokinetics or change in drug level with time. With a single ester, after so many hours or so many days blood level falls to one-half of what it had been; then by double that time that falls in half again resulting in one-quarter of the previous level; then by triple that time the level falls to one-eighth of what it had been, etc. This time period is called the half-life.

ForSustanon 250 half life,there is no such fixed time period. Information on most forum show that that after the last injection levels drop to one-half by the 4 day point; to one-quarter by the 10 day point; to one-eighth by the 16 day point; and to one-sixteenth by the 23 day point. Or if preferring to work with round numbers in terms of percent, as approximate values levels drop to 40% by day 6; to 30% by day 8; to 20% by day 11; and to 10% by day 18.

 

What other drugs will affect Testosterone Sustanon 250?

If you use other drugs or over the counter products at the same time, the effects of Sustanon 250 Injection may change. This may increase your risk for side-effects or cause your drug not to work properly. Tell your doctor about all the drugs, vitamins, and herbal supplements you are using, so that you doctor can help you prevent or manage drug interactions. Sustanon 250 Injection may interact with the following drugs and products:

• Anticoagulants
• Antidiabetics
• Cyclosporine
• Insulin
• Oxyphenbutazone
• Propranolol
• Thyroxine
• Warfarin

 

What’s Side Effects of Testosterone Sustanon 250 ?

All medications, steroidal and non-steroidal alike carry with them possible negative side-effects, Testosterone Sustanon 250 makes no exception. The possible side-effects of Testosterone Sustanon 250 are identical to every other testosterone form as the active hormone testosterone is what comprises Sustanon-250. As testosterone, regardless of form converts to estrogen via the aromatase process common anabolic side-effects of an estrogenic nature can occur such as Gynecomastia, increased blood pressure, as well as cholesterol issues and testicular atrophy. While testicular atrophy occurs in all who use testosterone it will reverse once use is discontinued when used responsibly. Testicular atrophy occurs because by administering exogenous testosterone our bodies are no longer required to produce their own; as testosterone is produced in the testicles, once production comes to a halt they simply shrink; once production begins again they return to their normal size. Beyond testicular atrophy, which will assuredly occur, other common side-effects are easily avoidable. As most side-effects are due to estrogen conversion by taking an aromatase inhibitor in conjunction with our testosterone we can prevent the estrogen from binding as well as reduce the amount in the body. Further and most importantly, with proper diet rich in healthy fats we can largely protect against blood pressure and cholesterol issues.

 

Warning of Testosterone Sustanon 250

Sustanon 250 will not bring any negative side effect when used in therapeutic purposes such as in TRT. However, using Sustanon-250 as a steroid will bring some negative side effects in estrogenic and androgenic.

One of the estrogenic side effects of Sustanon 250 is gynecomastia. Gynecomastia is a breast enlargement due to the rise of estrogen hormone. To avoid this side effect, you may want to use an anti-estrogen supplement or aromatase inhibitor such as Gynectrol and Arimidex.

For the androgenic side effects, acne and hair loss may appear in Sustanon-250 usage. It can also cause virilization in women. Yet, it is not recommended for women to use Sustanon 250. Women might suffer from low testosterone, but it can be treated by other supplements.

 

What's the difference between Testosterone Sustanon 250 Testosterone Enanthate?

When it comes to comparing Sustanon 250 and Testosterone Enanthate, the primary difference lies in the ester length.

Sustanon 250, being a fairly long-estered combination of Testosterone, takes a bit longer to "kick in" but benefits from this anabolic compound can be achieved with less of frequent injections.  Testosterone Enanthate, on the other hand, is required to be administered every week due to shorter esters though its effects are quicker than Sustanon.

Testosterone enanthate, when used for cycles of 10-12 weeks, is an ideal steroid as it is easier for athletes to determine and manage testosterone levels.  Though, this advantage may gets somewhat lost when the duration of the cycle is 4-6 weeks as effects of the steroid would start showing up after 2-4 weeks.  Because of the mixed esters, Sustanon is a difficult steroid to deal with when it comes to efficient management of blood levels.

However, Testosterone enanthate is believed to be more tolerable than Sustanon when it comes to estrogenic side-effect management. This is due to the fact that testosterone blood levels tend to build at a slow pace with Testosterone enanthate use and this also means that side effects do not show up early. The choice between Sustanon 250 and Testosterone Enanthate solely depends on expectations from steroid cycle and past experiences (if any).

 

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Proviron is a very unique anabolic steroid in cutting cycles

 

 

1.What is Proviron?

Proviron represents one of the oldest anabolic androgenic steroids on the market. Officially known as Mesterolone, it has appeared under numerous brand names over the years, but the Proviron name has continually remained dominant. It has also remained one of the most misunderstood anabolic steroids among steroid users.

In many ways, Proviron is a very unique anabolic steroid. It shares some strong similarities to Masteron (Drostanolone) and to a degree Anavar (Oxandrolone) and Winstrol (Stanozolol) but in totality it is its own unique animal. In a performance capacity, Proviron is not used to promote large buildups in mass, although it can serve an important purpose during such a phase of training. We will, however, find Proviron to be far more common in cutting cycles, but once again its purpose will be somewhat unique.

2.How Proviron works?

Mesterolone is a dihydrotestosterone (DHT) derived anabolic androgenic steroid. Specifically it is a structurally altered DHT hormone possessing the addition of a methyl group at the carbon one position. This allows the hormone to survive oral ingestion by protecting it from hepatic breakdown. This is one of the only oral anabolic steroids that is not C17-alpha alkylated (C17-aa) but instead carries the added methyl group. Oral Primobolan is the other most well-known oral steroid that carries this same methyl group. While the added methyl group does in fact protect it from breakdown, the total bioavailability of Proviron will be far less than most all C17-aa oral steroids. For this reason it has fallen out of popularity among many performance enhancing athletes but as we will see perhaps unjustifiably so.

Proviron carries an androgenic rating of 30-40 and an anabolic rating of 100-150. All ratings derive from and are measured against testosterone, which carries a rating of 100 in both categories. Despite having an anabolic rating that is potentially greater than testosterone, Proviron will display very low anabolic traits. This is very similar to Halotestin (Fluoxymesterone), which carries a massive anabolic rating but very little translatable anabolic activity. In the case of Proviron, while structurally very anabolic, the Mesterolone hormone converts and reduces to Diol metabolites, in turn reducing anabolic activity. However, Proviron’s androgenic rating is a different story. In fact, its translatable androgenic activity appears to commonly be higher than its structural rating would imply.

On a functional basis, Proviron carries four primary traits that largely define its mode of action. First and foremost the Mesterolone hormone has a strong binding affinity to Sex-Hormone-Binding-Globulin (SHBG). In fact, it appears to be one of the strongest anabolic steroids in this regard. By binding to SHBG, a hormone partially responsible for reducing free testosterone, binding SHBG will enhance the amount of circulating free testosterone. More importantly for the anabolic steroid user, it will make a larger percentage of the anabolic steroids used available in a free rather than bound state. A simple way to look at it is the anabolic steroids you’re taking become more powerful and potent.

Proviron also has the ability to interact with the aromatase enzyme, the enzyme responsible for the conversion of testosterone to estrogen. By binding to the aromatase enzyme, Proviron can actually inhibit aromatase activity, thereby offering protection against estrogenic side effects. It will not carry an anti-estrogenic effect near the level of power of an Aromatase Inhibitor (AI) but it will be notable. Depending on the nature of the cycle the individual undertakes it is quite possible for Proviron to take care of all your anti-estrogen needs.

The Mesterolone hormone will also carry a strong binding affinity to the androgen receptor. Once again this will promote the functionality of other steroids to a degree but more importantly promote enhanced metabolic activity through direct lipolysis. Then we’re left with the final issue that surrounds Proviron as a fertility medication. This is an anabolic steroid that does not suppress gonadotropins similarly to other anabolic steroids. With minimal suppression and its extremely strong androgenicity, this will enhance sperm production as androgens are necessary to spermatogenesis stimulation. This not only enhances the amount of sperm produced but greatly and equally important enhances the quality of the sperm. Before we go any further understand Proviron does have the ability to suppress gonadotropins, but there’s a line that has to be crossed for notable suppression to interfere with sperm production. This will make sense once we dive into the side effects section.

 

3.The Effects of Proviron

During a bulking phase Proviron is not going to be a foundational steroid, and for most men it will not have a place in an off-season cycle. There are exceptions and we’ll go over those here. Adding in Proviron could possibly help the individual breakthrough a sticking point during his cycle. At some point and time in all cycles the progress begins to wane, and in some cases come to a complete halt. By the way Proviron enhances the total free state of the other steroids being used in a stack, it could possibly help the individual breakthrough this sticking point. During the off-season, this is where most will use the largest amount of testosterone. Many will use large amounts during cutting cycles too, especially competitive bodybuilders but lower testosterone plans are more common during the cutting phase. However, there are those for numerous reasons who choose to run off-season cycles with limited testosterone doses. In such plans, including Proviron could give them a slight needed androgen boost. While it may not always be necessary it could prove to be beneficial.

Without question the best time to use Proviron will be during the cutting phase. This steroid has the ability to provide a bit of a hardening effect similar to Masteron, but more importantly the hardening effects of other steroids will be enhanced. Then we consider its strong binding to the androgen receptor, which will in fact enable the individual to burn body fat at a far more efficient rate. From here we must consider the anti-estrogen effect of Proviron. This will ensure the individual is less prone to water retention and as discussed, depending on the total cycle, it could negate the need for a traditional anti-estrogen. Then we’re once again left with the enhancement of circulating free testosterone. This can be a tremendous benefit when testosterone levels are often much lower during this phase of anabolic steroid use. In fact, with a low dosed testosterone cycle that includes other anabolic steroids, we can confidently say the total results will be greater for the individual who includes Proviron compared to the one who does not. In the end, the primary base benefit is the increased androgenicity of other steroids being used in order to promote a much harder and far more defined physique. It should be noted while Proviron can most certainly provide these traits they will not be noticeable unless you are lean.

4.Proviron Cycles and Uses

Being that Proviron is not an anabolic steroid and possesses extremely weak anabolic effects, it is not utilized in the form of cycles. It is instead normally utilized as an ancillary compound, as an adjunct to anabolic steroid cycles in order to minimize or mitigate the effects of Estrogen on the body. It is also used for its aesthetic effects in enhancing the ‘hard’ look of the physique both through its effects as an anti-estrogen, as well as its effects as a strong androgen.

When used as an ancillary, it can be taken by male athletes and bodybuilders all throughout their cycle length at 50 – 100mg per day, as there is no limit to how long it can be utilized for. Some individuals prefer to also run Proviron as a PCT (Post Cycle Therapy) drug in order to reduce Estrogen levels and boost fertility. Although this can be done, there are much better compounds with similar (and stronger) effects for PCT. When the risk of even weak endogenous Testosterone suppression is thrown into the mix with Proviron, it is advised to avoid the use of Proviron for PCT purposes unless there are no other options available. During a period in which individuals are attempting to recover their natural endogenous Testosterone levels, any threat no matter how minimal to endogenous Testosterone production should be unwelcome and avoided at all costs.

 

5.Proviron Dosing and Administration

Standard Proviron doses to treat androgen or male fertility will normally fall in the 50-75mg per day range. Normally the total dosing is split into 2-3 25mg doses per day. In androgen deficiency plans, the total dosing almost always starts at 75mg per day and slowly reduces to 25-50mg per day depending on patient need.

In a performance capacity, Proviron doses normally range from 50-150mg per day. Most men, however, will find 100mg per day to be the minimum beneficial dose with both 100mg and 150mg being highly effective. Total use will normally last between 8-12 weeks. However, in an effort to breakthrough a sticking point in a cycle, say towards the end of a cycle a 6 week course of Proviron may do the trick.

In the medical world for the treatment of insufficient androgenicity, a single tablet of 25mg taken three times per day (for a total of 75mg per day) is used at the onset of treatment, followed by a reduction in dose later on to maintenance levels of a single 25mg tablet per day. In the treatment of male infertility, the same dosages are normally used, though other fertility-boosting drugs are also included alongside Proviron.

In the case of bodybuilders and athletes, Proviron is normally used between 50 – 150mg per day to either control Estrogen levels, reduce water retention (caused by estrogen), or to increase fertility following the conclusion of a cycle.

Although Proviron is not approved for use in females, some females in the athletic and bodybuilding community do elect to use it. In this case, a single Proviron dosage of 25mg per day is enough to alter the look of the physique. This should be done no longer than 4 – 5 weeks in order to avoid virilization effects.

 

6.Proviron Side Effects

Because Proviron is a DHT-derivative, it carries with it no risks at any dosage for estrogenic side effects. In fact, as previously mentioned, Proviron acts as an anti-estrogen via its activity as an aromatase inhibitor in the body. This can result in the mitigation of estrogenic side effects from other compounds via the reduction of total circulating plasma levels of Estrogen. Research has demonstrated that because of this effect of Proviron, it has been utilized medically in the treatment of gynecomastia and breast cancers because of its strong androgenic nature combined with its anti-estrogenic capabilities.

Because Proviron is primarily an androgen, it does carry with it the risk of androgenic side effects, and they are more pronounced with higher dosages. Proviron’s androgenic side effects include: an increase in oily skin (as a result of increased sebum production/secretion), increased facial hair and bodily hair growth, as well as the increased risk of triggering MPB (Male Pattern Baldness) in those that are genetically sensitive or predisposed to it. Women are also prone to virilization through the use of Proviron, which is the development of male characteristics in females (i.e. deepening of the voice, facial hair growth, enlargement of the clitoris, etc.). It is also important to note that because Proviron is already a derivative of DHT, products such as Finasteride, Proscar, or Dutasteride will do absolutely nothing to reduce Proviron’s potential androgenic side effects.

Because Proviron is not C-17 alpha alkylated (it is instead methylated on its first carbon), research has shown that it is not known to produce hepatotoxic effects, and liver problems are extremely unlikely with this compound.

Proviron’s side effects do indeed include negative impacts on the cardiovascular system, however. Studies have shown that 100mg of Proviron daily for 6 months has shown very significant negative effects on cholesterol values, both increasing the bad (LDL) cholesterol and decreasing the good (HDL) cholesterol by 65% and 35% respectively.

It is also likely that Proviron may have a suppressive effect on endogenous natural Testosterone production (though this is considered to be very weak). Nevertheless, studies have demonstrated that 150mg or less per day of Proviron that no significant suppression of Testosterone results. In those same studies, higher dosages (300mg or higher per day) resulted in significant suppression of Testosterone levels.

7.Where to Buy Genuine Proviron raw powder online?

Proviron is not what we can call an extremely powerful anabolic steroid and we cannot really put it in a similar class that we would many other steroids. However, this is still a very beneficial anabolic steroid. It’s simply not beneficial in the traditional way in which we often view anabolic steroids. This is hard for many to accept, as message boards, while there are good ones many have brainwashed others into an improper view of anabolic steroids. In some ways, these individuals are just as guilty as the anti-steroid crowd when it comes to misinformation. Luckily for you, that should no longer be a problem when it comes to Proviron.

If used for the right purposes and with an understanding of the hormone, Proviron could potentially transform many of your cycles. Will this be the end all be all that sees a radical transformation acquired? Probably not, but it will provide benefits that others steroids cannot and simply round out your cycle in a way that will be hard to beat.

You can find many Proviron(Mesterolone) powder source online, but it is hard to buy Genuine Proviron(Mesterolone) raw online. There are many sources selling fake products at the market. so when you buy Proviron(Mesterolone) raw material online, you need to choose an realiable source.

Trenbolone hexahydrobenzylcarbonate:All things you should know!!

 

 

What Is trenbolone hexahydrobenzylcarbonate? 

Anabolic steroid Trenbolone Hexahydrobenzylcarbonate, brand name/trade name: Parabolan,for the commonly and informally abbreviated as Tren Hex or Trenbolone Hex. It is a longer acting esterified variant of the anabolic steroid(AS) Trenbolone, which is the most popular in the form of Trenbolone Acetate (a much faster acting esterified variant of Trenbolone). The Hexahydrobenzylcarbonate ester extends Trenbolone’s half-life to the extent of approximately 14 days rather than 3 days, which is the half-life of Trenbolone Acetate. Trenbolone in both formats saw very brief periods of use as an approved medical drug for human use, as Trenbolone Acetate was marketed for a brief time during the 1980s as Finajet and Finaject before being pulled from the market and disapproved for human use circa 1987. Parabolan was deemed more suitable for human use during its run on the prescription drug market due to its longer acting and slower releasing properties than Trenbolone Acetate, making it much more suitable and comfortable for clinical and medical use with less frequent injections required as a result. Trenbolone itself, no matter the ester attached to it, is known as the most powerful conventionally available anabolic steroid in use by athletes and bodybuilders today.

 

Trenbolone hexahydrobenzylcarbonate powder

Trenbolone hexahydrobenzylcarbonate raw powder,the material of Trenbolone hexahydrobenzylcarbonate,a kind of Yellow crystalline powder,many steroids products supplier usually buy high purity Trenbolone hexahydrobenzylcarbonate powder online,make it into all kinds of brand finished Trenbolone hexahydrobenzylcarbonate,the detail of the Trenbolone hexahydrobenzylcarbonate raw in SZOB as below:

Name: Parabolan (trenbolone hexahydrobenzylcarbonate)

CAS: 23454-33-3

Molecular Formula: C20H24O3

Molecular Weight: 312.4028

Melt Point: 90-92°C

Storage Temp.: RT

Color: Yellow crystalline powder

 

How Does trenbolone hexahydrobenzylcarbonate Works? 

Trenbolone hexahydrobenzylcarbonate is a very strong anabolic steroid and delivers a whole host of benefits to athletes.For those who already have good bulk, trenbolone hexahydrobenzylcarbonate can help to harden the muscles and add definition. This is ideal for bodybuilders prior to a competition or in a cutting cycle.

This drug was previously used to treat muscle wasting and cachexia, primarily due to its superior protein synthesis and retention of nitrogen. Both of these factors help to build lean muscle while preventing catabolism.more benefits of trenbolone hexahydrobenzylcarbonate are like:

Help gaining muscle

The anabolic activity with trenbolone hexahydrobenzylcarbonate is also enhanced by the increased rate of red blood cell circulation. The high red blood cell count means that more oxygen is delivered to the body, helping to improve endurance. This allows for longer and more intense training and faster recovery.

Help burning fat

Alongside increasing muscle, parabolan has the added benefit of helping to burn fat. Many types of anabolic steroid can raise the metabolic rate, which parabolan can also do. However, unlike many other anabolic steroids, trenbolone hexahydrobenzylcarbonate can also directly influence the burning of fat via its ability to bind with the androgen receptor. The net result is a vastly increased fat burning rate while simultaneously increasing muscle.

Used for veterinary industry

Trenbolone hexahydrobenzylcarbonate is still used within the veterinary industry, administered as Fina pellets to cattle not long before they are slaughtered. This is because tren hex has the ability to allow the body to process the nutrients in food far more efficiently making fats, carbohydrates and protein much more valuable gram for gram.

 

Trenbolone hexahydrobenzylcarbonate advantages

Trenbolone hexahydrobenzylcarbonate has no estrogenic effect as it does not aromatize. This is of great advantage to bodybuilders looking to create a lean and ripped physique as there’s no risk of water retention and bloating. Because there is no aromatization, gynecomastia is also not an issue.

 

How to Use trenbolone hexahydrobenzylcarbonate ? 

Cycle&dosage of Trenbolone Hexahydrobenzylcarbonate

Beginner Parabolan Cycle

Beginner Parabolan cycle example (12 weeks total cycle time)

Weeks 1-12:

– Testosterone Cypionate at 500mg/week

– Trenbolone Hexahydrobenzylcarbonate(Parabolan) at 228mg/week

Such a beginner Trenbolone Hexahydrobenzylcarbonate cycle is merely a starting point for those experienced anabolic steroid users just getting into the use of  Trenbolone Hexahydrobenzylcarbonate. Testosterone Cypionate, a long acting variant of Testosterone at a bodybuilding dose of 500mg/week is typically stacked alongside  Trenbolone Hexahydrobenzylcarbonate due to their almost seamless compatibility. Both compounds exhibit very similar half-lives and rates of release. This beginner  Trenbolone Hexahydrobenzylcarbonate cycle could be classified more as a bulking or mass gaining cycle due to the doses utilized.

 

Intermediate Trenbolone Hexahydrobenzylcarbonate(Parabolan)Cycle

Intermediate Trenbolone Hexahydrobenzylcarbonate(Parabolan)cycle example (14 weeks total cycle time)

Weeks 1-14:

– Testosterone Enanthate at 100mg/week

– Parabolan (Trenbolone Hexahydrobenzylcarbonate) at 350mg/week

– Equipoise (Boldenone Undecylenate) at 400mg/week

Weeks 1 – 6:

– Dianabol (Methandrostenolone) at 25mg/day

trenex 100This intermediate Parabolan cycle could be classified as another bulking or mass gaining cycle, and combines three anabolic steroids similar in their release rates and half-lives. Testosterone Enanthate is utilized at a TRT dose of 100mg/week, while Equipoise is utilized at 400mg/week. This cycle should present a low incidence of aromatization, with the exception of the possibility of Dianabol. Dianabol is inserted at the beginning of the cycle and run until week 6 in order to kick-start the cycle. Kick starting is an effort to throw in a compound (usually an oral anabolic steroid) that will achieve blood plasma levels fast during the first few weeks while the long acting compounds slowly build up in the user’s system. The use of a kickstarting compound is done so that the user can experience gains within the first several weeks when they otherwise wouldn’t experience fast changes from the long-acting compounds alone.

 

Advanced Trenbolone Hexahydrobenzylcarbonate(Parabolan) Cycle

Intermediate Trenbolone Hexahydrobenzylcarbonate(Parabolan) cycle example (12 weeks total cycle time)

Weeks 1-12:

– Testosterone Enanthate at 100mg/week

– Parabolan (Trenbolone Hexahydrobenzylcarbonate) at 500mg/week

– Primobolan (Methenolone Enanthate) at 1,000mg/week

Weeks 1 – 6:

– Oral Winstrol (Stanozolol) at 50mg/day

This intermediate Trenbolone Hexahydrobenzylcarbonate(Parabolan)cycle is easily classified as a pre-contest or cutting cycle where either fat loss or lean mass gain (with as little fat or water gain/retention as possible) is desired. Once again, similar acting compounds in terms of half-life are used together. Testosterone Enanthate is relegated toa support position of TRT once again.Trenbolone Hexahy drobenzy lcarbonate (Parabolan), a favourite among competitive bodybuilders (especially for pre-contest) is used and the benefits garnered from a high dose would assist in achieving the hard and dense look of the physique, especially when Parabolan is used. The use of Winstrol (oral format) is not only for the purpose of somewhat of a kickstart, but also to assist the user in achieving a dry, ripped, and hard look to the physique.

 

Type of PCT needed after the end of the cycle

Like any anabolic steroid, PCT is essential to help the body return to normal function. This is the case even if testosterone has been taken during the cycle because the body will suppress natural production while it is being supplemented.

Nolvadex or Clomid are often used as part of the PCT and will support the body to return to producing testosterone naturally once more.

 

How to store it after using Trenbolone Hexahydrobenzylcarbonate?

In case of expired Trenbolone Hexahydrobenzylcarbonate tablets or if the tablets or injections are not to be used any more, the same should be discarded after having consulting a pharmacist or local waste disposal company on how to safely discard Trenbolone Hexahydrobenzylcarbonate. It is highly recommended that Trenbolone Hexahydrobenzylcarbonate should not be flushed down the toilet or poured into a drain, unless specifically recommended by a qualified authority. Trenbolone Hexahydrobenzylcarbonate tablets or injections should be properly discarded, when expired or no longer needed. Trenbolone Hexahydrobenzylcarbonate must be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) and kept away from unauthorized use, pets, sunlight, moisture, and children.

 

Dosage of trenbolone hexahydrobenzylcarbonate 

The recommend dosage of Trenbolone Hexahydrobenzylcarbonate is usually 50-75mg a time,3 or 4 times a week.

Trenbolone Hexahydrobenzylcarbonate(Parabolan) is not generally considered to be a drug that is suitable for individuals who are completely new to using anabolic steroids, because of its potency. Therefore, the entry level dosage range is likely to still be too strong for those who aren’t used to anabolic steroids.

For those who have used steroids before but are new to Trenbolone Hexahydrobenzylcarbonate (Parabolan) dosage typically begins at around 152-220mg per week which equates to either half or one full ampoule. Very significant benefits can be seen at this dosage, particularly when the right training and diet regime is adhered to at the same time.

More experienced Trenbolone Hexahydrobenzylcarbonate(Parabolan) users may take 228-456mg per week, the equivalent of two ampoules.

The most advanced users could take in excess of 500mg but in many cases, this extremely high dose is not required for optimal results because of the sheer strength of Trenbolone Hexahydrobenzylcarbonate(Parabolan).

 

 Warning of trenbolone hexahydrobenzylcarbonate 

Trenbolone Hexahydrobenzylcarbonate(Parabolan) side effects can be a problem for some users, but in others the drug should not be taken at all.

Anyone with a history of any of the following conditions should refrain from taking tren hex without first obtaining medical advice:

• Testicular atrophy

• Prostate cancer

• Testicular cancer

• Breast cancer

• Impaired liver function

• Renal disease or dysfunction

• Stroke

• Cardiovascular disease

• Respiratory problems

Trenbolone Hexahydrobenzylcarbonate(Parabolan) is not recommended for use in women at any dose, due to the extremely high risk of virilization. This is due to the fact that parabolan is a very androgenic steroid.

 

What Are the Possible Side Effects of trenbolone hexahydrobenzylcarbonate? 

Trenbolone Hexahydrobenzylcarbonate(Parabolan), being a form of trenbolone, is one of the most powerful anabolic steroids, being five times stronger than testosterone. For this reason, it can cause side effects in some, and isn’t recommended for those who have never used anabolic steroids before.The Potential side effects of may include:

Androgenic effects

Trenbolone Hexahydrobenzylcarbonate(Parabolan) is a particularly strong androgenic drug and can affect men who are even moderately sensitive to it. Some of the effects that could be experienced include oily skin and excess body hair growth.

Acne can also be a problem but this tends to only occur in men who have a genetic tendency to develop it. In these cases, parabolan can exacerbate the problem.

Keeping clean, staying dry and changing out of workout clothes quickly can help with skin problems and reduce the incidence of acne.

Cardiovascular

The lack of water retention means that raised blood pressure does not occur with Trenbolone Hexahydrobenzylcarbonate(Parabolan) as a result of excess estrogen but nevertheless, there can be a very significant impact on cardiovascular health.

Any individual with a history of hypertension or raised cholesterol is not advised to commence Trenbolone Hexahydrobenzylcarbonate(Parabolan). In addition, a healthy lifestyle is important while taking the steroid, with a diet which is rich in omega fatty acids and low in saturated fats.

Hair loss

Because the androgenic effects of Trenbolone Hexahydrobenzylcarbonate(Parabolan) are so strong, there is a risk of hair loss amongst those that take the drug.

However, male pattern hair loss will only occur in those who have the gene for it. Rather than causing the hair loss, Trenbolone Hexahydrobenzylcarbonate(Parabolan) will simply accelerate the process. Once hair loss has occurred, it cannot be reversed even after use of the steroid has been stopped.

Liver toxicity

Trenbolone Hexahydrobenzylcarbonate(Parabolan)n is generally not believed to be a hepatotoxic steroid and is not linked to any side effects at a regular dose. It’s possible that when taken in a very high dose for a prolonged period there may be a degree of toxicity but this effect is not typically expected.

This is not the full list of all trenbolone hexahydrobenzylcarbonate side effects,please check more detail when you decide to use.

 

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Trenbolone Enanthate Raw Powder: All things you should know!!!

 

 

 What is Trenbolone Enanthate? 

Drug Trenbolone Enanthate

Trenbolone Enanthate is one of the most popular anabolic steroids(AS) used by bodybuilders due to its effectiveness.others like Trenbolone Acetate, or Trenbolone-Hex (Tren- hexahydrobenzylcarbonate) are also popular. Users of the drug find it beneficial for all cycles of bodybuilding, including cutting and bulking.

Trenbolone is a hormone that binds with androgen receptors, a long ester variant of the hormone Trenbolone.

Trenbolone, being a derivative of Nandrolone (the base hormone in Deca-Durabolin), is a 19-nor anabolic steroid. 19-nor compounds are characterized by their lack of a 19th carbon on the steroid structure, which also brings Trenbolone the classification of a progestin as well. Through it’s modifications from Nandrolone, it introduces two double-bonds between carbons 11 and 9, and it is this chemical modification that effectively makes Trenbolone totally immune to aromatization (conversion into Estrogen) by way of the aromatase enzyme as well as increasing the strength at which Trenbolone binds to the androgen receptor. That is to say that Trenbolone will not produce any estrogenic side effects alone, and that it is an extremely potent and very strong anabolic steroid with an anabolic:androgenic ratio of 500:500. Compared to Testosterone, this is staggering, as Testosterone expresses an anabolic:androgenic ratio of 100:100. Hence, we can see how and why Trenbolone is five times the strength of Testosterone. Its chemical modifications also allow it a stronger resistance to metabolism in the body, allowing even more maximization of its anabolic capabilities in muscle tissue. Lastly, Trenbolone Enanthate possesses the enanthate ester, affixed at the 17-beta hydroxyl group on the steroid structure. This, as mentioned many times already, slows the release rate and also extends Trenbolone’s half-life in the body to approximately 7 – 10 days.

 

What Is Trenbolone Enanthate powder?

Trenbolone Enanthate raw powder,the material of Trenbolone Enanthate,a kind of off-yellow color crystalline powder,many steroids products supplier usually buy high purity Trenbolone Enanthate powder online,make it into all kinds of brand finished Trenbolone Enanthate,the detail of the Trenbolone Enanthate raw in AAS as below:

Chemical Name: Tren E, trenbolone E

Molecular Formula: C25H34O3

Molecular Weight: 382.544

Purity: >98%

Grade: Pharmaceutical Grade

 

What’s the benefits of Trenbolone Enanthate

Trenbolone Enanthate is both an anabolic and androgen and is more powerful than the common testosterone. It works by binding the Androgen Receptor (AR) and doesn’t aromatize (turn to estrogen) leading to muscle gain. Besides binding to AR, Trenbolone also attaches itself to fat cells and activates the fat loss paths.

The binding potential of Trenbolone Enanthate is three times that of testosterone. As an anabolic, the steroid builds and retains muscle more effectively than testosterone and also works directly with glucocorticoid receptors to inhibit production of cortisol which burns muscles. 100mg of Trenbolone Enanthatewill have similar effect to 500mg of Trenbolone Enanthate.Exact benefits of Trenbolone Enanthate as below:

• Increasing muscle strength: High androgenic effects leads to faster growth of muscles and mass.
• Fat Burning: It also assists in burning calories and eliminating fat cells by binding to the fat cells.
• Improving stamina: The androgenic effect helps in cutting while at the same time improves your stamina.
• No aromatization: The steroid doesn’t turn into estrogen hence no muscle cells will be burned.
• Efficient: You require a smaller dose of Trenbolone compared to other alternatives. You can also vary the types depending on personal desires.cause it has a shorter half-life compared to other steroids.

Although Trenbolone may be found in oral form, you will experience the best results by going for the injectable variant. This is because it is quickly and easily absorbed into the body and will start working almost immediately. The risk of some of it being lost in the digestive system is minimized.

 

 How to Use Trenbolone Enanthate correctly? 

 

Recommend dosage of trenbolone Enanthate  

Trenbolone Enanthate is found on the black market in large quantities. It can be relatively costly, regardless of how and where it’s made. Its price can range from $15 per every gram of powder to approximately $150 per 10 ml bottle. Trenbolone’s dosage range is typically 75 mg- 100 mg one time,Due to its short ester length,you'd better take it every other day or 3 times a week through an intra-muscular injection.400 mg per week is generally considered quite a solid dose, but most people will find Tren E to be satisfactorily effective within the 300 mg- 500 mg per week range. 

Trenbolone Enanthate dosage &cycle

In market,the Trenbolone Enanthate was usually taken as injection forms.No matter what your purpose are, be it bulking or cutting most will find Trenbolone-Enanthate to be very effective in the 300mg-500mg per week range with 400mg per week generally being a very solid dose. Yes, you can use more but most will find doses that get much past 500mg per week to be more side effects,  especially if they enter the 600mg per week range and almost assuredly if they surpass 700mg per week. Regardless of dosing most will find 8 weeks to be decently effective with 12 weeks of use generally being as far as you want to go. If your cycle is extended past 12 weeks it’s normally best to substitute another anabolic hormone in Tren’s place in-order to keep progress alive; yes, our body will adapt.

Trenbolone Enanthate cycles are determined by the users’ needs and tolerance for the drug. How much mass and strength you gain depends upon how much you take.

As with most steroids, the effect is dose dependent, as are Trenbolone Enanthate’s side effects, the more you take the more gains you see; however, the greater the side effects you experience.So please be careful when taking.

As for what you should stack Trenbolone-Enanthate with, simply pick whatever you want as this hormone stacks well with all anabolic steroids. However, it is highly recommended that testosterone be part of your stack as Trenbolone in any form will greatly suppress natural testosterone production. Many individuals also find supplementing with the T-3 hormone to be very useful as levels generally fall when Tren is present. Further, as responsible use is important a good Post Cycle Therapy (PCT) plan should occur after the cycle’s completion. In the case of Trenbolone-Enanthate, if your cycle ends with this steroid in play your PCT will not want to begin until at least 2 weeks have passed since your last injection.

Trenbolone and Dianabol Combination

During the first three to four weeks, some bodybuilding websites recommend a Trenbolone and Dianabol combination or stack, and suggest taking approximately 50 mg daily. This intermediate Trenbolone cycle starts the dosages at a higher amount than the newbie cycles. Testosterone is used as a supplement instead of the main anabolic. Dianabol is included in this stack, but it is not because Tren is not strong enough to stand alone. The only thing that a Trenbolone Enanthate cycle needs is testosterone. When it comes to this particular cycle, Dianabol is often used as a kick starter for a person who wants to bulk up and get stronger.

Trenbolone Enanthate 800 mg and Drostanolone E Combination

During Weeks 1 through 12, bodybuilders may also recommend taking 100 mg of Testosterone enanthate and 800 mg of Trenbolone enanthate and 400mg of Drostanolone enanthate. These are weekly dosages. Everything stacked in this cycle contains enanthate esters. When the drugs all have the same ester it’s easier to inject and they can be placed in the same syringe. Trenbolone enanthate dosages will be higher, while the Testosterone is a supplemental replacement therapy, and the Drostanolone is there to supplement the Trenbolone.

Trenbolone Enanthate and Trenbolone A Combination

Note that the esters of Trenbolone do not have to have an anabolic steroid stacked with it. For example, Testosterone enanthate with Trenbolone enanthate. It is okay to combine Trenbolone acetate (Tren A) with Testosterone enanthate during your cycles. These cycles are not problematic. Be aware of timing and half-life of the esters and injection schedules to achieve maximum results. All the while, be aware that Trenbolone enanthate dosages can be – and often are – risky and can cause severe short and long-term side effects.

 

What Are the Possible Side Effects of Trenbolone Enanthate

Trenbolone Enanthate is a powerful steroid, but it also causes significant side effects.

The coomon side effects include:

• An increase in the effects of male pattern baldness;
• An increase in acne outbreaks;
• It is not recommended for female athletes due to its strong androgenic properties;
• A risk of oor sleep patterns;
• Profuse sweating;
• An increase in blood pressure;
• Trenbolone Enanthate Can Cause Liver or kidney damagesometimes

The list don't include all the side effects,you'd better check the other relevant side effects when you decide to take Trenbolone Enanthate.

 

 Warning of Trenbolone Enanthate 

Warnings And Precautions of Trenbolone Enanthate

Trenbolone Enanthate is a steroid which possesses strong androgenic properties. Sweating and a decrease in cardiovascular capability are often widely reported with Trenbolone Enanthate usage. Trenbolone Enanthate is not suitable for one who plays any kind of sports that require cardiovascular fitness. Sweating has been reported greatly at night time, with insomnia and even strange dreams might take place. It is recommended that water intake should be efficient while consuming Trenbolone Enanthate because it tend to causes loss of water.

However, it is said that Trenbolone Enanthate does not aromatise, but since the estrogen manifests progesterone related side effects, such as gynecomastia, it should be seriously kept in mind while stacking it with other androgenic anabolic steroids, such as testosterone. Trenbolone Enanthate is also reported to be very harsh on the HTPA function. Moreover, its recovery is also said to be harsher than steroids and because of this, the use of HCG is often advised.

 

 Where to buy Trenbolone Enanthate Raw Powder online 

In the market,there are different kinds purity of Trenbolone Enanthate powder, usually ranges from 60%-99%,the Trenbolone Enanthate powder with high purity like 98% are usually in Pharmaceutical Grade ,which is more safe to use,less side effects, can produce more drug Trenbolone Enanthate,where to buy Pharmaceutical Grade Trenbolone Enanthate powder,maybe this is a question.If you already

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Testosterone cypionate powder：Everything you should know about the amazing steroids!!!

 

 

What is Testosterone cypionate?/Testosterone cypionate overview

Testosterone Cypionate is one of the many esterified variants of Testosterone available,usually for bodybuilding and  treating ED,others like Testosterone acetate,Testosterone decanoate, Testosterone enanthate,Testosterone phenylpropionate,Testosterone isocaproate,Testosterone propionate,Testosterone Sustanon 250,are all part of the variants of Testosterone.

Testosterone Cypionate  is most likely the second most popular esterified variant (the first being Testosterone Enanthate). It is an injectable form of Testosterone with a slow rate of release and a longer half-life. However, the release rates and half-life of both Testosterone Cypionate and Testosterone Enanthate are very much identical and the two compounds are easily interchangeable (for example, an individual can easily run a 10 week cycle of Testosterone and switch between Testosterone Enanthate and Testosterone Cypionate seamlessly). Testosterone Cypionate possesses a half-life of approximately 12 days while Testosterone Enanthate possesses a half-life of approximately 10 days – hardly much difference. The interesting fact about Testosterone Cypionate, however, is that it seems to have a distinct favor of popularity among American bodybuilders and athletes over the Enanthate variant. These distinctions are not extreme, however, and the commonality of use and availability of both variants is almost equal with Testosterone Enanthate ever so slightly more popular. Neither variant possesses any advantages over the other.

 

History of Testosterone Cypionate

Testosterone Cypionate was first created in the mid-1950s, and was released on the prescription drug market under the brand name Depo-Testosterone and manufactured by UpJohn (however, its brand name at first was labeled as Depo-Testosterone cyclopentylpropionate but was shortened for obvious reasons). Unlike Testosterone Enanthate, which is primarily known as an international item, Testosterone Cypionate is known to be the US answer to the Enanthate variant (although Testosterone Enanthate is utilized almost just as equally in the US). Testosterone Cypionate has held such a positive track record that it is in fact still in production by Upjohn (who merged with Pfizer in 2009) today. As Testosterone Cypionate was the American response to the international product Testosterone Enanthate, many American bodybuilders and athletes throughout the 1960s, 70s, and 80s preferred the use of Testosterone Cypionate over the Enanthate variant for no reason other than the support of an American product, very much akin to an issue of pride (once again, the Cypionate and Enanthate variants of Testosterone are both almost 100% identical and there is no practical reason to prefer one compound over the other).

 

Testosterone is the primary androgen found in the body. Endogenous testosterone is synthesized by cells in the testis, ovary, and adrenal cortex. Therapeutically, testosterone is used in the management of hypogonadism, either congenital or acquired. Testosterone is also the most effective exogenous androgen for the palliative treatment of carcinoma of the breast in postmenopausal women. Testosterone was in use in 1938 and approved by the FDA in 1939. Anabolic steroids, derivatives of testosterone, have been used illicitly and are now controlled substances. Testosterone, like many anabolic steroids, was classified as a controlled substance in 1991. Testosterone is administered parenterally in regular and delayed-release (depot) dosage forms. In September 1995, the FDA initially approved testosterone transdermal patches (Androderm); many transdermal forms and brands are now available including implants, gels, and topical solutions. A testosterone buccal system, Striant, was FDA approved in July 2003; the system is a mucoadhesive product that adheres to the buccal mucosa and provides a controlled and sustained release of testosterone. In May 2014, the FDA approved an intranasal gel formulation (Natesto). A transdermal patch (Intrinsa) for hormone replacement in women is under investigation; the daily dosages used in women are much lower than for products used in males. The FDA ruled in late 2004 that it would delay the approval of Intrinsa women's testosterone patch and has required more data regarding safety, especially in relation to cardiovascular and breast health.

 

What is Testosterone cypionate powder?

 

Testosterone cypionate raw ,the raw material of drug Testosterone cypionate,is a kind of White or off white Crystal Powder,odorless or nearly so and stable in air. It is insoluble in water, freely soluble in alcohol, chloroform, dioxane, ether, and soluble in vegetable oils.Many bodybuilding supplement supplier usually buy high purity Testosterone cypionate raw powder,then make it into finished one.

Detail of Testosterone cypionate powder as below:

Name: Testosterone Cypionate

CAS: 58-20-8

Molecular Formula: C27H40O3

Molecular Weight: 412.6

Melt Point: 98 – 104ºC

Storage Temp.: 2-8ºC

Color: White or off white Crystal Powder

 

What form(s) does Testosterone cypionate powder come in?

Testosterone Cypionate is commonly used as an injected oil,also sold in the form of injection.In the market, there are 200mg/ml, 250mg/ml, 300mg/ml, some UGL even made 350mg/ml and 400mg/ml.

How does Testosterone cypionate work?

Testosterone cypionate belongs Testosterone,is the class of medications called androgens (male hormones). This medication is used to replace testosterone in men who have conditions caused by low testosterone levels, such as erectile dysfunction (difficulty getting or keeping an erection). There are other possible causes for erectile dysfunction, so testosterone is only used to treat erectile dysfunction that is caused by low testosterone.

Testosterone cypionate works by replacing the testosterone that the body is missing. Testosterone cypionate should only be used if testosterone deficiency has been confirmed by symptoms and blood tests.

Mechanism of Action

Endogenous testosterone is responsible for sexual maturation at all stages of development throughout life. Synthetically, it is prepared from cholesterol. The function of androgens in male development begins in the fetus, is crucial during puberty, and continues to play an important role in the adult male. Women also secrete small amounts of testosterone from the ovaries. The secretion of androgens from the adrenal cortex is insufficient to maintain male sexuality.

Increased androgen plasma concentrations suppress gonadotropin-releasing hormone (reducing endogenous testosterone), luteinizing hormone, and follicle-stimulating hormone by a negative-feedback mechanism. Testosterone also affects the formation of erythropoietin, the balance of calcium, and blood glucose. Androgens have a high lipid solubility, enabling them to rapidly enter cells of target tissues. Within the cells, testosterone undergoes enzymatic conversion to 5-alpha-dihydrotestosterone and forms a loosely bound complex with cystolic receptors. Androgen action arises from the initiation of transcription and cellular changes in the nucleus brought about by this steroid-receptor complex.

Normally, endogenous androgens stimulate RNA polymerase, resulting in an increased protein production.These proteins are responsible for normal male sexual development, including the growth and maturation of the prostate, seminal vesicle, penis, and scrotum. During puberty, androgens cause a sudden increase in growth and development of muscle, with redistribution of body fat. Changes also take place in the larynx and vocal cords, deepening the voice. Puberty is completed with beard development and growth of body hair. Fusion of the epiphyses and termination of growth is also governed by the androgens, as is the maintenance of spermatogenesis. When endogenous androgens are unavailable, use of exogenous androgens are necessary for normal male growth and development.

Pharmacokinetics:

Testosterone is administered intramuscularly (IM), to the skin as a topical gel, solution, ointment or transdermal systems for transdermal absorption, by implantation of long-acting pellets, or via buccal systems.

Testosterone is administered intramuscularly (IM); via subcutaneous injection; to the skin as a topical gel, solution, ointment or transdermal systems for transdermal absorption; by implantation of long-acting pellets, or; via buccal systems.

In serum, testosterone is bound to protein. It has a high affinity for sex hormone binding globulin (SHBG) and a low affinity for albumin. The albumin-bound portion freely dissociates. The affinity for SHBG changes throughout life. It is high during prepuberty, declines during adolescence and adult life, then rises again in old age. The active metabolite DHT has a greater affinity for SHBG than testosterone. Elimination half-life is 10—100 minutes and is dependent on the amount of free testosterone in the plasma.

Testosterone is metabolized primarily in the liver to various 17-keto steroids. It is a substrate for hepatic cytochrome P450 (CYP) 3A4 isoenzyme.1 Estradiol and dihydrotestosterone (DHT) are the major active metabolites, and DHT undergoes further metabolism. Testosterone activity appears to depend on formation of DHT, which binds to cytosol receptor proteins. Further metabolism of DHT takes place in reproductive tissues. About 90% of an intramuscular testosterone dose is excreted in the urine as conjugates of glucuronic and sulfuric acids. About 6% is excreted in the feces, largely unconjugated. There is considerable variation in the half-life of testosterone as reported in the literature, ranging from 10 to 100 minutes.2

Affected cytochrome P450 isoenzymes and drug transporters: CYP3A4, P-gp.

Testosterone is a substrate for CYP3A4 and is also both transported by and an inhibitor of P-glycoprotein (P-gp) transport.

 

Potential benefits of Testosterone Cypionate

The purpose of Testosterone Cypionate injections is to help regulate male hormone levels to help address problems related to low T. For men with low T or for Testosterone Cypionate bodybuilding, the benefits of Testosterone Cypionate injections can include:

1. an increased sex drive    
2. improved symptoms of ED   
3. more energy
4. improved mood
5. an increased sperm count
6. Maintain muscle strength and quality  
7. Maintain bone density and strength
8. Maintain libido and erections
9. Energizing and improving your fitness     

 

How should I use Testosterone Cypionate ?

Testosterone Cypionate doses are very flexible in terms of the user’s goals in question. Testosterone Cypionate doses can be tailored to any possible goal – cutting, bulking, lean mass cycles all alike. Variation between Testosterone Cypionate doses depending on the user’s goal.For example, the bodybuilding ranges of doses are generally required for an individual that wishes to bulk up or add lean mass. For the purpose of cutting and fat loss, it is generally not a requirement to venture very high in dose ranges due to the fact that the primary concern when engaging in fat loss is the preservation of muscle mass during a caloric deficit in which muscle loss is a risk without the use of anabolic steroids. In such a case, lower doses are usually all that is necessary.

Testosterone Cypionate dose for ED

Within the field of medicine, prescription guidelines for Testosterone Cypionate doses for the purpose of adult male androgen deficiency (hypogonadism and andropause) is determined to be 50 – 400mg administered once every 2 – 4 weeks. The specific dose will always depend on the individual in question,

Testosterone Cypionate doses also include that of Testosterone Replacement Therpay (TRT) doses. This is necessary in cycles where an individual wishes to stack an additional anabolic steroid with Testosterone Cypionate and have that anabolic steroid provide the muscle growth effects while Testosterone Cypionate takes on the supportive role of merely maintaining normal physiological levels of Testosterone. A dose of 100mg weekly of Testosterone Cypionate is considered a sufficient TRT dose. Any higher and the user begins to run the risk of increased aromatization from supraphysiological Testosterone Cypionate doses.

Testosterone Cypionate dose for bodybuilding

Base Performance Testosterone Cypionate Doses:

For the purpose of performance enhancement, base Testosterone Cypionate bodybuilding doses will fall in the 400-500mg per week range. In fact, for many men this is all they’ll ever need even if they’ve been using anabolic steroids for years. Testosterone Cypionate doses of this range are very well-tolerated by most healthy adult men and will work well continually cycle after cycle. If you’ve never run a cycle before, this is where you’ll want to start as it will help you determine your overall response.

Higher Testosterone Cypionate Doses:

Higher Testosterone Cypionate bodybuilding doses above the base performance level are not uncommon. You will find many men who supplement with 600-1,000mg per week. Most men will still find the 600mg range to be very tolerable, but as the dose increases beyond this point the probability of side effects begins to greatly increase. When Testosterone Cypionate doses surpass the 1,000mg per week mark this will dramatically increase the probability. For the average gym rat, his Testosterone Cypionate doses will never need to leave the 400-600mg per week range. For those who live a more hardcore lifestyle, such as a competitive bodybuilder or someone who simply lives that lifestyle, his doses will reach higher levels. Such doses can be run safely but it will take a concentrated effort and educated use; caution is advised.

Bodybuilding Testosterone cypionate is a long acting, single ester testosterone product. It has a length of 8 carbons, and is stored mostly in the adipose tissue when injected intra-muscularly. It is slowly and steadily released in the body after it is injected. The blood levels of cypionate peak 24-48 hours after injection and then decline slowly. The blood levels reach a steady point 12 days after initial injection and stay there for over three weeks. Cypionate is normally injected once a week, which makes the very lowest dose higher than half the peak dose at any given time. Any testosterone, as the king of mass builders, are cost effective products and important for any steroid stack. Used alone, the user can expect to see some significant gains. The long acting nature of cypionate allows the user to inject less frequently while maintaining stable blood levels. A long acting testosterone ester will be very helpful for your bulking needs, and cypionate is a product which is more simple than some of the other steroids out there. Not to say it is without its share of complications, but it's a good choice, especially for those new to enhanced bodybuilding. Discontinuing the product is not an option in case side effects occur, because it will continue to aggravate these side effects over extended periods of time due to the long length of action of this steroid. Ancillary drugs such as nolvadex, proviron, clomid and HCG may help, both during cycle and post cycle to help restore natural testosterone production. Testosterone cypionate does aromatize slightly more than sustanon, but when using either drug, one should be familiar with anti-estrogens such as nolvadex or clomid and use one of them when symptoms of gyno occur.

Female Testosterone Cypionate Dosage

The use of Testosterone Cypionate among female anabolic steroid users is very uncommon due to the fact that this is a strong androgenic compound, and virilization symptoms are of a high occurrence rate and tend to manifest very rapidly. Testosterone Cypionate, therefore, is not recommended for female use and there exists very little data on dosing practices with this compound.

 

What should I know before taking Testosterone Cypionate?

You are not allowed to use Testosterone Cypionate if：

• You have an allergy to testosterone or any other part of testosterone cypionate injection.
• you are allergic to any drugs like this one, any other drugs, foods, or other substances. Tell your doctor about the allergy and what signs you had, like rash; hives; itching; shortness of breath; wheezing; cough; swelling of face, lips, tongue, or throat; or any other signs.
• you are male and have breast or prostate cancer.
• you have any of these health problems: Heart disease, kidney disease, or liver disease.
• you are a woman. This medicine is not recommended for female use.

This is not a full list of all things you need to notice about the Testosterone Cypionate.

 

What should I know while taking Testosterone Cypionate?

There are some medicine,which is easy to interact with,please don’t use these products while taking Testosterone Cypionate:

• medicines for diabetes
• -medicines that treat or prevent blood clots like warfarin
• -oxyphenbutazone
• -propranolol
• -steroid medicines like prednisone or cortisone

 

What should I know after taking Testosterone Cypionate?

• Store this medication at 68°F to 77°F (20°C to 25°C) and away from heat, moisture and light.
• Keep all medicine out of the reach of children.
• Throw away any unused medicine after the expiration date.
• Do not flush unused medications or pour down a sink or drain.
• Do not share this medicine with anyone.
• Selling or giving away this medicine is dangerous and against the law.
• Testosterone Cypionate Cycles and Uses

 

What should I do if I miss a dose?

Use a missed dose as soon as you think about it.

If it is close to the time for your next dose, skip the missed dose and go back to your normal time.

Do not use 2 doses or extra doses.

 

Testosterone Cypionate Cycles and Uses

As with almost any Testosterone variant or derivative, Testosterone Cypionate cycles tend to almost always be utilized for the purpose of bulking, mass gaining, and strength gaining periods of training. Though its ideal use is for this purpose, this is not to say that it cannot be used effectively (albeit at a lower dosage) for cutting cycles where fat loss is the primary goal. For the purpose of bulking and/or gaining mass and strength, Testosterone Cypionate is usually employed at a higher dosage (approximately 500mg/week). It is usually utilized at this dosage for a period of 12 – 14 weeks due to its longer ester, and therefore longer half-life. Testosterone Cypionate possesses a half-life of around 10 – 12 days. By comparison, its close counterpart Testosterone Enanthate is almost the same, with a half-life of around 7 – 10 days.

No matter the cycle goal, whether it is cutting or bulking, Testosterone Cypionate is usually utilized with and stacked with other anabolic steroids that possess very similar characteristics for obvious reasons. It is a common companion to compounds such as Deca-Durabolin (Nandrolone Decanoate), which is usually run for the same 10 – 12 week length as Testosterone Cypionate, and a ‘kickstarting’ compound such as Dianabol (Methandrostenolone) is usually included from the start of the cycle until it is discontinued at around week 4 or 6.

 

What other drugs could interact with this medication?

There may be an interaction between testosterone cypionate and any of the following:

• adrenocorticotropic hormone (ACTH)
• corticosteroids (e.g., hydrocortisone, prednisone, methylprednisolone)
• cyclosporine
• dehydroepiandrosterone
• diabetes medications (e.g., chlorpropamide, glipizide, glyburide, insulin, metformin, nateglinide, rosiglitazone)
• propranolol
• warfarin

If you are taking any of these medications, you'd better not take Testosterone Cypionate,or speak with your doctor or pharmacist to change the dose of the drug.

Medications other than those listed above may interact with this medication. Tell your doctor or prescriber about all prescription, over-the-counter (non-prescription), and herbal medications you are taking. Also tell them about any supplements you take. Since caffeine, alcohol, the nicotine from cigarettes, or street drugs can affect the action of many medications, you should let your prescriber know if you use them.

 

The Side Effects of Testosterone Cypionate

As an extremely well-tolerated hormone for most men, the side effects of Testosterone Cypionate are in many ways easy to control. When it comes to such adverse reactions, keep in mind they largely fall into the realm of possible and are by no means guaranteed. Even so, total dosing, genetic predispositions and your overall state of health will play a role.

As for the side effects themselves, Testosterone Cypionate like all testosterone compounds carries a high level of aromatase activity; aromatization referring to the conversion of testosterone into estrogen. As estrogen levels rise, this can lead to gynecomastia (male breast enlargement) and excess water retention. This excess water retention can even negatively affect blood pressure. In-order to combat such effects, especially gynecomastia, many turn to Selective Estrogen Receptor Modulators (SERMs) such as Tamoxifen Citrate (Nolvadex) and for more serious protection Aromatase Inhibitors (AIs) such as Anastrozole (Arimidex). Without question, AIs are the most effective; however, they can also prove to be problematic when it comes to cholesterol and caution is advised.

Beyond these effects, Testosterone Cypionate can promote dihydrotestosterone (DHT) related side effects such as acne, hair loss and prostate enlargement; however, it should go without saying DHT steroids will be the prime culprits. In-order to provide protection, a 5-alpha reductase inhibitor such as Finasteride can be useful as it is an androgen suppressor and the androgen DHT is causing the problem. It must be noted; hair loss is only possible in men predisposed to male pattern baldness.

 

How to make drug Testosterone Cypionate from Testosterone Cypionate powder?

Here is the simple recipes of making Testosterone Cypionate(for reference)

 

Each mL of the 100 mg/mL solution contains:

Testosterone Cypionate……………………………………………………………………. 100 mg

Benzyl benzoate ……………………………………………………………………………… 0.1 mL

Cottonseed oil ………………………………………………………………………………… 736 mg

Benzyl alcohol (as preservative)………………………………………………………… 9.45 mg

Each mL of the 200 mg/mL solution contains:

Testosterone Cypionate……………………………………………………………………. 200 mg

Benzyl benzoate………………………………………………………………………………. 0.2 mL

Cottonseed oil………………………………………………………………………………… 560 mg

Benzyl alcohol (as preservative)………………………………………………………… 9.45 mg

Where to buy high purity Testosterone Cypionate powder online?

Testosterone Cypionate powder is a moderately popular compound within the anabolic steroid world, and often competes with Testosterone Enanthate for popularity. There should be no problems locating this product on the market, as it is quite common and also easily manufactured.

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Sibutramine in treating obesity: You must know more about sibutramine!!!

Sibutramine in treating obesity: You must know more about sibutramine!!!

 

What is sibutramine?

Sibutramine is a medication that assists with weight-loss by altering neurotransmitters within the brain. Neurotransmitters are chemicals that are produced and released by nerves in order to communicate with other nerves. Released neurotransmitters may attach to other nerves or they may be taken up again by the nerves that release them, a process termed reuptake. Sibutramine blocks the reuptake of the neurotransmitters dopamine, norepinephrine, and serotonin. Blocking the reuptake of neurotransmitters alters the balance of neurotransmitters within the nerve cells and thereby affect nerve function and interaction.

Meridia is found to be highly effective in the treatment of obesity as the medication is able to bring down the additional flab in the body in a gradual way spread over a period of time. If the weight loss program is accompanied by a proper diet and right medication like Meridia it leads to a definite reduction in body weight and also opens up the clear passage of healthy life. Obesity is a commonly reported problem affecting many people and it’s also understood by the patients how difficult it is shed the excess weight. When the body has excess weight it becomes a persisting problem for the individual to perform even simple tasks. With obesity as the main ailment, other issues also step into the body and make the affected person suffer on the whole.

Sibutramine Mechanism of Action

1. Sibutramine (the active ingredient in Meridia) is a powerful central nervous system stimulant similar to amphetamines, and chemically related to Phentermine ( the active ingredient in the weight loss drug Adipex).
2. Sibutramine works by increasing Serotonin and Norepinephrine levels in the brain, which leads to appetite suppression.
3. This drug was initially developed as an antidepressant, and later approved by the FDA for the treatment of obesity.

How does sibutramine works?

Sibutramine offers three types of benefit in weight management: by enhancing weight loss, by improving weight maintenance and by reducing the comorbidities of obesity. The clinical effects of sibutramine are explained through its known mode of action as a serotonin (5-HT) and noradrenaline reuptake inhibitor (SNRI). This dual mechanism of action results in two synergistic physiological effects–a reduction in energy intake and an increase in energy expenditure, which combine to promote and maintain weight loss.

How to Use Sibutramine hydrochloride?

Sibutramine is usually taken 10-15mg a time,once daily. Follow your doctor's instructions.Your doctor may occasionally change your dose to make sure you get the best results.Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.

Sibutramine can be taken with or without food.You should lose at least 4 pounds during the first 4 weeks of taking sibutramine and eating a low calorie diet. Tell your doctor if you do not lose at least 4 pounds after taking the medication for 4 weeks.

Sibutramine should not be taken for longer than 2 years.Store at room temperature away from moisture, heat, and light.Do not share sibutramine with another person. Keep the medication in a place where others cannot get to it.

Your blood pressure and pulse will need to be checked often. Visit your doctor regularly.Overdose symptoms may include headache, dizziness, and fast heart rate.

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Sibutramine Dosage

Usual Adult Dose for Obesity

Sibutramine was voluntarily withdrawn from the US market by the manufacturer in October, 2010 due to clinical trial data indicating an increased risk of heart attack and stroke. The following dosage information applies to when the drug was available in the US.

Initial Dose: 10 mg orally once a day.

Usual Geriatric Dose for Obesity

Sibutramine was voluntarily withdrawn from the US market by the manufacturer in October, 2010 due to clinical trial data indicating an increased risk of heart attack and stroke. The following dosage information applies to when the drug was available in the US.

Clinical studies of sibutramine did not include sufficient numbers of patients over 65 years of age. Sibutramine is contraindicated in this group of patients.

Usual Pediatric Dose for Obesity

Sibutramine was voluntarily withdrawn from the US market by the manufacturer in October, 2010 due to clinical trial data indicating an increased risk of heart attack and stroke. The following dosage information applies to when the drug was available in the US.

Based on one study (n=60)

14 to 17 years:

Initial Dose: 10 mg orally once a day.

The recipe of sibutramine(Making by yourself)

About sibutramine hydrochloride Customers use  feedback solutions(The recipe is for reference only):
1. Our products are sibutramine hydrochloride, purity 99%, pharmaceutical grade.
2. The commonly used method in the market is
  1). Mixed sweet potato leaves, lotus leaves, coffee powder and other plant extracts, such plant extracts are alkaline substances, with sibutramine hydrochloride mixed use, acid-base neutralization, reduce or lead to product weight loss effect instability.
  2). Direct use of sibutramine hydrochloride, each capsule content 20-30mg, daily dose not exceed 200mg.
  3). From the pharmacy, it is recommended that the use of grape sugar and sibutramine hydrochloride mixed capsules, recommended dose 30mg.
3. Recommendations on the production of equipment:
  1). The use of air pressure filling equipment to ensure that the net content of each capsule to achieve the specified value.
  2). The use of mechanical mixing equipment to ensure that the drug and other accessories fully mixed.
4. With regard to testing
Customers are recommended to use our products directly in the third-party laboratory or Annex University chemical laboratory testing, with a test report, can be reimbursed for testing costs and sample costs.

https://player.vimeo.com/video/244301098?badge=0

Sibutramine treat obesity(Sibutramine's application field)

Even if sibutramine has serious side effects, it is still a lot of weight loss products manufacturers, the most important raw materials in use, such as weight loss coffee, diet drink, jelly, etc., to lose weight is inseparable from the use of sibutramine.Adding proper sibutramine powder in these products can help improve the timeliness of medicine and help customers to achieve the desire to lose weight.

How sibutramine works in treating obesity?

Sibutramine(Meridia) has a direct influence on the brain as the very first step after the taking Meridia. As the nervous system acts as the center for controlling all the physical activities in the body, it becomes essential for the pill to propel its action in the brain. Meridia interacts with the chemicals in the nervous system that have a direct impact on the weight of the body.

The pill is suggested by experts to be taken as a blend with the daily diet to see the actual results within a specified time frame. Obesity is found to lead to other problems like spike in blood pressure, and other health issues like diabetes. The diet intake should be of low calorie along with an appropriate exercise regimen.

How effective is sibutramine in treating obesity?

Sibutramine(Meridia) is found to be highly effective in the treatment of obesity as the medication is able to bring down the additional flab in the body in a gradual way spread over a period of time. If the weight loss program is accompanied by a proper diet and right medication like Meridia it leads to a definite reduction in body weight and also opens up the clear passage of healthy life. Obesity is a commonly reported problem affecting many people and it’s also understood by the patients how difficult it is shed the excess weight. When the body has excess weight it becomes a persisting problem for the individual to perform even simple tasks. With obesity as the main ailment, other issues also step into the body and make the affected person suffer on the whole.

Pay attention on 3 things when making Diet Tea or others

Like this situation, it is said that not only in Singapore, there are many countries in Europe and North America, consumer reaction side effects, the actual effect is not obvious, were found to contain sibutramine, therefore, make the weight loss products manufacturers did not notice the control, the side effects of product after adding sibutramine not grasp good production proportion.

Here, we have to remind manufacturers of weight loss products (diet tea, weight loss coffee, diet jelly, etc.) that manufacturers should pay attention to the following issues:

1. Control the degree of acid and alkali of the product, so as to prevent the salt from being turned into salt in the acid base, resulting in the invalid product;

2. Sibutramine can not be mixed with plant extracts, plant extracts are generally strong alkaline, while sibutramine is strongly acidic, and it will also become salt after blending.

3. If you do not add other recipes properly, you will have obvious side effects: constipation, stain on your face, bad breath, etc.

Sibutramine side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Stop using sibutramine and call your doctor at once if you have a serious side effect such as:

1. fast, pounding, or uneven heartbeats;
2. new or worsening shortness of breath;
3. agitation, hallucinations, fever, tremor, overactive reflexes, nausea, vomiting, diarrhea, loss of coordination, dilated pupils;
4. very stiff (rigid) muscles, high fever, sweating, confusion, feeling like you might pass out;
5. easy bruising or bleeding (nosebleeds, bleeding gums, or any bleeding that will not stop);
6. dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, seizure);
7. chest pain or heavy feeling, pain spreading to the arm or shoulder, general ill feeling; or
8. sudden numbness or weakness (especially on one side of the body), problems with vision, speech, or balance.

What should I avoid while taking sibutramine(Warning of sibutramine)?

Sibutramine may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Do not take any other prescription or over-the-counter weight-loss products without your doctor's advice.

Avoid taking cough and cold or allergy medications while taking sibutramine.

Avoid drinking alcohol while taking sibutramine.

Sibutramine price
The price of sibutramine in the market is relatively expensive, especially for capsules and tablets, which will add a variety of materials to make, making its own value and price are out of proportion.
It is reasonable to choose the high purity of sibutramine powder, the powder is easy to test the purity, and can quickly distinguish the value of it.So sibutramine powder may be a better choice for users.
Here give a reference value，In general，sibutramine：USD50/10g,USD160/100g.

Buy sibutramine powder online

Visit our online pharmacy (AASRAW)and fill in an order of Meridia (Sibutramine). Define place of delivery, quantity of the product and the way of payment. In the period of 30 minutes, you will receive a confirmation of your order. It will be delivered within 10 business days.

100% Quality. We work only with licensed and reliable suppliers, which allow us to offer you best quality products at a very good price. Any product we offer (brand or generic) is a product which gained a very good reputation among our customers and was acknowledged by FDA.

Online order status check. We offer our customers a very convenient option to receive an update on order status. You can see the progress of your order beginning from the placement up to the delivery. Moreover you can contact our 24/7 support and receive any information you need without going online.

We accept bank transfer,WesternUnion Payment,MoneyGram Payment, Bitcoins….

We are able to ship to the following countries: United States, Canada, UK (Great Britain), Australia, Belgium, Denmark, Finland, France, Greece, Ireland, Italy, Spain.ect.

We have a guaranteed delivery. The standard shipping period takes from 14 to 28 business days. The order will be shipped via Registered airmail.

In case of any problems with the order we will offer you a free of charge re-shipment or a full refund of the amount.

More please read web site:www.aasraw.com.

 

Modafinil – Top Smart Drug with Nootropic Benefits

 

 

1.What are Smart Drugs?

Nootropics, or smart drugs, are being used around the world by students, entrepreneurs, small business owners, athletes, poker players and housewives. They are used to boost learning ability, improve memory function, enhance focus and concentration, and even to improve verbal and written communication skills.

 

2.What is Modafinil?

Modafinil is an wakefulness-promoting analeptic drug distributed by Cephalon Inc. and approved as a drug by the FDA (Food and Drug Administration) in the United States. While originally tested as a drug to treat certain sleep disorders, it is sometimes classified as a “smart drug” that is known to improve the performance of a subject who is impaired by fatigue and a lack of sleep.

You will also see it sold under the names Provigil, Sun Pharma Modalert, Alertec, Modapro, and Modiodal.

Modafinil was originally discovered in 1976 by a French medical professor Michel Jouvet in combination with the pharmaceutical company Cephalon. After it was seen to cause hyperactivity in animal studies it went on to be used for the first time in humans as an experimental treatment for narcolepsy in 1986.

Since then, the uses of Modafinil have expanded onto other sleep-related conditions, such as shift-work sleep disorder and chronic daytime sleepiness associated with obstructive sleep apnea.

Modafinil is also famously used by the British and American military for keeping soldiers awake and functioning at high levels for up to 40 hours at a time. Studies have also determined Modafinil to be effective at reducing or eliminating the damaging effects of short-term sleep deprivation on the brain.

For this reason, it is commonly used as a nootropic to enhance cognitive performance especially in individuals who otherwise do not get enough sleep.

 

3.How Modafinil Works?

The exact mechanisms of action of Modafinil in the body are unknown. Research has shown that this medication has effects on various neurotransmitters in the brain and central nervous system including Histamine, Dopamine, Epinephrine (Adrenaline), Norepinephrine (Noradrenaline), Serotonin, and Orexin (Hypocretin).

Taking Modafinil has been seen to raise histamine levels and and locomotor activity in the central nervous system. Modafinil’s effects are shown to wear off once the natural neuronal histamine concentration has been depleted by a powerful inhibitor. This runs counter to a similar drug called methylphenidate, which does not react in the same manner to fluoromethylhistidine, a histidine decarboxylase inhibitor.

Modafinil, the drug’s main active component of the same name, has not yet been fully researched to the extent that could reveal all the principles behind the way it operates. Several studies have discovered that it works by altering the CNS levels of histamine in the human body.

Controlled studies on mice revealed that the drug makes its way into the orexinergic system. Orexin is a peptide that acts as a neurotransmitter and is involved in the regulation of sleep/arousal states and the maintenance of vigilance. Test subjects that lacked the appropriate neuron failed to react as expected, pointing out the utmost importance of orexin in these processes.

In research Modafinil has been seen to affect Dopamine and its signalling pathways. In a study that looked at many different pathways and their neurotransmitters, Modafinil was seen to affect the Dopamine transporter, acting as a Dopamine reuptake inhibitor. An additional study using PET scans in human patients saw that by occupying the Dopamine transporter sites, Modafinil significantly increased levels of Dopamine in the brain.

 

4.Modafinil Uses and Benefits

Modafinil has been shown to help people stay awake and active, as well as make their mind much clearer if their memory has been previously worsened by the onset of sleep deprivation.

Studies have successfully shown a correlation between the use of this drug and retaining cognitive function in a healthy state against factors like a lack of sleep. However, not all of them could connect Modafinil to an improvement in psychomotor function in human test subjects.

 

Narcolepsy, Shift-Work Sleep disorder, and Sleep Apnea
Narcolepsy is a neurological condition that affects control of wakefulness and sleep. The condition causes excessive daytime sleepiness, and can even cause people to randomly faint and fall asleep throughout the day. The exact cause of narcolepsy is unknown, although there are several possibilities, and a strong link with certain genetic factors. Part of the mechanism is due to a loss of orexin releasing neurons in the brain.

In multiple double-blind placebo-controlled research studies, Modafinil has been seen to be an effective treatment for reducing daytime sleepiness in people with narcolepsy. Scores on the Multiple Sleep Latency Test and the Maintenance of Wakefulness Test are greatly improved using Modafinil over placebo. Nighttime sleep monitored during trials using polysomnography has been found to not be negatively affected using Modafinil compared to placebo.

Upon discontinuation of treatment, symptoms of narcolepsy were seen to return in patients to their baseline levels when not receiving treatment. There have not been reports of people developing withdrawal symptoms seen with other stimulants like amphetamines, and development of dependence does not seem to be an issue either. The most commonly reported adverse effect in studies of Modafinil for narcolepsy has been headaches, and the levels were not significantly greater than what was reported with placebo.

Researchers have therefore concluded that Modafinil is a generally well-tolerated treatment option for managing narcolepsy, and it most commonly prescribed for this original treatment purpose. Usage for other sleep disorders has grown as well, especially shift-work sleep disorder and obstructive sleep apnea/hypopnea syndrome.

Shift-work sleep disorder is a circadian rhythm disorder that occurs when people have jobs that they work during normal nighttime sleep periods. This can be people who consistently work the night shift of various jobs or those that have a rotating schedule that causes them to intermittently work night shifts. This is also seen in some people who work very long shifts, such as doctors.

Like narcolepsy, people with shift-work sleep disorder experience excessive daytime sleepiness. Additionally, they may experience insomnia when trying to sleep outside of normal sleep hours (i.e. during the daytime). If people are able to return to normal sleep patterns than symptoms will resolve themselves, however this is not an option for most people.

In one study, patients with shift-work sleep disorder were given either 200 mg of Modafinil or placebo before their shifts. Patients treated with Modafinil were seen to have a reduction in frequency and duration of attention lapses when tested on a vigilance test. A modest improvement in latency to sleep time was also seen.

However despite these improvements, patients continued to have some excessive sleepiness and impaired performance at night. Researchers have said that because of this residual sleepiness that still occurs that the development of even more effective treatments is necessary.

Obstructive sleep apnea/hypopnea syndrome (OSAHS) is a potentially serious disorder that occurs when the muscles supporting the tongue and soft palate in the mouth relax and cause the airway to be partially or completely blocked. Apnea refers to periods of total blockage and no breathing, while hypopnea refers to slow or shallow breathing that occurs with partial airway obstruction.

Symptoms of sleep apnea include loud snoring, observed periods of breathing cessation while sleeping, waking up choking, awakening with dry mouth and sore throat, morning headaches, and excessive daytime sleepiness.

Modafinil is therefore sometimes used as an adjunct therapy for treating the symptoms of sleep apnea. Its use is not to try and cure the disorder, but rather to improve the daytime sleepiness that often occurs due to the disrupted sleep patterns caused by breathing troubles at night. Multiple double-blind placebo-controlled research studies have shown that Modafinil significantly improves daytime sleepiness compared to placebo.

 

Attention Deficit disorder & Attention-Deficit Hyperactivity disorder
One of the most common off-label uses of Modafinil is for Attention Deficit disorder (ADD) and Attention-deficit Hyperactivity disorder (ADHD). Many people use Modafinil for these conditions because of the stimulant effect it has. Many user reviews online state that using Modafinil for ADHD helps them stay motivated and focused on the task at hand.

Other review also mention that Modafinil use doesn’t have some of the more serious negative side effects (e.g. anxiety, depression) experienced with traditional medication such as Adderall, Ritalin, dextroamphetamine, and dexmethylphenidate.

Multiple research studies have tested using Modafinil to manage ADHD in adults. Some studies compared Modafinil to a placebo, while others compared both Modafinil and conventional medications to placebo.

One study tested the effectiveness of Modafinil compared to the conventional drug dextroamphetamine. Patients who took either of the active medications were seen to have significantly improved scores on the DSM-IV ADHD Checklist when compared to placebo. The researchers concluded that Modafinil pills are a viable alternative to conventional stimulants in adults with ADHD.

A double-blind, randomized, placebo-controlled crossover study found that a 200 mg dose of Modafinil was able to produce a similar pattern of cognitive enhancement in patients with ADHD compared to healthy patients. The researchers concluded that Modafinil has potential as an alternative treatment therapy for ADHD compared to traditional stimulants.

Use of Modafinil in children for ADHD is not recommended at this time. A study conducted using a specific high dose form of Modafinil called Sparlon in children with ADHD ended with some serious negative side effects in a small number of the participants.

Stevens-Johnson syndrome is a rare and serious disorder of the skin and mucous membranes. Its primary symptoms are fever, fatigue, widespread skin pain, a red or purple spreading rash, and blisters on the mucous membranes of the mouth, nose, eyes, and genitals.

Multiple studies since that time have shown the efficacy and safety of Modafinil use in children for ADHD, however it is not approved for use in this group. Additionally, Modafinil is currently not approved by the FDA as a drug to treat ADD or ADHD in adults, and more research is still needed to determine its full effects on these disorders.

 

Symptoms of Fatigue in Depression and Multiple Sclerosis (MS)
One of the most commonly reported symptoms associated with chronic depression is fatigue. Even in patients who are successfully being treated with conventional antidepressants like Selective Serotonin Reuptake Inhibitors (SSRIs) and having improvement in other symptoms associated with depression, fatigue and excessive sleepiness can still persist.

Additionally, some patients do not respond as well as wanted to conventional medications, and the combination of those antidepressants along with Modafinil has been seen work in some cases.

Multiple double-blind placebo-controlled studies have looked at the Modafinil augmentation in patients with fatigue and sleepiness who are only partially responding to traditional SSRI treatment for depression. In three separate but similar studies, Modafinil was used as an adjunct treatment with SSRI antidepressants in patients who were partial responders or nonresponders to the SSRIs alone.

In all three trials, Modafinil was seen to significantly improve fatigue and sleepiness in patients in the short term (less than 6 weeks). The researchers concluded that Modafinil may be a useful adjunct treatment for some patients with depression, especially those with fatigue issues.

As seen in patients with depression, one of the most common symptoms associated with Multiple Sclerosis is fatigue. Less research has been done on patients with this condition, however what has been done is promising.

One study was a single-blind, phase 2, two center study that compared Modafinil to placebo in improving fatigue severity in patients with MS. The patients were first given placebo for weeks 1-2, then 200 mg Modafinil pills for weeks 3-4, 400 mg Modafinil pills for weeks 5-6, and then placebo again for weeks 7-9.

The investigators were not blind to treatment to ensure safety of the participants. To ensure unbiased results, efficacy of treatment was evaluated using self rating scales, the primary test being the Fatigue Severity Scale (FSS).

It was found that fatigue and daytime sleepiness was significantly improved using the 200 mg dose of Modafinil, compared to both the 400 mg Modafinil dose and the placebo. The researchers said it was unclear why the higher 400 mg dosage did not maintain the improvements seen with the 200 mg dosage, concluding that it may have been due to tolerance or possible dose-related adverse effects that masked any possible benefits on fatigue.

Overall the researchers concluded that Modafinil may be a well tolerated and effective treatment for improving fatigue and sleepiness in people with MS.

 

Nootropic Cognitive Enhancement Effects
Some of the most common off-label uses of Modafinil are using the drug as a nootropic drug for cognitive enhancement. Various people from university students to Wall Street bankers to entrepreneurs use Modafinil to improve memory, learning, focus, and attention span.

One review study that examined the findings of previous research studies found that Modafinil specifically shows improvement in working and episodic memory following use.

Another review concluded that Modafinil primarily improves cognitive function in relation to executive function, especially when planning and executing difficult and complex tasks.

One double-blind between-subjects research study looked at the potential cognitive enhancing effects Modafinil had on healthy adult males.

It was found that Modafinil use significantly enhanced the participants performance on various neuropsychological tests including visual pattern recognition, spatial planning, and a stop-signal reaction test. Conversely, responding to certain tests was seen to be decreased, suggesting that Modafinil may help inhibit impulsivity and improve response accuracy.

Similarly to user reviews found in online nootropic forums, participants in the study reported feeling more alert and attentive on Modafinil, and having improved energy levels.

More research is needed in this area to full determine the effects Modafinil may have on healthy individuals to improve cognitive abilities.

 

5.Modafinil Side Effects and Dosages

Modafinil is considered to be safe with no dangerous side effects when used as directed. There are some mild Modafinil side effects which you may encounter during the course of normal use.

Through careful medical studies of the drug, researchers have determined the following list of potential adverse effects that can be caused by Modafinil:

Headache
Nausea
Nervousness
Rhinitis (inflammation of the nasal mucosa)
Lack of appetite
Diarrhea
Rapid weight loss
Insomnia
Hypertension
Dry mouth
Vomiting
Some of the more rare but serious potential side effects of Modafinil are various different skin rashes and reactions, including the previously mentioned Stevens-Johnson syndrome, Drug reaction with eosinophilia and systemic symptoms (DRESS), and Toxic Epidermal Necrolysis (TEN).

If you encounter any of these side effects while taking Modafinil pills, you should consult your doctor or pharmacist. If you would like to use this medical product, ask your doctor for a prescription or investigate whether you are eligible to buy Modafinil online in your country without a prescription.

When used for on-labels uses, Modafinil is typically prescribed at doses of 200 mg per day. Sometimes a lower dose of 100 mg per day is used to start, and then the dosage is increased to 200 mg gradually in individuals who may be sensitive to the full dose to start.

There are no commonly recommended dosages for Modafinil for off-labels uses. Most people will follow similar dosages to prescribed dosages, typically around 200 mg per day.

It is a good idea to read Modafinil reviews and user experiences before you take your first dosage so that you know exactly how this drug may affect you.

 

6.Adrafinil vs. Modafinil vs. Armodafinil

Adrafinil is a compound that is very similar to Modafinil in structure and usage. The two compounds are very similar in molecular structure; the only difference in composition is Modafinil is lacking an amide hydroxyl group that Adrafinil has.

Adrafinil acts as a prodrug of Modafinil. This means that it converts to Modafinil in the body, and then acts in a similar manner. Adrafinil was actually discovered two years prior to Modafinil in 1974 by the same pharmaceutical company that first discovered Modafinil.

Because it needs to be converted into Modafinil in the body, Adrafinil is not as potent as Modafinil. Not all of the Adrafinil in a dose of this drug will be converted into Modafinil, most is converted into the inactive modafinilic acid.

Modafinil is technically a 1:1 combination of two enantiomers, R-Modafinil and S-Modafinil. Enantiomers are mirror image versions of the same compound; therefore they have the same molecular components, just the structure is different.

On its own, the R enantiomer of Modafinil is known as Armodafinil. As a drug, Armodrafinil is used for the same purposes as Modafinil, namely improving wakefulness in people with sleep disorders and excessive sleepiness. The half-life of Armodafinil is longer than Modafinil, which can make it more effective in some cases.

The most popular name brand version of Armodafinil is Nuvigil, which is produced by the company Cephalon, which also produces the most popular brand name version of Modafinil – Provigil.

 

7.Where to buy Genuine Modafinil raw powder online? 

You can find many Modafinil powder source online, but it is hard to buy Genuine Modafinil raw online. There are many sources selling fake products at the market. so when you buy Modafinil raw material online, you need to choose an realiable source. 

Primobolan is the most widely used anabolic steroid in cutting steroid cycles

 

 

1.What is Primobolan?

Primobolan is the trade name for the anabolic steroid Methenolone (also written as Metenolone). It is available in both an injectable oil-based format, as well as an oral form. Injectable Primobolan is known as Methenolone Enanthate, and the oral format is known as Methenolone Acetate. It is a very well-known and popular anabolic steroid due to its very mild nature as both an anabolic and an androgenic compound. 

Primobolan is an oral anabolic steroid that is a little unique compared to many oral anabolic steroids. Before we go any further, it’s important we distinguish the difference between Primobolan and Primobolan Depot. Primobolan Depot is an injectable version of the hormone that is attached to the large/long Enanthate ester. Primobolan is comprised of the same active steroidal hormone in Methenolone; however, it is attached to the small/short Acetate ester and designed for oral administration.

Primobolan is considered one of the safest anabolic steroids on the market and it carries an excellent safety rating to back this claim. In fact, this steroid has been used successfully to treat underweight children and premature infants without damage. It is also prescribed for osteoporosis and sarcopenia. However, the primary purpose of Primobolan is treating muscle wasting diseases and prolonged exposure to corticoid hormones. It has also proven to be extremely effective in treating malnutrition.

Playing an important role in therapeutic treatment plans, Primobolan is a very popular anabolic steroid among performance enhancing athletes. However, the injectable Depot version is far more popular as the oral version packs a much weaker punch. For bodybuilders, injectable Methenolone Acetate is the preferred form but a quality injectable Acetate version is very difficult to find. Further, the Methenolone hormone itself, while limited in oral form is one of the more commonly counterfeited anabolic steroids out there. It is also fairly expensive in many underground markets. This hormone is well-known for being one of Arnold Schwarzenegger’s favorites. How much truth is in that only he can say, but the story is enough for many to make inaccurate assumptions about his feelings on the hormone and how he used it. That we do know. It’s also been enough to keep the demand for this steroid fairly high, as well as plague the market with counterfeits.

An important note on demand; the demand for this steroid is also high due to its very female friendly nature. This is one of the few anabolic steroids women can use with a high rate of success. Steroids like Primobolan and Anavar carry very low virilization ratings making them perfect for female use.

 

2.The Effects of Primobolan

Primobolan is used to treat muscle wasting diseases in some cases; however, typically only in mild cases or where an immune boost is a benefit. This steroid is not going to pack on mass like Anadrol or Deca Durabolin and most men will not have much use for it in an off-season bulking cycle. We can, however, make an exception for females. Women are far more sensitive to anabolic steroids and a little of a mild anabolic steroid can go a long way. Just as important, most women are not looking to gain 30lbs of weight overnight. Small, moderate increases in weight can often be transforming on their own. Keeping the mild nature in mind, most men who use this steroid for a true off-season cycle will be disappointed.

Where Primobolan will truly shine is as a cutting steroid. In order to lose body fat, we must burn more calories than we consume. While absolutely necessary, this also puts our lean muscle mass at great risk. In fact, even if planned perfectly a fat loss diet will result in some lean muscle tissue loss unless an anabolic protectant is applied. Even with such protection a little tissue loss may occur, which should tell you how important an anabolic agent can be. The key to successful dieting is not simply losing weight, but losing fat while protecting your muscle mass; if these ends are not being met, your diet has not been successful. With a well-planned diet, Primobolan will help you achieve this goal. It has also been shown to have some fairly nice conditioning effects. Those who use Primo often appear harder and more defined. However, most will find the Depot version to be more efficient in the cutting phase, and this includes women.

Primobolan is also well appreciated in athletic circles. A moderate boost in strength is very possible with this steroid. Strength can refer to power and speed, both key elements to successful athleticism. However, where this steroid will truly be useful is in the promotion of recovery. Muscular endurance will also be enhanced and while such traits won’t be as strong as they are with many steroids, any bump is better than no bump at all. Further, as it’s a mild steroid, the athlete will not have to worry with massive buildups in size. In some cases, a lot of added size can be detrimental to performance depending the sport or position. In other cases, it can bring a lot of unwanted attention to the individual with prying eyes.

During a bulking phase Proviron is not going to be a foundational steroid, and for most men it will not have a place in an off-season cycle. There are exceptions and we’ll go over those here. Adding in Proviron could possibly help the individual breakthrough a sticking point during his cycle. At some point and time in all cycles the progress begins to wane, and in some cases come to a complete halt. By the way Proviron enhances the total free state of the other steroids being used in a stack, it could possibly help the individual breakthrough this sticking point. During the off-season, this is where most will use the largest amount of testosterone. Many will use large amounts during cutting cycles too, especially competitive bodybuilders but lower testosterone plans are more common during the cutting phase. However, there are those for numerous reasons who choose to run off-season cycles with limited testosterone doses. In such plans, including Proviron could give them a slight needed androgen boost. While it may not always be necessary it could prove to be beneficial.

Without question the best time to use Proviron will be during the cutting phase. This steroid has the ability to provide a bit of a hardening effect similar to Masteron, but more importantly the hardening effects of other steroids will be enhanced. Then we consider its strong binding to the androgen receptor, which will in fact enable the individual to burn body fat at a far more efficient rate. From here we must consider the anti-estrogen effect of Proviron. This will ensure the individual is less prone to water retention and as discussed, depending on the total cycle, it could negate the need for a traditional anti-estrogen. Then we’re once again left with the enhancement of circulating free testosterone. This can be a tremendous benefit when testosterone levels are often much lower during this phase of anabolic steroid use. In fact, with a low dosed testosterone cycle that includes other anabolic steroids, we can confidently say the total results will be greater for the individual who includes Proviron compared to the one who does not. In the end, the primary base benefit is the increased androgenicity of other steroids being used in order to promote a much harder and far more defined physique. It should be noted while Proviron can most certainly provide these traits they will not be noticeable unless you are lean.

 

3.Primobolan Cycles and Use

Primobolan cycles are commonly in the form of fat loss and/or cutting cycles. It is almost never used as a bulking or mass-gaining agent, and most of its use is in the form of a pre-contest drug in the final weeks leading up to a competition show or photo shoot. It is typically cycled with other compounds that hold similar qualities, properties, and half-lives. Many bodybuilders often stack Primobolan with Testosterone Propionate (or Testosterone Enanthate) and use it for the first 8 weeks of a cycle in order to assist in the retention of muscle mass during periods of low caloric intake.

Other bodybuilders will perform oral Primobolan cycles stacked with compounds such as Testosterone Propionate and Trenbolone Acetate, as all of the compounds involved work synergistically especially where half-lived are concerned. Some may opt to use Primobolan (either the oral or injectable) with some form of Testosterone and Winstrol (Stanozolol), typically the injectable form if it is with the oral Primobolan. It is important to remember not to utilized two different oral compounds within the same cycle.

Oral Primobolan (Methenolone Acetate) should normally be run for no longer than 8 weeks, and the injectable form (Methenolone Enanthate) can be run in cycle lengths of 10 – 12 weeks (or longer, depending on the individual’s goals and desires).

 

4.Primobolan Dosages and Administration

Primobolan dosage and administration depends heavily upon which form is being used: oral or injectable. Medical prescription Primobolan dosages outline 200mg as a first dosage, followed with 100mg every week for the complete duration of therapy. The medical condition being treated would determine what the actual full Primobolan dosage is. The range can be anywhere from 100mg every one or two weeks to 200mg every two to three weeks. Medical guidelines for oral Primobolan dosages call for 100 – 150mg per day for no longer than 6 – 8 weeks of consistent use.

Where bodybuilding, athletics, and performance enhancement is concerned, beginner Primobolan dosages for the injectable format normally start at about 400mg per week. Intermediate Primobolan dosages are usually in the range of 400 – 700mg per week, which should be adequate enough, and advanced users may venture as high as 800 – 1,000mg per week. Female Primobolan dosages in terms of safety and minimal virilization are usually in the range of 50 – 100mg per week. Injectable Primo tends to be used far less frequently by females than the oral variant, which is the preferred form.

Oral Primobolan dosages begin in the range of 50 – 100mg per day for beginners, 100 – 150mg per day for intermediates, and 150 – 200mg for advanced users. Female oral Primobolan dosages are usually recommended to be within the range of 50 – 70mg per day, and should present little risk of virilization.

Oral Primo should be administered once per day with no requirement to split up dosages throughout the day, as its half-life is about 2 – 3 days. Injectable Primobolan exhibits a half-life of 7 – 10 days due to the Enanthate ester, and should be administered twice per week, with each injection spaced evenly apart, in order to maintain stable and steady blood plasma levels.

 

5.Primo for Bulking or Cutting

Primobolan is one of few steroids that is ideal for both bulking and cutting.  The truth be told, there really is no such things as “bulking steroid” or a “cutting steroid” it’s just that some generate more water retention than others. That can work in your advantage if you’re looking to put on weight (even water weight) in order to get your body adapted to more mass. And the feeling of busting out of your shirtsleeves can be fun too.  But beyond water retention, bulking and cutting is more a matter of diet. Primo will not produce fast increases in weight weight by itself, but if calories are increased it’s a wonderful drug for bulking without the bloat. (What some people call a” lean bulk”). Of course, in a calorie deficit Primo will still create muscle growth, making it a favorite for  competitive bodybuilders in the last few weeks before a contest.

 

6.Stacking Primoblan

As great as Primo is, most guys feel they need to kick it up a notch by adding something stronger and in that regard, Primo is  very easy to stack since it goes with anything. There are no contraindications with other steroids and whatever else you’re using, Primobolan will simply add a greater anabolic impact to it.  The most logical stacking choice with Primo would be testosterone. Test goes with everything as well and the combination is a winning one. Not being particularly androgenic (even though, like all steroids, it’s based off of the testosterone molecule) Primobolan  can still cause some suppression since the androgenic quality would be just enough to suppress but not high enough to add more than the  body would produce on its own.  This is one of the criticisms of Primo. For maximum growth, some androgen elevation is needed.  The induced suppression along with the lack of androgen replacement can lead to a slight loss of libido. Adding a little testosterone  rectifies that potential pitfall plus increases greater muscle building potential. Together the two steroids provide all you want and need from a cycle. Stacking multiple injectable compounds is usually unnecessary.

If you’re looking for a “kick start” to you cycle Primo also stacks especially well with fast acting orals.  When using Primoboaln with Dianabol you’ll get the initial  impact of the D-bol along with the sustained solid muscle build up for the Primo. It’s the best of both worlds.  But when using an oral, ALWAYS use a proper liver protection supplements.  (N2GUARD, Protein Factory POST- CYCLE and LIV 52 are among the best and the most popular. Better yet – use all three).   Rumor has it that Arnold took a 100mg shot of Primobolin a day along with 25mgs dianabol tabs a day. That was regarded as pushing the envelope back in “the day” though by today’s standards it’s pretty mild.  It’s also a pretty good stack.  The two compliment each other well and you can get both the increased size and blood volume along with the superior nitrogen retention and relative safety.

 

7.Primobolan For Women

Primo is considered the best choice for women due to its low androgenic qualities and consequent lean gains.  Women tend to want to avoid excessive bulkiness and the smoothness that comes from water retention.  Also, since estrogen creates a “soft” look, steroids that aromatize can destroy the aesthetic they’re attempting to achieve. One drug which creates hardness without bloating or estrogen buildup is Masteron, but Masteron is a pure androgen. This can lead to the masculinizing side effects most women seek to avoid —  hair loss, body hair growth,  tougher skin, a deeper voice and most disturbing, enlargement of the clitoris.  Since Primo is almost purely anabolic, these sides are kept to an absolute minimum if dosages are kept reasonable. Women usually respond very well to a dosage of 50-100mg per week, although many opt for the oral version who feel it’s better at burning fat, though this is pure speculation and anecdotal. There’s no evidence to suggest as much, but empirical evidence is not without some merit.

Additionally, some woman choose to include other anabolics such as Winstrol or Anavar, but this just redundant.  Mixing too many steroids has no benefit and can be a detriment since it becomes unclear which are working best. If you like Primoblan, use Primobolan. And especially in the case of woman, there’s usually no need for add-ons. A popular recommendation for women would also be to first experiment by using Primobolan on its own, and later venture into a second steroid if necessary.

 

8.Primobolan Side Effects

The first thing to understand with Primobolan is that it is a DHT-derivative, meaning it is a modified form of DHT (Dihydrotestosterone). As such, it carries with it many similar properties and characteristics, including the inability to convert (aromatize) into Estrogen at any dose used. This should certainly be a comforting fact to most individuals who are concerned about Estrogenic side effects, such as bloating, gynecomastia, high blood pressure as a result of water retention, etc.

Although the oral format of Primobolan is C-17 Alpha Alkylated (also known as Methylation), which is a process that tends to make oral compounds present a degree of harm to the liver, Primobolan has never shown any measurable hepatotoxic effects to the body. Although oral Primo does not impose any measurable negative effects on the liver, it still presents some small amount of hepatotoxicity and this should still be understood, especially when it comes to extended cycle lengths and/or very high dosages. With that being said, one death of an anemic patient who was prescribed oral Primobolan has been linked to its use. Once again, high doses and/or very long cycle lengths of oral Primobolan may be a concern.

As much as Primobolan is touted by athletes and bodybuilders as being a"mild"anabolic steroid, it still exhibits suppression of endogenous Testosterone production and HPTA function. In fact, studies have confirmed that at even a very low dosage (30 – 45mg daily), test subjects experienced 15 – 65% suppression of natural endogenous Testosterone production[9]. Being that those dosages as far lower than what is required for performance enhancement purposes, it is still heavily recommended to perform a proper PCT (Post Cycle Therapy) following the discontinuation of Primobolan.

 

9.Where to buy Genuine Primobolan raw powder online?

You can find many Primobolan powder source online, but it is hard to buy Genuine Primobolan raw online. There are many sources selling fake products at the market. so when you buy Primobolan raw material online, you need to choose an realiable source.

Anavar is one of the best cutting steroid used by men and women

 

 

1.What is Anavar?

Anavar represents one of the most popular oral anabolic steroids of all time, and this is largely due to its well-tolerated nature. This is one of the few anabolic steroids that can be used safely by men and women, and it’s also one of the most side effect friendly. However, in some circles Anavar is greatly underappreciated due to its mild nature, but this is generally due to unrealistic expectations. Many tend to assume all anabolic steroids should yield a set of specific effects at a specific rate of power, but reality tells us varying steroids carry varying results and purposes. Anavar is without question an extremely beneficial anabolic steroid, but in order to appreciate its benefits we must understand it.

 

2.Effects of Anavar

[1] Muscle Growth

Bulking/Off-Season: As the Oxandrolone hormone does not aromatize, any weight gained due to use will be lean muscle mass. Water retention is impossible due to the use of this steroid. However, massive gains often associated with steroid bulking cycles should not be expected with this steroid, it simply isn’t cut out for it. The individual should be able to gain some solid lean tissue and many report Anavar gains are easier to hold onto. But it won’t provide gains similar to well-known mass agents like Anadrol, Dianabol, Nandrolone or Testosterone. Some may find despite moderate gains that is all they want.

While Anavar is not the best off-season bulking steroid for men, when it comes to female use we must make an exception. Women are far more sensitive to Anavar than men, and it can be a very effective off-season agent. Further, most women are not looking for gains in size anywhere near male levels; often a slight increase in muscularity can be transforming.

Regardless of sex, all who use Anavar for off-season mass gaining phases will appreciate its metabolic enhancing traits. Those who supplement with the Oxandrolone hormone will find they gain less off-season body fat than they would have otherwise. Due to the increased levels of free testosterone, individuals will also find other steroids being used to be more potent. It may not be by a lot, but every last bit helps.

[2] Cutting

Fat Loss: Without question, male or female one of the best times to supplement with Anavar will be during the cutting phase. This will also be the most common purpose of use as the vast majority who use anabolic steroids participate in no competitive sports taking them out of the athletic enhancement category in an official sense. Due to its powerful anabolic nature, Anavar is one of the best steroids on earth for preserving lean tissue during the dieting phase. In order to lose body fat, we must burn more calories than we consume. The key to successful dieting is losing the desired fat while maintaining as much lean tissue as possible; however, muscle loss will occur. It does not matter how well-planned your diet is, some muscle loss will occur if a powerful anabolic agent is not present. Anavar is the agent you need due to the facts discussed above regarding its effects.

Those who supplement with Anavar during the cutting phase will also burn fat at a more efficient rate. Regardless of how powerful the direct lipolysis trait is or isn’t, the metabolic rate will still be greatly enhanced. Once lean, the individual will also find he appears harder and more defined. This is often accompanied by enhanced vascularity, and an overall tighter look.

[3] Athletic Enhancement

Anavar is greatly appreciated by many athletes for a few specific reasons. This steroid will increase strength; the total increase will not be as significant as steroids like Dianabol and nowhere near the level of Halotestin, but it will be notable. Strength is one of the primary factors of successful athleticism as it translates into speed and power. Athletes also appreciate Anavar due to the fact that it won’t produce a large buildup in mass. In some cases, added mass might be a hindrance depending on the sport, and in other cases, it will bring about prying eyes that no athlete wants on them. When we further consider this steroid cannot lead to water retention, a possible burden to many athletes, Anavar rest as one of the top athletic choices.

[4] Enhanced Performance

Priority: Regardless of the purpose of use, all those who supplement with Anavar will find their rate of recovery is enhanced, as well as their muscular endurance. The individual will not tire out as fast, and he will be able to push longer and harder. This does not mean we should increase the duration of our training sessions, which may or may not be the case depending on the situation. However, we will make better use of each training session, we will make better use of our time on the field and all in all more quality work will be done.

 

3.Positive Effects for Men

1. The popularity of the product is secured by its great properties. The use of Anavar cycle brings multiple dividends for any athlete. Its major properties are as follows:
An anabolic effect of a huge potential. It is able to enhance the amounts of testosterone up to 400%.
2. Androgenic improvements. Due to the influence of the product, a man can gain about 25% of testosterone.
3. A total absence of estrogen. There will be no estrogen issues.
4. The improvement of hardness of muscles. The muscle toughness will increase for many a time.
5. A sufficient sustenance of performance. The athletes will be able to enjoy better results.
6. A significant enhancement of the presence of growth hormone. This component will improve merely all capabilities of the athletes.
7. An efficient and rapid melting of fatstores. The metabolic rate hugely increases.
8. A usability of both genders. Male and female athletes can almost safely use this product.
9. A lasting period of action. Anavar provides a long period of duration, which reaches 12 hours.

4.Positive Effects for Women

As it has been already mentioned, Oxandrolone can be used by both genders. Thus, Anavar for women has definite improvements as well.

It is obvious that men and women have various systems. Accordingly, the influence of different preparations will have various results. Therefore, the muscle growth will be more profitable for women athletes. They will gain muscle weight faster and easier.

Another advantage is a preserving function of lean muscle. Though the calorie amount might be limited, Oxandrolone enables an increased metabolic rate.

 

5.Anavar Cycles and Uses

Although Anavar has gained popularity as being a ‘cutting agent’ or ‘cutting steroid’ throughout the past, its capabilities are not limited strictly to this. Although it can perform and assist quite well in the area of achieving fat loss and physique definition, it is an excellent compound for mass gaining, strength, and bulking. Being that it is 3 – 6 times the anabolic strength of Testosterone, Anavar cycles can indeed be bulking cycles without issue.

However, because Anavar does impose some strain and toxicity in the area of liver function, it cannot be utilized for the same length of time as those core injectable compounds can. Therefore, it is often included at the beginning of any cycle for the first 6 – 8 weeks before it is discontinued. Anavar cycles can be extended to a maximum of 10 weeks at a reasonable dosage, however, due to its lower degree of liver toxicity than other oral compounds. For the purposes of bulking, Anavar cycles are normally run with similar compounds used for bulking, such as a long-estered Testosterone (e.g. Enanthate) and possibly a compound such as Deca-Durabolin (Nandrolone Decanoate).

For its use in fat loss and cutting, Anavar cycles are often shorter and utilized with compounds used for achieving similar goals. These can be anabolic steroids such as Testosterone Propionate, Trenbolone Acetate, Masteron (Drostanolone Propionate), etc. These compounds generally hold the same characteristics as Anavar and promote very little to no water retention or bloating that is often not desired during cutting and fat loss phases where it is important for the bodybuilder to observe changes in physique definition.

 

6.Anavar Dosages and Administration

Standard Anavar dosage for therapeutic treatment will normally fall in the 5-10mg per day range with 20mg per day normally being the maximum dose. Such use will normally last 2-4 weeks with a small break after use before implementing the next 2-4 week cycle. Such use will continue as long as deemed necessary.

For the male performance enhancing athlete, a 20-30mg per day dosing will provide athletic enhancement, but most will find 40-50mg per day to be far more efficient. 80mg per day is not uncommon, but this will increase the risk of side effects. Standard male Anavar cycles will last 6-8 weeks.

For the female performance enhancing athlete, regardless of the purpose of use, 5-10mg per day is normally the perfect dose. Very few women will need more than 10mg per day. If more is desired and 10mg per day has been well-tolerated, 15mg per day can be attempted the next go around. However, every increase in dosing will increase the risk of virilization. Doses of 20mg per day will strongly increase the risk with doses above this mark all but guaranteeing some level of virilization. Standard female Anavar cycles will last 6-8 weeks.

The vast majority of medical applications called for an Anavar dosage in the range of 2.5 – 20mg per day, which was of course heavily dependent on the type of sickness, disease, or disorder that Anavar was intended for. Within medicine, Anavar has been utilized as an example in AIDS patients within the range of 20 – 80mg per day in order to combat and/or reverse muscle wasting. The same has also been demonstrated with burn victims. This is a solid indication of the general dosage range that would be effective for muscle growth and athletics. As Anavar is a drug with plenty of experience with different ages of patients, the effects of Anavar are also not dependent on age.

anavar pills Balkan pharmaAlthough Anavar has been wrongfully touted as being a ‘mild steroid’ in the area of anabolic capability, studies have shown otherwise, and as previously mentioned thus far, it is a compound that is 3 – 6 times the anabolic strength of Testosterone. Therefore, in the athletics and bodybuilding world, Anavar dosages for beginners tend to start and stay in the 25 – 50mg per day range and should provide great results whether bulking up or trimming down the fat. Advanced users tend to venture between 50 – 80mg per day, and there is usually no need to exceed this range due to the dramatic results that such an Anavar dosage can provide. Very rarely, however, experienced advanced Anavar dosages venture within the 80 – 100mg per day range.

Being that Anavar is a great anabolic steroid for the female athlete and bodybuilder that wishes to minimize and eliminate androgenic virilization side effects as demonstrated in studies, most females will utilize an Anavar dosage within 5 – 10mg per day. Advanced female users that may want to push the envelope tend to rise up to 20mg per day, though it is recommended that any and all female use of Anavar for bodybuilding or athletic purposes be limited to no longer than 4 – 6 weeks at a time.

There is also something to be said about combining an Anavar dosage with caffeine. One study has demonstrated that just 300mg of caffeine administered alongside Anavar increased subjects’ blood plasma levels of Anavar by 15 – 20x compared to baseline levels.

 

7.The Benefits of Anavar

As a very mild anabolic steroid Anavar is not well-suited for bulking cycles or gaining phases; you will not produce a vast amount of lean muscle tissue through its use when speaking of performance enhancing purposes; however, what is produced will be solid muscle tissue. The greatest benefits associated with this particular steroid lie within muscle preservation and metabolic activity. This simply means Anavar has the ability to not only aid in reducing body-fat but preserving muscle tissue while on a calorie restricted diet; further, the more muscle tissue we have the greater our metabolic activity will be thereby increasing the rate in-which body-fat is utilized for energy. Because Anavar is apt for fat reduction and muscle preservation it is commonly used by physique athletes during their competition preparation, as well as by common gym rats who simply want to look leaner and tighter at the beach.

 

8.Anavar Side Effects

As previously touched upon, Anavar is hailed with praise among bodybuilders, athletes, and the medical community for its incredible side effect-to-benefit ratio and its general lack of negative side effects in comparison with many other anabolic steroids.

Estrogenic side effects are completely nonexistent with Anavar due to the fact that it is a derivative of DHT, which is an androgenic hormone that is already unable to convert into Estrogen. As such, Anavar retains this characteristic. In other words, the side effects typical of Estrogen (such as water retention, bloating, fat retention/gain, and development of gynecomastia) are completely unseen. In addition to a total lack of Estrogenic activity, Anavar also completely lacks any Progestogenic activity as well, thus negating any potential negative effects there too.

Although Anavar is comparably less androgenic than Testosterone by a great deal, side effects here can still surface especially in those individuals who may be sensitive to androgenic side effects. These can include increased oily skin, acne, hair growth increases in the face and body, and risks involving male pattern baldness (MPB) as well as benign prostatic hyperplasia (BPH).

Despite what is commonly touted about Anavar being “mild on the endocrine system”, there is evidence to the complete contrary where studies have demonstrated almost 40% suppression of endogenous Testosterone production and testicular function after only 5 days of use at 15mg per day in healthy young men. Therefore, Anavar should not be taken lightly in the area of suppressed and disrupted hormonal function. If it can suppress the HPTA (Hypothalamic Pituitary Testicular Axis) after a mere 5 days of use at 15mg per day, it can and will induce complete shutdown over weeks of use at higher ‘bodybuilding doses’.

In comparison with other oral anabolic steroids, studies have demonstrated that Anavar expresses the least amount of hepatotoxicity and strain on liver function of all of them. It should be noted that Anavar still expresses a degree of toxicity in this area, so it is still advisable not to utilize Anavar for an 8 – 10 week period at reasonable dosages. Proper supplementation with good liver support compounds is also always essential when utilizing oral anabolic steroids, no matter how mild they may be claimed to be.

 

9.Where to buy Genuine Anavar raw powder online? 

You can find many Anavar powder source online, but it is hard to buy Genuine Anavar raw online. There are many sources selling fake products at the market. so when you buy Anavar raw material online, you need to choose an realiable source.