Some things outgrow their original purpose. Researchers worked on nuclear energy in the 1940’s and 50’s hoping that it could one day produce electricity for commercial use. Sure, we now have many electric plants running on nuclear energy. But what we also have is the nuclear bomb.
Similar is the case with Arimidex. The FDA approved this drug in 1995 as a treatment for breast cancer in postmenopausal women. Arimidex fights breast cancer by decreasing the production of estrogen, the female hormone whose growth stimulates cancer tumors in females.
Many bodybuilders skip the last part in favor of the former. The moment they hear that there is an FDA-approved, estrogen-blocking drug, they pounce onto it. Want to know why? To treat the swelling of breast tissues (gynecomastia) among anabolic steroid users.
Anabolic steroids help increase muscle mass. That’s where the good news ends. Research has shown that our body converts anabolic steroids into estrogen. The elevated estrogen levels, in turn, lead to gynecomastia. That’s where Arimidex comes in.
What Is Arimidex?
Arimidex, known by its chemical name Anastrozole is an aromatase inhibitor. Why should that concern bodybuilders? The aromatase enzyme is responsible for the production of estrogens in the body. By inhibiting it, Arimidex lowers estrogen levels in the body.
Here’s why that is important. Many bodybuilders use anabolic steroids to build muscle, lose fat and improve athletic performance. What most anabolic steroid users may not know is that they increase estrogen levels in the body, exposing your body to serious side effects.
That is where Arimidex enters the picture. By inhibiting the aromatase enzyme and slowing the production of estrogen, this drug helps prevent gynecomastia. That’s because estrogen is to the breast tissue as gasoline is to your car. The latter needs the former to function.
Keep in mind that the benefits of Arimidex aren’t limited to preventing gynecomastia. This drug may also prevent infertility, erectile dysfunction, and depression in the male population. All of these are the side effects of the anabolic steroid cycles.
Overview of Benefits and Side Effects
If you’re in a hurry and want to have a quick overview of the benefits and side effects of Arimidex PCT, this section has you sorted.
Benefits
Prevents Gynecomastia
Might Treat Erectile Dysfunction
Might Treat Male Infertility
Side Effects
Headache
Vomiting
Hot Flashes
Allergic Reaction (In Rare Cases)
Remember that most of these side effects tend to be mild, as long as you stick to the recommended dosage (more on this below).
Also, if you’re looking for an alternative to anabolic steroids, one that could boost your body’s natural testosterone production, check out our guide on selective androgen receptor modulators.
Why Do Bodybuilders Use Arimidex?
Bodybuilders use Arimidex as a Post Cycle Therapy because it inhibits the production of estrogen. This hormone has many vital functions in the body, both male and female. But its elevated levels in men’s system lead to gynecomastia, or breast growth. That’s what Arimidex helps prevent.
Arimidex does that by reducing estrogen production in the body. This, in turn, lowers the supply of the female hormone to the breast tissue. With the incoming supply of fuel (estrogen) that it needs to grow depleted, the ability of the breast tissue to expand nosedives.
Arimidex Benefits for Men
One of the major benefits of Arimidex is that it might help or treat gynecomastia. However, its utility doesn’t end there. This aromatase inhibitor has also shown promise in treating erectile dysfunction, infertility and depression among the male population.
Here are the major benefits you may expect from Arimidex:
Prevents Gynecomastia
According to an estimate, gynecomastia is one of the most common male breast disorders. Up to 70% of boys and men develop ‘man boobs’ in early to mid-puberty. Most of them develop gynecomastia due to regular hormone changes. Some, however, get it due to anabolic steroids use.
Regardless of the cause, Arimidex helps prevent this condition. It does that by slowing down the production of the fuel (estrogen) that breast tissues need to grow. In doing so, this drug helps treat a ‘problem’ that has been nagging bodybuilders for ages.
Might Treat Infertility
Peer reviewed studies have shown that high estrogen levels might cause infertility in males. When your estrogen levels are high, they may cause sperm levels to drop. The resulting reduction in sperm count might lead to infertility. Estrogen control is thus necessary.
The good news is that Arimidex, originally developed as breast cancer treatment, has shown promise in getting male fertility back on track. It does that by a) inhibiting aromatase and b) by slowing the conversion of testosterone into estrogen. This helps Arimidex improve sperm production in males.
Might Treat Erectile Dysfunction
For bodybuilders who are suffering from erectile dysfunction, they aren’t facing this problem because they’re lifting weights. Instead, it’s their usage of anabolic steroids and similar unsafe drugs that might have hurt their ability to achieve and retain an erection firm enough for sex.
One study has shown that Arimidex Anastrozole might improve sexual dysfunction in men. Carried out on male subjects facing sexual issues with hypogonadism and epilepsy, the study found that 3-month treatment with Arimidex normalized sexual function in 72 per cent of the participants.
Arimidex Side Effects
As is the case with other drugs out there, there are side effects associated with Arimidex use. Keep in mind, though, that unlike research chemicals, Arimidex is FDA approved. This means you can count on it to be much safer than most other aromatase inhibitors out there.
Most of the side effects associated with Arimidex use are on the mild side. These adverse effects include headaches, fatigue, joint pain, hot flashes, weakness and nausea. Again, most of these side effects will be mild in nature and will go away on their own if you stick to the recommended dosage.
Having said that, it’s possible for you to develop an allergic reaction to Arimidex. That is not unusual as people out there have allergic reactions to drugs as benign as aspirin. Still, the fact that drug allergic reactions are common doesn’t mean their effects won’t be dangerous.
If you develop an allergic reaction to Arimidex, the symptoms you might experience include breast pain, chest pain, rapid heart rate, blurred vision, and rashes. If you experience these symptoms or they start to worsen, we recommend you immediately consult with your physician.
Arimidex Dosage & Cycles
Having looked at what Arimidex is, why bodybuilders use this aromatase inhibitor and the benefits it could offer to the general male population, it’s time we turn our attention to the most crucial question: how much Arimidex should you be taking on a daily basis?
Users indicate that you should aim for 0.5 to 1mg Arimidex or Arimistane per day. That is extremely easy given that this drug is mostly available in 1 mg tablets. If you feel that the recommended dosage is too much for you, you can take Arimidex every other day.
Since you’d be using it to prevent gynecomastia, make sure you continue your Arimidex cycle in tandem with your anabolic steroid cycle. That isn’t to say that you should start both cycles at the same time. In fact, users suggest starting your Arimidex cycle when you’re already two weeks into the steroid cycle.
Doing this will provide you with two benefits. The fact that you’re already on the steroid/supplement cycle by the time you start taking Arimidex will help you avoid this drug’s symptoms. At the same time, it will allow Arimidex to deliver the intended results.
Frequently Asked Questions
How much does Arimidex lower estrogen?
According to the FDA, taking 1 mg Arimidex tablet lowers estrogen by 70 per cent over the first 24 hours. After a fortnight of daily dosing, this drug can reduce estrogen by 80%. The suppressed levels won’t go back up for up to 6 days after you’ve completed the Arimidex cycle.
How fast does Arimidex lower estrogen?
Health experts tell us that Arimidex starts lowering estrogen within 24 hours of the first dose. Still, it might take the drug as much as seven days to attain peak levels in the blood plasma.
What is the recommended Arimidex dosage with testosterone?
Users on testosterone replacement therapy suggest taking 0.5mg to 1mg Arimidex once every three days. Keep in mind that this isn’t doctor advice. If you’re on testosterone replacement therapy, consult with your therapist before you start taking Arimidex.
Summary
Arimidex was initially developed to treat breast cancer in post menopausal women. Over the years, though, its aromatase inhibiting properties have caught the attention of bodybuilders, eager for a safe drug that could naturally lower their estrogen levels.
Multiple pieces of evidence suggest that it does precisely that. Keep in mind that there are yet to be any human studies to verify the effects of Arimidex on the male breast tissue. That’s why we suggest you consult with your healthcare professional before starting Arimidex post cycle therapy.
HCG is effective when used with other compounds rather than it being used alone and while it has seen some mainstream promotion as a failed (and illegal) weight loss ingredient, HCG’s real power lies in its ability to help steroid users achieve a major goal after a steroid cycle: to get natural testosterone back on track again.
What is HCG (Human Chorionic Gonadotropin)?
Human Chorionic Gonadotropin is a hormone naturally found in women and has an important role to play in pregnancy; in fact the hormone is only formed once a woman is pregnant as it is produced after implantation by the placenta and once HCG levels rise enough it is enough to confirm if a woman is pregnant.
Human Chorionic Gonadotropin Structure
If you’re a male steroid user you might then wonder how or why such a hormone could possible be of use to you. HCG does have a medical role for men: to treat low testosterone or hypogonadism.
Steroid users find HCG useful because it functions almost exactly like luteinizing hormone (LH). LH can be described as a pituitary analog to HCG because they are hormones produced in different parts of the body (luteinizing hormone forms in the pituitary gland) but have a similar function.
This is where HCG becomes very relevant to men: LH is vital for stimulating natural testosterone production. This is what makes HCG a popular option for PCT usage in particular, where the recovery of normal testosterone function following anabolic steroid suppression is required.
While SERMs and aromatase inhibitors are generally widely accepted as a necessary addition for any steroid user, HCG comes under much more debate with some anabolic steroid users swearing by its use, and others finding that it is not necessary or useful or comes with a greater risk than the other drugs.
In any case, when HCG is used it is rarely used alone but in conjunction with SERMs in post cycle therapy and only at low doses for short periods of time if used during a steroid cycle.
Although considered a side effect friendly hormone for most people, HCG comes with one particular risk factor that we need to be concerned about, and this revolves around dependence.
Thankfully this can be well controlled through sensible dosing and is a critical reason why HCG shouldn’t be taken until you’ve done adequate research into just how much you should be taking so you don’t put yourself at risk of dependence.
HCG and Steroids
For steroid users who make use of HCG while using anabolic steroids the intent is to use this hormone to address the suppression of natural hormones that takes place when you use most types of steroids.
During this time your normal testosterone production and levels will be extremely low or even non-existent and the use of HCG during steroid use can prevent the problem of testicular atrophy but more importantly, taking HCG during a steroid cycle helps prime the body for recovery once your cycle ends.
So what’s the downside to HCG and why doesn’t everyone just use it during a cycle? One of the commonly overlooked issues is the way the male body can become dependent on HCG’s supply of what is basically exogenous luteinizing hormone. Guys who take too much HCG or don’t seriously regulate use of it are at higher risk of dependence.
Those men who go overboard with their use of HCG during a steroid cycle, either through lack of knowledge or a false belief that more equals better, can quickly find themself suffering with a low testosterone condition. Those who know how to use HCG responsibly during a steroid cycle however will reap the benefits and avoid the problem of dependence occurring.
HCG vs Aromatase Inhibitors vs SERMs
HCG is very different from both SERMs and aromatase inhibitors (AIs).
Both SERMs and AIs are medications that have been designed to either block specific estrogen receptors (in the case of SERMs), or to lower overall estrogen levels (AIs). HCG on the other hand is a naturally occurring hormone produced in women once they fall pregnant.
HCG does not target estrogen in any way, but instead is able to directly help stimulate testosterone in men because it works in a very similar way to luteinizing hormone.
Both SERMs and AIs are mainly used to treat breast cancer in women. HCG is used medically to treat low testosterone and infertility and men, as well as fertility problems in women. All three categories of substances are therefore available with a prescription. While both SERMs and AIs are available as different products with slightly differing chemical structures and effects between them, HCG is the only one of the three that is a single hormone with no variation between products.
HCG is available in injection form only, while AI and SERM drugs are oral tablets that need to be taken more regularly than the once or twice weekly injections that HCG is normally administered by.
HCG is not intended to replace either SERMs or AIs at any point during or after a steroid cycle. Instead it is can be a very useful addition but one that needs to be used carefully and with knowledge of both how to dose it properly and what it can and can’t do both in benefits and side effects. Over-use of HCG can have the opposite of your intended effect: instead of improving or restoring your testosterone you could find yourself back in a low testosterone state.
HCG for Post Cycle Therapy (PCT)
Post cycle therapy use of HCG is the most common reason guys will use this hormone for the purpose of optimizing recovery after a steroid cycle. The power of this hormone for PCT use comes with taking it before starting a SERM cycle.
Most PCT plans will include either or both of the SERMs Nolvadex (Tamoxifen Citrate) and Clomid (Clomiphene Citrate) and while these are generally very effective on their own, many steroid users find that adding HCG to the PCT phase provides enhanced recovery benefits.
The strategy here is to make use of HCG prior to starting your regular SERM dosage, with HCG essentially acting as a kick start to the hormone production process thanks to the way it mimics luteinizing hormone. The SERMs then take over for the rest of your PCT cycle, providing a more efficient and effective recovery.
This type of PCT plan provides for the two main purposes of post cycle therapy: to help you maintain your gains and to speed up the restart of natural testosterone production; this hormone will be in a greatly suppressed state at the end of your steroid cycle in most cases and without a proper PCT plan the rate of recovery is extremely slow which puts you in the certain position of low testosterone and the associated symptoms and muscle loss.
HCG will usually be started within a 4 to 6 week period after the end of your steroid cycle but the timing will depend on the steroid compounds you’ve used. Those who are concerned about possible estrogenic side effects from using HCG during PCT, because of increased aromatase activity, might also choose to include an aromatase inhibitor into their PCT plan.
This is not always an effective idea because AIs come with their own set of issues when it comes to potentially negatively impacting on testosterone levels because of powerful estrogen suppression; in general, HCG is utilized for a short time frame during PCT so side effects are not a great concern for most users.
HCG Dosage
Whichever purpose you are using HCG for – on cycle or for PCT – the dosage and administration of this hormone is very sparse and controlled and unlike that of any other compound you will be using whether that be steroids themselves or drugs like SERMs and AIs.
When buying HCG from your chosen source you will normally receive a small packet of powder containing the active ingredients and another with sterile water in it. These two items are to be mixed together to form your injectable ingredient. Any left over must be refrigerated for later use – do not store the solution at room temperature.
HCG Dosage During Anabolic Steroid Use
When using HCG during your steroid cycle you will want to take it no more than once every 3 to 5 days at a maximum. This will come as some relief since HCG is an injection so you won’t have to be adding an extra injection to your steroid program too often.
A very low dose of HCG during this time is considered sufficient and this is usually in the realm of 250iu. There is no benefit to increasing the dose beyond this level, nor the frequency of administration.
This modest dosage is enough to give you all the benefits you want from HCG without putting your future testosterone restoration at risk by having the body become dependent on HCG which is an increased risk when you increase the dose – therefore, 250iu once every 5 days is suitable for the vast majority of male steroid users while on cycle.
HCG Dosage for Increased Endogenous Testosterone Secretion and PCT
HCG is most commonly used as a kick start to your PCT cycle in preparation for the use of SERMs afterwards. The length and dose of HCG during this time should be determined on how powerful your steroid cycle was and the level of testosterone suppression it is likely to have caused. This can be difficult for new steroid users to gauge initially so a lower HCG dose is advised in those circumstances.
Many users will take HCG for a period of two to three weeks with doses every 3 or 4 days starting at 1000iu at the low end right up to 4000iu. This higher dosage is advised only for advanced users who have used HCG previously and understand its effects. Following this short HCG cycle, SERM administration can begin to carry through the rest of your PCT phase.
Female HCG Dosage
HCG is very useful medically for females for the purpose of improving fertility, but it has no use for women who are using steroids. Men experience suppressed testosterone from most steroids but this is clearly not an issue that female steroid users need to be concerned with, therefore the use of HCG is not warranted by women outside of medical use.
HCG Side Effects
One of the great positive about HCG is that side effects are rare to non-existent. Unlike other substances used by steroid users like SERMs and AIs, HCG is not a drug developed in a lab but instead is a naturally occurring hormone. This means we don’t have to worry about adverse effects like headaches, upset stomach or other common problems that come about with the use of powerful medications.
HCG can raise testosterone levels so the main effects to watch out for relate to rising levels of the hormone and these can actually come in the form of an estrogenic nature. Water retention and gynecomastia are possible but are considered rare particularly because HCG is not often used on its own but instead combined with anti-estrogen drugs that will themselves mitigate these side effects when you are on a steroid cycle.
Because of the increase in circulating testosterone and DHT, androgenic side effects can be a concern and this might include increased oily skin and acne, increased body hair growth, and hair loss on the head but the risk of these adverse effects is highly individual and usually only affect men who are genetically predisposed to them, in the same way that androgenic side effects come about from steroid use.
With the use of HCG during post cycle therapy you are likely to be using it at higher doses, this is balanced by the fact that your use of HCG is also likely to be only for a short period of time so the risk of side effects during PCT is again quite low. All of these factors make HCG a hormone that is unlikely to cause you many or any problems at all and possibly is the most side effect friendly substance you will take at any time of anabolic steroid use.
The greatest risk with HCG is not in the form of traditional types of side effects that we see with steroids or other drugs, but rather whether the body starts becoming dependent on the external form of luteinizing hormone that you’re consuming.
When this happens you will have the reverse effect occur – instead of testosterone levels rising or maintaining at a healthy level with the help of HCG, you’ll be back down to low testosterone because the testicles have become reliant on the amount of HCG you’re taking in. This is avoided with low dosing and only using HCG for a minimal period of time.
In Conclusion:
HCG can be a short term and extremely helpful addition to any PCT regimen when used properly. But because of it’s tricky nature and it’s many nuances we think it wise to consult an experienced person in regards to it’s proper use!
For more information on to how to properly incorporate HCG into a post cycle therapy regimen (PCT) protocol, feel free to shoot us a message.
Please note – Post Cycle Therapy protocols are always evolving. The below article is a generalization, and may not cover every possible avenue of therapy that would be ideal for YOUR particular situation. We highly recommend contacting a qualified and experienced person for guidance as to the latest and most efficacious protocol for YOU and YOUR individual situation. For this, we strongly suggest that you email the experts here who will be glad to offer you assistance with this matter!
Post cycle therapy (PCT) is the phase when a bodybuilder utilizes medication(s) to restore endogenous (natural) testosterone production.
Anabolic steroids impair HPT (hypothalamic–pituitary–testicular) axis function, as the body detects excessively high serum testosterone levels.
Consequently, the body signals to cease testosterone production in a bid to keep homeostasis, by inhibiting GnRH (Gonadotropin-releasing hormone).
This decreases the release of LH (luteinizing hormone) and FSH (follicle-stimulating hormone) — two hormones crucial for testosterone synthesis.
Thus, when a bodybuilder comes off steroids and exogenous testosterone is removed, natural testosterone often becomes shut down.
This can result in various psychological and physiological side effects, such as:
Decreased well-being
Low libido
Erectile dysfunction
Catabolism (muscle loss)
Decreased sperm count
Testicular atrophy
The severity of the above effects depends on the anabolic steroids used, the dosages and the length of a cycle.
Low testosterone can persist for several weeks or months post-cycle, increasing the likelihood of addiction, due to strong withdrawal symptoms lingering.
The aim of a PCT is to dramatically shorten this process, thus accelerating the recovery of natural testosterone production. Bodybuilders typically utilize any or all of the following medications:
Clomid (clomiphene)
Nolvadex (tamoxifen)
HCG (human chorionic gonadotropin)
Best PCT Protocol
Referencing one of the leading medical experts in hormone therapy, having specialist knowledge in regards to ASIH (anabolic steroid-induced hypogonadism).
After treating hundreds of patients, the Dr. developed a PCT protocol that was used in a clinical report to treat 19 healthy men. All of these men had extremely suppressed testosterone levels, as a result of using Testosterone and Deca Durabolin for 12 weeks.
The following protocol successfully treated 100% of the male subjects, bringing their serum testosterone back to normal levels (within 45 days). This is quite a feat, considering it is common for bodybuilders to experience low testosterone for up to 4 months, following a steroid cycle.
hCG – 2000IU administered every other day for 20 days
Tamoxifen (nolvadex) – 2 x 20mg for 45 days
Clomiphene (clomid) – 2 x 50mg for 30 days
The above post cycle therapy plan should be viewed as aggressive. Thus, if potent AAS are used, it is necessary and very effective.
However, if milder steroids are used (such as Anavar, Primobolan or Turinabol), testosterone levels may only be moderately suppressed (rather than completely shut down).
In this case, all three of these PCT medications taken simultaneously may not be necessary. Instead, one or two of these drugs can be used with great success.
The timing of a PCT is crucial in regards to its effectiveness. If began too early, it may be ineffective, due to exogenous testosterone still being present in the body. If started too late, the body will have already entered a catabolic state, with withdrawal symptoms occurring.
The timing of a PCT should be tailored to the half-life of the steroid(s) taken. If users are taking multiple AAS simultaneously, then a PCT should begin after the last compound clears out of the body i.e. the slowest.
Here is a guide so users know when to start their PCT:
Clomid
Clomid is a SERM (selective estrogen receptor modulator), often prescribed to women as a fertility drug, acting as an ovulatory stimulant.
Clomid increases the secretion of gonadotropins (LH and FSH), via the inhibition of estrogen in various tissues, leading to an increase in endogenous testosterone.
Despite blocking estrogenic effects in many parts of the body, Clomid increases estrogen activity in the liver, causing a positive shift in cholesterol levels. This is particularly useful in regulating blood lipids and easing cardiovascular strain following a cycle.
Clomid Side Effects
Visual changes sometimes occur on Clomid, particularly in high doses or lengthy cycles.
This may include flashes or blurring; however, these are often temporary and subside within a few days/weeks post-cycle.
It is unknown what causes such changes, and in rare cases, they may even be irreversible. If such visual side effects start to occur, users should discontinue Clomid supplementation and visit an ophthalmologist for urgent examination.
More common side effects of Clomid, include:
Flushes
Abdominal discomfort
Nausea
Headaches
Liver stress
Impaired eyesight
Nolvadex
Nolvadex (tamoxifen citrate) is a SERM, commonly prescribed to women with breast cancer, and is regarded as one of the main reasons why the mortality rate for breast-cancer sufferers has significantly dropped in the last decade.
Nolvadex was first synthesized in 1962 and initially prescribed to treat female infertility.
However, it was later observed to have anti-mitogenic effects, reducing the stimulation of breast tissue — beneficial for slowing the growth of breast cancer.
Nolvadex also exhibited cancer-killing properties, due to the blocking of protein kinase C (PKC) via oxidative stress mechanisms.
Today, bodybuilders commonly use Nolvadex to prevent the onset of gynecomastia (accumulation of breast tissue).
As a PCT, Nolvadex works in the same way as Clomid, stimulating LH and FSH production, via the inhibition of estrogen’s negative effects in the hypothalamus (and thus restoring the HPTA axis).
Nolvadex Side Effects
Skin rash
Hot flashes
Decreased white blood cell count
Visual disturbances
Blood clots (deep vein thrombosis)
Liver stress
Uterine sarcoma and endometrial cancer have also been linked with Nolvadex use; however, the risk is very low, being approximately 1 in 500 cases. Such side effects are also correlated with long-term use (more than 2 years).
HCG
HCG (human chorionic gonadotropin) is a hormone produced by women in high quantities in the early stages of pregnancy, facilitating an increase in progesterone, helping to nurture the developing fetus and its surrounding environment (preventing miscarriage).
Bodybuilders take hCG post-cycle due to its ability to elevate luteinizing hormone (LH) levels, thus stimulating the Leydig cells to produce more endogenous testosterone.
HCG has not only been used in the treatment of male hypogonadism but also obesity. It was previously believed that hCG may have a stimulating effect on T3 levels; however, this is not known. Instead, hCG has an appetitive suppressant effect, meaning people could eat very-low-calorie diets, without feeling excessive hunger.
In 1957, hCG became the most prescribed medication for weight loss, due to this powerful (yet indirect) effect on satiety.
Thus, hCG may be particularly beneficial after a cutting cycle to minimize any potential weight gain following steroids.
HCG is regarded as the most effective post cycle therapy medication for treating testicular atrophy (shrinkage), due to its spermatogenesis-inducing effects.
PCT for Women
Post-cycle therapy is often deemed unnecessary for women, which may stem from them having smaller quantities of endogenous testosterone.
As with men, women’s endogenous testosterone production will also shut down, due to the body detecting an excess of this male hormone.
Testosterone remains a crucial hormone in females; greatly affecting their libido, well-being, energy and muscle mass.
With testosterone declining, estrogen will also drop significantly, due to less aromatization (conversion of testosterone into estrogen).
There is anecdotal evidence of female steroid-users experiencing: very low estrogen levels, low mood, diminished libido and depression post-cycle.
Nolvadex has been used as a PCT among women, in a dose range of 5-15mg for up to 4 weeks. Many women are reporting this to have a positive effect on their mood and to accelerate regulation in hormone levels.
However, some of these women are still experiencing 3-6 month delays before menstrual cycles return.
HCG is not an optimal PCT medication for women, with it potentially causing virilization and enlargement of the ovaries.
Clomid may also not be optimal due to ovarian hypersensitivity.
The medical treatment for women deficient in androgens is DHEA (dehydroepiandrosterone), which is one of the most critical hormones in females, being a key precursor of androgen and estrogen synthesis.
One study found that 50mg/day of DHEA ‘significantly increased’ libido in women over 70 years old when taken for 1 year.
Another study found that a 6-week cycle of DHEA improved sexual function in women, including arousal, orgasm quality and libido. They also found that depression symptoms decreased by 50%, significantly improving mood.
These women took 90mg/day of DHEA for the first 3 weeks, followed by 450mg/day of DHEA for the remaining 3 weeks.
Other research has shown that 50mg/day of DHEA when administered for 3 months, improves well-being in women by 82%. They also reported: greater relaxation, improved sleep, less stress and higher energy levels.
Thus, an effective post cycle therapy for women is:
50mg/day of DHEA for 12 weeks.
FAQs
Is a PCT essential?
A post-cycle therapy is not essential, as natural testosterone levels will eventually recover.
However, a better question may be: ‘Is a PCT optimal?‘. The answer to this is yes, as not only will users retain more of their gains from a cycle, but they will also improve their mental and sexual health.
A PCT may be deemed less essential when taking mild AAS, such as Anavar, with studies showing a moderate reduction of just 45% when taking 20-40mg/day for 12 weeks.
How Do I Know If I Need a PCT?
The most accurate way to know if you need a PCT is to get your testosterone levels checked.
However, if you have reasons for not wanting to see a doctor, you can often tell from the following signs:
Depression
Low libido
Testicular atrophy (shrinkage)
Where Do Bodybuilders Buy PCT medications?
Bodybuilders will either make an appointment with a doctor and hope they will be prescribed necessary PCT medications, or they will purchase them on the black market (in the same way they buy anabolic steroids).
The second method involves asking around and finding a source where you can pay with cash, or by making a payment online (which is riskier if entering your card details).
How Much Do PCT Medications Cost?
A reliable supplier of anabolic steroids has provided us with the UK market price for PCT drugs. We have done a rough conversion into dollars for our American readers.
Selective androgen receptor modulators (SARMs) are suppressive, thus a PCT is necessary. However, the severity of the decline in testosterone will determine the PCT protocol and how aggressive it should be.
As with steroids, some SARMs cause greater declines in endogenous testosterone than others.
However, as a general rule if users take one SARM, stick to a low to moderate dosage and cycle it for 8 weeks or less — only a moderate decline in testosterone is likely to occur.
In this case, 3 weeks of Nolvadex will be sufficient in bringing endogenous testosterone levels back to normal, with 30mg/day taken for week 1, 20mg/day for week 2 and 10mg/day for week 3.
If slightly higher dosages are taken or/and lengthier cycles are utilized, Nolvadex can be taken for 4 weeks, starting on 40mg for week 1, then decreasing the dosage by 10mg each week for the remaining 3 weeks.
For a high-dosed SARM cycle, a 4-week Nolvadex PCT may be necessary, being: 40mg/day during weeks 1 and 2, then 20mg/day during week 3 and 4.
Some individuals take more risks with SARMs i.e. stacking multiple compounds together, such as combining Ostarine, RAD-40 and LG simultaneously and utilizing excessive cycles, lasting 12-16 weeks. In this case a more drastic PCT protocol is needed, being Dr. Michael Scally’s combination of:
hCG – 2000IU administered every other day for 20 days
Tamoxifen (nolvadex) – 2 x 20mg for 45 days
Clomiphene (clomid) – 2 x 50mg for 30 days
Note: Some people mistake certain compounds as SARMs, such as cardarine and MK-677. These are not SARMs, and thus do not require a PCT, with cardarine being a fat burner and MK-677 a growth hormone secretagogue. Both of these products are not suppressive.
How Much Muscle Will a PCT Help Keep?
As a general rule, a PCT can help to retain anywhere from 50-75% of lean muscle gains from a cycle.
Mild compounds, such as Anavar or Primobolan, may enable users to retain high amounts of muscle tissue, due to less dramatic peaks in exogenous testosterone levels on-cycle (and thus less endogenous shut down).
Note: It is normal to lose some weight when coming off steroids, particularly when utilizing wet, bulking compounds; with users losing some intracellular and extracellular fluid (that previously accumulated due to high estrogen levels). This should not be confused with losing muscle weight.
PCT Diet & Supplementation
A person’s diet can also help to increase testosterone and anabolism post-cycle.
Doctors recommend eating a diet rich in meat and egg yolks, with cholesterol being a steroid hormone that synthesizes testosterone. Research has also found a link between higher HDL levels and high testosterone males.
Doctors also state that ZMA, D-aspartic acid, Tribulus Terrestris, Maca and Vitamin D3 and Bulbine Natalensis supplements can help to maximize natural testosterone production.
PCT Pros and Cons
Pros:
Increases testosterone production
Improves well-being
Enhances energy
Helps to retain lean muscle
Increases testicular size
Increases libido and erection quality
Improves fertility
Affordable
Cons:
More expense (on top of steroids)
Some medications come with side effects (in sensitive users)
AOD9604 is a peptide derived from human growth hormone (HGH) fragment 176-191, itself a derivative of human growth hormone. AOD9604 is a weight loss peptide in the truest sense of the term as it is a targeted fat burner (lipolytic) with limited additional effects. This peptide was specifically developed to maintain the lipolytic (fat burning) fragment of growth hormone without retaining any of the parent molecule’s ability to promote lean body mass accumulation. Research out of Australia shows that AOD9604 increases weight loss 3-fold compared to placebo. It affects beta-3-adrenergic receptors on white fat to boost fat breakdown and may indirectly activate apoptosis (programmed cell death) in white fat cells as well. AOD1604 is one of the most effective peptides for weight loss yet developed, with studies showing as much as a 50% reduction in weight gain over just three-weeks of administration.
This peptide is extremely safe, it is FDA approved, and there are no known health risks associated with AOD 9604 injections, especially when compared to traditional hormone-based weight loss treatments. As with any injection, some common side effects include pain, reddening, and swelling near the injection site.
Semaglutide (GLP-1 Agonist)
Semaglutide is similar in many ways to Liraglutide and is FDA approved for weight management and the treatment of metabolic syndrome. It acts as an agonist of the GLP-1 receptor. Research shows that semaglutide and similar peptides for weight loss work in two different ways. First, Semaglutide can delay gastric emptying and slow intestinal motility to increase feelings of fullness and decrease the rate of rise of blood sugar. Second, Semaglutide can act as a neurotransmitter to reduce the drive to eat in the central nervous system via reductions in the sensation of hunger as well as enhanced feelings of satiety. Semaglutide has been shown to produce a 5% weight loss over 6 months. At one year, average weight loss with semaglutide is 15% of total body weight.
You may know semaglutide as Ozempic, an injectable medication used in people with Type 2 diabetes. Ozempic can help manage blood sugar, and it can also lower the risk of heart attack and stroke if you also have heart disease. You can also find it as an oral pill, called Rybelsus. And Wegovy, a higher-strength version, is approved to help people lose weight.
Semaglutide works by mimicking a gut hormone that causes your pancreas to release insulin, blocks your liver from releasing sugar, and slows down how fast food leaves your stomach. While these actions can be beneficial for Type 2 diabetes and weight loss, they can also cause some side effects.
Some semaglutide side effects can be bothersome and make the medication difficult to tolerate. But the good news is that they usually subside over time. Although rare, there are also some serious side effects to know about. Keep reading to learn more about 10 semaglutide side effects to know about and how to manage them.
1. Nausea and vomiting
Nausea is the most common semaglutide side effect. Up to 20% of people taking it for Type 2 diabetes reported nausea in clinical trials. Nausea is even mire common if you’re taking the higher-dose version for weight loss. Vomiting tends to be less common than nausea.
You’re more likely to experience these side effects with higher doses of semaglutide. That’s why your healthcare provider will raise your dose slowly over a few weeks to minimize these effects. For most people, these side effects should improve over time as your body gets used to the medication.
Eating smaller meals, avoiding high-fat foods, and remaining upright after you eat can also help manage potential nausea and vomiting from semaglutide. But if these side effects are accompanied by severe stomach pain that may or may not spread to your back, get medical attention right away. This could be a signs of pancreatitus, a rare but serious side effect. More on that later.
2. Diarrhea
Diarrhea is another common semaglutide side effect. Around 9% of people taking it for Type 2 diabetes and 30% of people taking it for weight loss reported diarrhea during clinical trials.
Similar to nausea and vomiting, you’re more likely to experience diarrhea with higher doses of semaglutide. As mentioned above, your healthcare provider will slowly raise your dose over time to minimize this side effect. Constipation can also happen, but it tends to be less common than diarrhea.
3. Stomach pain
Mild stomach pain is another common stomach-related side effect of semaglutide. Similar to nausea, vomiting, and diarrhea, this should subside over time. Using the tips listed above can also help minimize this side effect.
Severe stomach pain can be a sign of other side effects, like pancreatitis or gallbladder problems (like gallstones). Contact your healthcare provider right away if this develops.
4. Fatigue
Fatigue is a common side effects of Wegovy, affecting 11% of people taking it in clinical trials. Fatigue was also reported in less than 5% of people taking Ozempic, and it wasn’t reported at all with Rybelsus.
Semaglutide works for weight loss by making you feel less hungry. And eating fewer calories may cause you to feel more tired. Feelings of fatigue should subside as your body adjusts to potential changes in your diet.
5. Low blood sugar
Low blood sugar (hypoglycemia) isn’t very common if you’re taking semaglutide on its own. That’s because it works by telling your body to release insulin in response to a meal specifically.
But taking semaglutide with other blood sugar-lowering medications, like insulin and sulfonylureas, raises the risk of hypoglycemia. So, your healthcare provider may need to change the dose of these medications when starting semaglutide.
If you have Type 2 diabetes, it’s important to regularly check your blood sugar levels to help avoid hypoglycemia. You may be advised to have an emergency glucagon or glucagon-like product to raise your blood sugar quickly if severe hypoglycemia happens.
6. Pancreatitis
Although rare, pancreatitis has been reported with semaglutide. If it happens, it can be life-threatening. Seek immediate medical attention if you develop severe abdominal pain, nausea and vomiting, and/or jaundice (yellowing of skin and eyes).
Let your healthcare provider know before starting semaglutide if you have a history of acute pancreatitis. They may recommend a different medication for you.
7. Gallbladder disease
Gallbladder disease, including gallstones, is possible with semaglutide, but it isn’t common. It was reported in less than 2% of people taking it in clinical trials.
Symptoms of gallbladder problems include upper stomach pain, fever, and jaundice. You may also notice clay-colored stools. Let your healthcare provider know right away if these develop.
Talk to your healthcare provider about ways you can avoid gallbladder problems while taking semaglutide. This may include dietary changes and routine physical activity.
8. Kidney damage
Studies have suggested that semaglutide may have some kidney benefits if you have Type 2 diabetes. But in rare cases, kidney damage has also been reported. This is more likely if you have severe nausea, vomiting, and/or diarrhea leading to dehydration.
Kidney damage is also more common if you already have kidney problems. Taking medications that cause you to get rid of excess water, like diuretics (water pills), also puts you at risk.
Your healthcare provider may monitor your kidneys if you’re experiencing a lot of stomach-related side effects. Let them know right away if you’re not urinating very much or at all, or notice swelling in your arms or legs.
9. Allergic reactions
Severe allergic reactions to semaglutide are rare, but possible. Call 911 or get immediate medical attention if you have swelling of the face, tongue, or throat, or shortness of breath after your dose.
Mild allergic reactions can include itching, rash, or redness at the injection site. Stopping semaglutide isn’t always necessary with mild reactions. But make sure to still tell your healthcare provider about your reaction.
Don’t use oral or injectable semaglutide if you’re allergic to any of their ingredients. And there’s a chance you could have an allergic reaction to semaglutide if you’ve had a reaction to a medication in the same class.
10. Thyroid tumors
Semaglutide has a boxed warning (the strictest warning) from the FDA about a risk of thyroid C-cell tumors. This is because animal studies found that rodents developed thyroid tumors when exposed to GLP-1 agonists. However, human studies have yet to confirm this risk.
Still, you shouldn’t take semaglutide if you or your family have a history of medullary thyroid cancer or multiple endocrine neoplasia (MEN) type 2. Contact your healthcare provider immediately if you notice signs or symptoms of thyroid cancer. These include a lump in your neck, and neck or jaw pain.
All this being said, and speaking strictly for myself (I know there will always be some who will argue to the contrary)… I personally feel it is a no-brainer which one to use if your looking for an EFFECTIVE, PROVEN and SAFE fat burning peptide… In my mind it’s AOD-9604 all the way!
Furthermore, there is a lot of evidence to back up these claims that AOD-9604 is the MUCH safer way to go. And truth be known, most of the resources I have personally checked seem to feel AOD-9604 is actually more effective than Semaglutide overall as well.
Safer… More Effective… You do the math.
I just felt it was important information to bring to you, being that these 2 peptides have gained so much attention in recent months… and these are definitely things you want to consider if you’re looking for such a product to help you with your fat loss goals.
Disclaimer: The following article is for educational purposes only and NOT to promote the use of illegal steroids. If you have any questions or concerns, our staff is available to help you with additional information.
Given the sensitive nature of this article topic, we’d like to clarify that no steroid can be considered 100% safe; especially when bought on the black market for cosmetic purposes.
Anabolic steroids are also illegal, thus unless utilized by a doctor in a strict medical setting; AAS have the potential to cause dangerous side effects to users.
However, certain steroids are safer than others, hence why several AAS are approved by the FDA in medicine (whilst others are not).
It’s worth noting that bodybuilders often consume significantly higher dosages of anabolic steroids, compared to in medical settings; thus increasing the risk of side effects.
Furthermore, bodybuilders often take steroids without having regular checkups with a medical doctor, which is a further risk.
However, below are the mildest and least destructive steroids a bodybuilder can take:
Testosterone
Anavar
Deca Durabolin
Testosterone
Testosterone is an FDA-approved injectable steroid, used to treat millions of men all over the world, who are deficient in natural testosterone.
This is known as testosterone replacement therapy or TRT.
Testosterone was included in the World Health Organization’s List of Essential Medicines, regarded as crucial for treating endocrine disorders.
In 2017, it was the 132nd most prescribed medication throughout the U.S; with over 5 million prescriptions.
From 2001 to 2011 testosterone prescriptions have tripled, indicating a current low testosterone epidemic.
In bodybuilding, testosterone is predominantly used in bulking cycles to add large amounts of muscle and strength; however, it’s also utilized in cutting cycles to retain muscle hypertrophy.
When injected correctly, it can be argued that testosterone is one of the safest steroids available.
Testosterone causes hefty gains in muscle size (20-30lbs) and remains one of the most popular steroids in bodybuilding; despite coming to market over 80 years ago.
If injected incorrectly, any steroid or medication can be dangerous (or fatal).
However, there is oral testosterone available (undecanoate) for those wanting to avoid needles. Oral testosterone is less commonly used in bodybuilding, compared to injectables, due to its higher market price.
Testosterone Side Effects
Testosterone poses little to no hepatic concern (liver stress), due to it being injectable and thus entering the bloodstream immediately; instead of the liver having to filter it.
Oral testosterone (undecanoate) is also safe for the liver, with it being absorbed via the intestinal lymphatic route; thus preventing hepatic strain. One study gave 2,800mg per week of testosterone undecanoate to male subjects for 21 days; yet none of them experienced any hepatotoxic stress, despite such an exceedingly large dose.
Blood Pressure
Testosterone is likely to increase blood pressure, due to a redistribution of HDL/LDL cholesterol levels. However, such cholesterol fluctuations are mild, compared to other anabolic steroids.
There are a couple of reasons why testosterone doesn’t negatively affect blood pressure significantly. Firstly, it converts to estrogen, with the female hormone having a positive effect on blood lipids.
Secondly, testosterone doesn’t pass through the liver, thus failing to stimulate hepatic lipase, an enzyme that can skew cholesterol levels in the wrong direction.
There is evidence oral testosterone may even improve cardiovascular health, when therapeutic doses are administered in overweight men. This however is likely to be correlative, with a reduction in fat mass likely being the culprit for such reductions in BP.
For most bodybuilders taking moderate to high dosages of testosterone, blood pressure will rise; with the severity depending on the dose and cycle duration.
In research, 280mg/week of testosterone enanthate had a very slight negative effect on HDL cholesterol, after 12 weeks.
300mg/week of testosterone (enanthate), when taken for 20 weeks, caused HDL levels to drop by just 13%.
Meanwhile, 600mg/week caused a reduction of 21%.
Note: Taking an AI (aromatase inhibitor) will further spike blood pressure, by inhibiting testosterone to estrogen conversion, thus further decreasing HDL levels.
Estrogenic Side Effects
Testosterone has the ability to cause gynecomastia and water retention, due to its estrogenic nature; however, a SERM (such as Nolvadex) significantly reduces the chances of gyno forming.
Incidents of gynecomastia are particularly rare when combining low doses of testosterone with a SERM.
Androgenic Side Effects
Androgenic side effects, such as hair loss on the scalp, prostate enlargement and acne are possible on testosterone.
Such side effects inspired Dr. Ziegler to create Dianabol, after understanding the Soviet strongmen had to use urinary catheters, as a result of cycling testosterone in the Olympic games.
Thus, Dianabol was formulated to be less androgenic than testosterone — yet more anabolic.
Therefore, despite testosterone’s mild properties, it may not be suitable for someone with existing prostate issues or someone looking to avoid hair loss.
Testosterone Suppression
As with all anabolic steroids, testosterone will decrease endogenous testosterone levels.
Low testosterone thus can be experienced for several months after, unless a PCT (post cycle therapy) is administered to shorten this recovery period.
HCG, Clomid or/and Nolvadex can be taken post-cycle to resurrect a male’s testosterone production.
Anavar (Oxandrolone)
Anavar is an oral steroid, often used in cutting cycles to enhance fat loss and lean muscle gains.
Anavar is one of the few steroids that is adept at building muscle and burning fat simultaneously.
Muscle gains are not extreme on Anavar; however, an increase of 10-15lbs is common.
Anavar is a mild steroid, that remains FDA-approved for medicinal purposes. It is commonly prescribed to patients suffering from bone pain due to osteoporosis; and those needing to gain weight quickly (as a consequence of trauma, infection or surgery).
Interestingly, Anavar can be prescribed to women and children, without them experiencing any notable negative effects.
This demonstrates Anavar’s mild properties, with other steroids causing masculinization in women or/and being too toxic for minors.
In bodybuilding circles, Anavar is nicknamed the ‘girl steroid’, due to it being generally safe for women to take (in low to moderate doses). Many AAS in comparison will enlarge the clitoris, shrink the breasts, cause hair growth on the body; and deepen the voice.
However, many men also take Anavar, not just for bodybuilding purposes; but to dramatically increase muscular strength, power and endurance.
Anavar Side Effects
Liver toxicity
Oral steroids generally don’t have a positive reputation when it comes to liver health.
This is because orals are c-17 alpha alkylated, meaning they are processed by the liver before entering the bloodstream. Consequently, the organ becomes stressed with ALT and AST liver enzymes rising.
However, Anavar is one of the few exceptions to this rule, with it posing considerably less liver toxicity (compared to other orals).
It is not entirely known why this is the case; however, the kidneys playing more of a role in processing oxandrolone, compared to other compounds, may be a reasonable explanation. Thus, decreasing the liver’s workload.
Cholesterol levels
Cholesterol levels will shift in a negative way, thought to be notably less than other steroids; albeit greater than testosterone.
For an oral steroid, Anavar is certainly not the worst compound for the heart; however, its effects are notable.
Research has shown that men taking 20mg/day of Anavar for 12 weeks, experienced a 30% decrease in HDL cholesterol (8).
A 40mg/day dose of Anavar only reduced HDL levels by a further 3% (33% in total).
When taking 80mg/day the reduction was severe, dropping by 50%.
LDL levels also increased in each of the groups, at a similar rate to the drop in HDL.
The typical bodybuilding dose for men is 20mg of Anavar per day. Also is not commonly taken for long periods of time (such as 12 weeks), but more often 6-8 weeks. Thus, a common Anavar cycle will likely yield less than a 30% decrease in HDL cholesterol; likely being closer to 20-25%.
This is not an alarming drop, however certainly something to monitor and take precautions against. Taking 4g/day of fish oil can help prevent such rises in BP, offering some level of cardiovascular protection on-cycle.
Virilization in Women
Although Anavar is viewed as a ‘female friendly’ steroid, virilization (or masculinization) can still occur in women taking high doses of it.
Doses over 10mg/day will increase the likelihood of undesirable effects, plus a cycle lasting beyond 6 weeks.
Doesn’t Aromatize
Anavar doesn’t convert to estrogen which is a positive in regards to body composition, as there will be no water retention. Consequently, this creates dry and full muscle bellies.
Also, there is no risk of gynecomastia on Anavar, due to a lack of aromatization activity.
However, low estrogen is one reason why cholesterol levels are worse on Anavar, compared to testosterone.
Testosterone Suppression
Significant decreases in natural testosterone production is a certainty when taking any steroid.
However, Anavar will not completely shut down users; but instead, cause moderate suppression.
One study reported a 45% reduction in testosterone when male subjects took 20mg and 40mg for 12 weeks.
This is a high dose and an excessive period of time, even by bodybuilding standards.
In comparison, a small dose of Dianabol (15mg), taken for 8 weeks can cause testosterone to drop by 69%.
Users can expect testosterone function to recover within several weeks post-cycle (without a PCT).
However, a PCT may be utilized to speed up this process, which also applies to female users.
Deca Durabolin
Deca Durabolin (Nandrolone) is an FDA-approved injectable steroid, used in medicine to treat anemia, osteoporosis and those suffering from various muscle-wasting diseases.
Deca Durabolin is favoured in medicine and the bodybuilding community, due to its mild nature; yet potent ability to add lean muscle and strength. It is anabolic, like testosterone, yet lacks strong estrogenic and androgenic properties.
In a trial in Sydney (Australia), 17 HIV-positive men took Deca Durabolin for 16 weeks.
They experienced ‘significant increases in weight’ (in the form of lean body mass), whilst ‘no subject experienced toxicity.
Deca Durabolin is one of the most heart-friendly anabolic steroids, with research showing it producing a subtle decrease in HDL cholesterol.
Studies administering 600mg/week of Deca for 10 weeks, saw a 26% reduction in HDL levels.
This effect is slightly worse than testosterone and similar to a moderate dose of Anavar.
Deca Durabolin has weak androgenic properties, thus male pattern baldness, prostate enlargement, and oily skin/acne are unlikely to trouble users.
Deca Durabolin Side Effects
Although Deca Durabolin is considered a ‘safer’ steroid in bodybuilding, it can cause some problematic side effects in other areas.
Arguably the most notorious side effect is ‘Deca dick’, which essentially is erectile dysfunction or impotence. There are two components affected, which are: the inability to get an erection and reduced libido.
One reason why Deca Durabolin may have a particularly negative effect on sexual libido/performance is due to it significantly increasing prolactin levels in the bloodstream.
Prolactin inhibits the production of GnRH (gonadotropin-releasing hormone), causing less endogenous testosterone production. This naturally leads to less desire for sex.
Due to Deca Durabolin’s low androgenicity, users can experience less nitric oxide production; which is crucial for optimal blood flow. Thus, erections may become less frequent, or more difficult to attain/sustain.
This is why some bodybuilders stack androgenic compounds with Deca Durabolin, such as testosterone, helping to keep nitric oxide levels high. Also supplementing with cabergoline can keep prolactin levels stable and thus prevent ‘Deca dick’.
Estrogen
Although Deca Durabolin is not regarded as estrogenic, it converts to estrogen at 20% of testosterone.
Deca however has strong progesterone properties, which can stimulate estrogen receptors in the mammary glands; thus still posing a risk of gynecomastia.
High progesterone can also contribute to water retention, causing the typical smooth look bodybuilders possess when taking Deca in the off-season.
Testosterone suppression
A common dose of Deca is 300-400mg per week, whilst stacked with other steroids.
Research has shown 100mg of Deca per week can reduce testosterone by 57%.
The same trial also found 300mg per week lowered test by 70%, thus a PCT should be of high priority post-cycle.
FAQ
What is the Safest Oral Steroid?
The safest oral steroid would be oral testosterone (undecanoate). However, Anavar and Primobolan are also very mild compounds with few side effects.
The most important organs to protect during a steroid cycle are the heart and liver, and these three oral steroids are the least destructive in this regard.
For women, the safest oral is Anavar, with it arguably being the most desirable compound for preserving their femininity.
What is the Safest Steroid Cycle?
Generally, the more steroids you stack together in a cycle — the greater the side effects.
Thus, a testosterone-only cycle is believed to be the mildest protocol, hence why it’s used as the first steroid cycle among beginners. Below is a cautiously dosed testosterone cycle, suitable for novices:
The above testosterone cycle would be classed as a bulking one, with users experiencing large increases in muscular strength and hypertrophy.
An Anavar-only cycle is another popular option for users prioritizing their safety. Male bodybuilders typically take the following dosages, to keep side effects at bay:
This would be seen as a cutting cycle, taken predominantly to enhance fat burning. Anavar is also suitable for users looking to gain small to moderate amounts of muscle simultaneously.
Note: Women on Anavar should take no more than 10mg/day. Below is a typical female Anavar cycle:
Summary
Although no anabolic steroid is 100% safe, some are classed as essential medicines from leading health organizations. Several steroids are also approved by the FDA, yet remain illegal today in most countries. Steroid use only becomes legal when they are prescribed by a medical doctor for underlying health problems.
IMPORTANT NOTE – Another steroid which could easily be added to this list is HEXADRONE. Given that it gives good results for lean muscle building… it is exceptionally mild to the body, plus it helps you shed a little bit of fat at the same time… but it also has the added bonus of acting as a mild aromatase inhibitor. to control estrogen side effects. A truly nice add to many cycle considerations!
A pet peeve of almost any supplier is “window shoppers”.
DON’T BE ONE!
Those are people who come to the supplier asking endless questions, with no intentions of ever really wanting to buy from them.
These are people who either have no real money, or are just looking for free information because they are too lazy to do all the hard research themselves.
Now, if you put yourself in the shoes of the supplier, who are often very busy performing the duties of their trade PLUS helping actual paying customers who deserve their help… this can be very frustrating.
And while most suppliers are good natured and want to help their fellow man with simple issues that they might know the answer to but the less experienced might not… that is all well and good. But savvy, experienced suppliers can and MUST quickly weed out these “tire kickers” and “window shoppers”… those who will ask a ton of questions, but never buy.
They are simply wasting the suppliers time!
So, before you go and start asking your local supplier a ton of endless questions to save yourself the effort of finding things out for yourself with proper research (often which leads to wrong info anyway)… take into consideration the supplier.
Make sure you are serious about buying from them, and are prepared to make your purchase BEFORE you start asking a supplier a bunch of questions!
If you are just looking for information to set up your next planned purchase… and as long as you are going to be BUYING from the supplier you are asking… tell that to your supplier up front so they know how to allocate their time. Many suppliers are very busy!
It isn’t right to ask any supplier a bunch of “help me” questions if you have no intention of BUYING from that supplier. You are just wasting their time. Time that supplier will definitely feel is better spent giving help to those who actually purchased from them.
In short… Don’t be a dick!
Have some common courtesy… if you’re not going to BUY from a supplier, don’t ask him or her a ton of questions looking for free help. You’re just rude and inconsiderate if you do.
Again, most suppliers don’t mind helping a little.. but if you have no intentions of buying from that supplier you should go away and do your research yourself. It’s not fair (or right) to bother a supplier if you are not going to give them your business.
Just think if the shoe were on the other foot… how would you like people swamping you with questions on what to do, how to do it etc… all day… every day… and then they give their business to someone else? That is totally wasting that suppliers time, and that’s screwed up!
If the people you buy from are not there to answer your questions and give you proper support… maybe you’re with the wrong supplier. You should be changing who you deal with!
And it is not unreasonable for a supplier to expect that you will order from him or her if you are there asking them a bunch of questions. Especially if you have done it on more than one occasion. That would only be fair! If they are kind enough to give you the benefit of their time and experience, you should pay back in kind by giving them your business.
If you can’t and don’t see it that way… there is something inherently wrong with you and you probably need your head examined. You’re simply not seeing things right.
Anadrol (Oxymetholone), is a DHT-derived oral anabolic steroid.
In bodybuilding, Anadrol is considered the most powerful oral steroid on the market.
Anadrol, also known as A-bombs or Oxy’s, is predominantly used by bodybuilders in the off-season (when bulking); significantly increasing muscular size and strength.
Anadrol first came on the scene in 1959, when studied for research purposes by a pharmaceutical company named Syntex. They found Anadrol to be a successful treatment for anemia, osteoporosis and muscle-wasting conditions such as HIV/AIDS.
2 years later, Oxymetholone became available in the UK under the brand name Anapolon. Other brand names also came to the fore, including: Adroyd and Anadrol (marketed in the U.S).
In the early 1960s, Anadrol was widely available for bodybuilders to use for cosmetic purposes.
As Anadrol’s harsh side effects became increasingly well-known, the FDA limited prescriptions of oxymetholone in the mid-1970s. Bodybuilders were now unable to obtain Anadrol from their doctor, with it now being predominantly prescribed to patients suffering from anemia.
Anadrol is one of the few steroids that is still FDA-approved for medicinal purposes today, alongside Anavar, Testosterone and Deca Durabolin.
Anadrol Benefits
Rapid weight gain
Muscle-building
Enhances strength
Oral form
Joint support
Fat loss
Rapid Weight Gain
Anadrol is quite possibly the best steroid in terms of weight gain, and blowing up a user’s muscles fast. This makes it a compound particularly coveted by skinny males who want huge gains.
The weight gained on Anadrol is typically comprised of muscle and water retention.
It is not uncommon for users to gain as much as 10lbs in the first week on Anadrol. By the 6th week, weight gain can increase to 30lbs. Roughly half of this is likely to be water.
Because Anadrol shifts a lot of water inside the muscle cells, muscle pumps in the gym can be described as ‘skin tearing. Pumps can become so huge where they are actually problematic, with some users describing lower back pumps as painful.
Muscle-Building
Anadrol will take a bodybuilder’s muscle size to a whole new level, with it being over 3x more anabolic than testosterone.
Some of this size will be temporary intracellular fluid retention, giving the muscles a constant pumped look.
However, the lean muscle gains on Anadrol are still significant, due to the steroid skyrocketing testosterone levels, protein synthesis and increasing nitrogen retention.
Scientists regard Anadrol as “one of the most potent steroids ever developed for building muscle“, with participants gaining 14.5lbs of muscle per 100lb of bodyweight in studies.
However, these results are based on high doses for excessive periods of time, thus results for a bodybuilder will be slightly less, assuming a shorter cycle and a more cautious dose.
18lbs of lean muscle is common for a first-time 6 week cycle of Anadrol. This will be roughly 60% of the overall weight gained.
Enhances Strength
Anadrol is arguably the greatest steroid in powerlifting and strongman circles. This is due to the sheer weight gain and the huge surge in testosterone.
It is common for users to add 30lbs to their bench press in the first 10 days on Anadrol.
By the end of a cycle, Anadrol has the ability to add approximately 60lbs to a user’s squat, deadlift and bench press.
Usually, the strength gained during these compound lifts will be double the bodyweight gained on Anadrol.
Strength levels can decrease by 40% post-cycle, which correlates with the same degree of weight loss.
Oral Form
Anadrol 50 essentially is a 50mg tablet. Thus, no injections are needed to reap the rewards from this steroid.
Injections can be very dangerous if the person doesn’t know what they are doing. One of the most common injection sites is the buttocks, which if done incorrectly can injure the sciatic nerve and cause paralysis.
Injections even when done safely, can be uncomfortable, which isn’t ideal when administering steroids with short half-lives (such as Anadrol), which require frequent injections.
Injecting into the buttocks may also mean users have to rely on friends or family to inject them.
Despite orals being more convenient and easier to take, there are drawbacks to taking pills, which will be detailed in the side effects section.
Joint Support
Anadrol is somewhat healthy for the joints, due to its water-retaining properties.
It lubricates the joints, increasing elasticity and decreasing inflammation or/and joint pain.
Thus, if a bodybuilder does have joint problems, taking a steroid such as Anadrol or Deca Durabolin may be more preferable to Winstrol for example; with the latter expelling water and creating more wear on the joints.
Fat Loss
Some people believe Anadrol causes fat gain; however, this isn’t accurate.
All anabolic steroids, including Anadrol, are different types of exogenous testosterone.
Testosterone will build muscle and burn fat. Thus, different steroids will build muscle and burn fat to different degrees.
Two studies have concluded that Anadrol burns significant amounts of subcutaneous fat when dosed at 100mg per day.
The reason why Anadrol may appear to cause fat gain is due to water retention. The puffiness and bloating from the excess fluid can give the appearance of a higher body fat percentage.
As it’s a bulking steroid, users are likely to combine Anadrol with a high-calorie diet, resulting in fat gain and additional water retention. This however is linked to the person’s diet and not directly related to Anadrol itself.
Therefore, if a maintenance calorie diet is adopted, the person will not gain subcutaneous fat.
However, Anadrol and other steroids can cause increases in visceral fat. This is not the fat you can pinch around your stomach, but instead located internally and wraps around your organs.
Side Effects
Generally, the better results experienced from a steroid, the worse the side effects are. Although Anadrol produces some of the best strength and mass gains, it is also a very harsh steroid. Thus, it is not recommended for beginners.
Anadrol’s side effects are:
Liver toxicity
High blood pressure
Water retention
Gynecomastia (possibility)
Shuts down testosterone
Hair loss
Acne
Increased risk of injury
Decreased well-being
Liver toxicity
One of the main concerns when taking Anadrol is that it is hepatotoxic.
It is a c17-alpha-alkylated compound, which essentially protects Anadrol from being deactivated via the liver. This allows a very high amount of Anadrol to remain active in the bloodstream when taken orally.
However, like all C17-alpha-alkylated steroids, they are straining on the liver.
Anadrol does have a saturated A-ring, which reduces its toxicity somewhat; however, studies confirm that liver health can deteriorate if high doses are used.
In a 2003 study, 89 men and women who were HIV/AIDS positive, took 100-150mg of Anadrol per day for 16 weeks.
25% of the 100mg group had their ALT/AST liver enzymes increase over 5 fold.
43% of the 150mg group’s ALT/AST increased over 5 fold.
Thus, Anadrol when taken in high doses for excessive periods of time is particularly damaging to the liver.
However, bodybuilders should have no reason to go above 100mg per day, as muscle/weight gains largely remained the same between the 100mg and 150mg groups in this study.
In another study, 31 elderly men took 50-100mg per day for 12 weeks. The 50mg did not experience any increase in liver enzymes, however the 100mg group experienced modest ALT and AST elevation. Although the 100mg group did not result in any cases of hepatic enlargement or cholestasis.
A 20-year-old Japanese woman who suffered from aplastic anemia was treated with Anadrol, taking 30mg/a day for 6 years (this is an incredibly long time). Despite developing multiple liver lesions, a lab evaluation found her liver function to be normal. This is astonishing considering she was taking this high dose (for a female) for 6 years!
Thus, given the resilient nature of the liver and multiple studies of Anadrol-abuse not resulting in liver failure; Anadrol does not seem to pose excessive damage to the liver.
However, users should still take precautions, utilizing low to moderate doses in relatively short cycles (4-6 weeks).
In another study 28 adults with chronic anemia were given a huge dose of Anadrol, being 5mg/per kg of bodyweight.
This translated as doses as high as 450mg per day for men. Surprisingly, hepatic toxicity was only observed in less than 10% of the patients.
Thus, liver toxicity with Anadrol may be somewhat exaggerated in the bodybuilding community. From medical research, it does not seem to be particularly dangerous, yet preventative measures should still be used.
TUDCA
To help ease the strain on the liver when taking Anadrol, users can supplement with TUDCA (Tauroursodeoxycholic acid). This is a naturally-occurring compound found in bile acid, produced in the liver.
The natural healing effects of TUDCA have been used to treat liver disease in Chinese medicine for the last 3,000 years; often in the form of bear bile (containing over 50% of TUDCA). In comparison, only small amounts of TUDCA exist in human bile.
In medical research, TUDCA has shown to be effective in treating chronic active hepatitis.
In one study, 53 patients took 500mg of TUDCA per day for 3 months. It was effective in lowering AST and ALT enzymes within the first month. This effect was dramatic by the 3rd month, with AST and ALT enzymes dropping by 44% and 49%. The patients also reported no side effects.
Therefore it would be wise to supplement with TUDCA during or/and after your cycle for maximum liver protection. Alcohol should also be avoided.
Effective TUDCA supplements can be bought online, here. It is an FDA-approved supplement.
High Blood Pressure
Anadrol is possibly the worst steroid in regards to blood pressure. All anabolic steroids will elevate a person’s blood pressure, due to exogenous testosterone causing a negative shift in cholesterol levels.
This results in a dramatic rise in LDL (bad) cholesterol levels and a decrease in HDL (good) levels.
With Anadrol, studies have shown an insignificant impact on LDL levels, but a dramatic decline in HDL levels.
In the previously cited study, the 31 elderly men taking 50-100mg of Anadrol per day experienced a reduction in HDL by 19 and 23 points.
Anadrol will also spike blood pressure due to it dramatically increasing red blood cell count. Anadrol users can experience up to 5x the number of red blood cells, compared to a normal person.
Consequently, blood can become more viscous, with blood flow to the heart potentially becoming impaired. When a person retains water, the same blood-thickening effect happens, further reducing circulation.
Due to Anadrol’s drastic effect on HDL cholesterol levels, water retention and red blood cell count, it is a steroid that has a very negative effect on the heart.
A diuretic may be used to lower blood pressure if a person experiences significant water retention. However, this will result in less muscle fullness and decreased strength gains, due to less ATP production inside the muscle cell.
Users with high blood pressure or a history of heart disease in their family should refrain from using Anadrol.
Those who are planning on cycling Anadrol should try and minimize this spike in BP, by performing regular cardio. This will improve blood flow to and from the heart.
Nosebleeds and headaches can occur whilst on Anadrol, which can be a sign of elevated blood pressure. If this happens, get a check-up and if your BP is very high, cycle off immediately.
Water Retention & Gynecomastia
Smooth, bloated muscles
Anadrol is a DHT derivative, thus it does not aromatize and convert into estrogen.
However, it does appear to be very estrogenic in real-life settings, having the potential to cause: gynecomastia, water retention and bloating.
It has been theorized that these estrogenic side effects are due to Anadrol acting as a progestin; however, studies show Anadrol to have little effect on progesterone levels.
Instead, Anadrol stimulates the estrogen receptors directly, similar to methandriol.
Water retention can be beneficial during a steroid cycle, as intracellular fluid can aid ATP production and thus increase muscular strength and size.
However, the downside to water retention, is the muscles look smooth and definition is reduced. Bloating is also common on Anadrol, especially in high doses or when taken in conjunction with a high sodium diet.
Due to Anadrol causing noticeable amounts of extracellular fluid retention, it’s not the best steroid for vascularity.
Why Anadrol Doesn’t Always Guarantee Water Retention
Some users do not experience much bloating or fluid retention on Anadrol if their diet is particularly clean and they are already very lean.
For example, Men’s Physique competitors often get away with taking Anadrol before a competition, helping them to look extra full; without any noticeable water retention or bloat.
The reason why they don’t experience water retention from Anadrol when preparing for a show is that the presence of high estrogen levels does not automatically guarantee water retention.
High estrogen simply increases your sensitivity to sodium, thus if a person’s sodium intake is moderate, and they take Anadrol; they will retain more water.
However, if a bodybuilder’s sodium intake is low and they consume large amounts of water (as bodybuilders typically do before a contest), sodium levels will remain low, and thus increased sodium sensitivity is no longer an issue.
Consequently, bodybuilders can appear extremely full and dry on stage.
Gyno
Anadrol can also cause gynecomastia via the direct stimulation of estrogen receptors in the mammary gland. Gynecomastia (gyno) is when additional breast tissue starts to form in a male’s breasts.
Mild gyno can resemble swollen nipples, whereas severe gyno can cause a man’s breasts to look like a woman’s.
To prevent estrogenic side effects from occurring, users can take an effective anti-estrogen, such as Nolvadex or Clomid. However, reducing estrogen levels may further decrease HDL levels, increasing blood pressure.
Note: Aromatase inhibitors, such as Arimidex or Cytadren will not be effective in reducing estrogenic side effects, as Anadrol does elevate estrogen levels via aromatization (but via direct stimulation).
Shuts Down Testosterone
All anabolic steroids will suppress endogenous testosterone production. The post-cycle crash can typically be hard on Anadrol-users, thus a PCT is essential in accelerating the restoration of mental well-being and natural testosterone production.
Low testosterone levels can cause:
Low energy
Low motivation
Decreased libido
Impotence
Decreased well-being
Because the ‘come down’ on Anadrol is severe, some steroid-users may opt to use a milder steroid such as Deca Durabolin after coming off it; to aid this transition. Such a protocol may also help users retain more strength/muscle gains experienced from an Anadrol cycle.
However, if a person opts to use a ‘lighter’ steroid following Anadrol, this will delay the time it takes for endogenous testosterone levels to recover. Thus, it is only typically implemented by individuals who have low well-being post-cycle.
Natural testosterone levels often recover within 1-4 months after coming off Anadrol (and other steroids). However, this is only a general rule that applies to those who do not abuse steroids.
If users take high dosages of Anadrol for excessive periods of time, they run the risk of developing hypogonadism, which may require medical intervention to get the testes functioning properly again.
Abuse of Anadrol, or other steroids, may also lead to infertility; due to decreased sperm count and quality. This effect can become permanent, preventing men from having children.
Discover how to increase your endogenous testosterone production (back to normal levels) in our post-cycle therapy section.
Hair Loss & Acne
Anadrol has a low androgenic rating of 45. This is less than half the rating of testosterone.
However, this mild score does not correlate in real-life settings, where Anadrol often produces androgenic effects, including hair loss (on the scalp), oily skin and acne.
This is due to increased sebum production which is secreted by the sebaceous glands. The role of sebum is to moisturize the skin; however, too much of it can block the pores, leading to acne breakouts.
This side effect is often genetic, thus if a person has experienced acne during puberty, they may be more at risk.
Anadrol is a DHT-derived steroid, but it also converts into dihydrotestosterone – the hormone responsible for hair loss on the scalp.
DHT causes miniaturization of the hair follicles, causing them to thin or even fall out. Hair loss is a concern when taking any steroid; however, it is often determined by a person’s genetics.
For example, some users may take Anadrol, Trenbolone and Testosterone together for several months and keep thick-looking hair. Whilst others can take a mild steroid such as Deca, and experience significant hairline recession or baldness from just a couple of cycles.
If you are predisposed to losing your hair, steroids will accelerate this process. Alternatively, if you have strong hair genetics, steroids will not cause you to go bald.
How Does Anadrol Produce Androgenic Side Effects, Despite Having a Low Androgenic Rating?
With Anadrol, the conversion of DHT isn’t through the usual pathway, being the 5-alpha reductase enzyme.
Anadrol uniquely contains an additional 2-hydroxymethylene group.
Once in the body, this is metabolized, reducing oxymetholone into 17-alpha methyl dihydrotestosterone (otherwise known as Mestanolone or Proviron).
17-alpha methyl dihydrotestosterone is a very potent androgen, which explains why androgenic side effects are possible, despite it having a low androgenic rating.
Because Anadrol does not convert into DHT via the 5-alpha reductase enzyme, medications such as Finasteride are ineffective for the treatment of hair loss. Also, it is not in a bodybuilder’s best interest to reduce DHT levels with such medications, as they can decrease strength and muscle gains.
Increased Risk of Injury
Rapid weight gain from Anadrol can place excessive stress on connective tissues. Thus, pectoral and bicep tears aren’t uncommon on Anadrol.
This is the side effect of fast and enormous increases in strength (+60lbs on compound exercises).
To reduce the risk of injury, bodybuilders can lift lighter weights and perform more repetitions. This will not reduce muscle gains, as lighter weights are just as effective for building mass and size as heavy weights.
Furthermore, performing a sufficient warm-up will help the muscles become more supple and decrease the risk of injury.
Decreased Well Being
Some users report Anadrol giving them mood swings and making them feel miserable. This can be attributed to the sheer power and toxicity of the steroid i.e. the combination of liver strain, water retention and high blood pressure.
In some individuals, Anadrol may not produce the constant euphoria feel, compared to Dianabol for example. This is because Anadrol is the harsher steroid, thus the side effects are also more profound.
However, individuals who genetically respond well to Anadrol, can experience increased well-being due to the huge increase in exogenous testosterone.
Note: Fluctuations in well-being may also be dose-dependent.
Is Anadrol Safe?
Anadrol remains FDA-approved in the United States for the treatment of anemia. Thus, when administered under a doctor’s supervision, Oxymetholone is deemed safe.
However, bodybuilders who take Anadrol remain at risk, as they are thought to be healthy individuals doing this in a non-medical setting. This opens the door for Anadrol to be abused, via high doses and excessive cycles.
Also when Anadrol is taken in recreational settings, it is not guaranteed to be real Oxymetholone, due to the purchase of this steroid on the black market.
Despite Anadrol being FDA approved, it is still one of the harshest steroids used in bodybuilding, thus extreme caution should be used.
Anadrol for Women
Because men experience androgenic effects from Anadrol, many assume that it also causes virilization side effects in women, which are:
Deepened voice
Clitoral enlargement
Body hair
Hair loss (on the scalp)
Masculine facial features (including more pronounced jawline)
However, research shows that Anadrol is actually a very female-friendly steroid, with a low affinity for masculinization side effects.
Study: female HIV patients suffering from chronic cachexia, were given 100-150mg of Anadrol per day for 30 weeks. This is a mega-dose by bodybuilding standards and an extremely harsh cycle.
However, virilization did not occur in any of the women. In fact, the only side effects reported were a lack of sexual desire and increased fatigue. Unlike men, the women also did not experience any hypertension or androgenic side effects either.
There are two explanations for why Anadrol does not cause virilization in women. Firstly, masculinization often occurs in women when androgen levels are high and estrogen levels are low. Anadrol is androgenic, but also very estrogenic; preventing this ratio from becoming imbalanced.
Another reason why Anadrol is female-friendly is due to its low affinity when binding to SHBG. High levels of sex hormone-binding globulin aren’t female-friendly, as it causes women’s natural testosterone production to become free, or unbound.
In comparison, Winstrol binds strongly to SHBG and consequently produces strong masculine side effects in women. Winstrol also does not convert into estrogen, creating an optimal environment for virilization.
Anavar is a very popular steroid among females; however, in clinical settings, Anavar can still produce virilization in higher doses.
Steroid expert, Bill Roberts (Ph.D.), states in his experience that;
“5mg of Anavar is roughly the equivalent of 25mg of Anadrol for risk of virilization”.
He also recommends splitting up the doses of Anadrol throughout the day, instead of taking 25mg in one go.
In another study, women were given Oxymetholone to treat anemia and bone marrow failure. They started on a dose of 1mg per kg, then it increased in monthly increments by 50%, up to 100mg per day. Every female was given a dose of at least 50mg of Anadrol per day.
Only mild side effects were reported. Only 4 women in the study showed slight virilization changes, despite being given huge doses. Such side effects also reversed after they stopped taking Anadrol.
12.5mg-25mg is considered an effective dose for women wanting to experience significant strength and muscle gains on Anadrol. These are very modest doses compared to the studies cited above, further preventing the risk of virilization.
Women should also be wary about liver toxicity on Anadrol. Therefore women should supplement with TUDCA and refrain from drinking alcohol.
Is Anadrol Legal?
Anadrol is illegal to take (for bodybuilding purposes) in most countries unless a doctor has prescribed it for medical reasons.
In the U.S, Anadrol is classed as a schedule III controlled substance, following the controlled substances act.
Thus, buying or selling Anadrol can result in prison time if caught. Possession of Anadrol (or other steroids) can result in a 1-year prison sentence and a minimum fine of $1,000. Prison time and fines increase for repeat offences.
Selling steroids can result in up to 5 years in prison and a fine of $250,000. This is applicable to first-time offenders. Fines and prison time can double for a second offence.
Anadrol can be legally bought in Mexico and Thailand (despite it being an ‘S controlled substance’ in the latter country).
Anadrol Results – Before & After Transformation
Due to Anadrol’s short esters, it kicks in very fast. Users often feel its powerful effects within the first few days.
As previously stated, one cycle of Anadrol can result in 30lbs of weight gain and 60lbs of added strength on the 3 big compound lifts. Additional cycles can lead to enhanced results, especially when stacked with other steroids.
Below are the results from a bodybuilder who took Anadrol and Deca Durabolin for 1 year.
In the picture on the left (above), the bodybuilder states that he was already taking SARMs, thus a user may experience even bigger gains than his if they transition from natural to taking Anadrol regularly.
From natural to using Anadrol
Huge back gains
As you can see, his muscles have blown up dramatically since he started taking Anadrol and Deca Durabolin. He hasn’t really gained any fat, but his muscles appear smoother and puffier due to some water retention.
These impressive results are typical after a few cycles of Anadrol.
Are Anadrol’s Results Permanent?
The leanmuscle gains experienced on Anadrol are often permanent. Just over half of the weight a user gains from Anadrol will be lean muscle (the rest will be water).
Thus, if a person gains 35lbs from a 6-week cycle, roughly 20lbs will be lean muscle (which will remain after coming off the steroid).
To increase muscle retention post-cycle, follow an effective post-cycle therapy protocol and continue training hard. Once a person stops lifting weights, lean muscle gains from Anadrol will diminish.
Injectable Anadrol vs Orals
Some people believe that by taking injectable Anadrol, you won’t strain your liver.
This however is false. Although it will bypass the liver upon entry into the bloodstream, it will have to process through the liver upon exiting your body.
Thus, it is believed that injectable Anadrol is less hepatotoxic than oral Anadrol; however, it still strains the organ.
With injectable Anadrol you are getting 100% of the true dose, as it is not being broken down by the liver.
With orals, they are C-17 alpha alkylated, thus a very high percentage of the steroid remains active. Although, your body won’t be utilizing 100% of the dose.
Furthermore, injectable Anadrol is more difficult to get hold of compared to orals, so there is no significant benefit to taking injectable Anadrol over oral Anadrol, other than slightly less liver strain.
Note: Liver strain is not particularly concerning on Anadrol if a moderate dose/cycle is performed.
Anadrol Dosage
Male bodybuilders will often take 50-100mg of Anadrol per day for 4-8 weeks.
An effective dose for women looking to build muscle is 12.5-25mg per day for 4-6 weeks.
Due to Anadrol’s short half-life of 5-9 hours, doses should be split up and taken regularly throughout the day. Anadrol typically contains pills in 50mg doses, thus by using a pill cutter you can give yourself 2-4 doses each day.
Important: Anadrol pills are fat-soluble, therefore eating them with food may decrease their biological availability and hinder results. Thus, for best results take Anadrol on an empty stomach.
The higher the dose, the more side effects a user will experience. Anything over 100mg per day will dramatically increase side effects, without much-added benefit in terms of results.
Anadrol Stacks & Cycles
Anadrol is commonly stacked with powerful injectable steroids, such as Testosterone, Deca Durabolin or Trenbolone.
Such stacks will lead to further mass and strength gains but also increased side effects. Stacking multiple steroids together will exacerbate testosterone suppression, cholesterol values and blood pressure.
With Anadrol being a particularly harsh steroid, it would be wiser to stack it with a mild injectable steroid such as Deca Durabolin, as opposed to Trenbolone. Testosterone is also suitable.
Like Dianabol, Anadrol can be cycled alone with good results, especially if the user is a novice to Oxymetholone.
Once users have built up a tolerance to Anadrol by cycling it once, users may stack other steroids with it.
Here are some sample Anadrol cycles that bodybuilders use today.
Anadrol-Only Cycle
This cycle is tailored for novices who haven’t used Anadrol before. Although Anadrol is not generally recommended for beginners, the above cycle may be tolerable due to lower doses.
Anadrol-Only Cycle (Experienced Users)
The above cycle is tailored for experienced steroid users, hence the higher dose and extended duration.
Anadrol and Testosterone Cycle
Anadrol and testosterone are one of the best duos to stack together for building size, strength and mass. This stack is suitable for experienced users only. With the addition of testosterone, the risk of gynecomastia increases greatly due to higher estrogen levels. Thus, it is advisable to take a SERM during this cycle, such as Nolvadex.
SERMS (selective estrogen receptor modulators) essentially block estrogen’s effects directly in the breast tissue, thus preventing the onset of gyno.
Anadrol / Testosterone / Trenbolone Cycle
Note: the above cycle is only utilized by very experienced steroid users.
This is an extreme cycle for incredible mass and strength gains. Rich Piana hailed it as his “best ever cycle”. The specific testosterone he used was Sustanon 250 and Trenbolone acetate. However, he stated that he didn’t utilize this cycle often, as it is very taxing on the body.
This cycle will be very estrogenic and androgenic. Thus, bodybuilders will often take an AI (aromatase inhibitor) to reduce testosterone’s estrogenic side effects. This is usually Letrozol or Anastrozol. A SERM such as Nolvadex may also be used to prevent the direct stimulation of estrogen in the mammary gland (from Anadrol).
Regular cardio should be performed throughout this cycle to lower blood pressure, whilst avoiding stimulants and high sodium foods.
It is difficult to prevent androgenic effects from occurring; however, these effects aren’t particularly damaging to a man’s health, such as acne or male pattern baldness.
You won’t find a trio of steroids that can produce the same level of strength and mass as this combination. Equally, it is one of the worst cycles for side effects.
Anadrol PCT (Post Cycle Therapy)
You will certainly need to utilize an effective post cycle therapy after taking Anadrol, as testosterone levels will become very suppressed; affecting mental well-being, energy levels, libido and gains.
In order to recover endogenous testosterone production quickly, an aggressive PCT protocol should be administered. This is especially true if a user is stacking Anadrol with other anabolic steroids.
The following would be an effective plan:
hCG – 2000 IU administered every other day for 20 days
Tamoxifen (Nolvadex) – 2 x 20mg for 45 days
Clomiphene (Clomid) – 2 x 50mg for 30 days
This PCT was created by Dr. Michael Scally, a hormone replacement expert. This trio of drugs has been effective in treating 19 men with low testosterone levels (from the use of anabolic steroids).
45 days after using this PCT, all of the men’s testosterone levels fully recovered back to normal levels.
Dr. Scally has treated over 100 men for hypogonadism, giving him specialist knowledge and experience in this area.
A PCT should begin as soon as Anadrol has left the user’s body. We can calculate this using Anadrol’s half-life (8-9 hours). To work out when the drug has fully left the body, you multiply the half-life by 5.5, giving us the following sum: 5.5 x 9 hours.
Thus, a PCT for Anadrol should begin 49.5 hours after the last dose. If other drugs are combined with Anadrol, you need to calculate when they will also leave the body. In this scenario, start the PCT when the last steroid has left your system i.e. the one with the longest half-life.
Using this aggressive PCT, endogenous testosterone production will typically recover after 2 months.
Where do Bodybuilders Buy Anadrol?
Anadrol is illegal in most countries, thus bodybuilders are forced to buy it through the black market.
Anadrol can be bought conveniently at a local store or pharmacy ONLY in countries where it’s 100% legal (i.e. Mexico).
Bodybuilders will often buy Anadrol from someone they know or an online website. There are 2 possible grades, being pharmaceutical grade and underground labs.
Pharmaceutical grade Anadrol is created by scientists in a lab for medical purposes. Thus when you buy genuine pharma-grade it is 100% legitimate. This can be purchased on the black market if someone has been prescribed Anadrol for their anemia. So if they haven’t taken their medication, they may decide to sell it.
Underground labs Anadrol essentially is someone formulating the Anadrol themselves. Thus, the risks associated with buying UGL steroids from unknown sellers are high, due to a lack of regulations and non-medical expertise.
Pharma Anadrol is rare, thus most of the Anadrol people buy is UGL. Pharma grade is also considerably more expensive than UGL, due to it being the real deal and more scarce.
Due to the possible risk of Anadrol containing dangerous substances or simply being a placebo pill; people are advised to only trust sources on the black market that can be verified (by someone they trust).
Buying from unknown websites with no reviews, or trusting someone down your gym, where no one can vouch for the product, increases the chances of being scammed.
Anadrol Price
The typical price of Anadrol on the black market is:
100 x 50mg pills = $85.
This will last just over 6 weeks, taking 100mg a day.
Or, it can last for 2 x 6-week cycles on 50mg per day.
This value has been established from an anonymous source. Prices will naturally be higher than this for pharmaceutical grade Anadrol.
Diet on Anadrol
A person’s diet is particularly important on Anadrol, in regards to water retention. Bodybuilders often report excessive bloating on Anadrol when eating ‘dirty’ foods in the off-season.
This combination of a high sodium diet and the estrogenic nature of Anadrol causes water to ‘spill’ outside the muscle cells, giving a puffy appearance. Facial and stomach bloating are also common.
In a bid to avoid this, it is important to drink lots of water and to eat clean. When a person drinks more water, it causes the body to flush out existing water in the body, as a self-defence mechanism.
Junk food (high sodium) not a good idea on anadrol
Eating unrefined carbohydrate sources, such as fruit, wholewheat pasta, wholegrain rice, oatmeal, wholemeal bread is a good idea, as refined carbs may exacerbate fluid retention, contributing to heightened blood pressure.
Some salty foods which shouldn’t be indulged in are salted nuts, bacon, sausage, anchovies, ham, baked beans and tuna. Fish sources such as haddock and salmon are better, lower-salt alternatives
It would also be a good idea to limit the intake of dairy products, as these can also contribute to bloating in some individuals.
FAQs
Does Anadrol Suppress Your Appetite?
Anadrol is designed to stimulate appetite, enabling users to gain weight fast. However, if doses are too high or the person doesn’t respond well, it can decrease appetite. This is usually the result of excess liver strain.
When the liver is being taxed, as a defence mechanism the body reduces appetite, in a bid to decrease the amount of food the organ has to process. This essentially reduces the liver’s workload.
Can You Use Anadrol for Cutting?
Anadrol can be used on a cut to increase fat burning, help retain muscle tissue and dramatically increase muscle fullness.
However, it is not generally taken during a cutting cycle, due to extracellular water retention. This has the potential to decrease muscle definition and increase bloating, which isn’t aesthetically pleasing when trying to burn fat.
However, some bodybuilders and men’s physique competitors will cycle Anadrol just before a show to blow up their muscles and come in exceptionally full. This can be done without significant increases in water retention if a person is extremely lean and keeps their diet clean.
Does Anadrol Negatively Affect Cardio?
In short: yes.
Due to the sheer weight gain on Anadrol, cardiovascular activities can become increasingly difficult.
Also on Anadrol, the blood becomes more viscous due to a dramatic rise in red blood cell count. Consequently, blood flow becomes impeded, making it easier to get out of breath.
However, cardio shouldn’t be avoided as it has the potential to reduce blood pressure and increase circulation. This can help negate some of the adverse effects of Anadrol (including strain on the heart).
Anadrol vs Dianabol
Anadrol and Dianabol are two wet steroids, being very estrogenic and typically causing significant water retention in the off-season. They are arguably the two best steroids for putting on mass quickly.
Anadrol is the more powerful steroid out of the two, in the typical doses taken. Weight gain is likely to be slightly more on Anadrol compared to Dianabol, with the same applying to strength gains. However, side effects are likely to be more severe on Anadrol.
Beginners will take often take Dianabol but are rightfully wary of Anadrol.
Despite Anadrol being ‘the more toxic steroid’, Dianabol mg for mg is actually the more potent drug. Typical doses of Dianabol range from 30-50mg per day. Whereas Anadrol requires double this dose to get similar results (50-100mg).
In summary, Dianabol is perhaps the better drug when weighing up the pros and cons of each steroid. However, people can respond differently to both compounds.
Anadrol vs Trenbolone
Anadrol and Trenbolone are very different steroids. Both are fast-acting; however, Anadrol 50 is an oral and Trenbolone is an injectable.
Anadrol causes significant amounts of water retention, whilst Trenbolone is a ‘dry‘ steroid. Therefore all of the weight gained on tren will be lean muscle mass, making it the more ‘aesthetically pleasing’ drug.
Trenbolone is the better steroid for cutting purposes, due to its superior fat-burning properties. Tren will also help users look more vascular, due to its diuretic properties (less water collecting between the muscle and skin).
Both are very harsh steroids that will elevate blood pressure, shut down testosterone, cause androgenic side effects and pose risks to the liver.
Trenbolone does have the ability to raise liver enzymes; however, this effect is thought to be less than Anadrol.
Both of these compounds complement each other very well in a stack together. However, this stack will also produce some of the worst side effects among all steroids.
Anadrol vs Deca Durabolin
Deca Durabolin is a bulking steroid like Anadrol, however a much milder compound.
Deca is an injectable steroid, whereas Anadrol is mostly in pill form.
Deca has long esters and is slow-acting, whereas Anadrol hits you like a train within the first few days of a cycle. Thus Deca cycles are typically longer than Anadrol (usually 8-10 weeks), as it takes longer to kick in.
Muscle and strength gains on Anadrol will be superior compared to Deca Durabolin, simply because it is more anabolic.
Deca is not estrogenic; however, some estrogen-like side effects are possible due to moderate progesterone activity. However, the risk of gynecomastia and bloating will be less on Deca.
Androgenic side effects will also be significantly less on Deca compared to Anadrol, so if you are prone to acne or are worried about hair loss — Deca is the better steroid.
Deca often needs to be stacked with other steroids in order to see tremendous gains in muscle mass, whereas Anadrol is a powerful drug by itself.
Anadrol vs Testosterone
Testosterone is mostly an injectable steroid, whereas Anadrol 50 is an oral.
These two steroids have somewhat similar effects. Both are powerful for adding lean mass and increasing strength; however, Anadrol will produce more water retention.
Weight gain will be more noticeable on Anadrol; however, lean muscle gains will be somewhat similar (with Anadrol having the edge). Anadrol is the better steroid for strength purposes.
Testosterone is more suitable for beginners as it’s less toxic to the body. A test-only cycle is better tolerated among novices than Anadrol.
Both steroids will produce estrogenic, androgenic and cardiovascular side effects. However, these will most likely be dialed up a notch or two on Anadrol.
Anadrol vs Anavar
Anavar is another oral steroid and a DHT derivative like Anadrol.
Anavar is predominantly used during cutting cycles, due to its fat-burning effects and being a ‘dry’ steroid, with no water retention. Anadrol however is a wet steroid, due to it being very estrogenic.
Anadrol will cause a lot of weight gain, whereas Anavar won’t.
Anavar is a better fat burner due to it stimulating T3 levels in the thyroid.
Anavar will increase lean muscle mass, however nowhere near to the extent of Anadrol.
Anavar is a very mild steroid, in regards to side effects, and thus is popular among beginners and women. In medicine, Anavar is even prescribed to children and is deemed ‘safe’.
Anadrol is a lot more toxic than Anavar, producing more severe side effects. Particularly in regards to blood pressure, testosterone suppression and estrogenic effects.
Should I Take Anadrol With Grapefruit Juice?
There was a study that measured whether grapefruit significantly increased the absorption and bioavailability of sex steroids – estradiol and progesterone.
Surprisingly, 200ml of grapefruit juice increased estradiol by 117% and progesterone 125% 24 hours after consumption.
In another study, researchers wanted to see if blood pressure medication, when taken with alcohol, had any interactions. To disguise the taste of alcohol they mixed it with grapefruit juice.
They concluded that alcohol had no interactions with the medications; however, grapefruit juice increased the absorption of the medication in the bloodstream by 5 fold.
The science behind grapefruit juice increasing the absorption of medications is due to it inhibiting an enzyme in the liver and intestines, known as CYP3A4.
CYP3A4’s job is to remove foreign molecules, by detecting toxins in the body. This process greatly decreases the biological availability of many drugs.
It is believed flavonoids and/or furanocoumarin present in grapefruit juice, are what inhibit CYP3A4 from functioning properly.
Another study found that grapefruit juice’s CYP3A4-inhibiting effect was most effective when drank 1 hour before taking the medication.
Research has shown that grapefruit can cause this effect for up to 24 hours, of which 1/3 of the effect still remains.
However, for optimal results 250ml of grapefruit juice should be drunk every 12 hours. Thus, users don’t need to drink 250ml of grapefruit juice with every single dose, but merely to keep CYP3A4 steadily deactivated throughout the day.
This is why many medications will say on the box: do not drink with grapefruit juice, as medications are obviously dosed based upon the CYP3A4 enzyme working as normal.
On a bodybuilding thread, one person shared his experience with grapefruit juice:
That’s very interesting, because I am in the 2nd week of my Dianabol cycle and I didn’t feel much difference at first, but this week I’ve been drinking a lot of grapefruit juice (instead of water) and I’ve had insane pumps which I’ve never experienced before, particularly in my legs.
There have been no studies conducted on mixing grapefruit juice with oral anabolic steroids, however theoretically this could work. Therefore, if users are going to drink grapefruit juice with orals, they need to be cautious of overdosing, as 50mg of Anadrol may effectively become 100mg with the inhibition of CYP3A4.
Thus, this methodology has the potential to increase results, but also increase the severity of side effects.
If this protocol is successful, the cost of an oral cycle may effectively decrease, as users will be able to lower the dose without it decreasing their gains.
Note: research shows that eating grapefruit is also effective in blocking CYP3A4.
Can I Use Anadrol All Year Round?
This isn’t recommended as Anadrol is one of the harshest steroids you can take. This will almost certainly cause excessive damage to the heart, suppress endogenous testosterone production enormously and place incredible strain on the liver.
Also, there is not much benefit to doing this, as gains will plateau, due to your body adapting to the steroid. You don’t want to condition your body to need mega doses of Anadrol in order to make further gains, which will be the case if someone chose to blast and cruise Anadrol.
Testosterone would be a safer steroid for blast and cruising.
I Have Taken 400mg of Anadrol and Felt Nothing, Why Isn’t It Working?
Never take more than 100mg of Anadrol per day (100mg is even a high dose).
Many bodybuilders will verify that Anadrol is one of the most powerful steroids on the market. You will certainly feel it, therefore the ‘Anadrol’ you have is almost certainly not authentic oxymetholone.
Will Anadrol Shrink My Testicles?
There is a good chance that a man’s testicles will decrease in size, signifying less sperm count.
This is the consequence of lowered endogenous testosterone production. This effect can be quite severe, hence why a powerful PCT protocol is needed to quickly restore normal test levels and sperm count. Several months after using Anadrol or other steroids, your testicles should return back to their normal size.
Will Anadrol Show on a Drugs Test?
This depends on the type of test.
For example, if someone is in the police or army, they are often tested for other substances such as amphetamines, cocaine and marijuana. Thus, steroids generally won’t cause a failed test. Hence how Ronnie Coleman was able to be a police officer and not have any problems.
However, if someone suspects you are taking steroids, from you talking openly about your use, it’s possible for them to order a steroid test specifically for you to take. Although, talking so abrasively about steroid use in such environments isn’t common, as people generally don’t want to get caught.
If you are a bodybuilder competing in a natural show and they conduct random testing, they certainly will be testing for Anadrol, among other anabolic steroids. Thus, as you do not know the date of the test, it is likely you will fail this test.
However, if there is a set date for a test, you can pass it by coming off Anadrol 2 months prior.
Anadrol’s detection time is 2 months. Thus, from your last dose until this time, trace amounts remain biologically present; which can cause a failed test. If a user leaves plenty of time and cycles off 2.5 months before a test they will be fine.
Note: If the person has taken any other steroids in the past, alongside Anadrol, they will need to calculate the detection times of those too.
Anadrol vs Superdrol
Superdrol is a very powerful oral steroid. Many people describe it as ‘oral Trenbolone’.
Superdrol, like Anadrol, is a DHT-derived steroid (despite being falsely marketed as a prohormone in the early 2000’s – later causing it to get banned).
Superdrol is the more powerful steroid mg per mg. For example, a high dose of Superdrol is 30mg, whereas a high dose of Anadrol requires over 3x that amount (100mg).
In terms of weight gain, Superdrol users will gain roughly 10lbs of lean muscle in a short 4-week cycle. In comparison, Anadrol will produce roughly 30% more lean muscle (in most users), once the water is flushed out post-cycle.
Both steroids are incredible for strength, with powerlifters known for using both compounds.
One bodybuilder even developed a hernia from the sheer strength gains of Superdrol, whilst performing heavy tricep pushdowns in the gym. This caused him to be hospitalized requiring emergency surgery.
The main difference between Superdrol and Anadrol is that Superdrol doesn’t cause estrogenic side effects. Thus, Superdrol is a dry steroid, causing no water retention or gynecomastia. This is the polar opposite of Anadrol, which has wet attributes.
Some bodybuilders will use Superdrol whilst cutting too, being a very aesthetic steroid, causing no water retention.
Therefore, with Superdrol users will retain a very high percentage of the weight gained, as this is almost all lean muscle tissue. However, a PCT is still needed to help keep your gains.
Superdrol is liver toxic like Anadrol, so bodybuilders don’t typically take them together or with any other orals. It will also shift cholesterol levels in a negative way, raising LDL’s and lowering HDL’s. Thus, blood pressure will rise significantly on both.
So, if it’s beach season and someone wants to gain some lean muscle without the risk of bloating or developing gyno, Superdrol is the better choice. But if someone is bulking in the off-season and wants to really pack on as much mass as possible, Anadrol is the better steroid.
Should I Take Anadrol Pre-Workout?
This is an effective strategy for immense energy, strength, pumps and motivation in the gym.
However, Anadrol should be divided into multiple doses throughout the day to keep maximum concentrations of the compound in your bloodstream. So, only 1/3 or 1/2 of your daily dose should be taken pre-workout.
I Can’t Sleep on Anadrol
Anabolic steroids, including Anadrol, may cause insomnia in some users. If this is greatly affecting sleep duration or quality for a sustained period of time, users should take Anadrol earlier in the day, or the dose should be lowered.
This is the best protocol rather than taking medications such as Diazepam, as they put further strain on the liver. Even natural supplements, such as valerian root, are capable of having an adverse effect on liver values.
Also if suffering from insomnia, completing your workout earlier in the day may help; as weight training stimulates the nervous system and increase adrenaline levels before bed.
Consuming tea, coffee, energy drinks or pre-workout supplements will also negatively impact sleep, due to the caffeine content. Thus, avoiding or decreasing the number of stimulants in a person’s diet will help.
Anadrol Summary: Pros vs Cons
Pros
Huge muscle gains
Incredible strength
Easy to take (oral)
Suitable for women (according to studies)
Cons
Very high blood pressure
Testosterone suppression
Water retention
Liver toxic
Gynecomastia risk
Extreme caution should be used when taking Anadrol, with it being one of the worst steroids for side effects. It will place a lot of strain on the heart, with blood pressure rising to high levels.
It will also cause a dramatic drop in natural testosterone levels. However, its virilization effects in women and liver toxicity are often exaggerated.
We do not encourage the use of Anadrol; however, if readers are going to use this compound, they should get regular checkups with their doctor to monitor their health.
Trenbolone as the base hormone is an extremely powerful hormone, approximately 5 times the strength of Testosterone in both anabolic and androgenic strength, making Trenbolone an extremely potent anabolic steroid. Roussel-UCLAF was the firm during the late 1960s to initially synthesize and investigate Trenbolone, first with Trenbolone Acetate, and then with other long-acting Trenbolone esterified variants. The interesting aspect of Trenbolone’s history is that Enanthate was not specifically researched by Roussel-UCLAF, though was metaphorically ‘on the backburner’. It was never officially manufactured as an FDA-approved (or any equivalent) pharmaceutical drug meant for human use or sale on the prescription market. The other two variants of Trenbolone (Acetate under the brand name Finajet/Finaject and Hex under the brand name Parabolan) both experienced brief periods of official sale and use on the pharmaceutical drug market, although briefly. Trenbolone Acetate’s life on the pharmaceutical market was short lived in the 1970s, while Parabolan reigned briefly during the 1990s. It was not long until they were pulled from the market and their status as human-use prescription drugs stripped. Trenbolone Enanthate, on the other hand, would surface much later on in 2004 as an underground lab (UGL) product, made by British Dragon and sold as Trenabol. British Dragon was the first to manufacture and offer this ester of Trenbolone, dosed at 200mg/ml, and eventually manufactured a full line of Trenbolone based products that were all underground products for sale on the black market. None were FDA-approved, manufactured by pharmaceutical companies, or sold in pharmacies.
Trenbolone Enanthate was never approved for either human or veterinary use, and is still to this day strictly an underground origin product that is only manufactured by underground laboratories. It is impossible to find any pharmaceutical grade Trenbolone Enanthate that is made to pharmaceutical standards and meant for human use. Its popularity is only as big as it currently is due to its popularity growth and boom on the black market and is extremely common among bodybuilders and athletes, probably because it is one of the few convenient long-acting Trenbolone esters. By the time Trenbolone Enanthate arrived on the scene, the vast majority of Trenbolone users were utilizing the Acetate ester, and still remains the most common form of Trenbolone even today. Although the original British Dragon laboratories shut down in 2006 and underwent a law enforcement bust, the legacy of Trenbolone Enanthate continues today and countless other underground labs continue to manufacture it, ensuring a steady and guaranteed supply on the black market.
What Is Trenbolone Enanthate?
As previously mentioned, Trenbolone Enanthate is 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.
As a result of its chemical modifications, there is little question as to why Trenbolone Enanthate is so popular and effective among bodybuilders and athletes. Because of its unique characteristics, Trenbolone Enanthate is quite versatile in terms of its capabilities of use. It can literally be utilized for any goal: bulking, lean mass gaining, cutting (fat loss), strength gaining, and other goals perhaps more specific to different sports. Trenbolone Enanthate is commonly utilized in longer cycles due to its longer half-life and slower activity in the body. Because of the long Enanthate ester, users will typical inject Trenbolone Enanthate approximately twice per week, with each administration spaced evenly apart. For example, an injection on Sunday and an injection on Wednesday would suffice. If an individual is utilizing 400mg/week of Trenbolone Enanthate, 200mg would be injected on Sunday and the following 200mg would be injected on Wednesday.
How Does Trenbolone Enanthate Work and How Is It Best Used?
Because Trenbolone Enanthate exhibits a half-life of approximately 7 – 10 days and is presently more common than its other long-ester counterpart Parabolan, it provides many users who are mostly needle-shy or find frequent injections inconvenient with a more convenient form of Trenbolone to use. In contrast with Trenbolone Acetate, which requires every other day injections at the very least, Trenbolone Enanthate requires administration only twice per week with each injection spread evenly apart (Monday and Thursday, for example). Because Trenbolone is considered an intermediate-advanced level anabolic steroid, the majority of users of this compound are usually well aware of the ins and outs of it. Many intermediates making their first step to Trenbolone will prefer Trenbolone Enanthate due to the convenience of less frequent injections. However, the disadvantage to this is the fact that Trenbolone is an anabolic steroid that is extremely powerful and does carry with it some potential side effects unseen with any other compounds. It has therefore been labelled as a ‘harsh’ anabolic steroid, and beginners to Trenbolone who are wondering which form to use might want to opt for Trenbolone Acetate instead. The reason being that the faster half-life of Trenbolone Acetate ensures that blood levels of Trenbolone rise quickly and fall quickly as well, ensuring a fast clearance from the body should any issues arise and the user wishes to stop. With Trenbolone Enanthate, two weeks is what is required before Trenbolone is completely clear of the body, during which time undesirable side-effects might persist.
It is therefore the prerogative of the individual to use this information and decide for themselves whether the convenience of less frequent injections is indeed worth the risk of having to wait two weeks before the drug is clear from the body if any undesirable effects arise. If the user is a well-experienced user of Trenbolone that already understands their body’s reaction, this decision should already be made.
It is important to understand that with long-estered anabolic steroids like Trenbolone Enanthate, the time required for the hormone to reach peak and optimal circulating blood plasma levels is considerably longer than short-estered variants. For example, many individuals report experiencing significant strength gains and/or physique changes by the second or third week with Trenbolone Acetate, but Trenbolone Enanthate might require upwards of 4 – 6 weeks (depending on the individual as well) before the hormone noticeably “kicks in”. Because of the long Enanthate ester, the hormone slowly reaches optimal levels over a period of a few weeks as each dose builds upon the last. Of course, those who wish to speed up this process can always decide to frontload. However, be aware that there are both benefits as well as risks/downsides to such a practice, and frontloading should thoroughly be researched and contemplated before doing so. This is especially true with a compound such as Trenbolone, and is doubly especially true if the user is a first-time Trenbolone user.
In general, Trenbolone Enanthate is what would be considered the advanced Trenbolone user’s Trenbolone. However, this is not to say that plenty of well-experienced Trenbolone veterans won’t utilize Trenbolone Acetate – many do, and many tend to stick with Trenbolone Acetate exclusively forever without touching Tren Enanthate. The take-home point here is that Trenbolone Enanthate use is much more common among experienced users rather than bare beginners to Trenbolone, who will most often elect to use Trenbolone Acetate due to the short half-life and therefore relatively quick clearance from the body. This is usually a security precaution in the event that the first-time user encounters a bad experience on Trenbolone and wishes to stop more abruptly than stopping Trenbolone Enanthate would.
Tren is best utilized with other similar compounds, but it is absolutely essential that some form of Testosterone be run with it, even if only for the sake of health. It might be a wise idea to limit the amount and/or dosage of aromatizable androgens used with it, as some times the Estrogen-related side effects can be exacerbated when high levels of a progestin is utilized in a high-Estrogen environment. Normally it is Testosterone Enanthate that is commonly combined in cycles with Trenbolone Enanthate, for very obvious reasons.
Trenbolone Enanthate Side Effects
Trenbolone is an anabolic steroid, and as such, it carries with it all of the typical side effects that are common among all anabolic steroids and more. “And more” refers to the additional unique side effects common to Trenbolone that are often discussed within the bodybuilding community (and frequently carried out of proportion) attached to very ridiculous and mostly-exaggerated horror stories.
Because Trenbolone does not aromatize into Estrogen at any dosage, there is zero risk of Estrogen-related side effects with Trenbolone alone. Estrogen Trenbolone Enanthate side effects are literally nonexistent. However, it is advised to closely monitor the dosage of aromatizable compounds run with it (i.e. Testosterone, Dianabol, etc.) as an Estrogen-rich environment in the body often leads to additional Trenbolone Enanthate side effects and complications due to complex hormonal pathways in the body that is related and linked between Estrogen, progestins, Prolactin, and the aromatase enzyme. Often times if an individual experiences Estrogen-related side effects during Trenbolone use, it is not the result of Trenbolone itself, but of the other compounds the individual is using alongside it.
Androgenic side effects are indeed a concern and definitely included as a part of the list of Trenbolone Enanthate side effects, as Trenbolone exhibits an adrogenic strength rating of 500. This means it is 5 times the androgenic strength of Testosterone. However, the up-side to this factor is that Trenbolone does not convert into any stronger androgenic metabolites in the body (unlike Testosterone, which is reduced into Dihydrotestosterone in the body). Therefore, any androgenic capabilities resultant from Trenbolone are what can be expected on average throughout its use. Individuals must take care to monitor and watch for androgenic side effects such as: increased aggression, irritability, acne (as a result of increased oil secretion on the skin), potential for male pattern baldness (if one possesses the genetics for it), and benign prostatic hyperplasia (enlargement of the prostate). Note that 5-alpha reductase inhibitors such as Proscar, Finasteride, Dutasteride, and Propecia do nothing to reduce or eliminate the androgenic Trenbolone Enanthate side effects.
There should be no concern for liver issues (hepatotoxicity) with Trenbolone Enanthate, as it is an injectable anabolic steroid that avoids the first pass through the liver. However, negative alteration of cholesterol and other cardiovascular concerns and issues can be a problem, as is the case with most, if not all anabolic steroids. Trenbolone Enanthate side effects also bring with it the typical HPTA suppression/shutdown that is common of all anabolic steroids. Therefore, users should either limit themselves to shorter cycles or ensure to engage in a proper PCT (Post Cycle Therapy) protocol following use, lest the secondary hypogonadism develops as a result of neglect in this area.
Trenbolone Enanthate side effects that are unique to Trenbolone itself include profuse perspiration (sweating), especially at night in bed for as of yet unknown reasons. Coughing fits that are normally more heavily associated with Trenbolone Acetate are very rarely reported or seen with Trenbolone Enanthate, though it still remains a possibility (dubbed the ‘tren cough’). The cough seems to occur more with Trenbolone Acetate rather than with the Enanthate variant, possibly because the incidence and severity of the cough have much to do with the rate of release of Trenbolone into the body. The true roots and cause of the ‘tren cough’ are currently not fully understood, but some valid and accurate hypotheses include the fact that Trenbolone itself causes varying degrees of anaphylactic reactions in the bronchial pathways, as well as some of the compound seeping into punctured capillaries/veins during the injection, which irritate the lungs. In the case of oil entering the bloodstream through capillaries/veins, this can occur with any oil-based anabolic steroid as well, which also results in coughing fits during or shortly after injection.
Finally, a small note should be made about one of the most commonly discussed Trenbolone Enanthate side effects: its seeming capability to induce larger amounts of aggression, anger, and impatientness in some users. Although there is a massive lack of clinical evidence to support the anecdotal claims that Tren exhibits this in some or most of its users, it is therefore the most important point of this whole profile to send the following message out to anyone willing to use Trenbolone in any form: those who have problems with their temper or patience must at all costs take responsible action and avoid the use of Trenbolone. If the use of Trenbolone Enanthate is too alluring, ensure to learn to exhibit self-control when one’s anger, temper, or lack of patience arises in any situations. It is irresponsible to utilize an anabolic steroid as potent as Trenbolone while knowing full well all of its potential effects, and allow oneself to get into serious trouble as a result of uncontrolled anger, and veer off blaming the anabolic steroid they had used as opposed to themselves for exercising poor self-responsibility. Trenbolone is a drug, and a very powerful androgenic anabolic hormone to be respected. Respect the hormone and it will respect you.
Trenbolone Acetate (Tren ace) is among the most potent anabolic steroids worldwide. This steroid was initially created to add muscles and increase appetite to aging horses and cattle while reducing body fat, but it ultimately made its way into bodybuilding; that alone tells you how potent this drug is when consumed. It is 5X as powerful as testosterone, and therefore, you should use it with caution.
Many people consider it a high-risk but high-reward steroid, usually used by bodybuilders, powerlifters, and athletes to refine and improve their body physique. Bodybuilders use an injectable anabolic to gain lean muscle and strength while enhancing fat loss.
Unlike other bulking steroids, Trenbolone is a dry compound, meaning it doesn’t convert to nitrogen when ingested; thus, you cannot experience water retention or fat accumulation during a cycle. It is a versatile compound that you can use as a bulking or cutting steroid.
Trenbolone Acetate Benefits
Trenbolone Acetate is popular among hardcore bodybuilders, fitness models, and physique competitors because of its many benefits. But if you want to try, ensure you buy from a reputable Trenbolone Acetate source for convenience and the best results.
Here are some of the critical benefits of Tren Ace:
Fast Bulking
Injecting Tren Ace creates a highly active anabolic environment where muscles are quickly repaired and grown, causing massive gains. Also, increased anabolic activity makes it easier and faster to cut fat and burn stored fat for energy while maintaining existing lean muscles.
Improves Nitrogen Retention
Trenbolone maintains a good balance of nitrogen to avoid the risk of muscle catabolism. It also helps in boosting your performance and lifting power while improving your recovery and growth.
Enhances IGF-1 Levels
The Trenbolone anabolic effects on the activity of androgen receptors increases the level of insulin-like Growth Factor-1. This causes the growth of skeletal muscle protein to rise. The hormone is critical for many body processes and fast muscle recovery.
Improves Food Uptake
Tren was initially developed to enhance diet in cattle; thus, it is not surprising that it has similar effects in humans. It helps the body make optimum use of the calories and nutrients from your food to gain muscle.
Enhance Recovery
Using Tren will make you gain muscle, strength, power, and endurance, making you push harder when working out, causing more stress on your muscle tissues. On the other hand, Tren ensures rapid recovery by repairing damaged muscle tissues quickly and increasing muscle growth. Also, Tren helps reduce or even avoid DOMS (delayed onset muscle soreness), so it allows you to get back to the gym sooner.
Typical Trenbolone Cycles and Dosages
Tren Cycle for Bulking
Tren for bulking is a 12-week cycle consisting of a steady 200 mg to 400 mg trenbolone per week for the whole 12 weeks period, depending on other compounds you are using and their potency. The common stacks are testosterone ester and Winstrol for the last weeks of the cycle.
Tren Cycle for Cutting
Tren Ace is the best form of Trenbolone for a cutting cycle. And for most users, the dosage is similar to that for bulking except for the experienced and advanced users who are comfortable consuming higher dosages.
A quality cycle for cutting involves taking 75 mg to 100 mg of Tren two to three weeks every week for four weeks. You then increase the dosage to 100 mg to 150 mg for the next eight weeks of the cycle.
Since Tren Ace leaves the body quickly, you’ll need more frequent injections. Also, using other compounds like testosterone and Dianabol will help keep side effects in check.
Beginner Tren Cycle
Tren Ace is not usually recommended for beginners because it is so powerful, but if you are determined to give it a try, you have to limit your dosage to a maximum of 200 mg per week for a 12-week cycle. This will allow you to evaluate your results and manage potential side effects.
Intermediate Tren Cycle
Intermediate users can use 300 mg to 500 mg per week for 10 to 12 weeks. You can also combine with other compounds like testosterone propionate for 12 weeks.
Advanced Tren Cycle
If you are at this stage of advanced Tren use, you can increase the dosage to 750 mg per week for 12 weeks or 1000 mg weekly. However, you should not exceed 1000 mg as it is an exceptionally high dosage.
An advanced cycle runs for 12 weeks, usually with a low dosage and increasing for the second half. You can also combine with other compounds like testosterone enanthate at 1000 mg per week and a low dose of Anavar at 100 mg weekly.
Trenbolone Post Cycle Therapy
PCT for Trenbolone is similar to that for other steroids. The main goal is to retain your gains and get the normal testosterone back to work.
A post cycle therapy (PCT) plan is critical to avoid a complete hormone crash after the Tren cycle. There is no one-size-fits-all PCT method for Tren or any other steroid. It is about trying one after another until you find the best way for you.
If you used Tren Ace alone in the cycle, you should start PCT 3 days after your last injection and run for four weeks. Nolvadex, Clomid, and HCG are the PCT drugs you can use together.
How to Take Trenbolone Acetate
Like other injectables, Tren Ace is simple to take, find a disinfected syringe, draw the correct dosage of the steroid from its container, and stick it to one of your major muscle groups (delts or buttocks). And slowly push the drug into your muscle tissue.
The ideal dose of Tren will depend on the product’s potency and body tolerance, which is unique to everyone. Always get the bestTren Aceto get value for your money and enjoy guaranteed effects.
Possible Trenbolone Side Effects
Tren is a drug with severe side effects when misused. Below are some of the side effects you may experience:
Trenbolone Acetate is more potent than testosterone and is the best steroid for bulking and cutting. It has beneficial effects such as improving robust anabolic hormone IGF-1, boosting lean body mass. Without water retention, it keeps you dry and lean. However, its side effects are more significant than testosterone’s; thus, you should use it cautiously.
Propionate is a fast-acting Testosterone ester, present in products such as Sustanon.
Testosterone propionate has the ability to produce impressive gains in the early stages of a cycle.
Although it kicks in fast, it’s not the most rapid form of Testosterone, with Suspension being superior in this regard.
As Propionate is absorbed quickly, frequent injections are required to maintain peak testosterone levels. It is thus recommended to be injected every other day.
Testosterone Propionate injections can be painful for many users, regularly leaving them feeling sore or even having to limp (after injecting in the leg).
One myth about Testosterone Propionate is that it’s cheap. This is because the price for a bottle is typically lower than other Testosterone products. However, Propionate is dosed at 100mg/ml, whereas other Testosterone esters such as Cypionate or Enanthate, are dosed at 250mg/ml.
Thus, if Propionate is priced at $50 and enanthate at $100; Propionate can work out 50% more expensive.
Testosterone Prop Benefits
The general benefits of Testosterone Propionate are typically the same as cycling any other Testosterone ester.
Thus, users can experience roughly 20lbs of lean muscle (combined with some fat loss), when taking Testosterone for the first time.
Strength will also go up dramatically in the first few weeks, then slowly continue increasing until the end of your cycle.
The main difference with Propionate is that results occur in the earlier stages of a cycle, compared to slower esters (such as Enanthate or Cypionate); taking more time to kick in.
However, the end result will be the same no matter what Testosterone ester you take; as they are all essentially the same steroid (they just peak at different times).
Testosterone Propionate Side Effects
The usual side effects associated with Testosterone also apply with Propionate, such as:
High cholesterol
Increased blood pressure
Risk of gynecomastia
Oily skin or/and acne
Hair loss
Testosterone suppression
LDL cholesterol levels rising and HDL levels falling is typical when taking any steroid; however, it’s worth noting that Testosterone is one of the least harmful steroids for negatively affecting cholesterol. Thus, blood pressure will rise, however, if moderate dosages are taken for reasonable lengths of time — this is often manageable.
Bodybuilders can also supplement with fish oil to control BP, taking 4 grams per day throughout a cycle.
Testosterone is estrogenic, thus water retention, bloating or/and gynecomastia are all possible.
Despite Testosterone causing some fat loss (due to its androgenic nature stimulating lipolysis); it is mainly used when bulking. Thus, many users do not mind a temporary ‘smooth’, watery look.
A SERM (such as Nolvadex) may be taken to reduce the risk of gynecomastia. AI’s (anti-aromatase inhibitors) are not recommended as blocking estrogen can worsen cholesterol and blood pressure; due to the female hormone having a positive effect on HDL cholesterol.
Oily skin and acne are possible for some users, which is the result of testosterone’s strong androgenic properties (causing increased sebum production).
Hair thinning on the scalp, or recession is possible due to elevated DHT levels.
Post-cycle, when DHT drops, hair on the scalp may become thicker again; however reverse effect is unlikely in regular, long-term steroid users.
It seems ironic that by taking Testosterone, your natural testosterone crashes. However, this is the reality (as is the case with all anabolic steroids. This occurs due to the body detecting exogenous testosterone; with total levels rising excessively high, the body halts natural production (to try and maintain homeostasis).
Thus, after a cycle ends users are left with shut down endogenous testosterone, needing a PCT to help resurrect testosterone back to adequate levels. An effective PCT can usually restore hormone function in approximately 4 weeks. Without a PCT, low testosterone levels can persist for several months.
Testosterone Propionate Cycle
Testosterone Propionate comes in bottles dosed at 1ml/100mg.
Beginner Cycle
100mg every other day, for 8 weeks.
Note: Testosterone Propionate generally isn’t advised for beginners, due to painful injections (and having to be administered frequently).
Intermediate Cycle
150mg every other day, for 8 weeks.
Advanced Cycle
200mg every other day, for 8-10 weeks.
Other supplements:
Fish oil (4g/day)
Nolvadex (20-40mg day)
Note: Intermediates and advanced steroid users may want to stack Testosterone Propionate with other compounds for maximum results; however, this isn’t recommended for beginners (due to additional side effects).
Testosterone Propionate Results
A first Testosterone cycle can produce the gains as seen above, in regards to muscle size and fat loss.
Users who follow the beginner cycle protocol (above) can expect a similar transformation.
Test Prop Vs Test Suspension
Testosterone Suspension is pure testosterone (no ester), thus it’s extremely fast-acting.
One benefit is Testosterone Suspension will produce faster results than propionate.
However, the downside is it requires very frequent injections (2x per day), to keep serum testosterone high. This is a lot more than propionate’s 2x per week.
Testosterone Suspension, like Propionate, can also be painful to inject.
The only situation where Testosterone Suspension might be advantageous is before a competition, where it clears out of the system quickly.
For example, someone might have a drugs test on a certain date, thus if they used Suspension they could stop taking it a few days before and not test positive. This is because Test Suspension’s detection time is 1-2 days, with a half-life of less than 24 hours.
However, Testosterone Propionate for example can be detected for up to 2 weeks, and thus you wouldn’t be able to use this closer to the competition (if being tested).
Other than for competition purposes and wanting it out of your system quickly, bodybuilders typically won’t use Testosterone Suspension; as there’s no need to inject 2x per day (when you can do so once per week).
Testosterone Prop vs Undecanoate
Undecanoate is the oral version of Testosterone, also known by the product name — Andriol or Testocaps.
Thus, for those who want to experience the benefits of Testosterone but don’t want to inject it; Undecanoate would be the ideal alternative.
Testosterone Undecanoate is also fast-acting, with testosterone levels peaking approximately 5 hours after a first dose.
Despite being an oral, Undecanoate is not liver toxic, being absorbed via the lymphatic route.
The only main advantage to taking Testosterone Propionate is that it’s a lot cheaper than Undecanoate; with Andriol being one of the most expensive steroids on the market.
Testosterone Prop vs Enanthate & Cypionate
Testosterone Enanthate and Cypionate are similar esters in many respects. They both are slow-acting, thus injections only need to be administered once every 4-5 days (compared to once every 2 days for propionate).
Due to Enanthate and Cypionate’s slower nature, results won’t happen as fast as Propionate.
However, Enanthate and Cypionate are known to be more pleasant injections, with users reporting less irritation and soreness.
Also, Enanthate/Cypionate are more affordable esters vs Propionate in the long run.
A bottle of propionate may be cheaper; however, it’s dosed at 100mg per 1ml, compared to 250mg per 1ml (for Enanthate/Cypionate).
Thus, when calculating the cost per ml, Propionate is considerably more expensive.
Cypionate and Enanthate remain the most popular esters for good reason; considering they produce the same results as Propionate, yet are cheaper and less hassle.
Summary
Testosterone Propionate is not a recommended ester, due to it being on the expensive side and often painful to inject.
However, in the right circumstance, users may opt for Propionate if they need it to clear out of their system quickly.