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Nolvadex (Tamoxifen) is one of the oldest and most popular selective estrogen receptor modulators (SERM’s) in the world. Tamoxifen Citrate was developed in 1961 by Imperial Chemical Industries (ICI) under the trade name Nolvadex. Later, AstraZeneca purchased ICI. Tamoxifen can be used to treat a large amount of dysfunctions, that’s why it was included in the World Health Organization’s list of essential medications. Nolvadex is also widely used by androgenic anabolic steroid users.
The drug was created to treat hormone-responsive breast cancer, then it turned out that it also can be used to prevent breast cancer. Nolvadex also can be used to treat women’s infertility, however studies have shown less effective results than from Clomid (Clomiphene).
In bodybuilding Tamoxifen can be used for two goals. The first option is as an anti-estrogen during an androgenic anabolic steroid cycle in order to prevent estrogen related side effects such as gynecomastia, bloating, high blood pressure, etc. However, similar to the case with Clomid (Clomiphene), I believe that there are more effective drugs such as Anastrozole or Proviron to prevent estrogenic side effects. The second most beneficial option is going through Post Cycle Therapy (PCT) in order to boost the Luteinizing Hormone and testosterone level.
Tamoxifen is a selective estrogen receptor modulator (SERM) with both estrogen agonist and antagonist properties. For the androgenic anabolic steroid users, one of the desired effects is in the prevention of gynecomastia. Tamoxifen also reduces other estrogenic side effects like water retention and blood pressure but not significantly. That’s why I recommend using other drugs to reduce the estradiol level like Anastrozole and Proviron, however Nolvadex can be used for a weak cycle and it has less side effects. Additionally, Nolvadex has a positive impact on cholesterol levels.
The most valuable effect of Nolvadex is boosting the testosterone level for Post Cycle Therapy (PCT). During the cycle your body stops producing its own testosterone because it realizes there are too many hormones. The rate of suppression depends on the steroid cycle, the more advanced the cycle the worse your natural testosterone level will be. Once the cycle is done the natural testosterone production will start slowly recovering again. However, after you’ve finished the cycle your natural testosterone level will be extremely low and it will take time to recover naturally.
No one, especially bodybuilders, would want to stay in a low testosterone condition because it can lead to high body fat, loss of muscles, etc.
Most athletes have a post cycle therapy plan in order to recover their testosterone level faster. Nolvadex one of the medications that is very effective in helping to recover the testosterone level. Nolvadex stimulates the higher release of both luteinizing hormone and follicle stimulating hormone. When the body indicates a rise in luteinizing hormone (LH) it starts producing testosterone. That helps in maintaining a higher testosterone level until your natural testosterone has completely recovered.
Dosages
In bodybuilding, for the purposes of post cycle therapy, your dosage should depend on the cycle. If the cycle was short (6-8 weeks) with one steroid or small steroids dosages you should use 20 milligrams for 14 days. If your cycle was advanced, the dosage of Nolvadex can be up to 50 milligrams per day for 6 weeks with gradually decreasing dosages. Also you can use a combination Nolvadex (Tamoxifen) with Clomid (Clomiphene) after advanced cycles.
The same as with Clomid it’s very important to start using Tamoxifen timely. After oral only cycles like Turinabol, Winstrol and Dianabol you should start using Nolvadex a day after your cycle is completed. If a cycle contains short duration esters, begin using Nolvadex 3 days after the cycle. If a cycle includes long lasting esters you should wait 14 days before using Nolvadex.
For the purpose of decreasing estrogenic side effects during an androgenic anabolic steroid cycle, the optimal dosage is from 10 to 20 milligrams per day. If this dosage does not help to protect from gynecomastia you should consider using aromatase inhibitors such as Anastrozole or Proviron.
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Viagra is used to treat erectile dysfunction (impotence) in men. Another brand of sildenafil is Revatio, which is used to treat pulmonary arterial hypertension and improve exercise capacity in men and women. This page contains specific information for Viagra, not Revatio.
Do not take Viagra while also taking Revatio, unless your doctor tells you to.
Some medicines can cause unwanted or dangerous effects when used with Viagra. Tell your doctor about all your current medicines, especially riociguat (Adempas) and nitrates.
Do not take Viagra if you are also using a nitrate drug for chest pain or heart problems, including nitroglycerin, isosorbide dinitrate, isosorbide mononitrate, and some recreational drugs such as “poppers”. Taking sildenafil with a nitrate medicine can cause a sudden and serious decrease in blood pressure.
Contact your doctor or seek emergency medical attention if your erection is painful or lasts longer than 4 hours. A prolonged erection (priapism) can damage the penis.
Stop using Viagra and get emergency medical help if you have sudden vision loss.
You should not use Viagra if you are allergic to sildenafil, or:
Do not take Viagra if you are also using a nitrate drug for chest pain or heart problems. This includes nitroglycerin, isosorbide dinitrate, and isosorbide mononitrate. Nitrates are also found in some recreational drugs such as amyl nitrate or nitrite (“poppers”). Taking sildenafil with a nitrate medicine can cause a sudden and serious decrease in blood pressure.
To make sure Viagra is safe for you, tell your doctor if you have ever had:
Viagra can decrease blood flow to the optic nerve of the eye, causing sudden vision loss. This has occurred in a small number of people taking sildenafil, most of whom also had heart disease, diabetes, high blood pressure, high cholesterol, or certain pre-existing eye problems, and in those who smoked or were over 50 years old. It is not clear whether sildenafil is the actual cause of vision loss.
Viagra is not expected to harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.
It is not known whether sildenafil passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.
Do not give this medicine to anyone under 18 years old without medical advice.
Take Viagra exactly as it was prescribed for you. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.
Viagra is usually taken only when needed, 30 minutes to 1 hour before sexual activity. You may take it up to 4 hours before sexual activity. Do not take Viagra more than once per day.
Viagra can help you have an erection when sexual stimulation occurs. An erection will not occur just by taking a pill. Follow your doctor’s instructions.
During sexual activity, if you become dizzy or nauseated, or have pain, numbness, or tingling in your chest, arms, neck, or jaw, stop and call your doctor right away. You could be having a serious side effect of sildenafil.
Store at room temperature away from moisture and heat.
Since Viagra is used as needed, you are not likely to miss a dose.
Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.
Drinking alcohol with this medicine can cause side effects.
Grapefruit and grapefruit juice may interact with sildenafil and lead to unwanted side effects. Avoid the use of grapefruit products while taking sildenafil.
Avoid using any other medicines to treat impotence, such as alprostadil or yohimbine, without first talking to your doctor.
Get emergency medical help if you have signs of an allergic reaction to Viagra: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Stop taking Viagra and get emergency medical help if you have:
Call your doctor at once if you have:
Winstrol is one of the most popular and well-known anabolic steroids on earth. Developed by Winthrop Laboratories in the late 1950’s, this is an anabolic steroid that has gotten a lot of media attention over the years. In fact, those who have never used anabolic steroids, if they can name a steroid it’s usually Winstrol or Stanozolol. The name Winstrol is actually the most commonly associated brand name of the Stanozolol hormone. This is an anabolic steroid that has garnered worldwide attention due to numerous athletic scandals over the years. When various athletes have been caught using anabolic steroids, Winstrol has been at the forefront of the scandal countless times. In fact, it is associated with the most important athletic steroid scandal in history.
In 1988, Canadian sprinter Ben Johnson tested positive for the steroid after taking the gold at that year’s Summer Olympics. Not only did Johnson destroy his competition, he handedly defeated the highly favored Carl Lewis with relative ease. This would lead to Stanozolol making countless news headlines for a very long time and more importantly truly usher in the U.S. government’s war on steroids. The Johnson scenario is not the largest athletic based steroid scandal to ever occur, which would probably belong to the decades long East German doping machine; however, the Johnson scandal would have the largest impact. When Ben Johnson destroyed the U.S. golden boy, many point to this as being the final nail in the coffin that the U.S. congress needed to justify classifying anabolic steroids as Schedule III controlled substances.
While one of the more well-known anabolic steroids, Winstrol is very popular among most in the steroid using population. It is in many ways a fairly mild anabolic steroid that can be safely used by men and women. Equally important, it has proven highly effective for numerous performance enhancement endeavors. It is a long standing favorite among competitive bodybuilders and physique based athletes during cutting or contest prep phases. It is also a top steroid of choice for numerous performance athletes due to its ability to promote strength and endurance without unwanted mass.
Beyond performance enhancement, Winstrol has had a lot of success in modern medicine. It has been successfully used to combat lean tissue wasting and has had a lot of success in preserving bone mass in cases of osteoporosis. Winstrol has also been used to combat prolonged exposure to corticosteroid treatment, given to burn victims and even used to aid in the healing of severe bone fractures. The steroid has also enjoyed a little success in treating obesity when hormonal assistance is needed, as well as treating delayed growth in some children. As the years have passed, Winstrol has remained available for treatment for most of these conditions as well as being proven highly successful in treating angioedema among a few other treatment plans such as specific forms of breast cancer. The steroid has never lost FDA approval and unlike many anabolic steroids has maintained approval for numerous therapeutic treatment plans.
Stanozolol is a dihydrotestosterone (DHT) derived anabolic androgenic steroid, or more specifically a structurally altered form. Stanozolol is the DHT hormone with two structural changes that give us the Winstrol compound. The first alteration is the introduction of an attached pyrazol group at the A-ring of the hormone replacing the 3-keto group. This modification officially classifies Stanozolol as a heterocyclic steroid. The hormone also carries an added methyl group in order to protect hormone after administration. This structural change takes place at the 17th carbon position officially classifying Stanozolol as a C17-alpha alkylated (C17-aa) anabolic steroid.
Due the combination of structural changes, this reduces the hormone’s androgenicity significantly and greatly increases its anabolic power. Officially Winstrol carries an anabolic rating of 320 and an androgenic rating of 20. More importantly, its ratings translate perfectly in real life effects giving us an extremely beneficial anabolic steroid.
Winstrol carries many positive steroidal traits, one of which is its ability to lower Sex-Hormone-Binding-Globulin (SHBG) significantly. This allows for more of the steroids being supplied to rest in an unbound state, as well as provides an increase in free testosterone. While many anabolic steroids lower SHBG Winstrol appears to have a much stronger affinity than most. In fact, studies have demonstrated nearly 50% reductions in SHBG in mere days of use and even at relatively low doses.
Beyond a reduction in SHBG, which is one of its primary traits, Winstrol will enhance protein synthesis and greatly increase nitrogen retention in the muscles. The steroid will also do a fairly decent job at increasing red blood cell count and inhibiting glucocorticoid hormones but not to the degree of many other steroids. In many ways, we have a mild yet evenly possession of some basic steroidal traits coupled with the dramatic SHBG reduction that gives us a controllable and unique compound. This really is one of the easiest anabolic steroids to understand.
When looking at the direct functions and traits of Winstrol there is one more issue we need to discuss. The Stanozolol hormone is both an injectable an oral anabolic steroid. Both forms are comprised of the same identical Stanozolol hormone. 1mg of one form is the same as 1mg of the other form. Some studies have suggested oral Winstrol may reduce SHBG a little more than its injectable counterpart, while others have said injectable forms may be slightly more potent on an overall milligram for milligram basis. However, overall these appear to be rather insignificant differences regardless of the direction they go. In fact, the individual should be able to receive the same identical benefits with either form.
Another important note often misunderstood about Winstrol forms is the C17-aa nature. Both oral and injectable Stanozolol are C17-aa anabolic steroids. Most oral steroids are C17-aa and while injectable steroids rarely are injectable Stanozolol is one of the exceptions. The injectable form is also commonly referred to as Winstrol Depot.
Although used to stave off lean tissue wasting, Winstrol is not what we’d call a bulking steroid. You will rarely find this steroid in an off-season mass gaining stack. However, it could be used in an effort to enhance the activity of the other steroids being used due to the strong SHBG reduction it will provide but this is generally not recommended. When we dive into the side effects of Winstrol, we will find it is very hepatotoxic and use should be limited to when it’s most valuable. For the male athlete, this will not be during the bulking phase.
When it comes to off-season bulking, we could make more of an exception with female use. Females are far more sensitive to the steroid and short burst plans could be very beneficial during this phase. But again, there are probably better options.
The effects of Winstrol are undoubtedly most beneficial to direct performance enhancement of an athletic nature. We’re talking about functional competitive athletes, not bodybuilders or physique athletes. This steroid has the ability to greatly increase strength and this can translate into both power and speed. Further, it will accomplish this without adding a lot of additional weight that could hinder some depending on the sport, as well as cause unwanted attention from prying eyes. There have been those who have said Winstrol isn’t good for competitive athletes, especially those athletes in explosive sports due to potential weakening of the tendons but this is more or less message board anecdotal hysteria that supports this claim. In fact, many studies have shown it can have a positive impact on strengthening tendons and we already know it’s good for the bones. If not, it wouldn’t be used to treat osteoporosis.
There are also some who complain of joint pain when using Winstrol. As a steroid that does not aromatize there will be no water retention but the “dry feeling” may not be what many think it is. Most who use the steroid will be physique athletes or gym rats during a cutting phase. They will also typically add it into a plan late in the diet once they’re already lean. Typically, when you become very lean, bodybuilding lean, this makes the joints a little uncomfortable. With or without Winstrol this discomfort could potentially exist. As for pro athletes who have nearly every last steroid at their disposal, remember, if Winstrol weren’t effective in competitive sports so many athletes wouldn’t make it a primary and favorite choice. In fact, the combo of Winstrol with low doses of Nandrolone is a very common stack among many athletes, and this stack will greatly eliminate any potential joint discomfort should it exist.
Beyond athletics, the gym rat or bodybuilding effects of Winstrol will be best displayed once you’re already somewhat lean. The steroid will help produce a dryer, harder look but only if you’re relatively lean. It will also aid in lean tissue preservation but not to a very strong degree that’s often needed in such a phase. It’s typically recommended that Winstrol only be used in this capacity as a secondary steroid, not a base or foundational steroid.
Both men and women can greatly benefit from Winstrol during the cutting phase. While it won’t be the best lean tissue preserver, many report maintaining more of their strength that is often lost when dieting when Winstrol is in play. Vascularity should also become more pronounced and overall the individual should enjoy an overall enhancement in definition.
The side effects of Winstrol most certainly exist, but they largely fall into the category of possible rather than guaranteed. The side effects of Winstrol can be controlled but it will take some effort on your part. There is also always the issue of individual response. We all respond to different things differently. This not only holds true with various anabolic steroids but all things we put into our body. Most of use can take Aspirin, but there are others who will experience horrible side effects if they touch the first pill. Most of us can tolerate dairy products, but there are others who become very sick if they even look at a glass of milk. Individual response dictates quite a lot. With that in mind, in order to help you understand the possible side effects of Winstrol we have broken them down into their separate categories along with all you’ll need to know.
Anastrozole
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 [R]
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. [R]
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.
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.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.
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:
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. [R]
Clomid (Clomiphene Citrate) is a powerfully effective anti-estrogen officially classified as a Selective Estrogen Receptor Modulator (SERM). In many ways, it is very similar to another popular SERM in Nolvadex (Tamoxifen Citrate). Clomid first gained worldwide attention in the early 1970’s as a strong fertility aid and is still used for that purpose today. It is also one of the most commonly used SERM’s by anabolic steroid users. No, it is not an anabolic steroid but can be used to combat estrogenic side effects sometimes caused by anabolic steroids. It can also be used as a Post Cycle Therapy (PCT) medication in order to stimulate suppressed testosterone production due to anabolic steroid use. PCT use of Clomid is the most common purpose and most beneficial point of use for the anabolic steroid user.
Clomiphene Citrate is a SERM that is specifically used as a fertility aid due to its ability to enhance the release of gonadotropins. Clomid has the ability to oppose the negative feedback of estrogens on the Hypothalamic-Pituitary-Ovarian-Axis. This will increase the release of Luteinizing Hormone (LH) and Follicle Stimulating Hormone (FSH) significantly. By increasing gonadotropin release, this can lead to the egg being released, thereby increasing the chance of conception.
Clomid also carries strong anti-estrogen properties that could be used therapeutically, but its anti-estrogen properties are most commonly associated with anabolic steroid use. Testosterone and many testosterone derived steroids have the ability to convert to estrogen through testosterone’s interaction with the aromatase enzyme. As estrogen levels rise, this can lead to gynecomastia and excess water retention. Heavy water retention can also promote high blood pressure. By supplementing with Clomid during anabolic steroid use, the SERM will bind to the estrogen receptors, therefore inhibiting the estrogen hormone from binding. This can be very useful in combating gynecomastia, as when Clomid binds to the receptor it prevents estrogen from stimulating the mammary tissue. It can also have a positive impact on water retention, but as it won’t actively reduce serum estrogen levels it’s sometimes not enough.
Clomid also possess functioning traits that are beneficial to the anabolic steroid user post anabolic steroid use. Specifically we’re referring to Post Cycle Therapy (PCT). In men, Clomid also has the ability to stimulate the pituitary to release more LH and FSH, which will in turn stimulate enhanced natural testosterone production. This is extremely beneficial to the anabolic steroid user post cycle as natural testosterone levels will be very low due to suppression caused by anabolic steroid use.
In a therapeutic setting as a fertility aid, the effects of Clomid are simple. The woman is having difficulty becoming pregnant, Clomid enhances the chance of conception and pregnancy occurs. It doesn’t always work and we’ll look at the process in the administration section, but it will greatly increase the odds of conception and is fairly successful.
As an anti-estrogen for on cycle steroid use, Clomid is fairly effective at staving off gynecomastia. It will not reduce estrogen levels or inhibit the aromatization process, but in many cases, binding to the receptors is enough protection for many men. In fact, while there are stronger protective agents, many men would be surprised as to how well a SERM like Clomid can work if they would give it a chance. More importantly, when using Clomid for this purpose it can also have a positive impact on cholesterol levels. While an anti-estrogen, Clomid actually acts as estrogen in the liver, which in turn will promote healthier cholesterol levels. This can be very beneficial to the anabolic steroid user as anabolic steroid use is notorious for promoting unhealthy cholesterol levels.
For many men, especially hardcore anabolic steroid users, Clomid is not enough for estrogenic protection. In this case, an Aromatase Inhibitor (AI) like Arimidex (Anastrozole) or Femara (Letrozole) will be needed. AI’s actively inhibit the aromatase process and will see serum estrogen levels reduced. By far they are the most effective at combating gynecomastia and will have more success in combating water retention. In fact, SERM’s like Clomid often do very little to combat water retention. However, in many cases, many performance athletes would do a better job controlling water retention if they did a better job controlling their diet. In off-season bulking plans this requires excess calories to grow. However, many take it too far, especially carbohydrate consumptions, and this will cause you to hold water with or without anabolic steroid use. Add in aromatizing steroids to the equation and water retention will be even greater. Further, AI’s while effective will have a negative impact on cholesterol, which leads us to only one sane conclusion. Control your diet and if you can control gynecomastia with a SERM like Clomid it should be your first choice.
Then we’re left with the effects of Clomid as they pertain to PCT. When we supplement with anabolic steroids, this will suppress natural testosterone production. The rate of suppression will be dependent on the steroids being used and to a degree the total dosing, but it will generally be substantial. For this reason, most men will always include exogenous testosterone in their steroid cycles. In fact, it’s not uncommon for it to be the only steroid used. This will protect the individual from a low testosterone condition while on cycle. Unfortunately, once steroid use comes to an end natural testosterone levels will be very low. Natural testosterone production will begin again on its own, but it will take a significant amount of time for levels to reach their previous high state. In fact, total recovery can take months to even a year. Further, natural testosterone recovery is dependent on no prior low testosterone condition existing and assumes that no severe damage was done to the Hypothalamic-Pituitary-Testicular-Axis (HPTA) through improper anabolic steroid use.
Due to natural testosterone levels being low post cycle, most men are encouraged to implement a PCT program. This will stimulate natural testosterone production greatly and shorten the total recovery time. It will not return your levels to normal on its own; there is no PCT plan on earth that can do this. However, a solid PCT plan will ensure you have enough testosterone for proper bodily function while your levels continue to naturally rise. Clomid is an excellent choice for this purpose and one of the most commonly used PCT medications. Highly successful PCT programs will often include Clomid and Nolvadex as well as the powerful peptide hormone HCG (Human Chorionic Gonadotropin).
Those who forgo Clomid therapy post cycle or any type of PCT plan and are going to be off cycle for an extended period of time will rest in a low testosterone condition for an extended period of time. Not only is this an extremely unhealthy state, it can come with all the traditional low testosterone symptoms. Many will find cortisol levels greatly increase as testosterone levels are low, and as a result, body fat levels go up and strength and muscle mass decrease. If you’re going to be off cycle for an extended period of time, 8 weeks or more there is no reason for forgoing a PCT program. If you are going to be off cycle for less than 8 weeks or bridging with a low dose of exogenous testosterone, which is very common in hardcore bodybuilding circles, this is the only time a PCT would be counterproductive.
Clomid is one of the most well-tolerated SERM’s and anti-estrogens on the market, and this applies to both men and women. While it carries a very high threshold of toleration, side effects of Clomid do exist and are possible. However, “possible” is the key word and a very important one. Anytime anabolic steroids are discussed as well as non-steroidal items used by anabolic steroid users, many seem to enjoy implying side effects are assured. This is not the case; in fact, most should be able to use Clomid side effect free.
When it comes to the possible side effects of Clomid, we will find most are fairly rare. Some women who have used the SERM as a fertility aid have experienced ovarian enlargement, but again this is very rare. Other possible side effects of Clomid use include:
The side effects of Clomid are also well noted for including possible visual disturbances. Data shows that approximately 1.5% of all those who use Clomid may experience some type of visual disturbance normally in the form of blurred or hazy vision. If this occurs, use should be discontinued and alternative medications should be examined. In most all cases, once use is discontinued vision will shortly return to normal. However, there have been a few reported cases over the years of visual disturbances that did not remedy post discontinuation. Normally, such cases have been linked to long term and extremely high dose use. Again, if visual disturbances occur, discontinue use immediately and choose another SERM to meet your needs.
A final note on the side effects of Clomid, some may experience acne. This appears to be most common when the SERM is used as part of a PCT program. In this case, it’s not really the SERM that’s causing the issue but rather the high influx of natural testosterone that is now being produced. Most should not have an issue, but those who are already genetically sensitive to acne may find a few pimples appear on their back, shoulders or chest.
For the purpose of fertility aid, Clomid doses will normally be at 50mg per day. The process is very simple; five days into the menstrual cycle a daily 50mg dose is administered every day once a day for five straight days. If this doesn’t result in conception, the dose is sometimes increased to 100mg per day. This cycle will be repeated 5-6 times over the course of the woman’s menstrual cycles until pregnant. If conception does not occur after 5-6 cycles of therapy, alternative treatments will need to be examined.
For the anabolic steroid user, standard Clomid doses for on cycle estrogenic protection will normally be 50mg per day throughout the duration of the cycle. If this doesn’t do the trick it’s unlikely any amount of Clomid will work. If this does not provide the protection you need, keep in mind many have reported greater success with the SERM Nolvadex for on cycle protection. However, you may very well need an AI like Arimidex.
Then we’re left with PCT Clomid use. Standard PCT Clomid doses will normally start at 100-150mg per day for 1-2 weeks. From here the dose will drop to 50-100mg per day for 1-2 weeks and finish with 1-2 weeks at 50mg per day. Total Clomid therapy should last 4-6 weeks, so dosing should be based and considered on that total schedule. Most will also be far more successful in their PCT recovery by including Nolvadex and HCG. Timing is also important when planning your Clomid PCT use, and this timing factor will vary depending on the inclusion of HCG: